COLUMBIA LIBRARIES OFFSITE HEALTH SCIENCES STANDARD HX64116638 RC111 .R42 Infection, immunity RECAP TJCiii T?42 (Culumbia Hninrriittit in tl|r (Eity nf Nfiu |InrU (tollrtjr nf ^Ijyairiaua auli ^itnirmta ^Atfnnut ICibrara Digitized by the Internet Archive in 2010 with funding from Open Knowledge Commons http://www.archive.org/details/infectionimmunit1906rick INFECTION, IMMUNITY AND SERUM THERAPY ' -^ In RELATION to the INFECTIOUS DIS- EASES which ATTACK MAN ; WITH CONSIDERATIONS of THE ALLIED SUBJECTS OF AGGLUTINATION, PRECIPITATION, HEMOLYSIS, ETC. H. T. RICKETTS, M.D. InUruBor in Pathology, Uni-versity of Chicago CHICAGO AMERICAN MEDICAL ASSOCIATION PRESS 103 DEARBORN AVENUE 1906 CuriltlGHT. lOU.j. Bi" Ami;i;[ca.v MEuiCAr. Associatu>.\. PREFACE, Immimity, in its present state of development, with its manifold new terms and special methods of experimentation, is a subject which appears dif- ficult to one who has not studied the newer litera- ture assiduously and grown into a knowledge of the . conditions through actual work in the laboratory. Much of the literature is technical in character and appears in journals not commonly found in the hands of the physician and student. Much of it also is comparatively recent, and its "essence" has not yet appeared in books which are in general use. The literature of immunitj^, moreover, grows so amazingly that the analysis even of current works is a -task of no mean proportions. At the same time, the subject is one of great interest and importance, and there exists a gen- eral wish, frequently expressed, to know more about the recent advances and the conditions which -A have operated against the success of serum therapy ■^ on a broader scale. ?5 The editor of The Journal of the American Med- ^ . . . ■f; ical Association^ appreciating the need which seemed to exist, requested the writer to prepare a If"*:, series of articles on the subject of "Immunitv," 405754 IV PREFACE. wliirh should present the genei'iil pi'ineijiles and the important theories and facts, in as simple a manner as possible. These articles appeared from Aveek to Aveek dnring the year of 1905 in the jour- nal mentioned, and after revision, and Avith such additions as Avould contribute to the completeness of the Avork, tliey are noAV collected, in larger type, in the present A^ohime and rmder a more suitable title. It Avas thought best to treat the subject broadly, to begin Avith the fundamental principles of in- fection and resistance and to introduce the reader to the more complex conceptions of the present time by taking him briefly over the main historical and developmental steps. It Avill be oljvious that the vicAVS of Ehrlich, concerning the production of antibodies, the nature of the reactions into Avhich the latter enter, and the methods by Avhich bacteria produce disease, haA^e l)een utilized extensively. This course demands no justification, Avhen it is appreciated that by no other means can one at the present "time corre- late a multitude of vi'ell-established facts Avliich bear on the problems of immunity. Whatever may be the eventual fate of the side-chain theory — and certain phases of it carry the aspect of finality — Ave should appreciate as much as possible the extent to AA'hich it has shaped modern thought, and recognize PREFACE. V that it has won an imperis]ia])lc })lar-c in tlio his- tory of biologic progress. It should also be understood that the utilization of the side-chain theory in no sense carries with it a negation of the importance of phagocytosis, a fact which is plainly set forth on pages 312-215. Without doubt the role of the phagocytes in recov- ery from a large group of infections is on a better and truer basis than it has ever been before, and for this condition the recent work on opsonins has been most significant. In relation to the grouping of the infectious diseases adopted in Part Two, attention is called to the explanatory paragraph on page 235. It will be noted that a complete bibliography of the subject of immunity has not been added, and this needs no explanation to one who is conscious of the massive proportions of the literature. A critical analysis of the entire literature, which would not have been in harmony with the endeavor to present the topics briefly and clearly, and which would have made detailed references essential, has not been attempted. The works cited in the bibli- ography are largely analytic in character and carry with them more or less complete references, through which those who are so interested may reach the original sources easily. This is true par- ticularly of the handbook of Kolle and ^Yasser- VI ]' in: FACE. inann and of the volume by ^letelinikoll'. Almost tlie entire fourth volume of the former is devoted to the subject of immunity, the enormous litera- ture of -which is analyzed by different persons of international repute. The most recent literature on the various subjects is accessible through the Index Medicus, or the index prepared semi-an- nually by The Journal of the American J\Iedical Association. Tlie index at the close of this volume serves as a glossary of terms, the explanations of which may he found on the pages referred to. H. T. ElCKETTS. Chicago, February, 190G. CONTENTS, PART ONE— GENERAL, Chapter I. Parasitism, Infectiousness, Contagiousness 1- (> Chapter II. Infectious Etiology 7- 10 Chapter III. General Considerations 17-2.3 Chapter IV. History and Development 24- 34 Chapter V. Natural Immunity : A. Protection Afforded by the Body Surfaces 35- 41 B. The Protective Nature of Inflammation . . 41- 46 C. The Antibacterial and Antitoxic Nature of Natural Immunity 46- 55 Chapter VI. Acquired Immunity 56- 64 Chapter VII. Toxins and Antitoxins 65- 77 Chapter VIII. The "Structure"' of Toxins and Antitoxins and the Nature of the Toxin-Antitoxin Reaction. . . 78- 91 Chapter IX. Tlie Plienomena of Agglutination 92-104 Chapter X. The Nature of the Substances Concerned in Agglutination 105-118 Till COXTlJyTS. Chapter XI. Precipitins 119-129 Chapter XII. A. General Properties of Bacterieidal Serum«. .. 130-141 B. Amboceptors and Complements 141-lGl Chapter XIII. Cytotoxins 102-175 Chapter XIV. Phagocytosis 17G-194 Chapter XV. The Side-Chain Theory of Ehrlich and Its Rela- tion to the Theory of Phagocytosis 195-217 Chapter XVI. Principles of Serum Therapy 218-234 PART TWO-SPECIAL, Group I. — Acquired Immunity Is Chiefly Antitoxic. A. — Bacterial Diseases: Diphtheria 235-244 Tetanus 244-25G Botulism 256-259 Bacillus Pyocyaneus 259-262 Otner Soluble Bacterial Toxins 262 B. — Intoxication hy Soluble Plant Toxins: Hay Fever 262-264 Other Plant Toxins 264 C. — Intoxication by Soluble Animal Toxins: Poisoning by Snake Bites 264-268 Other Zootoxins 268 Group II. — Acquired Immunity Is Chiefly Anti- bacterial. Typhoid Fever 269-284 Paratyphoid Fever 284-288 Acute Epidemic Dysentery 288-294 CONTENTS. IX Meat Poisoning by Bacillus Entoritirlis 204-208 Bacillus Coli Cominunis 298-304 Cholera 304-315 Plague 315-327 Anthrax 327-333 Malta Fever 333-335 Group III. — Acute Infections in Which Lasting Immunity Is Not Established. Pneumococcus Infections — Pneumonia 33G-349 Streptococci 349-370 Staphylococci 370-383 Micrococcus Catarrhalis 383-384 Gonorrhea and Other Infections with the Gono- coccus 384-388 Epidemic Cerebrospinal Meningitis 388-393 Influenza 393-399 Soft Chancre 399-401 Bacillus of Friedlander and Other Members of the Capsule-Forming Group 401-402 Relapsing Fever 403-406 Group IV. — Chronic Infections in Which Lasting Immunity Is Not Established. Tuberculosis 407-445 Leprosy 445-452 Glanders 452-458 Rhinoscleroma 458 Actinomycosis 458-462 Madura Foot 462 Infections by Streptothrix, Cladothrix and Lepto- thrix 463 Oidiomycosis 463-467 Group V. — Diseases of Protozoon Etiology. Malaria 468-483 Trypanosomiasis 483-497 "Spotted Fever" of the Rocky Mountain Stales. .497-498 Texas Fever as an Example of Pyroplasmosi-. . .499-500 Amebic i)ysentery 500-504 N VOXTIJNTS. SiUL'ospoiiilia 504 Jiahintidium Coli 505 Corc-onionas Intcstinalis 500 Trichomonas 507 Coccidiosis 508 Group VI. — J^iskasks oi- DouBTirL on Unknown lvriOLO(iY. Hydrophobia 510-521 Syphilis 522-520 Yellow Fever 529-538 Typhus Fever 538 Dengue Fever 539-541 Acute Articular Klieuniatism 541 Smallpox and Vaccinia 541-555 Chickenpox (Varicella) 555 Scarlet Fever 550-55!) Measles 559-562 (ierman Measles ( Kiitheln) 502 Whooping Cough 502-50(1 Mumps 5(10 Appendix 507-571 Bibliography 572 Index 573-599 Corrections 600 PART ONE—GENERAL. CHAPTER I. PARASITISM,, INFECTIOUSNESS, CONTAGIOUSNESS. Parasitism is the condition in which a plant, or Parasitism. an animal being, lives on or within another living organism. A true parasite always derives its sus- tenance from the tissues of its host. Some parasites may live on a host without causing appreciable damage, that is, they are non- pathogenic parasites. In this case they may de- rive their nutrition from some of the excreted non- living products of the host, living as pure sapro- ]:)hytes,^ or the amount of nutritious substance which they 'obtain from the host may be so little that the health of the latter is not impaired. There is another large class of parasites, how- ever, which under proper conditions cause severe diseases in the host. Many pathogenic microbes live in and on the skin without doing harm, but if cer- tain ones reach the deeper tissues, they may insti- tute pathologic processes (e. g., staphylococci). Any organism Avhich is able to cause pathologic tissue changes or to set up abnormal s3miptoms is classed as a patliogenic parasite. The abnormal processes which they set up are our infectious diseases. 1. A .saprophyte is defined as a vegetable organism which lives on dead organic matter. An organism which is liabitually saprophytic may become pathogenic under the proper conditions (bacillus of malignant edema). And. on the other hand, a patliogenic parasite lives a saprophytic life, when it grows in our artificial culture media. IXFECTIOy AMJ 1.UMLMTY. Infectious Disease. Infestation and Infec- tion. Contagiousness and Infectious- ness. Au inl'eelious di^ea^;e is oue whic-li is caused by living organisms which in some way have been introduced into the tissues of the body. Accord- ingly the word lias reference to the nature of the cause of the disease. It is from the Latin inficire, meaning to place in or into. Where living organisms exist on a body sur- face, as the skin or intestinal tract, the surface is .>^aid to l)e infested; the skin, for example, is in- fested with pediculi. One may also say that the intestinal tract is infested with tape worms, but here the distinction between infestation and in- fection is not to be draAATi so sharply ; surely when the larvfe penetrate the intestinal wall and reach the circulation or distant organs we must speak of infection. But even the adult tenia as it ex- ists in the intestines may cause erosions of the mucous membrane or may perhaps burrow a slight distance into the wall, a condition which approx- imates the action of the larvfe in passing through the wall; accordingly at some point the distinc- tion between infestation and infection becomes an arbitrary one. Confusion sometimes arises in using the words infectious and contagious. A contagious disease is one which may be transmitted from one indi- vidual to another by direct or indirect contact; the word has reference to the manner of transmis- si(m of an infection. Non-infectious diseases are never contagious. Contagiousness is well illus- trated in those disease in which the transmi:=6ion takes place through the air. as seems to be the case in smallpox and scarlet fever. Here there may be a contagious zone of atmosphere surround- ing the patient, in which the Airii^; i.^ ]")roscnt. and Contact Infection. CONTACT INFECTION. 3 by which tlie agent reaches the lungs oC one within the zone. Contagiousness is even more striking when it takes place through the medium of some inanimate substance, such as clothing or toys, which were previously within the contagious zone or in direct contact with the patient. Such sub- stances, fomites, were formerly thought to he of great importance in the extension of yellow fever; a theory which has been entirely exploded by the proof that the disease is transmitted through the bite> of infected mosquitoes. Typhoid fever is not highly contagious. There probably is no infected zone of atmosphere about the patient in the sense that there is about a scar- let fever patient. Yet it frequently happens that the nurse contracts the disease while caring for her patient. It is likely that she has in some way transferred the bacteria from the patient's sputum, urine, feces or fekin to her lips or hands so that eventually they found their way into the intes- tines. At the same time it is not improbable that the point of entrance for the germs, i. e., the in- fection atrium, may at times be the lungs, the Jil'Jr^*" bacteria having been inhaled. However, t}T)hoid fever is usually a 'Svater borne" disease, seldom "air borne.'' We are to look on malaria as a strictly non-con- tagious disease, although no doubt is possible as to its infectiousness. Ko amount of personal con- tact with the patient will transmit it to another. To accomplish transmission the parasite must be actually injected into an individual, an event which happens exclusively, it is believed, through the bite of a mosquito which has previously fed on the blood of a malarial patient. IM'ECTIOX AXD IMMCMTY Pathogenesis. Mechanical and Toxic Injuries. Tetanus is anothci- iiuled example of an iufee- tioiis disease which is not acquired by contact with one sufl'ering from it. The various parasites have ditl'erent ways of in- juring the body. Tlie itcli mite burrows into and honeatli the oiiidermis, causin^ii' nieelianical ii-rita- lioii ;w well as tlio inilammatory reaction pnxhieed by its toxic excretions. Tlie loss of blood caused by some intestinal ])arasites, and the hemorrlu:ige which follows from the Avounds, often lead to grave anemias and the general changes wliich are caused by such anemias. This is especially the case in the duodenal infection Avitb uncinaria dunden- alis (uncinariasis). A certain variety of Fihirin smigainis Jioininis produces disorders l)y mechanical ly blocking the lymph channels. The Plasmodium of malaria causes anemia by the destruction of blood cells. The febril disturbances of infectious diseases are certainly due to toxic influences. Tt is generally said that bacteria produce dis- turbance* in both a mechanical and a toxic way. However, the more we learn about bacterial infec- tions the more important do the toxic pheno- mena become. It is doubtful if any pathogenic bacterium is entirely devoid of toxic powers. It is probable that the bacterial eml)oli which are sometimes found in capillaries and small ar- teries cause disturbances through the shutting off of so much circulation, but still greater damage may result from the action of toxins which are formed by the microbes making up the emboli. In lobar pneumonia we have a good example of a mechanical disturbance of importance. The KFFECTii OF TOXfjXH. r, alveoli become filled with a fibrinous and purulent exudate which makes a large area of pulmonary tissue unavailable for respiration. Yet, even here, the mechanical disturl:)ance lias arisen only as a result of the previous toxic action of the pneumo- cocci on the capillary walls and the alveolar epithe- lium, permitting the escape of the Idood and serum. The toxins of bacteria often show a remarkable Effects of selective action on one organ or another. Some destroy the red blood cells to a great degree (staphylococcus and streptococcus) ; other toxins have a special affinity for the nervous tissue (tet- anus) ; some attack particularly the endothelium of the vessels^ causing many minute hemorrhages. Frequently bacterial toxins cause areas of necrosis in the lymphoid and parenchymatous organs, and the granular degenerations of the latter, in acute infectious diseases, are Avell known. The albumin and casts which appear in the urine in many acute febrile diseases are the result of toxic action on the epithelium and endothelium of the kidneys. It is said that in anthrax all the glycogen may disappear from tlie liver; toxins may disturb the functions of various organs to similar degree. Some chronic infections are characterized by the ■ development of new connective tissue and vessels ; this is seen especially in tuberculosis, syphilis and actinomycosis. The import of the new connective tissue depends on its location. A large amount of it may form in pre-existing connective tissues with no consequent harm ; but even a small scar, gTimma or tubercle in the brain may cause serious results. It has been stated above that infectious diseases infectious are caused by living pathogenic organisms. In- ^"''**"""*- vestigations have shown, however, that the toxic G lyFECTlOX A.\L) IMMLMTY. proiliicts of .some organisms can be prepared and separated from the organisms themselves by filtra- tion, and that such microbe-free toxins when in- jected into animals may cause the same symptoms that are produced by the bacteria themselves (teta- nus and diphtheria). Accordingly, for the sake of convenience, these toxins also may be considered among the infectious agents, even though sepa- rated from their corresponding bacteria. The va- rious infectious agents, including these toxins, find their proper places in the following classification, which, for the most part, is that of von Behring: I. Living (i. c., pathogenic parasites). A. Macroparasites (e. g., intestinal worms, pediculi). B. Microparasites. 1. Bacteria (fission fungi : each cell divides into two in proliferating) . 2. Fungi of more complex organiza- tion (e. g., aspergillum, oidia). 3. Protozoa (e. g., plasmodium mala- ria, ameba coli). 1\. Xdii-living (i. e., toxins). A. Animal toxins (e. g., snake venom). B. Vegetable toxins. 1. Xon-bacterial (e. g., abrin, from the jequirity bean; ricin, from the cas- tor oil bean; these are strong red corpuscle poisons, chiefly of experi- mental interest). 2. Bacterial. a. Soluble bacterial toxins (diph- theria and tetanus). b. Intracellular bacterial toxins, which are not secreted by tlie cells in a soluble form. CHAPTER II. Koch's Laws. INFECTIOUS ETIOLOGY. The microbic cause of a disease must he in hand before a logical attempt can be made to prepare a specific immune serum. It is not in all cases nec- essary that the organism be cultivated artificially, however ; the conditions in rinderpest may be cited in which the body fluids of a diseased animal, known to contain the infectioiis agent, are used for immunization, although the microbe itself can not. as yet be cultivated or recognized. There are so many possibilities of error, and so many errors have actually been made in regard to infectious etiology, that certain requirements in the way of proof are now habitually demanded be- fore a particular organism can be accepted as the cause of a disease. These requirements are most frequently expressed in the form of Koch's laws, which may be stated as follows 1. The suspected organism must be found constantly in the proper tissues of an animal suffering from the disease, or which has died from it. 2. The organism must be cultivated artificially in a pure state. 3. It must be possible to reproduce the disease in a suitable animal by inoculation with the pure culture. 4. The organism must again be cultivated in a pure state from the tissues of the experiment animal. Since these laws were formulated another proce- Agglutination Test dure has been developed which may give valuable evidence as to etiology. This pertains to the ag- glutination test, or, as we speak of it in connection with typhoid fever, the Gruber-Widal reaction. S IXFKCTIOX AM> IMMl'MTY. 'J'his principle, that in the aequinn-- of iiumiinily to a niicrobic infection the serum of an individual gains in agglutinatino- power for the micro-organ- ism, has been found to hold trne in many infec- tions. Consequently, if one has in hand the speci- fic micro-organism for a disease, he would expect the serum of a patient sick of this disease to have a stronger agglutinating power for this micro-or- ganism than for others which were accidentally present; and this power would also be greater than that posse>sed by the serum of one who had not had this particular disease. In spite of some pos- sibilities of error the a^'glutination test lias been of distinct value in the recognition of the specific micro-organisms in certain diseases, as in the case of the germ of epidemic dysentery (Shiga). Obstacles AH Koch's laws have not been complied with in Laws, certain cases, because of various difficulties which have been encountered. First, the patho- genic protozoa can not be cultivated on artificial media (we must except the success of Xovy and ]\IcXeal with certain trypanosomas, and of Strong with the ameba coli under symbiotic conditions) ; second, certain bacteria which may be found con- stantly in a given disease have not been cultivated artificially (spirillum of recurrent fever) ; third, there are a few diseases which are peculiar to man and accordingly can not be reproduced in experi- ment animals (leprosy, influenza, scarlet fever, measles, etc.) ; fourth, some infectious agents are pathogenic for experiment animals, but do not reproduce in them a clinical or anatomic condition identical with that found in the original animal (typhoid). Furthermore, failure to com])ly with all the re- KOCIVH L.nV'.S'. 9 quirements enumerated does not, in sonic cases, disqualify tlie organism as the causal factor. If an organism is found constantly in characteristic sites in a given disease and not in other infections, and if at the same time other microbes are not present or are present inconstantly or through ac- cident, there could be little or no hesitation in ac- cepting this organism as the cause of the disease, even if it were impossible to cultivate it or to trans- fer the disease to animals. The typhoid bacillus has been cultivated from characteristic foci (stools, blood, spleen, urine, rose spots) in such a large number of cases, and the bactericidal and agglu- tinating powers of the patient's serum against this organism are so distinctive, that compliance with the third law, though desirable, is not now essen- tial. The conditions are similar in reference to cholera and the cholera vibrio. The conditions are so imique in some diseases that, although all Koch's laws have not been met literally, certain equivalents have been met. To illustrate, we may consider an anopheles mosquito which has become infected with the plasmodium of malaria by biting a malarial patient, as a cul- ture medium: and the transferring of the infection to another patient by the bite of this mosquito as the inoculation experiment which is desired. The term "specific infectious disease" has come specific to have a very special meaning. It is applied to a Diseases. disease having characteristic clinical and anatomic phenomena, which can be caused only by one par- ticular micro-organism. Among the diseases which come within the limits of this brief defini- tion, the following may be enumerated (the micro- organism which is the cause of each disease being also given) : 10 IXFECTIOX Ayn IMMVyiTY. Lnknown Etiology. Diplitheria Tetanus Typlioid fever Cliolora Anthrax Tuberculosis Leprosy Plao'ue Bacillus dijih ih cricv Bacillus tctani Bacillus iyphosus Vibrio cliolerce Bacillus anthracis Bacillns tuberculosis Bacillus Icprce Bacillus pcstis Dysentei-y (bacillary) Bacillus dysenteriai Intluenza Glanders (farcy) Chancroid Recurrent fever (lonorrhea Bacillus influenzae Bacillus mallei Bacillus cliancri mollis (Ducrey) 8p irillu m oh crmcieri Micrococcus gonorrhece P^pidemic cerebrospi- Diplococcus intracellula- ris mcningiiidis (of Weichselbaum) Actinomyces hovis et ho minis Blastomycetes and Oidia Plasmodium malarice A large number of animal diseases have their specific microbe.^, as do certain other human dis- eases which hardly concern us as to the subject in hand. In addition to the diseases mentioned, there are several, of unknown etiology, which from analogy we must recognize as specific. Scarlet fever, measles, German measles, chickenpox, smallpox, yellow fever, typhus fever, hydrophobia and syphi- lis, are undoubtedly due to micro-organisms. Mal- lory recently found in the skin of four scarlet nal meningitis Actinomycosis Blastomycosis Malaria UNKNOWN ETIOLOGY. 11 fever patients a protozoon-like body which he be- lieves to be the cause of the disease, although he admits that much desired proof has not been ob- tained. The Diplococcus scarlatince of Class, which a few years ago acquired some notoriety, has not been able to stand as the cause of scarlet fever in the face of rigid investigation. Parker, Beyer and Pothier have announced the discovery of a protozoon (?) Myxococcidium stegomyice, in the mosquitoes which infect man with yellow fever; but Carroll maintains that this organism has no relation to the production of the disease. The Bacillus icieroides, which Sanarelli found in a rather high percentage of cases, is now generally considered as a contaminating organism. It is possible that smallpox and vaccinia will be eliminated from the diseases of unlcnown causa- tion, owing to the evidence of protozoon etiology that Councilman and his colaborers have obtained ; however, for the present, the question may be con- sidered sub judice in view of the fact that the forms described bear a close resemblance to cer- tain well-knoAvn types of cell degeneration. The following animal diseases, of unknown etiology, may also be mentioned in this connec- tion: Foot and mouth disease, peripneumonia, bovine pest, sheep-pox (clavelee), chicken-typhus or chicken-pest and epithelioma contagiosum of fowls. The following appear to be the chief reasons for obstacles to DiscovGrv OT the failure to discover the organisms of these dis- Microbes. eases : 1. Inability to cultivate the microbe. 2. Mixed, or symbiotic infections. It is conceivable that in some case the combined action of two micro-organisms may be necessary to cause the 12 /.\ Fi:cTI()\ .1 A /' / \IML MTY. Filterability of Viruses. Non-Specific Infectious Processes. disease. The non-toxic pi'oducts of the two may synthesize to form a toxic sul)staiice (Hektoen.) 3. Unstained ability of ihv microbe. 4. Ultramiscro- scapic size. The organism of the peripneumonia of cattle was cultivated by Nocard and Eoux by grow- ing it in a closed collodion sac which was placed in the ]:)eritoneal cavity of suitable animals. It is so small that its form can not be made out. and growth is recognized only by clouding of the culture medium, and the increased virulence of the latter for animals. Some valuable information has been obtained l)y observing whether the infectious agents are so small tliat they will pass through dense filters of porcelain or infusorial earth. It has been found that the viruses of foot and mouth disease, peri- pneumonia, rinderpest, sheep-pox, chicken-typhus, horse sickness, epithelioma contagiosum of fowls, and yellow fever are filteral)le, i. e.. they pass through the filter. This is determined by inject- ing the filtered culture medium or serum into sus- ceptible animals. The viruses of smallpox and vaccinia are said to be non-filterable. Success in filtering the hydrophobia virus has recently been claimed by Eemlinger. Inasmuch as scarlet fever, measles, chicken-pox, typhus fever and syphilis* can not be produced in animals, the filteraljility of their viruses is not at present susceptible of dem- onstration. There is a marked tendency in many diseases, typhoid, cholera, malaria, etc., for characteristic organs or groups of organs to be involved in some particular manner. These are features which * Uecently syphilis lias been iuocnlalefl sMcccssf\illy into antln-opoid apes. (Metchnikoff and Konx.) NON-BUSVErrinf/JTy. \ ■'. stamp them as specific diseases. On the other hand, a large nnniber of iiiicro-organisms cause no Avcll-deflned clinical and anatomic disease, l)ut, depending on various accidents, cause an intlam- ination now in one organ, now in another. Suppuration is not a specific disease, because the pyogenic power is common to a large number of microbes. A diphtheritic or pseudo-diphtheri- tic process in the mouth and throat may be caused by the diphtheria hacillus, streptococcus, staphylo- coccus, oidium or yeasts; bronchitis may be caused by the influenza, tubercle, plague and typlioid bacilli, and by the infecting agents of the acute exanthemata, etc. ; pulmonitis by the pneumococ- cus, streptococcus, tubercle, plague, Friedlander and influenza l^acilli, oidium, actinomyces, etc. ; meningitis by the tubercle and influenza bacilli, streptococcus, staphylococcus, pneumococcus, go no- coccus, diplococcus of epidemic meningitis, the syphilis virus, etc. ; arthritis by the streptococcus, staphylococcus, tubercle bacillus, gonococcus, the virus of rheumatic fever, etc. ; endocarditis by the streptococcus, staphylococcus, gonococcus, pneu- mococcus, tubercle bacillus, etc., and septicemia by a whole host of organisms aside from those mentioned as causing specific diseases. Within certain limits, however, there is often a degree of specifi.city in the processes produced by some of the organisms mentioned, which some- times allows of clinical and anatomic differentia- tion. The infiltrating and rapidly extending in- vasion of the subcutaneous and connective tissues caused by the streptococcus can often be distin- guished clinically from the slower, more circum- scribed process of the staphylococcus. The condi- 14 INFECriOX AXD IMMUNITY. tioii.s induced by the Bacillus aerogcncs capsulatus, the bacillus of malignant edema, are, in turn, dif- ferent from those of tlic streptococcus and staphy- lococcus. The pneumococcus commonly causes the consolidation of rather extensive areas of tlie lung, whereas the streptococcus and the bacillus of Friedlander are more often found in the lobu- lar consolidations. The membranous inflamma- tion of diphtheria may in favorable cases be distin- guished from that of the pyogenic organisms with- out bacteriologic aids ; in this possibility, however, there lies no justification for neglect of tlie bac- teriologic examination. Mixed The coexistence of two or more micro-organisms Infections. . , . , ti • • j? j? , ]n a morbid condition is of frequent occurrence, and some of the most interesting and important phenomena of infectious diseases are referable to mixed, secondary or superimposed infections. Two exogenous infections may attack an indi- vidual at the same time. ^leasles and scarlet fever and diphtheria and scarlet fever have been known to coexist. Pneumococcus pneumonia and typhoid fever, chancre and soft chancre with pus cocci, syphilis and gonorrhea, diphtheria with strepto- cocci, tetanus with gangrene-producing organisms, are common observations. One organism may in- tensify the virulence of another. Diphtheria ac- companied by streptococcus infection seems to l)e more virulent than diphtheria alone. It is also believed that the presence of aerol)ie organisms (those which demand oxygen for their develop- ment) in a wound infected with the tetanus bacil- lus or the bacillus of malignant edema (anaeroliic organisms), may increase the virulence of these infections. Streptococci are probably important MIXED INFECT ION f^. 15 organisms in scarlet fever, for they are present in nnusual nnmbers in the throat lesions and are often found in fatal cases in all the organs, yet it is believed that they constitute only a mixed or secondary infection superimposed on that of the scarlatina virus. The conditions are somewhat similar in smallpox, the pustules of which invari- ably contain streptococci, staphylococci, or both. In both scarlatina and smallpox these secondary infections may be responsible for many fatalities. Pneumococcus pneumonia occurring during the course of, or during convalescence from the erup- tive fevers, diphtheria, typhoid fever or erysipelas ; a streptococcus septicemia developing during typhoid (giving rise to an irregular temperature curve), streptococcus infection of tubercular cavi- ties, and the development of acute tuberculosis during measles — rthese are important examples of secondary infections. We should naturally expect that the presence of a severe secondary infection might embarrass at- tempts at serum therapy. Experience on this point is practically limited to diphtheria, and there is no lack of evidence to show that the dis- ease when complicated by severe streptococcus in- fection often can not be controlled by antitoxin treatment. It may be emphasized that there are certain dis- infectious eases in which a wide dissemination of the bac- teria is not necessary for the production of morbid phenomena; where, in fact, they may be entirely localized (diphtheria, tetanus), and the symptoms are produced by virulent toxins which are readily dissolved in the body fluids and carried to impor- tant organs. More especially are those microbes 10 rXFKCTlOX AXn IMMIXITY. placed in this class wliidi ihmIiut their spofitic disease-producing toxins in a soluhlc foi'ni when grown in our artificial cnhuiT media (houillon). The bacilli of diphtheria, tetanus, botulism and the pyocyanous liaeillus belong distinctively to this group. Snake venom and araclinolysin (spider poison) are the best known exam])les of soluble animal toxins. As will appear later, the serums of all animals probably contain a variety of toxins which are injurious to one or more species of animals. CHAPTEE III. GENERAL CONSIDERATIONS. By imirmnity we "understand that condition in Definition. which an individual or a species of animals exhib- its unusual or complete resistance to an infection for which other individuals or other species show a greater or less degree of susceptibility. Immune is from the Latin immunise which originally ap- plied to one who was exempt from a public service, exempt from tribute, or free. Although the word retained this civil meaning for centuries, and still retains it in certain connections, it also had, even in ancient times, a limited application to the pro- tection which an individual might possess against poisons. It is seen, for example, in descriptions of a tribe inhabiting Northern Africa, the Psylli, who possessed a natural immunity to the bites of poisonous snakes. Although we may be certain from this and other references that a condition of immunity was recognized in very ancient times, the present significance of the term has developed largely from a better understanding of the nature of infectious diseases and of the conditions upon which the resistance of the body depends. As the definition suggests, we do not think of Diseases ... ^ T-, . T , , T. Concerned In immunity to such processes as Bright s disease, immunity. arteriosclerosis or the metabolic diseases, but only to those which we have learned to recognize as in- fectious. Immunity has no necessary relationship to the degree of contagiousness of an infectious disease. 18 INFECTION AND IMMUNITY. Acquired Immunity. Natural Immunity. Family Suscep- tibility and Immunity. although some of the most striking and certainlj^ the most common examples of immunit}^ are seen in relation to such infections (as scarlet fever and smallpox). Tetanus, on the other hand, which is absolutely non-contagious, can likewise give rise to a high degree of immunity. iSTo medical fact is more widely" known among intelligent people than that an attack of certain of our infectious diseases brings about some kind of change in the patient's tissues which protects him, or renders him immune, against further at- tacks of the same disease. Inasmuch as he was previously susceptible, the new property is an ac- quired one, and he is now said to possess an ac- quired immunity against this infection. It is also well Iniown that many diseases which attack man can not be inoculated into animals, and biologists are. familiar with many examples of immunit}^ which are confined to particular spe- cies. The lower animals apparently can not be in- fected with scarlet fever or measles, nor man vidth chicken cholera. The negro is less susceptible than the white man to 3^ellow fever. The resist- ance which these examples illustrate has occurred naturally, not through having the disease; it is a natural immunity. Natural immunit}^ is, for the most part, an in- lierited condition; this certainly is the case where a whole class of animals is involved. Similarly, the susceptibility which is peculiar to a species must be he^editar5^ It is often said of some dis- eases that they run in families ; e. g., carcinoma, gout, insanity. This appears to be just as true of some infectious diseases, the most noteworthy ex- ample of which is probably tuberculosis. In con- NATURAL IMMUNITY. 19 trast to this inherited susceptibility is an inherited immunity, which may also run in families. It is not so easy to adduce examples of thisi. We are in the habit of thinking of the individual who can resist all infections as representing a standard. He, however, is above the average in resistance, and the average is our proper standard for esti- mating the resistance of a species or race of ani- mals. It is undoubtedly true that some families possess an unusual resistance to tuberculosis. Furthermore, experimental work with animals has proved that, within limits, an immunity to cer- tain infections (e. g., tetanus) acquired by a. fe- male may be transmitted to her offspring. Even in a given family, however, there are often marked variations in susceptibility and resistance. One child may contract scarlet fever, while his brother, living under exactly the same conditions, may escape it. There is, moreover, much reason to be- lieve that the same individual varies greatly in his resistance at different times and under different conditions. Hence, the personal equation, as rep- resented by individual resistance or individual sus- ceptibility, is of no small consequence. The facts mentioned were familiar long before anything was known regarding the principles on which they depend. Subsequent to the discovery of some of these principles (to be considered later), it became convenient and necessary to rec- ognize other special types of immunity, although any type which can be conceived must still find a place under either natural or acquired immunity. Although such diseases as typhoid and cholera Antibacterial . T 1 ' T , • , and Antitoxic are accompanied by pronounced toxic symptoms, immimity. the poisonous substances seem to be integrally as- 20 INFECTION AND IMMUNITY. sociated with the bacterial protoplasm and not secreted in a soluble or diffusible form by the liv- ing cell ; the}^ are spoken of as intracellular toxins or endotoxins. Observations point to the belief that the endotoxins are liberated only after the bacteria are killed and dissolved. When one, through infection, has acquired immunity toi ty- phoid or cholera, his fresh serum is able to kill the respective bacterium, but apparently is not able to neutralize its toxic substance. Hence, on the basis of the nature of the serum, immunity to such dis- eases is spoken of as antibacterial rather than antitoxic. On the other hand, the symptoms which are so characteristic of tetanus are produced not by contact of the bacteria with the nervous system, but rather through the specific soluble toxin which is secreted by the bacilli in the wound where they reside. This poison, or toxin, is carried from the wound to the nervous system through the lymph- atic or blood circulation, the bacterium itself not being transported. Therefore, although tetanus is a bacterial disease, it is at the same time and in a peculiar sense a toxic disease. The serum of an animal which has acquired im- munity to diphtheria or tetanus neutralizes the cor- responding soluble toxin, but does not necessarily injure the micro-organism itself. That is to sa)^, the immunity is antitoxic. Experience has shown that this distinction between antibacterial and an- titoxic immunity is an important one, and the differentiation is very sharp in some instances. In many examples of natural immunity, the re- sistance can not be attributed so specifically to anti- bacterial or antitoxic serum properties. This is re- ferred to later. ACQUIRED IMMUNITY. 21 Immunity. Immunity which results from an infection de- ^'^*'^® pends on a specific reaction on the part of the tissue cells in response to the chemical injury pro- duced by the bacteria or their toxins. The indica- tion of the occurrence of such a reaction lies, first, in the recovery of the patient, and, second, in the new antitoxic or antibacterial power which may be demonstrated in the serum. In view of the active part played by the body in establishing this new resistance, the condition is referred to as an active immunity. In the preparation of various anti- toxic and antibacterial serums for commercial pur- poses, a condition of active immunity is deliberate- ly produced in the animals (the horse, for ex^ra- ple) by the injection of the toxins or of the bac- teria. Contrariwise, the resistance which is established Passive ' Immunity. in an individual through the injection of an im- mune serum (such as diphtheria antitoxin)' is a passive immunity, since it depends on the intro- duction of ready-made immunizing substances rather than on their production through an active process on the part of the one injected. Active and passive immunity, then, are varieties of ac- quired immunit}^ Depending on the disease which caused the immunity, or on the character of the serum injected, they may be either anti- bacterial or antitoxic. Any one of the types mentioned may be either Relative and relative or absolute; synonyms are partial and immunity. complete. If absolute, infection is impossible. If only relative, different conditions may be made to prevail which would render infection possible; for example, a large number of bacteria will often cause an infection where a smaller number fails - 22 IXFECTIOX AXD IMMUXITY. to do so. Tlicre may also be a temporary decrease in one's resistance through overwork, hunger or ex- posure. Immunity is usually relative. ^'**t>f'"*(M ^y proper combinations of the terms which have been enumerated, one may describe somewhat accurately the different forms of immunity. Thus, a child which has received a prophylactic injec- tion of diphtheria antitoxin is in a state of ac- quired passive antitoxic immunity to diphtheria. If immunity to t}^hoid has developed as a result of the disease, the condition is that of an acquired active antibacterial immunity, etc. Accordingly, although the terms may be somewhat confusing, .it is seen that they are in no sense contradictory. The following classification of immunity is con- venient, although in giving it, we must recognize that it probably does not include all types of im- munity. At this point the single example may be cited, that the chicken is very resistant to tetanus toxin, although its serum contains no antitoxin ; hence in this instance we could hardly speak of antitoxic immunity to tetanus, but rather of non- susceptibility to the toxin. f Natural. T The inherited immunity of species and Anti- varieties of animals. I bacter- Inherited family or individual immunity. !- ial or rVcquired. Anti- Active. I toxic. Passive. J „ L. ".'■ug In many of these conditions proper biologic ex- Habituation. , -n n i ^ i periments will demonstrate the presence of the antibacterial or antitoxic substance in the serum of the animal which possesses the immunity. The technic of such experiments will be illustrated later. There is another kind of acquired resistance which properly may be mentioned here. It is a Immun- ity. DRUG HABITUATION. 23 well-known fact that one may gradually accus- tom himself to enormous closes of morphin, ar- senic, alcohol and some other drugs. A priori, it would seem that this condition of resistance should be analogous to that which is present in antitoxic immunity. But, on the contraTy, the seriim of a morphin or alcohol habitue has no power of neutralizing the effects of morphin or alcohol. Tlie conditions on which this resistance depends are not understood. CHAPTER IV. HISTORY AND DEVELOPMENT. Early Times and The Conception of the nature of immunity Practices. ^ . ,i "« which was current at one period or another of history had some relationship to the conception of the etiology of diseases at those times. It will be remembered that at one time diseases were supposed to be imposed by an angry deity, and to ■ avert them various mysticisms were resorted to, such as the utterance of incantations and the wearing of talismans. On the other hand, a more logical attempt to explain the natui'al immunity of the Psylli against snake poison was made by Pliny, who suggested that it might be due to their habit of drinking water from wells in which pois- onous snakes dwelt. This is not unlike our pres- ent conception of active immunization. Von Behring quotes literature to show that among some primitive races of to-day, artificial immunization is carried on; a Mozambique tribe is said to inoculate against snake poison by rub- bing into a small cutaneous incision a paste which contains venom. Probably non-fatal quantities are introduced in this wa}^, resulting in the forma- tion of venom antitoxin, a method comparable to that used in the production of diphtheria anti- toxin. At a very early period the possibility of habitua- tion to poisonous drugs was recognized. We learn that ]\Iithridates by taking gradually increasing doses of poisons established in himself resistance EARLY CONCEPTIONS. 25 of this sort. It is stated also that he fed ducks with poisons and then proposed to use their blood as an antidote (serumtherapy). The importance of antidotes in the minds of the ancients may be appreciated from the fact that epidemic diseases, such as plague, cholera and smallpox, were at one time considered as diie to unknown poisons, which might be comparable in nature to some known poisons, as aconite. Mercury for syphilis, quinin for malaria, and salicylic acid for rheumatism would certainly have fallen into the category of antidotes, and mercury may have been so con- sidered. A historic illustration of the treatment of dis- ease on a supposed etiolo.gic basis is found in a theory which was prevalent in the seventeenth century, according to which diseases were either acid or basic in character, and hence should be treated, the one with an alkali, the other with an acid. Sylvius considered plague to be of acid nature and administered alkalies, while Etmiiller took the opposite view. Manifestly, rational treatment and prophylaxis of the infectious diseases could not be undertaken until their etiology was correctly understood. Yet here, as so often happens in medicine, empiricism preceded rationalism. For example, protective inoculation did not become a principle until the time of Pasteur, yet it had been practiced against smallpox for centuries, and the method put on its present basis by Jenner long before there was any idea as to the principles involved in the pro- tection. The belief that invisible "animalcules" are able Micro to cause morbid processes in man is a very old organisms. , 2G IXFECTIO^^ AXD IMMUXITY. one. A passage from Yarro (116-37 B. C.) reads as follows : "There are swampy places in which grow animals never so small which may not be recognized by the naked eye, and which gain ac- cess to the body through the air and bring about severe diseases." Microscope^ TliG discovery and use of the compound micro- scope in the seventeenth century disclosed the reality of the minute living forms^ which had been suspected so often. Ivircher, with his first crude microscope (1646), examined the tissues of va- rious diseases, and was the author of many the- ories as to their etiology. It is now believed that the magnification of Kircher's microscope was so small that many of the "worms" which he saw were really larger fungus cells and in some in- stances the as yet undiscovered blood and pus cells. Leeuwenhoek (1632-1723), a Dutch naturalist, with his compound microscope magnifying 1,000 diameters, described accurately many microscopic forms, but made no application of his discoveries to medical problems; nevertheless, such applica- tion was not wanting, and the succeeding century and a half saw such voluminous descriptions of microbes, so many contradictory theories and statements concerning their relationship to in- fections, that the "infinitesimally small" fell into disfavor in many quarters as the cause of diseases. The attractions and reasonableness of the theory, however, were such that it continued to gain ex- ponents, and in the early part of the nineteenth century reached a degree of definiteness. In 1855, the great French ph}'sician, Bretonneau, affirmed that a specific germ was the cause of every con- MICROBW SPECIFICITY. 27 tagious disease: "An epidemic disease can orig- inate and extend only through the agency of the germ producing it." Yet at this time no infec- tion had been definitely proved to be of microbic origin. In 1850 Eayer and Devaine made an observa- -^"^hrax. tion^, which might have fallen into the oblivion of many preceding ones had it not been confirmed by later investigators. They found "small filiform bodies" in the blood of sheep which had died of anthrax, and were ■ naturally inclined to believe that these forms caused the disease. Other stu- the study of anthrax, with the result that the the study of anthrax, with the result that the small rods of Devaine were scientifically proved to be its cause. Two great minds dominated medical research Fermentations. at this time — Pasteur and Koch. Pasteur, in his early career as a chemist, had had his attention called to the processes of fermentation. He re- curred to this subject at a time when the theory of the spontaneous generation of small living forms was widely discussed, and in 1857-1861 proved be3^ond any possibility of doubt that lactic acid, alcoholic and butyric acid fermentations were due to the action of minute living cells; and, fur- thermore, that * each particular kind of . fermenta- tion had its own peculiar microbe as the cause. This was an example of what we term to-day microbic specificity. Pasteur then applied what lyjic^obic he had learned about fermentations to the study specificity. of the diseases of wines and beers. He found their causes, and devised a preventive measure, which consisted merel}' in the destruction of the germs by heating the wine to a suitable temperature be- 2S lyPECTIOX AXD IMMUNITY. Vaccination. AnthraX' fore it was stored. At the instance of tlie French government, he then studied certain diseases of silk worms. His success in discovering their causes and prevention must always remain for us one of the landmarks of the world's progress. It was during the latter investigations that he took up the study of anthrax. The specific mi- crobe having been discovered, and the methods of transmission of the malady having been made clear through investigations by both Pasteur and Koch, Pasteur turned his attention to methods of prevention and, if possible, of cure. Pasteur pondered the question of smallpox vac- cination. He came to believe that vaccinia was smallpox, the virus of which had been attenuated by its passage through the cow, and that conse- quently when man was vaccinated he was inocu- lated with a benign form of the disease. Might not this be an example of a law which would be general in its application? The protective inocu- lation (active immunization) against the pleuro- pneumonia of cattle which had long been prac- ticed gave encouragement to this hope. Some work by Toussaint was important in the answer to this question. It was evident that a weakening or attenuation of the bacteria or virus must first be obtained before it could be safely injected into animals for the purpose of producing immunity, for if the. unaltered virus were injected the viru- lent infection would result. Accordingly, Tous- saint heated the blood of a sheep which had died of anthrax, to a temperature of 55° C. for ten minutes, then injected it into a number of sheep. Some of the animals died of anthrax, while others suffered only a mild attack from which they re- HYDROPHOBIA. 29 covered; the latter were found to be immune to a subsequent inoculation with virulent blood. In- asmuch, however, as some of Toussaint's animals had died of anthrax, Pasteur concluded that there was some grave error in technic. He considered that Toussaint's method probably killed or atten- uated the fully-developed bacilli, but did not in- jure the spores of the parasite (Koch had pre- viously shown the existence of anthrax spores). After much experimentation, Pasteur hit on the plan of growing the bacillus at a temperature of 4:2° C, obtaining 'in this way a culture of the fully developed organism which had a low viru- lence, but which did not form the dangerous spores. When sheep were inoculated with the proper amount of this culture, which became known as anthrax vaccine, they had a mild attack of the disease, which rendered them immune to virulent inoculations. With the possibility of protective inoculation Hydrophobia. with a known virus actually demonstrated, sim- ilar procedures were tried with other animal dis- eases of known bacterial etiology, with the result that successful vaccines against chicken cholera and swine plague were developed. Somewhat later, having failed in their attempts to discover ■ the microbes of plague and cholera, Pasteur and his co-workers turned to the study of hydropho- bia. All efforts to cultivate the virus from the spinal cord of rabid dogs, which surely is its seat in the affected animal, failed. The unique idea then occurred to consider the infected spinal cord as a fully developed culture of the virus. It re- mained to subject such a culture to the proper attenuating conditions for the purpose of weaken- 30 INFECTION AND IMMUNITY. Two Important Principles. Theories of the Cause of Immunity. Exhaustion Theory. ing or nctnally destroying its virulence in order to make it tit for protective injections. Tliis was ac- complished by drying the cords in a closed ve?sel over a hygroscopic substance (solid potassium hydroxid), the final virulence of the cord depend- ing on the length of time it had been subjected to the drying process. The technic of the protec- tive injections, the success of which is household knowledge, will be the subject of later considera- tion. Of primary importance, during this period, was the work of Koch on the specific bacteria of tu- berculosis, cholera, typhoid and the pyogenic dis- eases; and not least his improved methods of ob- taining pure cultures through the use of solid media (gelatin) on j)lates. Through his work and that of Pasteur two great principles had been set in motion : the microbic specificity of infectious diseases, and protective inoculation in its general- ized form, through the use of attenuated virus. The scientific mind turned at once to the in- quiry, What changes in an animal body are re- sponsible for the immunit}^ which is acquired as the result of protective inoculations? Also, upon what properties of the tissues or bod}'- fluids does the natural immunity of an animal depend, and does the susceptibility of one species dejDend on the absence of those properties which characterize the natural immunity of another species? Pas- teur had observed that if he grew the microbe of chicken cholera in a liquid medium for some time, then removed the bacteria by filtration, the fluid became unfit for the further growth of the organ- ism on subsequent reinoculation. That is, the nutrient material had been used up; and he sug- PHAQOCYTO^IH. 31 gestecl that this is the case in. the body of an ani- maL Having nndcrgone the infection, suitable nutrient material for the microbe is used up, and recovery ensues. The prolonged absence of the proper nutritious substances would account for the more or less permanent nature of the acquired immunity. This conception, the exhaustion theory, at one time shared by Koch and EHebs, is still represented in an altered form by Baumgar- ten, who sjDcaks of an unfavorable culture medium as representing the condition of the immune body, which, of course, is. broadly true. Chauveau was the aiithor of another historic Rete'lfon theory of acquired immunity (the noxious reten- Theory. tion theory), which maintained that during the course of a disease the bacteria produce substances in the presence of which they can not develop further; consequently recovery takes place, and the continued presence of these noxious sfubstances renders another attack of the disease impossible. Although it is true that bacteria do not grow well in their own metabolic products, theories of im- munity on this and similar bases are not in ac- cord with the fact that immunity may be of great duration, and that it may be conferred by the injection of the killed bacteria, or, in some cases, of their non-living soluble products. Metchnikoff may be credited with having first Phagocytosis. offered a plausible explanation of natural resist- ance, founded on observation. As a zoologist he had studied the .subject of intracellular digestion in the lower animals, and it was while working on this problem that he observed the fate of a yeast fungus (Monospora), wliich caused epidemics among the daphnia, small, transparent animals 32 INFECTION AND IMMUNITY. • M-itli -which he was workiug. Kear the alimentary tract, Avhich was tlie infection atrium, some hirge mesoblastic cells, which are perhaps analogous to the white blood cells, were seen to ingest the para- sites and dissolve them. If this took place to a sufficient extent the animals recovered; if, how- ever, the infecting organisms were too numerous or the reaction on the part of the animal insuffi- cient, the body Ijecamc overwhelmed with para- sites and death resulted. Since that time Metch- nikoff has evolved his well-known theory of pha- 2:oc-\i;osis as the essential factor in both natural and acquired immunity, a theory which Pasteur, in his later years, looked on with favor. "We may speak of this as the cellular theory of immunity; a theory which has had to imdergo important modications in order to bring it into accord with new facts. Investigation Considering that natural or acquired immunity ties of Serums, must exist because of certain qualities of the body cells, or of the body fluids, or possibly of both, investigators began to make analyses of the tis- sues; and of all the analyses, that which we may term the biologic has been the most fruitful. In this case biologic analysis means the detection of reactions -^'hich may occur when bacteria or their products are placed on contact with tissue cells Bactericidal or fluids, either in the living animal or in test- glass experiments. The chief of these are the de- termination of the ability of the serum of an ani- mal to kill bacteria or to neutralize bacterial toxins. These important investigations, still in their infancy, were inaugurated by the findings of Fodor, Nuttall, N"issen, v. Behring and Buch- ner, which showed that fresh defibrinated blood. PROPERTIES OF SERUMS. 33 and the blood serum of various animals, were able to kill bacteria in the reagent glass. In contrast to the action of ordinary antiseptics, this power is often selective, killing one variety of bacterium and leaving another unharmed. This was of enor- mous importance, as it seemed to identify the factor on which natural antibacterial immunity depends. Then followed the discovery of Nissen and V. Behring (Vibrio metchniJcovi) , and of Bouchard (B. pyocyaneus) , that if an animal is systematically injected, i. e., immunized, with a micro-organism, the power of its serum to kill the bacterium used in the immunization is greatly increased ; from which it would seem that acquired immunity depends on the increase of powers which are normally present to a certain degree. These observations have to do with the bactericidal power of serum. Further progress was made through the disco v- Tox/nsand ery that the tetanus bacillus (Brieger and Frankel) '^"*"®*'"«- and the diphtheria bacillus (Eoux and Yersin) secrete each a powerful, specific, soluble toxin, which may be separated from the bacteria by fil- tration. Immunization with these bacterium-free toxins was undertaken (Behring and Kitasato, 1890) with the familiar result of the production of the specific antitoxins. Other investigations in this direction soon showed the independence of the antibacterial and the antitoxic properties of serums'. With these facts in hand, the vigor with which investigations have been pushed may be readily imagined. The hope naturally prevailed that phy- sicians might become the masters of all infectious diseases, through the possession of specific anti- :14 IXFKCTIOX AM) HI M I MTY. l>;iet('rinl and aiilitoxie serums. JJut raihires, with which we are only too familiar, met tlie attempts to prod nee adequate antiserums for many diseases. Xevertheless these failures, through stimulation to closer study, have resulted in the accumulation of much additional knowledge concerning the pathogenic jn-operties of different bacteria, the nature of the immune serums and the various pro- tective factors of the body. Ehrlich has evolved a new theory of immunity from facts which were discovered in his laboratory, the "side-chain" theory, which it is the ])urpose to utilize in the interpretation of many reactions which will come up for consideration. CHAPTEK V. NATURAL IMMUNT'l'Y. A. PROTECTION" AFFORDED BY THE BODY SURFACES. Virulent organisms (e. g., staphylococci and The streptococci) exist normally on the skin or be- tween the superficial horny cells, some exceptional circumstance being necessary, e. g., wounds, to en- able them to penetrate deeper and to cause disease. It is evident, then, that the physiologic shedding of the superficial horny cells and their continual refonuation at a deeper level is a process calcu- lated to rid the surface of the body of many micro- organisms. The question whether micro-organisms can ever penetrate the unbroken skin has been much dis- cussed. Although experiiuents have shown that traumatism is not absolutely necessary, clinical experience indicates that these so-called crypto- genetic infections are not of ready occurrence. When they do occiir. the infection atrium is prob- ably one of the glandular orifices. The SAveat glands with their ducts, and the hair Cutaneous Orifices. follicles with their appended sebaceous glands, are vulnerable points in the defense which the cutaneous surface represents. Although they are protected somewhat by the flow of their excretions, especially in warm weather, and although the en- trance of germs is made more difficult by the con- traction of the skin and consequent narrowing of the orifices in cold weather, yet various incidents may lead to the introduction and retention of Subcutaneous Connective 36 INFECTION AND IMMUNITY. virulent inicro-orgaiiisms in these structures. When tliis occurs there is little difficulty in the way of their producing necrosis of the epithelium, invading the surrounding tissue and causing a pustule, boil, carbuncle, cellulitis, or even a gen- eralized infection. The secretion of the sebaceous glands appears to be not germicidal. On the other hand, the acid nature and certain salts found in perspiration render this fluid antagonistic to the development and virulence of certain micro-organ- isms. The serous exudate, and the crust which forms subsequent to an abrasion, antagonize infection. The serum itself contains germicidal substances. Avhile the crust mechanically prevents microbic invasion. Soluble poisons such as aconite and bacterial toxins are not absorbed through the unbroken skin. Even after germs penetrate the epidermis, the Tissue, subcutaneous connective tissue is often an obstacle to their further extension. The subcutaneous in- jection of some micro-organisms (e. g., cholera) is tolerated better by animals than one given into the abdominal cavity or blood vessels. We are also familiar with the benign course of lupus compared with visceral tuberculosis; the same is true of cutaneous and visceral glanders. This re- sistance is explainable, at least in part, by the rapidity with which new connective tissue forms in the subcutaneous tissue, offering a mechanical limitation to the infection, and by the rich lymph supply which makes possible the rapid accumula- tion of bactericidal lymph and of phagocytic cells. On the other hand, it must be mentioned that in some diseases the subcutaneous tissue offers no SURFACE PROTECTION. 37 perceptible resistance to bacterial invasion (plague), and that toxins may be more virulent when introduced into this tissue than when in- jected into the abdominal cavity or the general circulation ( tetanus ) . The moist condition of mucous membranes has J}"*^""' been found to favor the multiplication of many microbes, although mucus itself is said to atten- uate the virulence of some micro-organisms, as the pneumococcus ; mucus, however, is not actively germicidal. A laver of mucus, on the other hand, is a mechanical protection, and its constant excre- tion is a means of steadily removing bacteria from mucous surfaces. The conjunctiva is protected against infection Conjunctiva. by the mechanical interference of the eyebrows, eyelashes, eyelids, irrigation of the conjunctival surface by tears which carry germs through the lachrymal duct into the nasal cavity, the ability of the conjunctival epithelium to repair itself rapidly, and the mild germicidal action of the salts which are present in the tears. These pro- tective agencies, however, are often surmounted by' micro-organisms, such as the pneumococcus, staphylococcus and the influenza bacillus. Many soluble poisons, aconite, diphtheria toxin and the toxin of hay fever are readily absorbed from the conjunctiva. Compared with the anterior nares, the posterior Nasal are poor in micro-organisms. This is no doubt due to the filtering of the air by the hairs, the tor- tuosity of the channel causing dust and bacteria to strike the walls where they are held by a moist surface, and the action of the ciliated epithelium in carrying them imbedded in mucus, again to- 38 IXFECTION AXD fMUUXITY. ward the anterior nares. Nevertheless, the nasal niueou^; membrane is a common infection atrium for streptococci, staph3'lococci, diphtheria and in- tluonza bacilli, the diplococcns of epidemic men- ingitis, and, probabh', for other infectious agents, Mouth. At least thirty species of micro-organisms flour- ish in the oral cavity, some of tliem being jjatho- genic : staph3dococci, streptococci, pneumococci. and often diphtheria bacilli. They are constantly removed Avith the saliva, and tlu'ougli the exten- sive desquamation of the epidermis occasioned by mastication. Saliva is not germicidal, but in- liibits the growth and weakens the virulence of some bacteria. The fetid breath and the sor- didity observed in fevers where the mouth is dry are attributable at least in part to tlie lack oL' saliva with its anti-infectious properties. The great rapidity "with whicli wounds of the mouth lieal is a potent factor in preventing serious infec- tions. Langs. Micro-organisuis do not readily reach tlie ulti- mate ramifications of the bronchioles. In ordinary respiration the velocity of the inspired air is so reduced as it nears the alveoli that the further movements of the gases is one of gradual diffusion more than of violent admixture. Consequently there are greater o.p])ortiinities for gcrm,> to come in contact with the lironchial walls where they l)ecome iml:)edded in mucus with Avhich they may be expelled by coughing and the action of the ciliated epithelium. Both the alveolar epithelial cells and (he leucocytes wliicli enter the air sacs and bronchioles have been shown to take up bac- teria. The conditions in the lungs Avhich favor the develo])inent of infections. l)i'oncl]itis, pneu- HTOMAiJlL AM) INTEHTiyEH. :','.) nionJa, influenza, tuberculosis, etc., arc hy no means clearly understood. Variations in indi- vidual resistance, here as in other parts of the body, are certainly of great importance. It is probable that the lung is the infection atrium for a nmnber of our acute infectious diseases. It has been demonstrated that systemic infections, as with anthrax bacilli, may be caused l)y the inhala- tion of the germs. The gastric juice, through the hydrochloric stomach. acid it contains, is able to kill anthrax, typhoid, tubercle bacilli, cholera vibrio and other organ- isms. Clinical and experimental evidence shows that this power is often inadequate, virulent micro-organisms reaching the intestines in spite of it (typhoid, cholera, dysentery, tuberculosis, etc.). It is probable that bacteria in the stomach are often protected against the action of the gas- tric juice to some extent by being imbedded in solid particles of food. Certain acidophilic germs, as Avell as yeasts and torulge, seem to flourish in the gastric secretions; these are largely non-patho- genic, but the regularity with which peritonitis follows perforating wounds of the stomach indi- cates that it probably always contains pathogenic bacteria, though it may be only their temporary habitat. The gastric juice may render some bac- teria harmless by digesting their toxins; one gram of the gastric juice of a dog will neutralize fifty fatal doses of diphtheria toxin, or 10,000 of tetanus toxin, using the guinea-pig as the test animal. On the other hand, the toxin of the bacil- lus of botulism (causing a form of meat poison- ing) seems to .be uninfluenced by the stomach eon- tents, as the development of the intoxication indi- 40 INFECTIOX AND IMMUNITY. cates. Vomiting is often a means of ridding the stomacli of toxic substances, including bacteria. The stomach itself is exceptionall}^ free from in- fections. Intestines. Tlie bile is moderately bactericidal for some germs, but. on the whole, the intestinal secretions have low germicidal powers; this is indicated by the fact that the colon contains many more bac- teria than the duodenum. On the other hand, the pancreatic juice destroys some toxins (diph- theria, tetanus) more powerfully even than the gastric juice. This ability of the pancreatic juice to destroy toxic bacterial products may explain the more frequent occurrence of enteritis in the ileum than in the duodenum. The bile also has a neu- tralizing power for some toxins. Although a num- ber of pathogenic bacteria inhabit the intestinal tract (colon bacillus, streptococci, etc.), they do not often set up inflammatory processes in the adult. The tissues become accustomed to their presence. The pathogenic bacteria which do not normally exist in the intestines are those which, on introduction, are most likely to cause disease (typhoid, cholera, dysentery, etc.). The intesti- nal tract of the infant, on the other hand, is fre- quently attacked by some micro-organisms (strep- tococcus, colon bacillus, bacillus pyocyaneus), which in the same locality in the adult appear harmless. The fact that many individuals are not stricken in an epidemic, in which all are equally exposed to infection, points to the probability that pathogenic organisms (t^^hoid. cholera and dys- entery) often traverse the intestinal canal without inducing disease. ISraturally, microbes are elimi- nated in enormous quantities in the feces, and in INFLAMMATION. 41 inflammatory states this elimination is increased by diarrhea. It is also not to be forgotten that the intestinal tract is, to a considerable extent, a lymphoid organ, and that consequently in the presence of infection enormous quantities of phagoc}d:es can quickly be called into action. The protective properties of the genito-urinary surfaces are not different in principle from those already mentioned (vaginal acidity, urinary irri- gation) . B. THE PROTECTIVE NATURE OF INFLAMMATION". Although there are many chemical and physical Nature of _ , , . , . r, ,• ^ '^ . Inframmation. agents which may cause miiammation, we are in- terested here only in those of an infectious na- ture. Inflammation may be considered a? a reactive condition on the part of the tissues, which devel- ops in response to the action of some injurious agent. The process may be beneficial in some in- stances, while in others it may be pernicious from the beginning to the end. The thickening of the endothelium of the cerebral vessels as one sees it in syphilis is a progressive, reactive change which in no sense can be of benefit to the individual, and which can have no conceivable function in over- coming the s;\nphilitic infection. Likewise, the new formed connective tissue seen in alcoholic cirrho- sis of the liver is of no benefit to the hepatic tissue, though it may serve in some degree to protect the liver cells from the alcohol which continues to be ingested. In an ulcer of the cornea the presence of serum and of leucocytes, as well as the prolifer- ation of connective tissue, may be the sine qua non for the healing of the ulcer, vet the resultinsf scar 41 lyFKCTlOX AXD IMMUXITY. may liTeatiy i!iii>air the vision. The intiainmation ill the instances cited is injurious because of tlie functional importance of the tissues involved. On the other hand, an extensive scar Avhich has formed in tissues of less functional importance, as in the skin and suhcutaneous tissue, may he harmless. It is then to he recognized that there are certain consequences of the inflammatory reaction, the seriousness of which depends on the situation, severity, duration and extent of the ])rocess. and that these consequences are independent of any ]'»rotective function the inflammation may have exercised. Variations in The amouut and character of the reaction are tfc« Reactions. subject to many variations, depending on a num- ber of conditions : 1. It varies Avitli the nature of tlie microbe. Xon-pathogenic organisms induce little more in- flammation than so many minute, inanimate, non-toxic particles. The tubercle bacillus causes especially the formation of connective tissue, giant cells and the accumulation of lymphoid cells, aside from some retrogressive changes char- acteristic of the disease. Organisms similar to the streptococcus and pneumococcus lead to the formation of ]-)us and fibrin, to the accumulation of serum and of polymor])honuclear leucocytes more than mononuclears, Avhereas the prolifera- tion of fixed tissue elements is secondary. The tetanus bacillus alone causes almost no local in- flammatory change. 2. The reaction is influenced by the virulence of a particular bacterium. A streptococcus which has lost its virulence is disposed of liy the animal PIIA aoOYTOSfS. 43 tissues with a niiniiniu)] tissue reaction, perliaps no more than slight congestion and edema and the wandering in of a few leucocytes; one of liigh- er virulence causes an intense reaction, mani- fested by congestion, edema, hemorrhages, necro- sis and pus formation; then streptococci of such great virulence that they destroy life in the course of a few hours are occasionally encountered in wound infections and in peritonitis, having in the meantime elicited a minimum inflammatory reac- tion. 3. It has a relation to the resistance or the nat- ural immunity of the individual. Metchnikoff, in particular, has shown that animals of high re- sistance to a particular microbe destroy the germ quickly by phagocytosis (the ingestion of parti- cles by cells, especially the leucocytes), while in susceptible animals the accumulation and activity of phagocytic leucocytes are deficient. The occurrence of leucocytes in inflammatory Leucocytes. conditions is so characteristic that one naturally seeks to associate their presence with some in- fluence which is exerted by the toxic substance or the bacteria which cause the inflammation. It is a long-known fact that some microbes attract one kind of leucocyte, that others attract another kind, and that in still other instances the leuco- cytes appear to be either uninfluenced or actually are repelled by the infecting agent. Tliis phenomenon of living cells moving toward chemotaxis. or away from certain other cells or substances is termed chemotaxis ; the former is positive, the lat- ter negative, chemotaxis. There is a somewhat general law, but one to which exceptions exist, that, regardless of the microbe involved, the more 44 INFECTION AND IMMUNITY. acute the inflnnimatorv process the more do poly- inori)hoiiuc]ear leucocytes accumulate, while in the more chronic infections, with much connec- tive tissue formation, the mononuclear leucocytes predominate. Thus in tuberculosis one finds lymjDhocytes and plasma cells — mononuclears — predominating greatly over the polymoi'phonu- clears. In the acute purulent infections, on the other hand — streptococcus, staphylococcus, pneu- mococcus — the latter type of leucocyte predomi- nates, the mononuclears being fewer and remain- ing at a. distance from the center of action. There is reason to believe that the mononuclear leuco- c^"tes play an important, though perhaps indirect, role in the formation of the connective tissue. Phagocytosis. The ingestion of particles by living cells, phago- cytosis, is a property which many cells possess. Although micro-organisms and inanimate parti- cles are sometimes found in epithelial cells, cer- tain of the mesoblastic cells have this function pre-eminently : Pol3^morphonnclear leucoc3i;es, large mononuclear leucocytes (lymphocytes), ameboid connective tissue and endothelial cells. Of these the pol^miorphonuclear leucoc}d:es, the microphages of Metchnikoff, have the greatest phagocA'tic power; the others, the macrophages, are more exceptionally phagocytic. Now, the mere ingestion of the bacteria by such cells would not be of necessity injurious to the microbes; in- deed, opponents of MetchnikofE's phagocytic theory of immunity hold that phagocytosis by wandering cells may be, and often is, pernicious, in that the cells may return to the circulation and spread the infection to other parts. But when we learn that after ingesting the bacteria the phago- PLASMA, SERUM AND FIBRIN. 45 cytes are often able to kill and digest them, it is realized that the process may be a genuine pro- tective factor. This being true, the importance of positive chemotaxis in recovery from an infection becomes manifest. It is also represented that phagocytic cells have the power of excreting their germicidal substances into the plasma and serum and lending to the latter a bactericidal power. Furthermore, it is held that they may absorb liquid poisons, bacterial toxins, and in some manner de- stroy their toxicity. As shown later, these are es- sential points in the j)hagocytic theory of immun- ity. Serum, even when entirely free of leucocyte?, influence of has bactericidal powers; it need not be discussed serum. at present whether this power exists primarily in the serum or is one conferred on it by the leuco- cytes. In view of its presence, however, it is evi- dent that the serous exudate which is usually present in inflammations, especially the acute, may be of influence in combating the infection. Serum often contains natural antitoxins, and, in addition, it may be of value in lessening the tox- icity of poisons by diluting them and aiding in their elimination. The abundant deposit of fibrin seen in some in- Fibrin. fiammations is of mechanical value by hemming in the infection and in offering a barrier to the rapid diffusion of toxins. We are all familiar with the part pla3^ed by fibrinous and fibrous ad- hesions in preventing a localized peritonitis from becoming generalized. In prolonged inflamma- tions fibrin furnishes a ground substance into which new connective tissue and vessels grow (or- iranization). 4t; lyFECTIOX AM) IMMi'MTY. Inflammatory Tlio iicw fomiefl coiinective tissue seen in many Connective . • n ,i i • • i. i ' Tissue, inllamniations, especially tlie clironic, as m tuher- oulosis and actinomycosis, offers an important l)arrier to the extension of an infection. Perhaps no l)etter example of this conkl he cited than the ■ dense tissue which forms aroinid a luticMvulous sinns or ahscess. To Slim up. the inllamiiiatory reaction antago- nizes infections. 1. mechanically, through the formation of new connective tissue around the focus, and dense accumulations of leucocytes and iihrin; 2, through the bactericidal and antitoxic actions of the lymph and serum; 3, through the ]diagocytic action of amehoid cells. The value of hot applications in local inflam- mations, in that they increase congestion, Avhich hastens the exudation of plasma and leucocytes and the proliferation of cells, finds: a logical ex- planation in view of the facts mentioned. Also increase in local temperature probably favoi-s chemical actions. The special features of the phagocytic theory of immunity are considered in a later chapter. For many details in regard to inflammation, the reader is referred to the classic article of Adami on this subject in the first vol- ume of x\llbutt's System of Medicine. C. THE ANTIBACTERIAL AND THE ANTITOXIC NATURE OF NATURAL IMMUNITY. In a previous page it has been stated that nat- ural immunity may be either antibacterial or anti- toxic. We have seen that the protection afforded by the body surfaces may be effective against both microbes and their toxins, and that local inflam- matory processes, although most certainly antago- NATUMAfj .\NTII',.\(!Ti:h'l.\L IMMIMTV. 47 nizing tIic hacicna, mn}- at the same time have some antitoxic value. The term natural irnmimity, however, as indi- JJ^J-barteriafl cated ill the first chapter, lias a peculiar applica- immunity. tion to tlio natural resistance of some species or races of animals to infections to which other spe- cies or races are susceptible; and to an unusual in- dividual resistance, often seen in members of a given race or species. This condition depends on properties residing in the tissues or fluids of the liody, and consequently is independent of any pro- tection Avhicli the body surfaces afford. Its pres- ence is demonstrated in the most striking man- ner by tlie experimental method, when microbes or toxins are injected directly into the tissues or circulation. At the same time every-day observa- tion provides many examples. In determining the antibacterial nature of im- munity in a given case there are two conditions which must be proved : 1, that the body cells or fluids are able to destroy the microbe, and that this power is s.uJ0Liciently strong to make it reason- able that the immunity depends on it; 2, that the immunity does not depend on non-susceptibility to a possible toxin of the microbe, nor on a nat- urally existing antitoxin. To prove the first condition, three procedures may be resorted to : First, the microbes are in- jected into the subcutaneous tissue, the peritoneal cavity or the blood vessels. If the animal does not become ill after a dose which, in proportion to weight, is pathogenic for some other test animal, an immunity is indicated. At a proper interval all the tissues and fluids are examined to deter- mine the fate of the microbes. This may be done 48 INFECTION AND IMMUNITY. by staining the fluids and cells for bacteria and examining with the microscope, or by inoculating culture tubes with tlie fliiids, the growth or non- gro^^ih of colonies determining wliether or not the microbe^^ have disappeared. Examinations of this nature often disclose the fact that many of the bacteria have been phagocytized by the leucocytes, while others have apparently succumbed to the germicidal action of serum or plasma. It is often desirable to determine the extent to which mi- crobes are eliminated through the excretions (urine or feces) ; this is best done by the culture method, but is a difficult technical problem. Second, the animal's serum or plasma may be mixed with a suspension of the microbes in a number of test tubes, using varying amounts of serum with constant amounts of the bacteria in the different tulies. and at a f^ubsequent period, from tbree to twenty-four hours later, cultures are made from these mixtures to determine the bactericidal power of the serum. Tlie numbers of colonies which appear in these cultures, minus the number which appear when ?erum is not added, is an index of the bactericidal power of the serum. If this power is found to be high, it is, in the pres- ent state of our knowledge, considered as pre- sumptive evidence that the natural immunity of" the animal depends on it. It is, nevertheless, a fact that the antibacterial immunity of an animal does not always go hand in hand with the bac- tericidal power of its serum. A well-loiown illus- tration of this is the following: Both the dog and the rat have a rather high degree of immunity against infections witli the anthrax bacillus; vet it has been found tliat the serum of the dog has NATURAL ANTITOXIC IMMUNITY. 49 almost no bactericidal effect on this microbe, while that of the rat has a very strong effect. At the same time we should remember that the bacterici- dal power of the serum does not necessarily repre- sent the entire antibacterial function of the body. In the serum we have none of the body cells, and especially none of the phagocytes, the destructive action of which on some bacteria is well known. Third, it is now possible to perform test-tube experiments with the leucocytes of an animal, whereby the phagocytic power of these cells for a given microbe may be determined. This may be done by counting in stained specimens the num- ber of bacteria which are englobed; or the bac- tericidal power of the leucocytes may be deter- mined approximately by performing the culture experiments described in the preceding paragraph, in this instance, however, substituting fresh defib- rinated blood for the serum. If the bactericidal power of the defibrinated blood (containing leu- coc5rtes) is greater than that of the serum alone, the effect of the leucoc}i:es becomes apparent. This receives further consideration in the chapter on phagocytosis. At a time when the antitoxic action of serums Alexins. was not appreciated, Buchner gave the name of alexins (from the Greek, aX^^eiv, to ward off) to the protective substances of the serum, i. e., to the bactericidal substances, making the observation that they were very labile substances, losing their power spontaneously in a few days when exposed to the air and light, or when they were heated to 55 C. for thirty minutes. In determining the presence or absence of anti- ^^^»f^K toxic immunity, the toxin of the microbe, of immunity. 50 INFECT I Oy AND IMMUNITY. course, must first be in hand. The methods of ob- taining toxins will be referred to later. If the animal resists a dose of toxin which, in proportion to weight, produces disease in some other suscepti- ble animal, the tissues or fluids of the first animal may contain antitoxin. It will be indicated later how this result may be obtained even without the jDresence of antitoxin, the immunity being due to some other obscure cause. If the resistance is referable to the presence of antitoxin, the latter may be detected in the following manner: The animal is bled, its serum collected from the clot, then mixtures of the serum and of the toxin are injected into animals of known susceptibility for the toxin. If the test animal is in this way pro- tected from an otherwise fatal dose of the toxin, it is evidence that the serum contains an antitoxic substance. Following this method of experimentation, if antibacterial properties are found to the exclusion of antitoxic, the immunity is considered to be an- tibacterial ; and -with the converse result it is anti- toxic. It is, of course, conceivable that in a given case it might be both antitoxic and antibacterial. In dealing with diseases of which the specific mi- crobe is known and cultivated, the existence of antibacterial or of antitoxic substances can usual- ly be found by the methods described. If the eti- ologj is unknown, as in scarlet fever, measles, s}qohilis, etc., that is, if the virus and its toxin can not be obtained in quantities, the nature of the resistance is not at present open to determination. Examples are kno"^vn in which, in spite of rather high resistance on the part of the animal, it? serum contains neither strong antitoxic nor Relative Immunity. NON-8 USCIJ/'Tf/ifLITY. 5 1 bactericidal properties. This relationship exists between a number of animals and such bacteria as the pneumococcus, staphylococcus and strepto- coccus. It is possible that the phagocytes are im- portant factors in immunity to these infections. It is seldom that natural resistance is absolute. Pasteur found that the great immunity of the chicken for anthrax could be overcome by im- mersing the animal in cold water, the reduction in body temperature supposedly decreasing the re- sistance. It was stated in a previous chapter that physical exhaustion, hunger and exposure to cold may also reduce natural resistance. Pestilence and famine often go hand in hand. Similarly, antitoxic immunity usually is rela- tive. The chicken, which withstands a large quan- tity of tetanus toxin when injected into the skin, muscles or circulation, succumbs when the toxin is injected directly into the nervous tissue. As an illustration of natural immunity to toxins, the following table serves a good purpose. The horse is the most susceptible animal for tetanus toxin. If the minimimi fatal amount for one gram of horse weight is taken as a unit, this scale of re- sistance for some other animals is obtained (Knorr) : For 1 gram of guinea-pig weight 2 units are fatal For 1 gram of goat weight 4 units are fatal For 1 gram of mouse weight 13 units are fatal For 1 gram of rabbit weight 2,000 units are fatal For 1 gram of chicken weight 200,000 units are fatal In view of the high immunity of the chicken tib^'ft"**^®"' against tetanus, one may be led to suppose that its serum would contain a large amount of antitoxin, yet experiments show that it possesses practically no tetanus antitoxin. This fact suggests that there is a distinct type of natural immunity 52 INFECTION AND IMMUNITY. which, it is tliouglit, may be independent of both the antibacterial and the antitoxic properties of tlie body. Receptoi^s! ^^ ^^ ^^^^ thought that the toxic elements of bac- teria are chemical substances (very complex, surely) which are able to injure the tissues, i. e., to cause disease, only by entering into chemical union with substances which the cells contain. ■ Such chemical substances of groups pertaining to the cells will be referred to later under the name of cell receptors. Accordingly, if the cells of an animal do not possess groups or receptors which are capable of forming a chemical union with the toxin, the latter would be unable to pro- duce injury, i. e., the animal would be immune even in the absence of all bactericidal or antitoxic properties. This condition, however, is not one which is capable of experimental demonstration, at least at present, but the conditions point irre- sistibly to its existence in some cases. We are accordingly led to the conclusion that immunity to toxins is not in all cases antitoxic, in the sense that the serum contains demonstrable antitoxin; and likewise that immunity to bacteria is not in all cases antibacterial, in the sense that the serum contains substances which are able to kill the bacteria in test-tube experiments. N'on- susceptibility and phagoc5i;osis may be of impor- tance in resistance of this t}'pe. Importance of There is another factor, however, which mav the Tissue ti, ,i p , i- •, • \ Attacked, throw light on the type ot natural immunity ]ust considered. We know that tetanus toxin causes tetanus through its power of uniting with the nerve cells, and we may consider that tetanus is a very fatal, disease, primarily because of the vital NUMMARY. 53 nature of the tissue which it attacks. Now, if the toxin, instead of uniting with the cells of a vital organ, were to combine with cells of less impor- tance to the economy, as, for example, the cells of the subcutaneous tissue, it is probable that we should have no tetanus. In some of the lower ani- mals there is reason to believe that the toxin of tetanus does unite with such tissue (Metchnikoff). Eoux and Borrel believe that the greater degree of immunity which the rabbit has over the guinea- pig is due largely to the fact that the rabbit's liver is able to fix a great deal of the toxin. And Metchnikoff has found that the liver of the scor- pion, which has an absolute immunity to tetanus, absorbs the toxin and retains it for months. By way of summary, then, we may say that the Summary. natural blood immunity and tissue (histogenic, Behring) immunity depend on the following fac- tors: Bactericidal and antitoxic powers of the serum and plasma, the destructive effect of the cells, especially the phagocytes, on both bacteria and toxins; a possible absolute non-susceptibility in some cases (the absolute non-existence of suit- able cell receptors) ; the overwhelming distribu- tion of the suitable receptors for the toxin in or- gans of less vital necessity for the individual, thus diverting it from more important organs. In order that a pathogenic organism produce a progressively fatal disease in a susceptible animal, the following obstacles must be surmounted: The strong defenses of the body surfaces must first be overcome; a local inflammatory reaction which may have been excited must first prove itself to be inadequate for the limitation of the infection; there must be an insufficient supply or insufficient 54 INFECTION AND IMMUNITY. activity of antiruicrobie and antitoxic processes in the body fluids and cells. In view of the wide variations in the nature of different infectious agents, it is possible that the defensive means wliieh would counteract one might be inadequate for another; and inasmuch as animals appear to differ as much in the charac- ter of their defensive as microbes do in their of- fensive powers, there is abundant room for the display of the various phenomena of natural im- munity and of natural susceptibility with which we have become familiar. OTHER PROPERTIES OF NORMAL SERUMS. Hemolysis. In addition to the bactericidal and antitoxic ac- tion of many normal serums, they often possess other characteristics which are of the highest in- terest in the study of immunity. In earlier days it had been noted that the transfusion of blood from one species to another was often fatal to the injected animal. Later investigations showed that this w^as due to toxic substances in the trans- fused blood ; substances which, above all, de- stroyed the red blood cells of the injected animal. This action, in which the hemoglobin is dissolved out of the red blood cells, may be reproduced m test-tube experiments .by mixing the blood cells of one animal with the serum of another which is toxic (e. g., rabbit blood -j- goat serum). This is the phenomenon of hemolysis, and the appearance of such a tube is exactly like that seen when blood is mixed with distilled water or even with tap water; i. e., it is a laking of the blood, it loses its opacity and assumes a beautiful cherry-red color. The serum of practically every species contains a HEMOLYSINS, ETC. 55 hemolytic substance (a serum hemolysin) for some kind of erythrocyte. Some serums also contain toxic agents for other Cytotoxins. cells; they are generally called serum cytotoxins. The serum of the eel not only contains a strong hemolysin, or hemotoxin, but also a powerful poison for nervous tissue, neurotoxin. Similarly we have normal leucotoxins for leucocytes, nephro- toxin for kidney tissue, etc. Another property of many normal serums is Agglutinins. that which causes- agglutination or clumping of bacteria, as one sees it in the Gruber-Widal test for typhoid. Even normal human serum may ag- glutinate the typhoid bacillus, but to a less degree than that of a typhoid patient. One serum often causes a precipitate in the serum of another animal, or in a bacterial culture filtrate. In considering these facts, one becomes con- scious of the great complexity of that substance which plays so important a part in immunity and its studv — i. e., the blood serum. Precipitins. CHAPTER Aa. Immunity ACQUIRED IMMUNITY. Immunity which is acquired as the result of infection is said to have been acquired natm-all)', a very different thing from natural immunity. Immunity which is acquired artificially may be active, as in vaccination; or passive, as when diphtheria antitoxin is injected prophylactically. Active One who has recovered from scarlet fever, small- pox, plague, typhoid fe'ver, etc., becomes possessed of lasting protection against subsequent attacks. On the other hand, the immunity afforded by an at- tack of certain other diseases usually is of shorter duration: cholera, diphtheria, pneumonia, etc. So far as known, the acquired protection is very spe- cific in character: e. g., a person who has had measles may still have scarlet fever; or an attack of cholera does not protect against a later attack of typhoid. In a number of diseases one attack confers no evident protection against a second; gonorrhea, influenza, recurrent fever and malaria. Some dis- eases may create a predisposition for recurrence: erysipelas, influenza, diphtheria in some instances, although a natural susceptibility of the individual may explain repeated attacks. A very important factor for progress in artifi- cial immunity was the knowledge that evem a light attack of an infection (scarlet fever, cholera, typhoid, smallpox) may be efficient in conferring immunity. Such light attacks are frequently noted sporadically and in epidemics, while occa- sionally an epidemic is mild in character through- VACCINATION. 57 out. An epidemic of benign smallpox recently prevailed in the middle Western states and the • mild character of the plague which was endemic in San Francisco will be remembered. In these instances it seems probable that the mild charac- ter of the disease depends on the low viriilence of the organism which causes the epidemic ; and the condition suggests the possibility of artifLcial at- tenuation of virulent micro-organisms for the pur- pose of inducing at will infections of a benign character. It might be possible to' so modify the virus that vaccination. protection could be established vsdthout setting in motion the actual disease even in a mild form. An attenuation of this nature had long been prac- ticed with smallpox virus. Before cowpox was resorted to as a source of vaccine, it had been the custom to inoculate the genuine virus of smallpox, for the purpose of producing immunity. Con- trary to the natural expectation, this method, instead of reproducing severe smallpox, often caused the modified disease which we call varioloid. This phenomenon may depend on the fact that the virus finds the skin and subcutaneous tissue an unfavorable medium for the development of virulence; a condition which would be equiva- lent to an attenuation of the microbe. The patho- genicity of the cholera vibrio in animal experi- ments is affected similarly in subcutaneous injec- Attenuation. tions. It is now generally considered that cowpox is smallpox which has suffered a decrease in viru- lence because of its passage through the cow. Consequently, when this weakened virus is planted in the skin of man, where it may undergo further attenuation and produce the mildest possible form of modified smallpox, we have an ideal vaccine. 58 INFECTION AND IMMUNITY. Passage. In a similar manner the virulence of tlie anthrax bacillus for sheep may be lessened b}^ passing the organism through the dove. This metliod of de- creasing, or in some cases of increasing, the viru- lence of a micro-organism is known as passage. No single method of attenuation is suitable for all organisms. Pasteur found tliat cultures of the bacillus of chicken-cholera become so weak- ened when exposed to the action of light and air that the}' may safely be used as vaccine; also that the anthrax bacillus when grown at 42° C. is at- tenuated and does not form spores, and conse- quently becomes a suitable vaccine for sheep and cattle. Of no less interest to us is Pasteur's method of attenuating the virus of hydrophobia by desiccating the spinal cords of infected ani- mals (ral)bits) ; the altered cords are then suitable for the immunization of individuals who have been bitten by a rabid animal. Work of the past decade has sho'mi that suc- cessful vaccination is possible against cholera, tj'phoid and plague by the inoculation of avirn- lent cultures, or those which have been killed out- right by heat. In so far as we know the immunity Avliich is caused by vaccination or protective in- oculation is antibacterial, or, better, antimicrobic. If the canse of the disease is unrecognized, as in smallpox and hydrophobia, there is no means of determining whether it is antibacterial or anti- toxic. Nature of One may ask if acquired immunity to bacteria immunit^v. and to toxins is due to the presence of the anti- bacterial and antitoxic substances which were mentioned in connection with natural immunity. Although normal serum is strongly bactericidal LEUCOCYTES. 59 for the typhoid bacillus, the serum of one who has recovered from typhoid fever possesses this power to a much greater degree. As this is true in many other bacterial infections, the new resistance is held to depend on the increase of bactericidal sub- stances in the serum. Similarly in acquired im- munity to diphtheria and to tetanus, the most conspicuous change is a great increase in the cor- responding antitoxins. The result is the same, regardless of whether the immunity be produced by a natural attack of the disease, or by artificial immunization with the specific microbe or toxin. Accordingly it seems probable that acquired im- munity in these instances depends on the presence in the sertim of an increased amount of properties which, to a certain degree, may be present nor- mally. It was stated in the section on natural immun- The Leucocytes ity that the leucocytes, acting as phagocytes and immunity. as resorptive cells, seem to be. responsible, at least in part, for natural resistance to an infection. Metchnikoff and his followers have provided us with many observations wliich are interpreted as showing that the importance of these cells is con- tinued into acquired immunity. These investiga- tors state that in acquired immunity the phago- cytes have a much greater capacity for ingesting and killing bacteria and for absorbing and de- stroying toxins than when the animal is in a state of greater susceptibility. It is also concluded that the serum in active immunity owes its new or more powerful antibacterial, antitoxic and other properties to the leucocytes, w^hich under the in- fluence of the infection have overproduced and ex- creted these substances into the plasma. CO rXFECTIOX AND IMMUNITY. Passive immunity. The Leucocytes in Passive Immunity. It will appear later that recovery from certain infections (streptococcus, staphylococcus, pneumo- coccus, etc.) is not characterized by tlie formation of antibacterial or antitoxic substances. In these instances it seems probable tliat the temporary immnnit}', of which recovery is the outward mani- fest-ation, is due to destruction oi the bacteria by phagocytic cells. This conception seems all the more plausible when we remember the hyperleu- cocA'tosis which characterizes these infections. Inasmuch as it has proved possible by tlie pro- longed immunization of animals with bacteria or toxins to induce a high concentration of antibac- terial or antitoxic substances in their sennn, it was the natural expectation that if such serums were injected into other animals the latter would thereby be endowed with an increased resistance to the infectious agent against which the serum had special activities (passive immunization). This has been- found to be the case with many antibacterial (typhoid, cholera, plague, dysentery, etc.) and some antitoxic serums (diphtheria, teta- nus). Unfortunately the protection afforded by the injection of an immune serum is of short dura- tion (from two to several weeks) ; it is as if a for- eign substance had been injected, the fate of which is to be eliminated rapidly. This is in contrast to the condition in active immunity in which the protective substances are often formed over a long period by the body cells. The school of Metchnikoff brings the leucocytes into relation with passive as well as active im- munity. It is held that the immune serum which is injected is potent, because it stimulates the leu- cocytes to a greater phagocytic activity in the case Opsonins. BACTERIOLYTIC ENZYMES. 61 of antibacterial iramiinity, or to a greater absorp- tion and destruction of toxins in the case of anti- toxic immunity. Our knowledge of poisons (see Chapter XIV) is as yet so limited that positive statements can not be made as to the part they play in acquired im- munity, although it is thought that immunization with some microbes causes an increase in the quantity of opsonins. Mention may be made here of the well-known but curious phenomenon that resistance may vary with the age of the individual. Typhoid fever at- tacks the adolescent or middle-aged rather than the very young or very old. Active tuberculosis grows less common in the later decades of life. Then we have what are distinctively the diseases of childhood: after 15 years of age diphtheria, for example, is uncommon. Some of these instances of acquired immunity may be referable to differ- ences in the character of the cell receptors at dif- ferent ages, while perhaps others are due to a slow immunizing process occasioned by the prolonged presence of non-pathogenic amounts of the proper micro-organisms. Emmerich and Loew found that many bacteria Barterioiytrc produce in culture media, as well as in the animal body, substances which apparently act as ferments and which are able to kill not only the bacterium which secretes the ferment, but many others. For example, pyocyanase, the bacteriol3i;ic enz3'nie of Bacillus pyocyaneus, dissolves pyocyaneus, anthrax, diphtheria and typhoid bacilli, the vibrio of cholera, the streptococcus and staphylococcus. These enzymes usually are not toxic, and it is sup- posed that during the course of an infection they Enzymes. Immiine Cytotoxins. Immune Agglutinins. 02 INFECTION AND IMMUNITY. reach such a concentration in the blood that they destroy the bacteria which produced them, thus bringing about recovery. It is claimed also that they, either during infection or as a result of re- peated injection of the ferment, enter into a some- what permanent combination with the albumin of the body, forming the so-called "immune-pro- teidin,'' on which acquired immunity depends. It is -also stated that with "pyocyanase-immuno- proteidin^^ it is possible to so immunize a rabbit that a subsequent (12 days) otherwise fatal dose of the anthrax bacillus is harmless. Although the effects of these "enzymes" on anthrax and on some other organisms have been confirmed by a number of investigators, their im- portance in acquired immunity and in the recov- ery from infections is very doubtful. There is the special objection to this theory tliat it puts im- munity on a non-specific basis; i. e., pyocj'anase will protect against anthrax, diphtheria, etc.. while, in reality, all our clinical and experimental data point to the high specificity of acquired immunity. The serum acquires antibodies not only for bac- teria and toxins, but also for many other cells and sulDstances which may be used for immunization. There are many immune c}ix)toxins, such as the serum hemolysins, leucotoxins, neurotoxins, nephrotoxins, etc., which are formed as the result of immunization with the corresponding cells. (See Chapter XIII.) By systematically injecting an animal with a bacterium or with any tissue cell, agglutinating substances (the agglutinins) are formed and may be demonstrated in the serum. Like other anti- I'liEClPITl'NH. 03 bodies, they are highly specific for tlie cell used in the immuiiization. (See Chapters IX and X.) It has been found that toxins, other than those of bacterial origin, will yield antitoxins by im- munization. Such toxins are snake venom, yield- ing antivenin; ricin, a hemagglutinating toxin from the castor oil bean, yielding antiricin, etc. Eecentlv what is termed the biologic test for '"""?".« o Precipitins This test may a"** „. , . •^ The Biologic Test for species has assumed prominence, be illustrated : A goat is injected repeatedly with the serum of man. . After a number of injections a very minute amount of this goat's serum will cause a precipitate when mixed with human serum, but not when mixed with the serum of any other animal (except, perhaps, that of anthropoid apes). The test is so delicate that when a small amount of old dried human blood is dissolved in salt solution and treated with the goat serum the precipitation will still occur, and in view of this fact, the test has become of medicolegal impor- tance. The wide distribution of this phenomenon among all kinds of animals gives it great biologic significance. Kraus found that by immunization with cer- tain bacterial filtrates substances are formed in the serum which cause precipitates in the filtrates. It is further interesting that other albumin-con- taining substances, as egg albumin or milk, will on immunization, yield specific antibodies. The serum of an animal which has been immunized with goat's milk will cause a precipitate in the latter, but not in coat's milk. (See Chapter XL) It has also been possible toi obtain specific anti- bodies for ferments : for the peptonizing ferments Species. Antiferments. G4 IXFECTIOy AND IMMUNITY. of bacteria, for emiilsin, lab, fibrin ferments, etc. There are, however, very many substances for which serum antibodies can not be obtained; this is true for all substances of knoAvn chemical com- position, as acids, bases, salts, and for the alka- loids (strychnin, morphin, aconite, etc.) CHAPTER VII. TOXINS AND ANTITOXINS. Through Ehrlich the word toxin has come to thriich's have a special significance, being applied only to a of Toxin. certain type of toxic substances. Toxins have the following properties (Ehrlich) : 1. They are extremely labile substances which occur as secretion products of vegetable or of ani- mal organisms. 2. Their chemical nature is uuinown. The im- possibility of obtaining them in pure form and their great lability render them insusceptible to ordinary chemical analysis. 3. An analysis of a toxin may be reached at present only through the medium of animal ex- periments. 4. Immunization with toxins yields antitoxins. It has not been possible to obtain antitoxins for inorganic poisons, glucosids and alkaloids (morpliin, strychnin, etc.) 5. In contrast to well-defined chemical poisons, the action of toxins is characterized by a latent or incubation period. That is, following the introduc- tion of a toxin, a certain period of time elapses before toxic symptoms appear, and this period is greater than the time logically required for the absorption of the toxin through the circulation.'^ The incubation period may be shortened experi- 1. Recent work indicates that the long incubation period of tetanus may depend, at least in part, upon the length of time required for the toxin to reach the ganglion cells through the axis cylinders of the motor nerves. Preparation of Toxins. GG INFECTION AND IMMUNITY. nientallv by tlic inject iou of large quantities of toxin, but it can not be eliniinatcd ontirel_v. Snake poison appears to act without incubation period, but it is still to be classed with the toxins, because of its power to cause the formation of an anti- toxin. (). "The facts make it necessary to assume, as a condition for the poisonous action of toxins, a spe- cific chemical union of the toxin with the proto- plasm of the cells in certain organs." . . . "The affinity of other poisons, as the alkaloids, for tissues, depends not on chemical union, but on some such process as solid solution or loose salt formation.'^ The preparation of soluble toxins is relatively simple. It is necessary only to inoculate a suitable fluid culture medium with a culture of the micro- organism, to allow growth to take place for some days at body temperature, then to pass the fluid through a porcelain or some equivalent filter. The soluble toxins usually may be precipitated from the filtrate by some precipitant, as ammonium sulphate, and preserved in a dried state for a long period. Such a |)recipitate does not represent the toxin in a pure form, but various proteid sub- stances of the culture medium, as well. The bacilli of diphtheria and tetanus Bacillus pyocyaneus, and Bacillus hotulismus, are the princi" pal micro-organisms which produce soluble toxins. When the toxins of these organisms are injected into a suitable animal, phenomena similar to those produced by an infection with the organisms themselves are produced. They are in a particu- lar sense specific toxins. Some micro-organisms, however, produce more than one toxin. The teta- MULTIPLICITY OF TOXINS. 07 nus bacillus, for example, secretes, in addition to the toxin causing the nervous symptoms of tetanus, another (tetanolysin, or tetanus hemolysin) which has the power to destroy red blood cells. Ehrlich holds that the diphtheria bacillus produces not only the toxin which causes the acute intoxication of diphtheria, but another of long incubation period which may cause paralysis. Cobra poison has at least two toxins, one which attacks the nerv- ous tissues^ — a neurotoxin — and'anotlier which at- tacks the erythrocytes ; the two may be separated by appropriate measures. As previously stated, the serum of the eel has a strong neurotoxin and a hemotoxin. Some micro-organisms produce one or more Secondary soluble toxic substances, Avhich it is often difficult or impossible to consider as the actual disease- producing elements of these organisms. Concern- ing a disease which is so well characterized clini- cally as tetanus, it is not difficult to determine by inoculation experiment whether one has in hand the specific toxin. The proof is naturally much more difficult in relation to streptococci and staphylococci, for example, where the group of symptoms and the pathologic conditions are not entirely unique for the infection. We are by no means certain that the hemolysin or the leucoci- din (toxin for leucocytes) of the staphylococcus, or the hemolysin of the streptococcus are the para- mount disease-producing toxins of these organisms, although these substances are true toxins. An important test for the pathogenic signifi- cance of a toxin lies in its ability or inability to cause the formation of an antitoxin which is •efficient in the treatment of an infection by the GS IXFECTIOX A\D IMAIUXITY Intracellular Toxins, or Endotoxins. The McFadyen Method. corresponding organism. This is not the ea.'^e with the ioxins jufit mentioned. However, one should not place too much importance on such a test, for it is quite possible that we are not able on artificial culture media to obtain the toxiti in such concentration that the production of an effi- cient antitoxin is possible. There is a large class of organisms the members of which apparently do not produce soluble toxins ; such organisms, however, cause highly toxic diseases (e. g., t}'phoid, cholera, plague). The dead or ground-up bodies of such bacteria are very toxic; also when the germs disintegrate by a process of autolysis or self-digestion the culture medium be- comes toxic because of the cell contents which are set free. Such organisms are said to contain in- tracellular toxins or endotoxins. In infections by them it is supposed that toxic symptoms are pro- duced when a pathogenic amount of the intracel- lular toxins is liberated by the bacteriolytic action of the body fluids or cells (phagocytes). Nothing is known of the nature of such toxins. They certainly are very different from the soluble toxins of diphtheria and tetanus, since immuniza- tion with them has not as yet resulted in the pro- duction of efficient antitoxins. In spite of this fact, however, it is none the less probable that they are the disease-producing constituents of the organisms. Buchner gave tlie name of "plasmin" to the cell juice wliich he was able to express from some micro-organisms. McFadyen, by grinding large masses of typhoid bacilli which had been rendered brittle by the tem- perature of liquid air, obtains from this organism a toxic cell juice. The efficiency of the antitoxin PREPARATION OF ANTITOXIN,^. 69 wliich he is said to obtain by immiimzation with this material has not been demonstrated practi- cally'. It seems improbable that immimization with this "toxin" will yield a serum differing in propertiQs from that obtained by immimization with the living organisms. Toxic substances obtained from bacteria by the Accidental • a • ^ Toxic Sub- action of strong chemicals and extracting fluids, stances. may not represent the essential toxic substance of the organism, but perhaps some clisintegration product which iiappens to be toxic. It is, of course, common knowledge that an anti- toxin is the blood serum of an animal, after the latter has been rendered highly immune by re- peated injections of the corresponding toxin. The horse is chosen for immunization because of its marked ability to yield antitoxins (diphtheria, tetanus), because of its size, withstanding much loss of blood, and because of the readiness with which it submits to manipulation. Manufacturing plants which produce antitoxins Preparation and other antiserums on a large scale have splen- didly equipped stables, which are kept in the maximum hygienic condition, and from which rats in particular are rigorously excluded.- The horses are carefully groomed and fed and given such ex- ercise as will keep them in a healthy condition. The toxins, in solution, are injected subcutane- 2. The importance of this is very great if, for example, horses are receiviDg injections of some virulent living niicro-organism (as the plague bacillus). In this case living micro-organisms reach the general circulation, and a rat having bitten the animal could well contract the plague and be an evident source of danger, not only to other animals, but to the community at large. Even fly- proof stalls are properly instituted in such cases. Attenuation 70 INFECTION AXD IMMUNITY. ousi}'.^ Grave and even fatal reactions ma}^ follow the first injections;, if the toxin has been given in too large closes or in too concentrated solutions. This is especially true when injecting tetanus toxin. It is of great importance first to establish what the Germans call a '^Grundimmunitdt" which means a primary immmiity in the animal itself so that the immunization may then be pushed vigorously until the blood contains anti- toxin in high" concentration. For tliis purpose it ]]as been found necessary to weaken tlie first tox- ins injected. This may be done by heating the 'of'ToTins! toxin solution to 65 or 70 C. for an hour; by add- ing to it from 0.05 to 0.4 pei- cent; of the trichlo- rid of iodin; or by adding a solution of laotassiura iodid in which iodin has been dissolved (Lugol's solution). High dilutions of the unaltered toxin may also be used. Gradually the virulence and amount of the toxin injected may be increased until finally the full virulent toixin is given in large doses. The increase in dosage must be very gradual. Eventually as much as a liter or more of diphtheria toxin is tolerated. Following each injection a reaction occurs. With diphtheria the local swelling may be great, and sloughing may occur. Following an injection of tetanus toxin, tetanic symptoms may appear. In either case, there is some loss of weight and often fever, and another injection must not be given until the original weight is regained and the general behavior of the animal indicates that its former healthy condition is re-established. Several months of such treatment are necessary 3. For the production of antivenln the snake venom Is best injeoted intravenously. PRESERVATIVES. 71 for the production of diplithoria antitoxin in liigii concentration. At the end of this time blood is drawn from the jugular vein by means of a large trochar to which a rubber tube i,s attached. The tube leads to a tall glass cylinder holding from one to two liters, and into this the blood is allowed to How. Six liters may be drawn safely from a horse of average size.* The most rigid asepsis is observed in taking the blood. The glass cylinders, appropriately covered to prevent contamination, are then set in a cool, dark place, and after the serum has separated from the clot samples are taken to be tested for their antitoxic value. The serum, in bulk or after being bottled for orsmlms.^^* the trade, is preserved at a low temperature and in the dark, 0.5 per cent, of carbolic acid having been added to insure sterility. The addition of the acid may cause harmless cloudiness in the serum, but does not destroy the antitoxin. Serums may be preserved perfectly in a dried or frozen state. Many facts of scientific and practical impor- tance have been brought to light through the im- munization of animals on a large scale. It has been found, for example, that following each in- jection of toxin the amount of antitoxin in the blood suffers a reduction, and only equals or rises above the previous amount eight or ten days later. This decrease is explained by assuming that the toxin has, to a certain extent, united chemically with the circulating a.nti toxin. It indicates also 4. Some horses may be bled as many as forty times without suffering a conspicuous deterioration in health. In time, however, an animal becomes less valuable as an antitoxin producer. 72 IXFECTIOX AXD IMMVXITY. the period at which the liorse should be bled in order that the greatest amount of antitoxin may be obtained. It might even be dangerous to draw the blood before this time had elapsed, since some free toxin might still be in the circulation. It is noteworthy that all horses are not equally good producers of antitoxin. One may yield a serum of three times the value of another, al- though the two have been treated identically and seem to be equally immune to the toxin. Another most interesting fact is that, although the blood of an animal may be very rich in anti- toxin, he still may have a disproportionate sus- ceptibility to fresh injections of the toxin. Many of these phenomena have not been ex- plained satisfactorily. standardiza- The nccessity of standardizing antitoxins so and Antitoxins, that dosagc may be controlled accurately is self- evident. To meet tMs need the antitoxic unit familiar in practice was devised. Behring, and also Ehrlich, decided arbitrarily to consider as the antitoxic unit that quantity of a serum which would protect a guinea-pig from 100 fatal doses of the toxin. Ehrlich's original method of testing a serum was to mix difEerent quantities with 10 fatal doses of the toxin and inject each mixture into a guinea-pig of 250 to 300 grams' weight. That- quantity of the serum which pro- tected the animal against the ten fatal doses of toxin contained 1/10 of an immimity unit, and from this result the number of units in a cubic centimeter could be calculated. This method in- volved the use of toxin as the standard by which the value of the antitoxin was measured, and it was found to be unreliable. A toxin degenerates ANTITOXIC UNIT. 73 rather rapidly, retaining- at the same time its binding power for the antitoxin; hence two tests made with the same serum two months apart •might indicate different antitoxic values for the serum. Also 10 fatal doses of one toxin often re- quired more antitoxin for neutralization than the same quantity of a second toxin. These phenomena are due to the formation of toxids. (See next chapter. ) On accoumt of these sources of error, Ehrlich devised a new method in which a standard anti- toxin or test-seram is used as the starting point for the valuation of a new serum. The test-serum standard T I • 1 I (• T-i Antrtoxiits. used at the Eoyal Prussian Institute tor Experi- mental Therapy at Frankfurt, of which Ehrlich is the chief, is a dried and powdered serum of such strength that 1 gram contains 1,700 immun- ity imits; i. e., 1/1700 of a c.c. would protect a guinea-pig against 100 fatal doses of a diphtheria toxin.^ Any other high-grade serum would have answered equally well. The institute keeps in stock a large number of 5. In Germany the various sei'ums are prepared by pri- vate individuals or corporations and manufacturers are re- quired to send a sample of every lot of serum intended for the trade to the Frankfurt Institute that its exact value may bo determined. Each bottle eventually receives a stamp sig- nifying the value in antitoxin units of the contained serum. Moreover, samples of every lot of serum are retained in the in&titute, and from time to time these are tested ; and when it is found that the samples have degenerated beyond a cer- tain value the order is sent out to call in all serum belong- ing to the degenerated lot. When a manufacturer thinks the serum of one of his horses has a high value he may draw a small amount of blood from the animal and send the serum to Frankfurt for a preliminary test. If the serum is sufficiently strong he may then bleed the horse freely ; if it is weak he will be advised to continue th? immunization for a time. 74 IXFECTlOy AND IMMUNITY. viaJs, each containing two grams of this dried serum. The air and moisture are exhausted from each vial and the latter is then sealed in the flaine. Once in three months one of these vials is broken open carefully and the serum dissolved in 200 c.c. of a solution made up of equal parts of glycerin and 10 per cent, salt solution; hence each cubic centimeter of the solution contains 17 units. Dur- ing the succeeding three months this antitoxic solution is used in the comparative valuation of new antitoxins; the solution retains its strength unaltered for this period. For individual tests the serum-solution just described is again diluted seventeenfold, so that each cubic centimeter con- tains one unit. This adds to convenience and ac- curacy. The first .step in the process is to standardize some diphtheria toxin in which the degenejative changes (toxoid formation) have come to a stand- still. This is done by adding so much of the toxin to 1 unit (1 c.c.) of the test serum that an excess of one fatal dose of the toxin remains unbound ])y the antitoxin. The quantity of the toxin which gives this re- sult is called the L+dose.^ The LO dose of the toxin also is determined, this being tlie amount which is exactly neutralized by the imit of anti- toxin. The use of the two doses serves to eliminate, subjective errors on the part of the observer. The L-f- and LO doses of toxin are then used to de- termine the value of new antitoxins. That quan- tity of the new serum which, when mixed with the L-f- dose of toxin, causes the animal to die in 6. Ij=T.imps (Limit) ; + is commonly used to indicate a fatal rosTilt. NATIONAL REOULATIONH. 75 four to six dayS;, contains 1 .unit of antitoxin. If, for example, 1/100 c.c. accomplishes this result, the serum is of one hundredfold strength i. e., 1 c.c. would contain 100 antitoxic units. For therapeutic purposes, it is desirable to have a serum of high value in order to avoid giving too large quantities. Several diphtheria serums are on the market Avhich have a value of 500 units to the cubic centimeter. It is difficult to immunize above this' point. In addition to" the need of knowing the exact Pur'ty of '-' Serum. antitoxic value of a serum, it should be determined positively that there is no contamination of the serum, and especially that no adventitious toxin (tetanus) is present. The sterility of the serum is determined by both a.erobic and anaerobic cultures, and itsi freedom from toxins by Injecting considerable quantities into animals. The serum should not have more than 0.5 per cent, of carbolic acid as a preserva- tive. A convenient method of determining this point is the injection of 0.5 c.c. of the serum into a white mouse. If more than this quantity of the acid is present the mouse dies. Similar principles prevail in the standardiza- tion of tetanus antitoxin, the mouse being used as tlie test animal. Unfortunately tetanus antitox- ins practically go without standardization in this country. This would seem to be for commercial reasons only, for they may be standardized with a low percentage of error. That the United States government is attempt- ing to guard the quality of diphtheria antitoxins 76 IXFECTIOX AXD IMMVXITY. on sale in our markets is apparent from the fol- lowing statement :' ••EX\MIXATION OF SERUMS MADE BY LICENSED MANUFAOTUKERS. "Tho fict of Congress, approved July 1, 1902, entitled 'An net to regulate the sale of viruses, serums, toxins and analogous products in the District of Columbia, to regulate interstate commerce in said articles, and for other pur- poses," and the regulations framed thereunder, approved Feb. 21, 1003, imposed upon the director of the Hygienic Laboratory the duty of examining vaccines and antitoxins for purity and potency. "Accordingly purchases are made for the Hygienic Lab- oratory from time to time on the open market by officers of the Public Health and Marine-Hospital Service stationed in various parts oC the country. The antitoxin is always ))onght from reliable druggists, who keep the product under pi'oper condilions of liglit. temperature, etc. Several grades of diphtheria antitoxin made by each licensed manufac- turer are bought and sent to the Hygienic Laboratory by mail for the purposes of these tests. "The serums are tested not only for potency, but also to determine their freedom from contamination by foreign bacteria, and finally to insure the absence of chemical poi- sons, especially tetanus toxin. Note is made of the phys- ical appearance of the serum, and tests are made to de- termine whether an excessive amount of preservative has been added. "A careful memorandum is made of the facts given by the manufacturer, as stated on the label, as to the num- ber of units contained in the package, and the date beyond which the contents can not be expected beyond a reasonable doubt to yield a specific result. Note is also made of the manufacturer's compliance with the law requiring that the product be plainly marked with the name of the article, and the name, address and license number of the manu- facturer. "Delinquencies that occasionally come to light in these examinations are at once reported to the Surgeon General, U. S. Public -Health and Mariue-Hospital Service, who 7. Taken verbatim from Rosenau. "The Immunity Unit for Standardizing Diphtheria Antitoxin," Bulletin No. 21 of the Hygienic Laboratory of the Public Health and Marine Hospital Service of the United States. M. J. Rosenau is Director of the Hygienic Laboratory. OFFICINAL ANTITOXIN. 77 takes the necessary stops reciuiring the immofliate with- drawal of the particular lot of serum from the market and institutes measures to prevent a repetition of similar errors." •'SEIRUM ANTIDIPIITHERICUM IN THE I'lIARMA- COPEIA. •'The next edition of the United States Pharmacopeia, being the eighth decennial revision, 1900, which is to ap- pear shortly, will contain an antitoxic serum for the first time. The serum will be known officially as antidiphtheric serum or Serum anticliphthericvm, and the unit will be recognized as that approved or established by the United States Public Health and Marine-Hospital Service. "The ofHcial text, which has been kindly furnished by Professor Remington in advance, will be as follows : "SERUM ANTIDIPHTHERICUM. ANTIDIPHTHERIC SERUM. DIPHTHERIA ANTITOXIN. "A fluid separated from the coagulated blood of a horse Etjuus cahaUiis, Linue, immunized through the inoculation of a diphtheric toxin. It should be kept in sealed glass containers, in a dark place, at temperatures between 4.5° and 15° C. (40° and 59° F.). "A yellowish ,or yellowish-brown, transparent or slightly turbid liquid, odorless or having a slight odor, due to the presence of the antiseptic used as a pre- servative. "Specific gravity: 1.025 to 1,040 at 25° C. (77° P.). "Antidiphtheric serum gradually loses its power, the loss in one year varying between 10 per cent, and 30 per cent. Each container should be furnished with a label or statement, giving the strength of the anti- diphtheritic serum, expressed in antitoxic units, the name and percentage by volume of the antiseptic used for the preservation of the liquid (if such be used), the date when the antidiphtheric serum was last tested, and the date beyond which it will not have the strength indicated on the label or statement. "The standard of strength, expressed in units of anti- toxic power, should be that approved or established by the United States Public Health and Marine-Hospital Service. "Average dose : 3',000 units. "Immunizing dose for well persons : 500 units." CHAPTEE VIII. Biologic Analysis Neutralization of Toxin by Antitoxin. THE STRUCTURE OF TOXINS AND ANTITOXINS AND THE NATURE OF THE TOXIN-ANTI- TOXIN REACTION. Because of tJie impossibility of obtaining bac- terial toxins in pnre form, no conception can be gained of their composition in terms of atoms or molecules, although it is convenient to assume that they have some imknown molecular sti'uc- ture. Inferences as to their nature and structure can be gained only by means of the biologic ex- periment, i. e., their effects on animals and animal cells under arbitrax}^ conditions. Wlien a toxin and its antitoxin are mixed in suitable proportions, ' the mixture becomes non- toxic as the result of chemical union of the two substances ; each molecule of toxin has combined with a molecule of antitoxin to form a new non- toxic molecule which may l)e spoken of as the toxin-antitoxin molecule. It was at one time sup- posed that antitoxin had the power of destroying the toxin, perbaps by a ferment-like action. In two instances it has been possible to show that this is not the case. Ordinarily toxins are more susceptible to heat than antitoxins, but in the case of pyocyaneus toxin and snake venom the anti- toxins are the more susceptible. Wasserman found that when a neutral mixture of pyocyaneus toxin and its antitoxin was heated to a certain temperature tJie mixture again became toxic, and Calmette made a similar observation concerning venom and antivenin. If the toxin had been de- TOXIN-ANTITOXIN REACTION. 7!J stroyed b}^ the antitoxin the solution certainly would not have regained its original toxicity on the application of heat. The following facts add support to the view Chemical that neutralization consis.ts of chemical union be- Reaction. tween the two substancas : First, neutralization takes place according to the law of multiple proportions, i.e., ten times a given amount of antitoxin will neutralize a pro- portionate amount of toxin; second, neutralization is more rapid at warm than at cold temperatures; and, third, more rapid in concentrated than in di- lute solutions. These are some well-known laws of chemical reactions. "Emil Fischer has shown that in the ferments, ferments. definite atom-groups of special configuration are present which above all else are requisite for the whole phenomenon (of fermentation). Only such substances as possess a group to which the ferment group corresponds, as lock to key, are subject to the action of a particular ferment." This applies to the action of a particular ferment on only one kind of substance. Having this conception in mind, Ehrlich as- Haptophores sumes that union occurs between toxin and anti- toxin through a special group of atoms which the toxin molecule possesses, and which fits into, or corresponds specifically to, another group of atoms in the antitoxin molecule. These are spoken of as the binding or haptophorons groups (hapto- phores) of the molecules. The haptophorons group of the toxin molecule is highly specific since a toxin can be neutralized only by its own anti- toxin, and naturally the haptophotrons group of the antitoxin molecule must be equally specific. so INFECTION AX D I MM U XI TY. Toxophore. The toxiii iiioleciile contains not only a hapto- pliorus group, through which it unites with anti- toxin in one instance or with tissue cells in the production of disease, but also certain constituents in which the specific activity of the substance re- sides. Toxin is able to work a change in tissue cells after it has combined with them. The toxic prop- erty is said to reside in a toxophorous group. The toxophorous and haptophorous groups are parts of the toxin molecule. Toxoids. It is a peculiarity of toxins that they lose a cer- tain amount of their toxicity in the course of time, although their binding power for antitoxin remains practically unchanged. In the language of the terms which were used above, the toxophorous groups may degenerate or disappear and leave the haptophorous groups intact. Toxins which have undergone this change are called toxoids. Further evidence of the existence of toxoids lies in the fact that when used for immunization they cause the formation of antitoxins. This is possi- ble only when the substance is able to unite with the tissue cells; therefore, the non-toxic toxin or toxoid has retained its haptophorous groups. A toxin entirely free from toxoids has never been observed, since even during the few days re- quired for its preparation a certain amount of degeneration occurs. Partial Additional information concerning the nature Method of of toxiu has been gained by experimenting witli mixtures of toxin and antitoxin, in which the two are present in var\'ing proportions. This is the "partial saturation" method of Ehrlich. Through a vast number of experiments Ehrlich obtained in- The Toxirf ''TOXIN SPECTRUM." 81 formation which permitted liJm to estimate that 300 "binding nnits" are represented in that amount of diphtheria toxin (hypothetically pure) which is exactly neutralized by one antitoxin unit. If the entire amoimt of antitoxin, i. e., 200/200, is added to the quantity of toxin in question, com- plete neutralization of the latter, of course, occurs. In case the toxin is entirely pure, 199/200 of the antitoxin unit would destroy all but 1/200 of the initial toxicity; and 150/200, or 100/200, or 75/200, etc., of the antitoxin when added would permit corresponding degrees of toxicity tO' be demonstrated through animal inoculations. It was found, however, that neutralization did not take place according to this simple scale. The re- siJecirumV suits were complicated, and Ehrlich has found it convenient to express them graphically in the form of a "toxin spectrum'^ (Figs. 1, 2, 3 and 4). For example, let 199/200 of the antitoxin unit be added to the proper amount of the toxin, 198/200 to another similar amount, 197/200 to another, etc., -down to 150/200. In the last mixture, 50 out of the 200 binding units which the toxin pos- sesses are free, and these 50, rather than some Epitoxoids. other 50, are free because they have less aiEnity for the antitoxin than the 150 units which were bound. It has been foimd that those units which first become free have a low degree of toxicity. It was thought that they might have lost their toxo- phorous groups, i. e., that they were toxoids; and because of their weak affinity for antitoxin they were called epitoxoids. It was found, however, that they possessed a rather constant though low degree of toxicity and that the toxic action was characteris- 82 INFECTIOX AX J) IMMLMTY. tic. Injection was followed b)' some local edema, Toxon. ^^^^^ ^y ^ ^^^S incubation period, and finally by cachexia and paralysis. On account of this char- a.ctcristic toxic action and the long incubation period, Ehrlich has concluded that the so-called epitoxoid is in reality a second toxin which is se- creted by the diphtheria bacillus. This he now designates as toxon^ in order to distinguish it from that other constituent of diphtheria bouillon, the toxin, which causes the acute phenomena of diph- theria. Protoxoids. Lot ouc uow add still sniallor amounts of the antitoxin unit to the 200 binding units of the toxin. When 149/200 are added it is found that a certain amount of true toxin remains free, the quantity which is unbound being in direct propor- tion to the amount of antitoxin withheld. Conse- quently when but 50/200 antitoxin unit is added the amount of free toxin corresponds to 100 bind- 1. The existence or non-existence of toxons has created a great deal of discussion among investigators. The Swed- isli chemist, Arrheniiis, lias recently attempted to apply oen.ain principles of physical chemistry to the study of toxins and antitoxins. It is a v/ell-known fact that some chemical substances, when in solution, have the power of breaking up into their constituent parts: thus sodium clilorid breaks np in part into sodium and chlorin, as so- dium or chlorin Ions or electrolytes. The dissociated so- dium or chloi-in may then enter into combination with any other suitable substances which may be present. Arrhenlus holds that this is the case with the toxin-antitoxin molecule, that it may to a certain extent again break up into sep- arate toxin and antitoxin. He believes that this dissociated toxin is the substance which Ehrlich has been calling toxon. Madsen. who formerly had done much work with toxons, has now joined with Arrhenius in support of the dissociation theory. In spite of the reasonableness of this theory, Ehrlich and his followers continue to uphold the toxon as an independent toxic substance, and have pub- lished additional experiments to support their position. J'JiOTOTOXINS, ETC. 83 Jng units. If true toxin only remained it could then be said that the constitution of this toxin is : toxin 150 and toxon 50. However, it may be found that as 49/200, 48/200, etc., to 0/200 anti- toxin unit are added, no increase of free toxin is found, although the antitoxin added has been bound. In this case, the 50 binding units of toxin which have the greatest affinity for antitoxin are non-toxic; i. e., they are toxoids, and since they have the maximum affinity for antitoxin they are called protoxoids. . It has been assumed also that a toxoid may Syntoxoids. exist which has an aihnity for antitoxin exactly equaling that which toxin possesses; this, as yet purely hypothetical constituent, bears the name of syntoxoid. Figure 1 is a grapliic representation of the toxin just described (Madsen). Probably no two toxins have the same constitution. The toxon zone, for example, could well be much larger in one diphtheria toxin than in another. Eefinements in experimentation show that even Proto-, ^ Deutero- and the true toxin is not uniform in its virulence and Tritotoxins. its affinity for antitoxin. Accordingly a proto- toxin, a deuterotoxin and a tritotoxin may be rec- ognized by this same partial saturation method. (See Fig. 2.) For example, it may be found that when a portion of the antitoxin unit, between the limits of 149/200 and 125/200. is withheld, a toxin is left free which is less virulent than that re- maining free between the limits of 124/200 and 100/200 ; and from this point on the new unbound toxin may be still more virulent. The first would be tritotoxin, the second deuterotoxin and the third prototoxin. 84 lyFECTIOK AND IMMUNITY VTotot{>;(o( Jo to 10 i» n to f« /«> 110 1X0 /to /yj /fo Ao /7» /»* /f« l«o Fiiiuro 1. i i m w//i'M i 'm 7~o >f o n e ^ toxt-n , Figure 2. ^ JJfutero- yz-ti- ■ t ioxcn> p Figure 3. TratatoxoiJ g^eutfrp JTritotoxoidj a oxone 2huTerQ- TritoToxin |9 Tox( n ■_■ p Figure 4. Figures 1, 2, 3 and 4 are taken from Aschoff's "Bhr- llch's Seitenkettentheorie. etc.," Ztschr. f. Allgem. Physiol., vol. i, 1902. Figure 1 is a toxin spectrum worked out by Madsen. Figures 2, 3 and 4 are spectra representing the changes in qualitative and quantitative structure which a toxin may undergo with age, as described in preceding para- graphs. ORIGIN OF ANTITOXIN. 85 The "spectrum" of a toxin changes with its age. The prototoxin, and portions of the deutero- or tritotoxin maj^ disappear because of toxoid forma- tion. Such changes have led to the recognition of an alpha and a beta modification of the toxin. The alpha modifications of all three toxins readily become toxoids. Only the beta modification of the deuterotoxin remains constant. The toxon also remains relatively intact (Figs. 2, 3 and 4). This very complicated method of investigation was also undertakeai by Madsen in the study of tetanus toxin, for which a somewhat similar "spectrum" was constructed. Such spectra have not been worked out in de- tail for some of the vegetable toxins, as ricin and abrin, but it is known that they form toxoids. Snake venom differs from the bacterial toxins in structure (See Part II, Chapter III). The idea was originally advanced that antitoxin The Formation was transformed toxin, a change in the latter hav- ing been effected through some action of the tissues. In that case, the amount of antitoxin pro- duced should be roughly equivalent to the amount of toxin injected. This, however, was found not to be the case. A single injection of tetanus toxin may yield 100,000 times the amount of antitoxin necessary to neutralize the toxin injected. An in- teresting experiment is on record which shows the fallacy of the view just mentioned. An animal, the serum of which was rich in' antitoxins, was bled repeatedly until an amount of blood which equaled the total quantit;\^ normalh^ present in the animal's body was drawn. Yet the antitoxic power of the new formed blood was practically un- changed. 8{j IXFECTIOy AND IMMUNITY. Ehrlich's "Side-Chain" Theory. Receptors. Multiplicity of Receptors. Met-chnikoff, to explain this "overproduction" of antitoxin, has suggested that the toxin molecules may be taken up b}' phagocytic cells and broken up into an indefinite number of smaller molecules, each of which then is altered in some obscure man- ner so as to constitute a molecule of antitoxin. The views of Ehrlich have found wide accept- ance, and have provided a valuable working h)-- potliesis for many investigations. A considera- tion of this subject introduces one at once to the well-known side-chain theory of immunity of Ehrlich. It may be considered briefly at this point, in so far as it involves the origin and nature of antitoxin. Ehrlich considers it fundamental, in regard to the metabolic activity of cells, to assume that the cell constituents must enter into chemical combination with food substances in order that the latter may be made available for the use of the cell. It is supposed that cells contain cer- tain atom groups of unknown chemical nature which make possible the binding of food sub- stances. The name of receptor was given to such groups, since substances are received into the cell through them. Inasmuch as the foods and some other substances which penetrate the cells differ in their chemical nature, it is probable that there are various receptors for the various types of sub- stances. The binding, however, is but a prelimi- nar\^ step to profound changes which the substance may next undergo, through the action of other, more vital, cell constituents. That is to say, the receptor is but a link to bring the substance into relationship with the vital activities of the cell, which Ehrlich supposes may reside in a hypotheti- cal "Leistungsl-prn^ (action center or nucleus). ACTION OF TOXINS. 87 In view of this conception one readily un(]erstands the propriety of considering the receptor as a side- cbain of the "Leistungslccrn," jiLst as the chemist speaks of the various cronps Avhich may be at- Side-Chains. Fig. 5. — Graphic representation of receptors of the first order and of toxin uniting with the cell receptor, a. Cell receptor ; 6, toxin molecule ; c, haptophore of toxin mole- cule ; d, toxophore of toxin molecule, e, haptophore of the cell receptor. From Ehrlich's "Schlussbetrachtungen," Nothnagel's System of Medicine, vol. viii. This cut is not to be taken as representing the actual morphology of toxins or cell receptors. Nothing is known of their morphology, if, indeed, they have any. The cut is intended merely to represent, in a graphic manner, the supposed chemical structure and mode of action of these substances. This statement applies also to Figures 6 and 7. tached to the benzol ring, or benzol nucleus, as side-chains (See Chapter XV). In preceding pages it has been emphasized that Action of a toxin, in order that it may injure a cell, must enter into chemical combination with its constitu- 88 . INFECTION AND IMMUNITY. ents, and it is a fundameutal tenet of the Ehrlieh theory that this union is one which takes place between the toxin and a cell receptor (side-chain). Tlie cell receptor, then, either is a haptophore or possesses a haptophore as a part of its complex. As the physiologic demands are probably re- sponsible for the character of the various recep- tors, it is not likely that special receptors are created when some unusual substance, as a bac- terial toxin, is introduced into the body. Conse- quently, when toxin unites with a cell, it probably occupies receptors which, under normal circum- stances, are employed in some physiologic process. If some inert, non-toxic substance should com- bine extensively "with cells, a corresponding num- ber of receptors, which ordinarily are used for normal metabolism, would be thrown out of func- tion. Union of this nature would be equivalent to an injur\^ of the cell, and it is possible that the action of toxoids is of this mild nature. When toxin unites with cells there is involved not only the diversion of cell receptors from their customary functions, but in addition the destruc- tive action of the toxin on the vital parts of the cell (perhaps on the "Leistungshern") . The more toxin introduced, the greater the number of cell receptors bound, and the greater the injun^ to the cell. Hypothesis In casc a non-fatal amount of toxin lias been bound, but sufficient to cause some injury, how does the cell respond to the injury? Weigert, a few years ago, gave expression to a hypothesis which is held to have some bearing on this ques- tion. In studying regeneration following injury he concluded that tissues have the tendency to STRUCTURE OF ANTITOXIN. 89 reproduce not only to the extent of making good the injury, but that an excess of new tissue re- sults. The clearest example of this occurrence is that of scar formation, in which a seeming excess of new connective tissue cells is formed, . which later disappears in part. Similarly, when of side-chains. a non-fatal amount of toxin unites with the receptors, a cell defect or injury is created. The cell has for practical purposes lost so many recep- tors. This loss affects the vital activities of the cell, the "Leistungshern" and new receptors, iden- tical with those occupied, are reproduced. Follow- ing the law stated, they are reproduced in excess of the number injured, and the excess may be so great that the cell may be overfilled with them — so overfilled that many are discharged and reach the general circulation. These cast-off receptors, or side-chains, still retaining their power of unit- ing with toxin, constitute our antitoxins. As Behjnng has stated it, the receptor, when attached to the cell, is. the agent through which the latter is attacked, but when cast off from the cell becomes its protector (Fig. 5). As" regards the structure of the antitoxin (cast- Receptors of ~, I \ .. • , in the First Order. on receptor), it is necessary to assume only the presence of the proper haptophorous .group. Ehr- lich designates all receptors of this simple type as "receptors of the first order." In following sections we will have to do with receptors of the second and third orders. Wassermann gives the following list of anti- toxins: ANTlTOXIIs^S FOR BACTERIAL TOXIXS. Diphthei'ia antitoxin. Tetanus antitoxin. 90 IXFECTIOX AXD JMMUMTY. Botulism antitoxin. P3'0cyanens antitoxin. Symptomatic anthrax antitoxin. Antileucocidin, an antitoxin for the leucocytic poison of the staphylococcns. Antitoxins for the blood dissolvino: toxins of a number of bacteria. ANTITOSINS FOR ANIMAL TOXINS. Antlvenin for snake poison. Antitoxin for scorpion poison. Antitoxin for spider poison. Antitoxins for certain poisons of fish, eel serum, salamander, turtle, and for wasp poison. ANTITOXINS FOE PLANT TOXINS. Antiricin, for a red blood corpuscle poison of the castor oil bean. Antiabrin, for a similar poison of the jequirity bean. Antirobin, for robin, a locust tree poison. Anticrotin, for crotin, a toxin froni the bean of Croton iiglium, the croton oil bean. Hay fever antitoxin, for the toxin of pollens \\'hich cause hay fever. ANTTFERMENTS. Antirennet. Antipepsin. Antitrypsin. Antiiibrinferment. Antiurease, for urease, a urea splitting- ferment. Antilaccase. Antityrosinase. Antisteapsin. Antiferments agvainst the ferments of bacterial cultures. OTHER ANTlTOXlNf^. 91 The above are true antitoxins. There are other substances, however, which occasionally exert an antagonistic action on toxins, although they prob- ably are not true antitoxins. For example, it has been found that cholesterin neutralizes the action of tetanolysiin, the hemolytic toxin of the tetanus bacillus. The discovery of Hektoen that certain salts are able to neutralize the toxic action of some serums, by combining with the so-called complement, may also be mentioned in this connection. CHAPTER IX. Specificity. Wjdal and Griinbaum. Normal Agglutinins. THE PHENOMENON OF AGGLUTINATION. Agglutination, in the bacteriologic sense, refers to the clumping and sedimentation of a homogene- ous suspension of micro-organisms by the action of a serum. Although a number of investigators had ob- served the phenomenon of agglutination, Gruber and Durham first saw its significance. They found that the reaction was a specific one, i. e., that the serum which would cause the strongest agglutina- tion of a micro-organism was that of an animal which had been made immune to it by repeated injections. Widal's service consisted in the utilization of the phenomenon as an aid in the diagnosis of typhoid fever. He is the originator of clinical serum diagnosis. It is perhaps largely a matter of acci- dent that we speak of the Widal reaction rather than the Griinbaum reaction. Griinbaum was car- rying on the same work at the same time, but Widal preceded him in the publication of his more extensive work. In the chapter on natural immunity it was stated that normal serums often are able to ag- glutinate bacteria. ISTormal human serum may ag- glutinate the typhoid, colon, pyocyaneus, and dys- entery bacilli, and occasionally the staphylococcus and cholera vibrio; it does not agglutinate the streptococcus and some other organisms. In cer- tain cases it may agglutinate the typhoid bacillus NORMAL AND IMMUNE AGQLUTININH. 93 even when the serum is diluted to one in thirty, a point of practical importance in the clinical use of the test. When a normal serum is found to liave a high agglutinating power, a previous infection by the micro-organism is to be thought of. This pos- sibility receives emphasis from the fact that the serum of a new-born child is devoid of many of the agglutinins which are found in later life. Hence, of the so-called normal agglutinins, many, after all, may be acquired properties. The term immune agglutinin is applied to the agglutinating substance in a serum, when the property has developed as a result of infection, or of systematic immunization with the organism. They are formed during infections with the organ- isms of typhoid, cholera, dysentery, plague, etc. For the artificial production of agglutinins, the bacteria may be injected into the veins, subcutane- ous tissue, or peritoneal cavity ; in some cases they may be fed to animals, rubbed into the skin, or sprayed into tlie lungs. If certain micro-organ- isms are sealed up in a collodion sac and placed in the abdominal cavity of an animal, an agglutinat- ing serum will be formed ; the necessary substances diffuse through the sac and reach those body cells which produce the agglutinin. It is not necessary that living bacteria be injected ; in fact, the strong- est agglutinin is said to be formed by the injection of bacteria which have been killed by a tempera- ture of 62 C. In certain instances agglutinins are produced by immunization with disintegration products of bacteria or with bacterial extracts. Nearly all bacteria, even when non-pathogenic, will give rise to agglutinating serums when in- jected ; but not all have the power equally. Mcolle Immune Agglutinins. Agolutinin Producing Organisms. 04 INFECTION AND IMMUNITY. and Trenell distinguisli three groups of bacteria in regard to their aggiutinability by the homolo- gous antiserums.^ The first group includes easily aggiutinable organisms, for the most pathogenic: Typhoid, dysentery, cholera, plague, glanders, and the colon, psittacosis, pyocynneus bacilli, and B. enteritidis. Tliey yield agglutinating serums read- ily either as a result of infection or by immuniza- tion. The second group comprises organisms which, during infection or convalescence, do not cause the formation of agglutinins, but may be forced to do so by systematically injecting them into animals. In the third group are included those which, even during prolonged immunization, rarely cause the formation of agglutinating serums: the Friedlander bacillus. These facts may be taken as an index of the diseases in which we may expect to obtain the agglutination reaction by the serum of the patient. Variations in The degree of agglutinating power which may Agglutinogenic , i , • -, ^ • *" . , . ^ . ,-, ^-r ' Power of be obtained by immunization varies greatly, van rganisms. ^:|^^. Yg^(:]g gpeaks of a tjQDhoid serum which in a dilution of one in one million was agglutinating, and Durham had a cholera serum which was ef- fective in a dilution of one in two millions. Such powerful serums are rarely obtained. Even two different strains of the same organism may differ in their ability to cause the formation of agglutinins. It is generally said that a typhoid strain, which is agglutinated with difficulty, gives rise to a weak agglutinating serum, while an easily 1. The homologous organism for a typhoid serum, for ex- ample, is the typhoid bacillus, and vice versa ; other organ- isms, or other serums, are heterologous. These are commonly used terms. DISTRIBUTION AND VARIATIONS. 95 agglutinable strain gives a strong agglutinin. The logic of this will become apparent when we con- sider the nature of the bacterial substance which causes the body to produce agglutinin. That the agglutinating power of the serum of a variations in i 1-1 ^- 1. • T 1 J. 1 • £ 1. Quantity of typhoid patient varies irom day to day is a tact Agglutinin. of practical importance. It may be thirty times as strong one day as the next, and may even disap- pear entirely for a day or two. Hence the impor- tance of making more than one test in a suspicious case, when the first trial has been doubtful or negative. There is no adequate explanation for this great variation. It is said that mixed infec- tions, intestinal hemorrhage, or a sudden pouring out of t}^hoid bacilli into the circulation may cause a reduction in the agglutinating power. This occurrence has an important bearing on the possi- bility of using the agglutinating power of the serum as a prognostic sign. Although it has often been noted that in fatal infections agglutinins may be absent from the serum, the variations just men- tioned indicate that prognosis could not be based safely on the result of a single agglutination test. The agglutinating substance is found in the Distribution of highest concentration in the blood serum, but it in^Bo"dy?'"' may be demonstrated in the various body fluids and in extracts of the organs ; it is said to be par- ticularly rich in the milk. It is present in the serum of an artificially produced blister, and it has been recommended that blistering be resorted to in order to obtain serum for the test. The bile often agglutinates the typhoid bacillus, but the power has no necessary relationship to a pre-exist- ing infection ; it is possible that the agglutination in this case is due to obscure chemical causes 90 IXFECyi'WX AND IMMIMTY. Inheritance. Agglutination and Immunity. rather than to the usual serum agghitinin. The administration of pilocarpin causes a rise in the agghitinating power of the tears, sputum and some other body fluids; the drug increases cell secre- tions. "When typhoid fever occurs during pregnancy, agglutinins may appear in the serum of the fetus. On the one hand it has been held that agglutinin passes from the mother to the fetus, or, on the other hand, that the presence of agglutinins arises from infection of the fetus itself. Although the milk may be very rich in agglu- tinin, it is doubtful if the serum of a breast-fed child undergoes much increase in its a2:2:lutinating power because of the ingestion of the milk. The intestinal Juices (trypsin) digest agglutinin?. The origin of agglutinins in the animal body is not loiOT^m. One of tlie most interesting and important phe- nomena in the study of immimity is the so-called Pfeiffer reaction. An animal which has been rendered immime to cholera by repeated injections of cholera vibrios has the power of digesting or dis- solving the latter when they are placed in the fresh serum or in the peritoneal cavity of the immunized animal. Gruber and Durham were studying this phenomenon in the test tube when they first ob- served the agglutination reaction. It was found that the agglutinating property, as well as the bac- tericidal power, was the result of immunization. Inasmuch as an increase in the bactericidal power of a serum points to the existence of an acquired immunity, the question naturally arises : Does the associated property of agglutination have a similar significance ? RELATION TO IMMUNITY. 97 Many observations indicate that the two activi- ties are distinct; that they depend on different substances in the serum. The following are the important points involved: 1. The bactericidal power is destroyed at 56 C, while agglutinins resist a temperature of 62 C. 2. In certain cases it has been possible to cause the bacteria to absorb the agglutinin from the serum, leaving the bactericidal substance intact. 3. A serum may be bactericidal, but not agglu- tinating. 4. During the course of natural or experimental typhoid fever or cholera the development of the agglutinating and bactericidal powers may not be parallel. In cholera, the agglutinating power may disappear soon, but the bactericidal power remains for a long time. 5. Micro-organisms which have been killed by a bactericidal serum may lose their toxicity; ag- glutinated bacteria remain virulent. Besredka found an apparent relationship be- tween agglutination and immunit}^; if t3^phoid bacilli were agglutinated before they were injected into the abdomen of a guinea-pig the animal would recover, but if they were not agglutinated death resulted. The explanation offered for this loss of virulence is that the bacilli being agglutinated and immobilized are more readily taken up by the phagocytes; if phagoc^^tosis is inhibited by some means the agglutinated organisms are found to be still virulent. Koch has attempted to use the agglutination test with the tubercle bacillus as an index of im- munity against tuberculosis. This is not accepted as a reliable test for the immunity, but is perhaps- 98 INFECTION AND IMMUNITY. Technic of the Agolutinatlon Test. The Bacterial Suspension. a general index of the ability of the individual to form antibodies for this organism. This method was devised inasmuch as the bactericidal action of a serum on the tubercle bacilhi? is not readily de- termined. One may use two methods of determining the agglutination of bacteria: 1. The macroscopic or naked eye observation of the clumping and sedi- mentation of a homogeneous suspension of the bacteria in test-tubes; 2, the microscopic observa- tion of the clumping of the organisms when the latter are mixed with serum and mounted as a "■hanging-drop" preparation.^ ^Vl'len the organism to be tested grows rapidly, it is the custom to use a young culture, one which has grown on an agar surface or in bouillon for from eighteen to tAventy-four hours. Older cul- tures of the typhoid bacillus or of the cholera vibrio are agglutinated with more difficulty than a young culture. If an agar culture is used, the bacteria may be washed from the surface by pour- ing five or ten cubic centimeters of physiologic salt solution into the tube and shaking vigorously ; the resulting suspension is then ready for use. For either the macroscopic or microscopic test it is absolutely essential to have a homogeneous suspen- sion of the bacteria, in order to avoid misinterpre- tations which may be occasioned by the accidental 2. For fi hanging-drop pTpparation it is necessary to have a slide with a saucer-shaped depression on one surface. -A drop of the solution to be examined is mounted on a cover- glass, and the latter is then mounted, drop side down, over the depression and the edges of the cover-glass sealed with vaselin or paraffin. There is ample room for motile organ- Isms to swim about in such a preparation, and the loss of "motility incident to agglutination is readily observed. TECHNIC. 99 or natural clumping of some of the organisms; the tubes should be shaken thoroughly before the emulsions are used. This uniformity of suspen- sion is readily accomplished with such organisms as the typhoid bacillus and cholera vibrio, motile organisms, but when they grow in chains (strep- tococcus) or in coherent masses (diphtheria and tiibercle bacilli) more violent measures must be resorted to. Daily shaking of a liquid culture of the diphtheria or tubercle bacillus is fairly effec- tive, but the medium must be passed through a paper filter before it can be used safely; in this way the larger clumps are removed. Some inves- tigators dry a large quantity of tubercle bacilli, grind them up thoroughly in an agate mortar and suspend the particles in salt solution; the frag- mented condition of the organisms does not inter- fere with their participation in the reaction. One should have a uniform technic in preparing a bac- terial emulsion in order to obtain as nearly as pos- sible the same number of bacteria in a given vol- ume of solution, on different occasions. For exam- ple, one may uniformly suspend a twenty-four- hour agar culture in ten cubic centimeters of salt solution. A uniform technic makes it possible to observe the quantitative relationship which exists between the mass of bacteria to be agglutinated and the agglutinating power of the serum. To obtain serum for the test one may resort to To obtain blistering; place a cantharides plaster from one- half to three-fourths of an inch square on the ab- dominal skin, protect it with a dressing, and in about twelve hours remove the serum with a steril- ized hypodermic syringe. Or, one may collect in a small test tube .5 to 1 c.c. of blood from the lobe Serum. 100 INFECTION AND IMMUNITY. of the ear or finger-tip, and draw off the. serum after it has separated by clotting. It is the cus- tom in some well-equipped laboratories to fill sev- eral U-shaped capillar}^ tubes with blood from the lobe of the ear and to separate the blood from the serum at cmce by centrifugation. The custom of drying a few drops of blood on a covorglass or on filter paper, and of sending this preparation to a laboratory for the agglutination reaction, has been practiced quite extensively, and is a justifiable procedure when it is not possible to collect the pure serum. It has the disadvantage that the experi- menter never knows exactly how much blood has been collected, and consequently can not perform the test with exact dilutions of the serum, the im- portance of which will be pointed out l^elow. Tlie red corpuscles and debris in such a preparation also interfere with the clearness of the field in micro- scopic examination, a difficulty which may be partly overcome by filtering the dissolved serum. _ Serum When only a small amount of serum is available, it is necessary to use the microscopic method. Normal human serum, when concentrated, and even when diluted to one in ten or higher, some- times agglutinates the typhoid l^acillus and some other organisms; the same serum, when diluted to one in forty or one in sixty, may not agglutinate. The serum of a typhoid patient, however, or of a typhoid convalescent rarely fails to agglutinate in these higher dilutions. It is generally held that a dilution of one in forty or fifty is sufficiently high to eliminate the possibility of agglutination by a non-t^^hoid serum, and sufficiently low to render the serums of all, or nearly all, t\'phoid pa- tients agglutinating. The necessity for dilution of MEASUREMENT. 101 the serum is emphasized by the additional fact that infections with related organisms, as the colon bacillus, cause a slight increase in the agglutinat- ing power for the typhoid bacillus along with a relatively large increase of colon agglutinins. A test with a low dilution of this colon serum might give a positive reaction with the typhoid bacillus and lead to an incorrect interpretation; but if a dilution of one in forty were used, the non- agglutination of the typhoid bacillus would speak against a typhoid infection. This will be consid- ered under "group agglutination'^ (Chapter X). A convenient method of measuring small The "Loop" , . -, , -, . ^ . Measurement. amounts of culture and serum is by means of a fine platinum wire which is bent at its tip to form an eyelet or "loop."^ If one places one loop of serum into a small watch glass or hollow-ground slide, and adds nine loops of bouillon or of salt solution, a dilution of one in ten is reached. Five loops of this mixture with five of the diluent gives a dilution of one in twenty. One loop of the sec- ond dilution, to which is added one of the culture suspension, gives the desired dilution of one in forty. The last may be mixed directly on the coverglass, and then inverted on a hollow-ground slide. It is readily seen how with even a minute quantity of serum, one may make the test with di- lutions of one in ten, one in twenty, one in thirty, one in forty, etc., details which are necessary for a correctly performed test. It is important that in the different dilutions the same amount of bac- terial emulsion be used. 3. PfelfEer Introduced a conventional "loop" of such dimensions that it holds 2 milligrams of bacterial cells as they g^re taken from a solid surface, like that of agar. 10-J INFECTION AND IMMUNITY The Microscopic Reaction. The Macroscop- ic Reaction. In the macroscopic test, more serum is neces- sary, though the quantity need not be large, and the dilutions are made in test tubes of suitable size. One should always deal with definite quan- tities of the serum dilutions, and should always add the same amount of bacterial emulsion in tlie various tubes involved in a test. If agglutination occurs in the microscopic prep- aration described above, one sees, with the high power, in the course of from fifteen minutes to a lialf-hour, that two or more micro-organisms whicli come in contact have a tendency to remain in this position. In the case of a motile organism (typhoid) the movements may be exaggerated for a time. In the course of the next few hours, other cells are added to incipient groups and new groups originate. Motility becomes less and less and event- ually ceases, in a characteristic reaction. The maximum change has taken place in from six to eight hours. Not less than four or five cells which are permanently agglutinated are considered in- dicative of a positive reaction; the test is most decisive when large masses are formed, so large that they are seen readity with a low magnification. A similar preparation to which no serum has been added should always be made, in order to eliminate spontaneous or "auto-agglutination" as a possible source of error. In a macroscopic test, the uniform cloudiness of the mixture of serum and hacteria becomes changed by the formation of smaller and larger flakes or clumps of bacteria, which in the course of a few hours sink to the bottom as a white precipi- tate, leaving a clear overlying fluid. Here also a UNIT OF A(J(1LUTININ. 103 control tube, to wJiicli no scrinii lias been added, should be preserved for comparison. The body temperature, which may be obtained in a thermostat, facilitates the reaction. The value of an agglutinating serum can not be expressed in units with the exactness that is at- tained in measuring diphtheria antitoxin for the following reasons : 1, The limits of the reaction are not sufficiently definite ; 2, a given mass of bacteria has the power of absorbing varying amounts of the agglutinating substance, depending on the con- centration of the latter; and 3, it is impossible to obtain standard bacterial emulsions. One may arbitrarily decide on a unit similar to that of Zilpnik, in which a serum which is able to agglutinate a given mass of bacteria in a dilu- tion of one in forty is taken as the standard. If a similar amount of a serum aggkitinates in a di- lution of .1 in 120 it is said to be of threefold strength. The value of the agglutination reaction as a clinical diagnostic aid will be considered later in connection with the individual diseases. A consideration of agglutination would be in- complete if one did not mention the phenomenon as it occurs with cells other than those of bacteria, in particular the red blood cells. The serums of many animals, as stated in a previous chapter, are toxic for the erythrocytes of some other species. In some instances, the corpuscles lose their hemo- globin under the influence of the serum (hemoly- sis) ; in other instances, or even with the same serums, the corpuscles are throAvn into clumps and settle to the bottom of the test tube, leaving a clear overlying fluid. The analogy with the bacterial The Agglutinin Unit. Agglutination of Red Blood Corpuscles. lOi INFECTION AND IMMUNITY. agglutinins goes still further, in view of the fact that the formation of these 'liemagglutinins" may be induced artificially in the body of an ani- mal by the injection of erythrocytes from another species. An animal does not form agglutinins for its own cells (auto-agglutinins), and rarely, if ever, for the cells of another member of the same species (iso-aggiutinins). "Wliat is said in the next chapter concerning the specificity of the bac- terial agglutinins also holds for the hemaggluti- nins. Plant Hemag- Certain plant toxins, true toxins with hapto- phorous and toxophorous structures, agglutinate red blood cells: ricin, abrin, crotin, etc. Some of the earliest and most important work which Ehrlich has done in the field of immunity was ac- complished with these plant toxins. glutinins. CHAPTEE X. THE NATURE OF THE SUBSTANCES CONCERNED IN AGGLUTINATION. Two substances are concerned in agglutination : Terms. one, the active or agglutinating substance, exists in the serum, while the other, the substance acted on or the agglutinable substance, is present in the bacteria. The agglutinable substance is generally supposed to be passive in the reaction, while the agglutinating property seems to possess a ferment- like element, which acts on the agglutinable sub- stance. Agglutinin, the term used in the preced- ing chapter, is now generally applied to the sub- stance in the serum. Eecently the bacterial con- stituent has been called agglutinogen, because of the belief that the agglutinable substance, when introduced into the animal body, stimulates the latter to the formation of agglutinin; hence ag- gutinogen means, not agglutination-producing, but agglutinin -producing. These shorter terms will be used for the sake of convenience. The presence of agglutinogen in an organism AggiutiaogRn. may be demonstrated in three ways : 1. The mere fact of its agglutinability by a serum is evidence of the presence of an agglutinable substance. 2. If during infection or immunization the serum ac- quires agglutinating properties, the bacterium pos- sesses an agglutinogenic substance. 3. If a cul- ture is mixed with a serum containing the specific agglutinin, and after a period of contact is re- moved by centrifugation. the resultant disappear- lOG IXFECriON AND IMMUNITY. Distribution of Agglutinogen. The Precipita- tion Reaction. ance of agglutinin from the scrum, which may be demonstrated, shows that something in the bac- teria (agglutinogen) has combined with the ag- glutinin. The location of agglutinogen in the bacterial cells has received some discussion. There is a tend- ency to believe that it exists in the cell envelope or perhaps on its surface. It appears to be formed in the cell, and, in some cases, it may be excreted into a surrounding medium; certainly when bacteria die and disintegrate agglutinogen is liberated. The filtrates of certain cultures (entirely free from bacterial cells), when injected into animals, will cause the formation of agglutinins. Also, just as a micro-organism is able to absorb agglutinin from the corresponding antiserum by a process of chemical union, so a filtrate of the type mentioned is able to neutralize the agglutinating power of the serum. In these instances agglutinogen becomes free as a consequence of disintegration of some of the iDacterial cells. The filtrates of certain cultures exhibit another phenomenon when they are mixed with their spe- cific antiserums; this has to do with the bacterial precipitins of Kraus. If, for example, the filtrate of an old typhoid bouillon culture is mixed with antityphoid serum, a distinct precipitate is formed which eventually settles to the bottom of the tube. This is a specific reaction, and does not occur if the filtrate is mixed with some other immune serum. It is thought by some that this so-called precipi- table substance in the filtrate is identical with the agglutinable substance (agglutinogen), but this point is still the subject of investigation. Agglutinogen may be extracted from micro- AOaLUTlNOGEN AND AOULUT/NIN. 107 organisms by chemical processes. The presence of the substance in the extracts becomes manifest when immunization with them causes the forma- tion of an agglutinating serum. This, again, is the "test of immunization." The agglutinogen of one bacteriiim is not iden- tical with that of any other. If they were identi- cal, immunization with the one would yield an ag- glutinating serum of equal power for both cells; this, however, is not the result obtained. On the other hand, the agglutinins of two difEerent organ- isms may coincide to a certain degree, as will be shown under the subject of "group agglutination." Certain experiments gO' to show that the agglutin- ogen of even a single micro-organism is not uni- form substance. One portion is heat-susceptible, being destroyed at 63 C, while another portion is said to resist a temperature of 165 C. Such tech- nical questions continue to be investigated. Agglutinogens are said to pass through semi- permeable membranes, while agglutinins do not. Smith and Eeagh distinguish two kinds of ag- glutinogen in those bacteria which possess fiagellge, one peculiar to the cell body, and the other to the flagellse. Agglutinin may be precipitated completely from a serum by the sulphates of magnesium or ammo- nium, when the salts are used in proper concentra- tions. Because of their reaction to such precipi- tating agents, agglutinins are thought to belong to the globulin fraction of serums ; whether globulins or not, they are precipitated with them. Agglutinins resist digestion with pepsin and papayotin, but are destroyed after prolonged ex- posure to the action of trypsin. An agglutinating Multipficity of Agglutinogens. Flagellar and Somatic Agglutinogens. Properties of Agglutinins. 108 IXFECTION AND IMMUNITY. Structure of Agglutinogen. Structure of Agglutinin. Zymotoxic Group. scrum which is dried and kcjDt free from moisture and the action of light retains its power unaltered. Similar to agglutinogen, agglutinin is thought not to be a uniform substance, one portion being sus- ceptible to heat, and another portion resistant; these have been called alpha and beta agglutinins. It is convenient to speak of the reaction between agglutinin and agglutinogen, and of the process in the body through which agglutinins are formed, in terms of the side-chain theory. Accordingly, if that constituent of micro-organisms which we have termed agglutinogen is the substance which stimu- lates the tissues to form agglutinin, we must as- sign to it a haptophorous group through which it may unite with the receptors of the tissue cells. This haptophore comes into play again in the union between agglutinogen and agglutinin, which pre- cedes agglutination. There is no reason for as- signing to agglutinogen any other structure than this single haptophore ; it is a passive bod}^, similar to antitoxin, and has no other function than that of uniting either with cell or with agglutinin. Agglutinin also must have a haptophorous or binding group, inasmuch as it enters into combina- tion with agglutinogen. In addition to this bind- ing group, experiments have showm that agglutinin possesses a toxic constituent, which is analogous to the toxophorous group of the toxin molecule. In this case, however, it is called a zymotoxic, zymophorous or agglutinophorous group ; suppos- edly it has a ferment-like activity (Fig. 6). The analogy with toxins goes further, in that the zATuotoxic group of agglutinin may degenerate or may be destroyed, leaving the haptophorous group with its binding power for agglutinogen practi- A0GLUTIN0ID8. 109 cally unaltered; these are agglutiuoids, just as Aggiutinoids. toxins when changed in a similar way are called toxoids. A serum which is rich in agglutinin may be changed into one rich in agglutinoid by expo- sure to a temperature of from 60 to 75 C, and by the action of acids or alkalies; the change also takes place spontaneously in the course of time, when the agglutinin is in solution. Agglutinoids are detected by methods analogous to those used in the recognition of toxoids. If toxoids unite with all the antitoxin in a solution, there naturally remains no antitoxin to unite with true toxin which may be added subsequently. Sim- ilarly, if all the agglutinogen in a mass of micro- organisms has united with inactive agglutinoid, agglutinin which is added subsequently would have no point of attack and the reaction of agglutina- tion would not occur. So we may say that when bacteria are treated with a serum which has lost its original agglutinating power, and the bacteria are thereby made insusceptible to the action of a fresh agglutinating serum, the former serum con- tains agglutinoids. Sometimes it is found that even a fresh serum, Proaggiu- when concentrated, will cause less agglutination than when diluted. This has been referred to the presence of agglutinoids which have a stronger affinity for agglutinogen than has the agglutinin; when of this character they are called proagglu- tinoids, and accordingly are analogous to the pro- toxoids mentioned earlier. As the serum is diluted the concentration of the proagglutinoids becomes less, and at a time when they are so dilute that they have no influence on the reaction, the agglutinins 110 INFECTION AM) IMMUNITY. Two Stages in Agglutination. Group Agglutination. are still present in such quantity that tion is brought about. The presence of some salt is necessary agglutina- for the occurrence of agglutination. Bordet found that if the salts were removed from the serum and from the suspension of bacteria by dialysis, and the two were then mixed, agglutination did not occur; if a small trace of sodium chlorid was added the re- action took place promptly. Furthermore, if the serum was completely removed from the bacteria by repeatedly washing them in distilled water, it was found that the microbes had absorbed the ag- glutinin, but the latter remained inactive until the salt was added. This experiment not only suggests a haptophor- ous as distinguished from a z^^motoxic group, but also indicates that agglutination consists of two phases. The first phase represents the union of agglutinin vrith the bacteria, while in the second are included the other changes necessary for the clumping of the organisms, in which the activity of the ZAanotoxic group is represented. The action of the salt, just cited, is unknown. The properties of serums which are of interest in immunity are now being studied by chemists, notably by Arrhenius. The study of mass action, of chemical equilibrium between agglutinin and agglutinogen, for example, and of the dissociation of the compound after it has once formed, are subjects under investigation, but which are too technical to be entered on here. "Group agglutination" has been referred to. By this is meant the ability of an antimicrobic serum to agglutinate certain other organisms which mor- phologically, biologically and often pathogeneti- GROUP AGGLUTINATION. Ill cally, are closely related to the homologous bac- terium. In these instances, the agglutinating power is greatest for the homologous organism, and the degree to which the heterologous organisms are agglutinated is, to some extent, an index of the proximity of the relationship of the latter to the former. Antityphoid serum has been found to agglutinate the psittacosis, colon, paracolon, and paratyphoid bacilli and Bacillus enteritidis, but the action is never so strong as on the typhoid bacillus itself. We are to understand that this power to agglutinate related organisms represents something more than the normal property of the serum; there has been an actual increase in agglu- tinin for the heterologous bacteria as a result of infection or immunization by the primary organ- ism. Having typhoid fever in mind, this is a rule which works both ways. Infections with the colon bacillus and related organisms, and sometimes with organisms not closely related, as the staphylo- coccus, may cause an increase in agglutinin for the typhoid bacillus. The importance of this fact is evident, and it may explain the positive Gruber- Widal reaction sometimes found in infections other than typhoid. Inasmuch as the highest agglutinating power is chief Aggiutinii always manifest against the homologous organism, finins?"^^^ "' this is spoken of as the chief agglutinin {Haupt- agglutinin) of the serum, while the weaker agglu- tinins for other organisms are called partial or ad- ventitious agglutinins, or coagglutinins {MUag- glutinin). The phenomenon of group agglutination would SpecifichV. seem to violate the specificity which we are in the 112 INFECTION AND IMMUNITY. habit of attributing to the reactions of immunity; yet a reasonable explanation has been offered for the occurrence. It is probable that the proto- plasms of all cells have certain constituents in common, and that the closer the relationship be- tween two different cells the greater is the simi- larity of their constituents. In view of this prob- ability, Durham has used the following illustra- tion in the explanation of group agglutinations : The typhoid bacillus contains certain constituents, agglutinogenic molecules, which one may desig- nate as a, b, c, d, and e; these differ among them- selves in unlcnown respects, but each is able to stimulate to the formation of a corresponding ag- glutinin. The serum, then, would have the ag- glutinin molecules A, B, C, D and E, also differing among themselves, but having at least one property in common — that of causing agglutination of the typhoid bacillus by uniting with the correspond- ing agglutinogenic molecules. In this sense noth- ing could be more specific. The Bacillus enteri- tidis, closely related to the typhoid organism, may possess the agglutinogenic molecules c, d, e, f, g, and h, and following the principle expressed above would stimulate, in the body, to the formation of the agglutinin molecules C, D, E, F, G and H. Inasmuch as the agglutinogens c, d and e are com- mon to the two bacilli, the agglutinins C, D and E, which are present in both serums, would affect either of the two organisms. The typhoid serum, however, would contain five agglutinins for the typhoid bacillus and only three for the Bacillus enteritidis, consequently the action would be stronger against the typhoid bacillus; mutato mu- tandis, the same applies to the enteritidis serum. SEBUM DILUTIONS. 113 The same line of reasoning would explain the in- creased agglutinating power of an anticolon serum for the typhoid bacillus. A further elaboration of this principle may be made in a case in which two different strains of the same organism (typhoid bacillus) have some- what different agglutinogenic molecules; Conse- quently the homologous immune serums for the two organisms might not coincide in their ag- glutinating powers for a third strain of the bacil- lus. In view of the points mentioned, it is clear that importance specificity of a given serum may be determined Dilutions. only by diluting the serum to such an extent that the coagglutinins practically are eliminated, the chief agglutinin being present in so much greater concentration that it is still able to agglutinate the homologous bacterium. Theoretically, it is also important for the spe- cificity of the reaction that the particular strain of the organism to be used for the test correspond in its agglutinogenic molecules or receptors with those of the strain used for the immunization ; the agglutinogenic receptors should be typical for the organism. It is doubtful if group agglutination occurs among all closely related bacteria, inasmuch as Kolle found that it did not exist among the vib- rios. It is thought possible that the multiple agglu- tinating power of a serum may be caused by mixed infections in some instances. Although this is to be kept in mind, one should not overestimate its diagnostic importance, because a similar multi- Mixed Infections. 114 rXFECTIOX AXD IMMUXITY. plicity ma}' result I'rom infection l)v a single micro- organism. Production of Thc explanation of the production of aggluti- ^^''"thrlkh "ii^s by the body, according to the conception of Theory. Eijpiich, Is similar to that already given for the production of antitoxins. That is to say, the ag- glutinin molecules are cast-off cell receptors, the overproduction of which has occurred as a result of their union with the agglutinogenic molecules of the bacteria. The antitoxin receptors were rela- tively simple, having no other demonstrable struc- ture than that of the haptophorous groups through which they unite with the corresponding toxin. Receptors of We have recognized in the agglutinin receptor two Second Order. i i ^ t~ ^ i • groups, a haptophorous and a zymotoxic; conse- quently it must have this same structure when it is still a part of the cell. Ehrlich designates it as a receptor of the second order, which, being de- fined, is a receptor in which a haptophorous and a zymotoxic group exist as integral parts of the molecule (Fig. 6). In accordance with the side-chain theory, the ability of an animal to form agglutinins for a cer- tain organism would depend on its possession of re- ceptors of the second order which are able to unite with the agglutinogenic receptors of the bacterium. It is well established that different animals may not form serums with equal agglutinating powers for an organism. The follovdng is a concrete ex- ample: Wassermann immunized rabbits, guinea- pigs and pigeons with a strain of the colon bacil- lus, and tested the three serums with fifteen other strains of the same organism. The serum of the guinea-pigs readily agglutinated the strain which was used for immunization, but scarcelv affected INAOGLUT/XAJilL/ry. 115 the others. The serums of the rabbits and pigeons also agglutinated the homologous culture, but the coagglutinins which they possessed did not affect other strains equally. Consequently, it was sup- posed that the cells of the three animals contained a limited number of receptors in common, whereas Fig. 6. — Graphic representation of receptors of the second order and of some substance uniting with one of them, c, ceU receptor of the second order ; d, toxophore or zymophorous group of the receptor ; e, haptophore of the receptor ; f, food substance or product of bacterial disintegration uniting with the haptophore of the cell receptor. From Ehrlich's "Schlussbetrachtungen," Nothnagel's System of Medicine, vol. viii. other receptors which were present in one of the animals were largely wanting in the other two. Inagglutinability was mentioned as a charac- teristic of certain bacteria, especially the bacillus of Priedlander. This condition is much more im- portant when it involves an organism which Inagglutinabil- ity of Some Organisms. IIU IM'ECTIOX AM) IMMUXITY. usually is agglutinated with ease. In some in- stances, the typhoid bacillus when freshly culti- vated from a patient, or, indeed, from contami- nated water, has been found to resist agglutination by a strong serum; the same organism after a period of existence on artificial media becomes ag- glutinable. Widal and Sicard noted that often the serum of a typhoid patient would not agglutinate the bacillus which had been cultivated from the patient's own body, although the same serum would agglutinate laboratory cultures. Cultiva- tion of the typhoid bacillus at 42 C. will cause it to lose its agglutinable property, but it may be re- established by subsequent cultivation at lower temperatures. It seems that this variation must be due to some change in the bacteria, i. e., in the agglutinable substance. It is possible that the organism, during its existence in the animal, be- comes immimized against the action of the agglu- tinin just as the animal becomes immunized against the toxic action of bacteria. This condi- tion in the micro-organisms would then be repre- sented by a great excess of agglutinogenic recep- tors, so that a much greater amount of agglutinin would be required to cause clumping. It is read- ily seen how the use of an inagglutinable strain of the t}'phoid bacillus would affect serum diagnosis. Thftoriesof We are to consider that in the phenomenon of agglutination a reaction of a chemical or physico- chemical nature takes place between the agglutinin of the serum and the agglutinogen of the micro- organisms, the actual clumping following as a consequence of this reaction. It is not a "vital'* reaction, for dead bacteria may be agglutinated. Agglutination. THEORIES OF A(J(JLUTINATION. 117 Theories of agglutination have to do, not with the existence of agglutinin and agglutinogen, but rather with the nature of the reaction between the two, and the influences which bring about the clumping after the reaction has occurred. The original theory of Gruber supposed that the serum so affected the bacteria that they became sticky; consequently, as they came in contact, they were, so to say, glued together. Dineur thought changes occurred in the flagells of the organisms, a theory which is untenable because some bacteria are ag- glutinable which do not possess fiagellse. Em- merich and Loew refer agglutination to the action of an enzyme which is produced by the bacterium itself, a theory which is not given general credence. Bordet excludes the vitality or motility of the or- ganisms as factors, and believes that the process is purely a ph5^sical one, because of the fact that some laiown chemical substances may be made to precipitate or to agglutinate certain other sub- stances (precipitation of colloids by salts) ; the theory presupposes some change in the molecular attraction between the microbes and the surround- ing fluid. Other theories have to do with the question of precipitation. As previously stated, when the fil- trates of cultures of certain organisms are mixed Avith their corresponding immune serums, precipi- tates occur in the mixtures. It was mentioned that the substance in the filtrate which takes part in the precipitation may represent, in part, the ag- glu tin able substance which has been excreted by the bacteria. Mcolle supposes that the agglutin- able substance resides in the external layer of the bacteria and that when the serum is added a coag- lis IXFECrfOX Axn immtxity. ulation occurs in tlie envelope, rendering coales- cence with the envelopes of other individuals pos- sible. The theory of Paltauf that the agglutinable substance finds its way to the surface of the bac- terium and is precipitated by its union with ag- glutinin is somewhat similar. The shell of the co- agulated substance accounts for the sticky charac- ter which the envelope acquires, according to the theory of Gruber. Paltauf cites observations which tend to show that some substance actually is extruded from the micro-organisms during ag- glutination, and that in properly stained speci- mens it can be seen as a precipitate surrounding and between adjacent organisms. The multiplicity of theories leads one to suspect that the true nature of the process remains obscure. CHAPTER XI. Precipitins. PRECIPITINS. Because of their scientific importance and cer- tain practical features, the serum-precipitins should receive something more than the incidental mention which has been given them under agglu- tination and in other chapters. In 1897 Kraus discovered that bouillon cultures Bacterial of the organisms of typhoid, cholera and plague, from which the bacteria had been removed by fil- tration, would cause precipitates when mixed with their respective antiserums. The reaction is spe- cific. As stated later, however, this specificity holds only when those quantitative relationships are observed which were found so essential for the agglutination test. The precipitins of Kraus are the bacterial precipitins. He proposed their use for the identification of micro-organisms. If, for example, one has in hand a culture which he sus- pects to be that of the typhoid bacillus, it may be gro^\ai in a liquid medium, the cells removed by filtration, and the filtrate mixed with a Icnown antityphoid serum; if a precipitate occurs when the serum is sufficiently diluted, the reaction indi- cates that the organism in question is the typhoid bacillus. Inasmuch as precipitins are formed dur- ing the course of some infections it may be possible to use them in clinical diagnosis, but for either bacterial or clinical diagnosis the agglutination test is more readily performed and interpreted. 120 INFECTION AND IMMUNITY. Phytoprecipi- tins and Zo- oprecipitins. Lactoserum. Precipitogen, Precipitin and Precipitate. Pli}'toprecipitins are produced by immtmiza- tion with albuminous substances of plant origin, as ricin and albumin from grains, and their action is specific for the homologous substance. Zooprecipitins are obtained by immunizing with animal albumins. Through the work of Wasser- mann and Ulilenhuth, of ISTuttall, and others, it luTs been demonstrated as a general law that im- munization with an albumin from whatsoever source gives rise to the formation of a precipitin which manifests its action only against the par- ticular albumin used for the immunization. Hence, the albumin of a particular serum, in some un- Icnovm respect, is different from that of all others ; it is special to the species. Immunization with milk causes the formation of a precipitin which throws down the casein of the milk used for injection, but not that of milk from another species. The milk of the goat may be differentiated from that of the cow by the use of the lactoserum. Likewise, after the injection of egg-albumin a precipitin is formed which is specific for the type injected. Three substances are open to study in the pre- cipitation reaction. First, the fluid or substance which is used for immunization ; it bears the name of precipitogen, i. e., the precipitin-producing sub- stance. Second, the specific constituent of the precipitating serum, i. e., the precipitin. Third, the precipitate, which is a consequence of the reac- tion between precipitogen and precipitin. We are able to recognize in this instance the actual end- product of a reaction, a condition which is not so easilv realized in other "immunitv reactions." Tt PEECIPiriN. 121 is true, of course, that little has been learned con- cerning the nature of the end-product ; its chemis- try is as dark as that of the proteids in general. As stated in the chapter on "Natural Immun- Formation of ity/' normal serums occasionally have the power *'''^*^""t'"- to cause precipitates in other serums. Precipitins for egg albumin and goat serum have been found in extracts of organs, although at the same time they were absent from the serum of the animal. In this case the active bodies exist in the cells as "sessile receptors/' and by the process of extraction they are brought into solution. During immuniza- tion these same receptors are stimulated to over- production and are thrown into the circulation as free precipitin receptors. The power of forming precipitins may be widely distributed among the organs. This function has been assigned to the leucocytes (Kraus and Leva- diti, Moll), and in one case they were formed locally in the anterior chamber of the eye (v. Dungern. Eomer). For the artificial production of precipitins the precipitinogenous fluid may be injected into the veins, peritoneal cavity or the subcutaneous tissue. Within from four and a half to five days the pre- cipitin has been formed to such an extent that it may be demonstrated in the serum of the im- munized animal. As in the case of agglutinin formation, not all animals have equally the power of forming a pre- cipitin for a given albumin. This point, as re- lated to serum precipitins, is of particular impor- tance, and involves a factor which is of no conse- quence in bacterial agglutinins. In the first place, an animal will not form a precipitin which Concerning Autoprecipi- tins and Iso- precipitins. ill IXFKCTION AM) IM.MCMTY. ' is active against its own serum, i. e., by bleeding an animal and reinjecting the serum a specific pre- cipitin is not formed. If formed it would be an autoprecipitin, and, as a rule, animals do not form antibodies for their own tissue constituents. Again, animals are unlikely to form antibodies for the tissue constituents of other members of the same species; these, when formed, are called iso- bodies. Schiitze immunized thirty -two rabbits with serum from the rabbit and obtained an iso- precipitin from only two of the number. In the third place, animals do not readily form anti- bodies for the tissue constituents of other animals which zoologically or biologically are closely re- lated. Immunization of the guinea-pig witli the serum of the rabbit, a pigeon with that of a chicken, or a monkey with human scrum, are pro- cedures which usually do not yield precipitating scrums. Nature of Chemically, little is laiown of precipitins. They Precipitins. ^^,^ thrown down by ammonium sulphate in con- jimction with the euglobulin fraction of serum, and are destro^'ed by those substances whieli alter al- buminous bodies, as acids, alkalies, pepsin and trypsin. Specific When serum is heated to from 50° to 60° C. its ability to cause a precipitate in the homologous ]n*ecipitogen is destroyed, although it may be dem- onstrated that the power to combine with the lat- ter is unchanged. Hence precipitin, like agglu- tinin, is composed of two groups, a binding or haptophorous. and a ferment-like group in which the active property reside: the latter is the cnag- ulin of the molecule. Wlien precipitin has lost its coagulin it becomes prccipitoid. and as precipitoid Inhibition. SPECIFIC INN fJilTION. 123 it may unite with precipitogen and thoreljy inhibit the action of a fresh precipitin which may be added later. When a precapitating serum has partly degenerated into precipitoids, that is, when it consists of a mixture of precipitin and precipi- toid, it is found that the latter have the greater affinity for precipitogen; hence, in concentrated solutions of the serum, precipitoid may be present in sufficient quantity to bind all the available pre- cipitogen, and the reaction w^ould not occur in spite of the presence of active precipitin. This is spoken of as specific inhibition. The action is analogous to that of toxoids and agglutinoids, and the phenomenon is mentioned again in this in- stance in order to emphasize the fact that certain principles of action are common to many of the immune substances. Precipitoids, like toxoids and agglutinoids, are formed by long standing, by the action of heat and light and by other injurious in- fluences. The molecule of precipitin, like that of agglu- tinin, is a receptor of the second order (Fig. 6). The attempt has been made to produce antipre- Antiprecipitins. cipitins by immunization with precipitating serums ; this is immunization with an immune serum. It is reported that antibodies have been obtained for lactoserum, but not for bacterial pre- cipitins. There is a limit to the cycle of antibody formation. Precipitogen may be defined as any albuminous substance immunization with which will cause the formation of a specific precipitating serum. In addition to those mentioned above, albuminous urine, pleural exudates, ascitic fluid and that from hydrocele are precipitogens. The same is true of Nature of Precipitogen. 124 INFLCTIOX AMJ IMMLMTY. ■ some albuminous fractions of scrums, as globulin. the precipitating serum for which may be called antiglobulin. Kraus believes that the precipitogen of bacterial filtrates is associated with albuminous molecules. Jacoby obtained by tryptic digestion of ricin, a precipitogen which gives no albumin reaction. On the other hand, certain precipito- gens are destroyed by pepsin and tr^npsin, a fact which indicates their albuminous nature. Certain precipitogens are said to consist of a thermolabile and a thermostabile portion, the dif- ferentiation of which we need hardly consider. Precipitoid It is of no little interest that precipitogen, simi- Precipitogen! lar to precipitin, consists of two groups, through one of which it unites with precipitin, whereas the other has a coagulating function. Egg albumin, for example, when heated to rather high tempera- tures, loses its ability to participate in the pre- cipitation reaction, although it retains its binding power for precipitin. Tn view of the fact that the two substances which enter into the reaction have similar structures, it is difficult to say which as- sumes the passive and which the active role. De- generated precipitogen is also called precipitoid. Tn order to distinguish the two precipitoids one mnst speak of the precipitoid of precipitogen. and the precipitoid of precipitin. The precipitoid of precipitogen yields precipitin by immunization; hence, it is all the more analogous to the toxoids. Precipitate. The •|)recipitatc which is caused when a bacterial filtrate is mixed with its specific antiserum forms in from one-half hour to several hours, and appears as a coherent white sediment which in the course of twenty-four hours has left the overlying fluid quite clear. The action of the precipitins for FORENSIC TESTS. 125 serums is more rapid, and in either case sedimen- tation is hastened by placing the fluids at body temperature. As intimated above, the occurrence of the reaction depends on an intact condition of the coagulin groups of both substances. A low concentration of organic acid favors, whereas min- eral acids and alkalies inhibit or prevent precipi- tation ; a neutral reaction is indifferent. The pre- cipitate contains albumin, which, however, has be- come so changed that it is not susceptible to the action of trypsin. The two in combining have in some way shut off the point of attack for tr}'psin. A lactoserum precipitates the casein of the corre- sponding milk. The presence of salts is necessary for the reaction of precipitation. Group precipitation is not so pronounced as group agglutination, yet it exists to a certain de- gree and is of the utmost practical importance in attempting to differentiate serums by the precipi- tation method. Although bacterial precipitins are highly specific, it is important to observe the prin- ciple of serum dilution which was emphasized under agglutination, in order to obtain the adven- titious precipitins in such small amounts that they do not interfere with the chief precipitin. That feature of the precipitation reaction which has the most practical bearing has to do with its medicolegal use in the detection of human blood. For this purpose it has supplanted the specific hemolytic serums, which are to be referred to later. In the course of investigations it was found that even the smallest dried blood stain, although months old, would cause the formation of a sedi- ment when mixed with its homologous precipitat- ing serum. It remained for certain important de- Group Precipi- tation and Specificity. Forensic Use of Precipitins. l-2() IXFECTIOy AM> IMMl XITY tails to be worked out in order to render the test sufficiently reliable for forensic work. The spe- cificity of the reaction appeared to be threatened somewhat wlien it was learned that the serum of monkeys under i i i i i_ • by Cells. combmed action ol amboceptor and complement is necessary for the cytotoxic action of a serum. In view of the fact that the toxic power is lost by ex- posure to that temperature which destroys comple- ment, it seems that the latter is the actual dis- solving or toxic substance, whereas the ambocep- tor must play some intermediary role. Investiga- tions have shown that the two act together in a very definite manner in that the absorption of the amboceptors by the cells is a prerequisite for the absorption and action of the complement. This may be verified by simple experiments. Mix erythroc3i;es with the homologous amboceptors, and after a period of from twenty to thirty min- utes centrifugate the mixture and remove all the free serum from the cells by repeated washings with isotonic salt solution. If the cells are again suspended in salt solution and a small amount of MECEAISIIBM OF HEMOLYSIS. 145 complement is added and thoroughly mixed, the hemoglobin is dissolved out; a control must, of course, show that the complement alone has not the dissolving power. The result indicates that the erythrocytes during their contact with the im- mune serum had absorbed or combined chemically with the amboceptors, and that the latter remained attached to the cells in spite of the washings to which they were submitted. < It would seem that the union of amboceptor Sensitization with cell has the effect of rendering the latter sus- ceptible to the action of complement, and for this reason amboceptor-laden cells are spoken of as sensitized cells. Hence, according to the cells and serums employed, we may refer to sensitized erythrocytes, sensitized bacteria, etc. The experi- ment is called the sensitizing, absorption or bind- ing experiment. An immune serum may be de- prived of all its amboceptors in the binding ex- periment if a sufficient quantity of cells has been used, and it would thereby be rendered incapable for further reactivation by the subsequent addition of complement. If, instead of performing the experiment in the Order of Action T ., T ,1 -, ,11 of Amboceptor manner described, the process is reversed so that andcompie- the corpuscles are first treated with the solution of complement and then with the amboceptors, the corpuscles are not hemolyzed. During the wash- ing process the complement is entirely separated from the cells, and from this fact it is clear that direct union between corpuscle and complement does not occur; only sensitized cells take up com- plement. The question as to whether the corpuscles in taking up amboceptors do so by chemical combina- ment. 14G IX FECI! 0\ AM) IMMIXITY. Cytophilous Haptophore of the Am- boceptor. The Absorption Experiment in the Cold. tion or by physical absorption has been contended with some vigor. Elirlicli believes tliat the process is one of chemical nnion, and if one adheres to this view it becomes necessary to assign binding or haptophorous groups both to the red blood cells and to the amboceptors. In contrast to another haptophore which the amboceptor possesses and which will be described below, that one which unites with the cell is called the cytophilous hapto- phore. The haptophore of the erythrocyte which enters into the union is an essential part of a re- ceptor of the red cell, consequently we say that tlie amboceptor unites with a receptor of the corpuscle. The heating of serum to 56° C. provides one means of apparent isolation of the amboceptor from the complement, but this is not a true isola- tion in that complement is merely rendered inac- tive by the heat rather than totally eliminated. Ehrlich and Morgenroth devised a method liy which the amboceptors may be separated from a fresh immune serum without in any way injuring the complement. This is accomplished by per- forming the binding experiment, already alluded to, at a low temperature. The serum, containing both amboceptors and complement, is cooled to 0° C. or slightly above, by means of a freezing mix- ture of salt and ice. A suspension of the homolo- gous corpuscles is cooled to the same point, the serum is added and the mixture maintained at 0° to 4° C. for fifteen to twenty minutes. At the end of this time the sensitized cells are removed bv immediate centrifugation at a low temperature, and are washed entirely free from serum by the use of ice-cold salt solution. If the low tempera- ture has been adhered to rifforouslv and the w^ork UNION WITH CELLS. 147 done quickly, the corpuscles are not laked during the manipulations in spite of the presence of both amboceptors and complement. Furthermore, the washed sensitized cells remain intact even when their temperature reaches that of the thermostat, whereas if some fresh normal serum or the serum from which the amboceptors were absorbed is added, they undergo hemolysis as readily as when treated with the active immune serum. The original immune serum is now a solution of com- plement, and fresh corpuscles which are added to it are not dissolved because of the absence of ambo- ceptors. These results show the following important facts : Amboceptor and complement exist side by side in an immune serum, not as a united sub- stance. Union of amboceptor with cell is inde- pendent of complement, the latter being taken up only after the amboceptor-cell reaction has oc- curred. Amboceptors unite with cells at a low temperature, whereas complement requires a higher temperature for its union and for the fer- ment-like activity by which it dissolves or kills the cells. That constituent of the amboceptor which compfemento- unites with the cell has been referred to as the phore of Am-** cytophilous haptophore. Ehrlich and his follow- •'*•"'»**»'■• ers believe that complement in establishing con- nection with the cells does so by combining with a second haptophore of the amboceptor, after the latter has sensitized the er>i;hrocyte or bacterium. Hence, an amboceptor has, as the name implies, two receiving groups or haptophores, the second being the complement ophilous haptophore (Fig. 7). It is hardlv desirable to discuss various ex- Amboceptors 148 lyFECTlOX A\D LMMIXITY. periments which I'urnisli additional evidence of the amboceptor nature of the therniostabile body. The observed phenomena allow one to assign to it the two liaptophores mentioned. Action of There is a conflict of ideas as to the nature of the change produced b)^ the amboceptors, as a re- sult of which the cells are made susceptible to the action of complement. Bordet speaks of the am- boceptor as the substance sensibilisatrice, the sen- sitizing substance; and his conception of the ac- tion of the two substances he has compared rough- ly to the opening of a lock for which two keys are demanded. One key, amboceptor, is needed to prepare the lock for- the action of the second key, complement, the latter being the one which really opens it. Metchnikoff applies the name fixator to the therniostabile body, having in mind the action of a mordant in preparing tissues or other substances for the reception of a dye; this differs little from preparator, the word used by Gruber. The idea of Ehrlich, however, is distinctly at variance with the conceptions mentioned, for he sees in the union of amboceptor with cell nothing more than the introduction of a new chemical affinity, i. e., one which attracts complement, and this new affinity does not lie in the cell itself, but rather in the amboceptor (complementophilons haptophore) after the union has occurred. Hence, the terms intermediary body {Zwisclienkorper) , copula of Milller, and desmon of London, are words which carry with them the meaning that the amboceptor first unites with the cell and then acts as a linking substance through which complement finally is put in relation to the cell. This also is COMPLEMENTOID. 149 the meaning embodied in the amboceptor of Ehrlich, the word indicating more accurately his conception of the method by which the substance acts as an intermediary body. If we consider it established that in the process structure of of cytolysis union occurs between complement and ""* *"'^" " amboceptor we must at the same time assign a haptophorous group to complement. Union would be impossible without it. Corroborative proof of the existence of this haptophore lies in the fact that immunization with complement results in the formation of anticomplement, a prerequisite for which is union of complement with cell receptors in the immunized animal ; and this union, it seems necessary to assume, takes place through a binding group. The mere possession of a haptophore, how- ever, does not account for the ferment-like activity of complement. The latter characteristic resides in the so-called zymotoxic group; hence, comple- ment, having a binding and a toxic group, has a structure like that of a toxin. Somewhat loosely we have said that the inactiv- Compiemen- ity of a serum which has been heated to 56° C. depends on destruction of the complement. This is not strictly true, however, for such treatment destroys only the zymotoxic group, the haptophor- ous constituent remaining uninjured. Comple- ment altered in this respect is called complemen- toid, and it is analogous to toxoid, agglutinoid and precipitoid. Two essential facts go to show that this is the principle change wrought b}^ heating. First, the fact stated above, that immunization with complementoid, causes the formation of anticomplement. Second, complementoid may exceed true complement in its affinity for the Amboceptors. 150 ISFKVTIOy AyO IMMUNITY. amboceptor, and if sensitized cells are treated with a serum containing a mixture of complement and complementoid, the latter may occupy completely the complementophilous haptophores of the ambo- ceptors and thus may block the way for action on the part of complement. This is again the spe- cific inhibition which has been mentioned in con- nection with toxoids, agglutinoids and precipi- toids. This is the Complementoid-Verstopfung of Ehrlich. formationof Tho amboceptor, as the characteristic property of a bactericidal or of a hemolytic serum, is a spe- cific product of the immunization, whereas the amount and character of complement in the im- munized animal undergoes little or no change. We are, of course, obliged to consider the ambo- ceptors as a product of the cells of the body. In the terminology of Ehrlich, they are discarded cell receptors, and with their two haptophores repre- sent a more complex structure than either the re- ceptors of antitoxin or agglutinin ; the latter are uniceptors; the former amboceptors, and because of their higher differentiation Ehrlich has called them receptors of the third order (Fig. 7). Wlien micro-organisms gain entrance to the body they are killed and dissolved in considerable masses. As a result of the solution, certain bac- terial constituents reach the circulation, and among them are molecules or receptors which pos- sess haptophores capable of uniting with a par- ticular type of amboceptor, the latter being an in- tegral part of some tissue cells. This union hav- ing taken place, an affinity for circulating com- plement may be created as in the test-tube experi- ments. We have thus the possibility of stimula- FORMATION OF AMBOCEPTORS. 151 tion of the cell by the bacterial constituent itself as a toxic or unusual food substance, or the toxic action may be caused by products of disintegra- tion of the bacterial substance, the disintegration having been accomplished by the digestive action Fig. 7. — Graphic representation of receptors of the third order, and of some substance uniting with one of them. c. Cell receptor the third order, an amboceptor ; e^ one of the haptophores of the amboceptor, with which some food sub- stance or product of bacterial disintegration, f, may unite ; g, the other haptophore of the amboceptor with which com- plement may unite ; K, complement ; li, the haptophore, and !s, the zymotoxic group of complement. From Ehrlich's "Schlussbetrachtungen," Nothnagel's System of Medicine, vol. viii. of the complement which was taken up by the am- boceptor. The effect is that of an unusual stimu- lation, in response to which the cell, if not fatally injured, reproduces many amboceptors correspond- ing to the type which was occupied or injured. As in the formation of other antibodies, the new- 151 IXFKCTIOS A\D /.l/.l/r.V/7'I'. Specificity of Bactericidal Amboceptors and Comple- ments. Bacterial Receptors. foniicil ;iinlioco]iti"iTs riMcli tlu^ iiriicral llniils of llio ( "iiiiri'i'iiiiiL;' till' s|)('rillrit\' of sci'uiii-licmolysin? ami >i'ruiii-li;iclci'iolysin!^ for llicii- liomolo,u"ous cells, wo, of course, refer to tlic spocifieitv of the wliolo nniboceptor-comploinoiit ooniplox. Tt is noc- cssarv to tlirow tlio rpsponsibilitv on both sub- staiicos. l)eeiUise of tlio variations wliicli exist amono^ complements as well as amons; ambocep- tors. Tnasmnch, however, as the heat-resistant body alone is increased dni'in.u' iinmnnization or infection, the a'l'eater ]y,\vi of the sj^ecifieiiy wonld seem to depend on the nature of the ainhoceplor rather than on that of complement. .Ml bacteria which stimulate to the formation of bactericidal serums do so because of certain re- ceptors which they possess. These are, of course, analoofous to the receptors of erythroc}i;eR which cause the production of the hemolytic bodies in serum. Bacteria have, in addition, many otliei- re- ceptors, some of which cause the development of ao-glutinins. In the latter instance we speak of the agglutinogenic receptors of the cells, but there is no name of equal eonvenience which is used to designate the receptors which stimulate to the formation of amboceptors. No two micro-organ- isms contain an identical receptor apparatus : if the contrary were the case their antiserums wonld coincide in their bactericidal action. Therefore, the cell receptors (amboceptors) with wdiich they nnite during immnnization differ correspondinglv in their c^i;ophilous haptophores. The c\i:ophilous haptonhore of the typhoid amboceptor finds its specific counterpart in the tvphoid bacillus, and finding no such counterpart in the vibrio of chol- Complements. COMPLEMENT AND ANTWOMPLEMENT 153 era, the latter can not be sensitized by the anti- typhoid serum; on this fact depends the specificity of the serum. This conception does not interfere with the explanation of the group reaction among bactericidal serums, for it is conceivable that the colon bacillus, for example, has, in addition to those receptors which characterize the organism, a small percentage of receptors which are identical with those characterizing the typhoid bacillus. In accordance with this possibility an antityphoid serum may well, as it does, show some increased bactericidal power 'for closely related organisms. Hence the explanation of group bacteriolysis is identical with that of group agglutination. There is a wide difference of opinion regarding Multiplicity of the unity of complement, or alexin, its S3Tionym. Bordet and his followers stand for the unity of the alexins, and their position rests on the fact that a given normal serum may be used to activate many different amboceptors. We should appreciate that this phenomenon might depend on the broad range of action of a single complement, or on the pres- ence of different complements each being specific for a particiilar amboceptor. Ehrlich and his school take the latter view and have actually dem- onstrated a multiplicity of complements in a few instances. Ehrlich and Sachs treated fresh nor- ■mal serums (complement) in various ways, such as digestion with papain, partial destruction with alkalies, heat, etc.. and were able by these methods to destroy the complement for one kind of ambo- ceptor, while the serum still retained its power for activating other amboceptors. Accordingly, it seems clear that the ability of a normal serum to activate a given amboceptor depends not only on 1.5-1 I\FECT10.\ A.\D IMMl .MTY ' the presence of complement in a ^iciiLTal sense, but on the presence of a suitable complement, 1. e., one the haptophore of Avhicli corresponds to the com- plementophilous haptophore of tlie amboceptor. This point is of great importance in reference to the treatment of infectious diseases with antibac- terial serums, for the efficacy of the serum would seem to depend on the introduction of suitable complement in conjunction with the amboceptors, or on the existence of such complement in the l)ody of the patient. Anticom- Added proof of the multiplicity of complements lias been obtained by experiments with anticom- plements. As stated, the latter are obtained by immunization of suitable animals with normal or immune serums which contain complement or com- plementoid. When they are mixed with the liomolo- gous complements the haptophores of the latter are bound by means of the haptophores of the anti- complements. The evidence of this union lies in the fact that a complement which has been treated with its specific anticomplement is no longer able to activate the appropriate amboceptor. With properly selected serums, it may be shown that a given anticomplement will neutralize a comple- ment which is specific for one amboceptor, but will have no effect on another complement which acti- vates a different amboceptor. Hence, complements differ at least in this respect that not all have iden- tical haptophores. Immunization with leucocytes, ceils which contain complement, also causes the formation of anticomplement. Both natural and acquired antibacterial immunity may be lowered by the injection of anticomplement which is ho- mologous to the complement of the animal. POLYCEPTORS. 155 Some time ago Ehrlich expressed the opinion that an amboceptor in certain cases may have more than one complementophilous haptophore; in other words, that it may be a polyceptor rather Fig. 8. — Illustrating the amboceptor with more than one complementophilous haptophore (a polyceptor). a. Cell re- ceptor ; l)j cytophilous haptophore of the amboceptor ; c, the dominant complement ; d, the non-dominant complements oc , The haptophore of the amboceptor for the dominant com- plement; /3, those for the non-dominant complements. (From Ehrlich and Marshall.) than an amboceptor. This has again been empha- sized recently by way of explaining the ability of an amboceptor to absorb from a normal serum not only the complement which serves to activate the l.-it; INFECTION AND IMMUNITY. ■ amboceptor, but also others whieli ]iapi)eii to be present in the serum. The former is spoken of as tlie dominant complement and the latter as non- dominant complements. Figure 8 is an illustra- tion of such a polyceptor. Antiam- Tf oue immunizes with an immune scrum the boceptors. n j. • i j • i x* ]no(luct is spoken of m a general wa)^ as an anti- immune serum. The latter contains, as stated, anticomplement, and through the agency of this substance the antiserum antagonizes the action of the serum which was used for the immunization. Inasmuch, however, as the immune serum contains amboceptors also, the antagonistic action of the antiserum may depend, in part, on the presence of antiamboceptors. DifTerentiation between the ac- tion of anticomplement and antiamboceptor is dif- ficult, but it may be accomplished in certain cases by appropriate binding experiments. Serum 1, an inactive hemoh^ic serum, i. e., a solution of ambo- ceptors and complementoid, is treated with serum 2. Serum 2 has been obtained by irhmunization of an animal with serum 1, and contains anticomple- ment and possibly antiamboceptors. If serum 2 contains only anticomplement, it will have no ef- fect on the amboceptors of serum 1, when the two are mixed. The amboceptors are free to sensitize corpuscles which may be added, and the latter when sensitized undergo hemolysis in the presence of complement. Tf, however, serum 2 contains anti- amboceptors, either the C3iophilous or the comple- raentophilous haptophore of the amboceptor will be bound. In either case corpuscles which are added subsequently would not appear as sensitized, for if the cytophilous haptophore had been bound by antiamboceptor union between cell receptor and DIVERSION OF COMPLEMENT. 157 amboceptor could not occur; and if the comple- inentophilous liaptophore had been preoccupied complement would have no effect even if the ambo- ceptors had united with the cells by their unbound cytophilous haptophores. Ehrlich and Morgenroth demonstrated such antiamboceptors for certain hemolytic serums, and it was their belief that they combine with the cytophilous rather than with the complementophilous haptophore of the ambo- ceptor. However, Ehrlich has recently been able to prove the occurrence of an antibody for the com- plementophilous haptophore in one case. Pfeiffer also reports the demonstration of antiamboceptors Danger of for the specific amboceptors of anticholera serum, of Antiam- The possibility of antianiboceptor formation is one **"" °^^' of practical bearing, in view of the fact that the prolonged treatment of a patient with a bacteri- cidal serum may result in the development of such antibodies. If present in sufficient amount they would combine with new amboceptors which were injected and thus deviate the latter from the bac- teria. A phenomenon equally of theoretical and prac- Diversion of tical importance has to do with the so-called diver- and it's Theo- sion (Ahlenkv/ng) of complement. It has been reticai Danger. found that the action of a bactericidal or hemoMic serum is lessened, if a great excess of amboceptors* over complement is added. To explain this fact ISTeisser and Wechsberg have supposed that when so many amboceptors are present that all can not be taken up by the cells, those which remain free are able to combine with some of the complement which is present and thus prevent the accession of the latter to the sensitized cells ; that is to say, the complement is diverted from its natural course of 15S IXFECTlOy AXD IM.UUMTY. aetiou (Fig. 9). This amounts to a protection of the sensitized cells from the action of the comple- ment. The phenomenon led Wechsberg to sug- gest that in the therapeutic administration of bac- tericidal serums it may be possible to give too mucli of the serum. Although diversion of com- plement is a demonstrated fact, its importance in serum thera])v is perhaps not definitely settled. Hemolytic Am- It is of interest that amboceptors are widely dis- ""^^"venom. tributcd in the animal kingdom, and that in cer- tain instances they may be demonstrated in the secretions. It has lone; l)een Icnown that the Fig. 9. — Illustrating diversion of complement. The free amboceptors have combined with the available complement, and thereby prevented the latter from activating the am- boceptors which have united with the bacterial cell. (From Neisser and Wechsberg.) venoms of serpents owe a great deal of their tox- icity to their power of destroying red blood cells.* A given venom may contain several toxic sub- stances, and the poisons of different serpents by no means coincide in their toxic properties. Cobra venom has at least two distinct toxins, one for the nervous tissue and one which dissolves erythro- cytes, the neurotoxin having the greater patho- genic significance; it, moreover, agglutinates red blood corpuscles. The venom of the rattlesnake, on the other hand, is neurotoxic to a less degree, but has a pronounced influence in causing capil- * See also part IT, Chapter Z. concerning venoms. ENDOGOMPLEMENT. 159 lary hemorrhages. The latter power Flexner as- cribes to a toxin for endothelial cells, which he calls hemorrhagin. Through the works both of Flexner and Koguchi and of Kyes, facts were learned concerning the hemolytic toxin of cobra venom, which may be of great importance in prob- lems of general immimity. It seems that the hemolysin of venom is an amboceptor rather than a toxin of the usual nature, and that the aid of complement is necessary for its toxic action. The venom itself contains only the amboceptors, hence the toxicity of the substance depends on its being complemented after it is introduced into the body. The possession of suitable complement, therefore, is a source of danger in this instance rather than a means of protection for the individual. One may very well suspect that a similar relation- ship is possible in connection with other sub- stances which are as yet unknown. A fact of additional importance is that the am- Endocom- boceptor finds suitable complement not only in the serum of the animal but it may also be activated by a complement which the erythrocytes them- selves contain. Kyes speaks of the latter as endo- complement, i. e., endocellular complement. In attempting to discover the nature of the com- Lecithin. plement which is present in the erythrocytes, vari- ous substances existing normally in the red cells, as cholestrin and lecithin, were obtained in pure form and their activating power for the cobra am- boceptors was tested in reagent-glass experiments. From this work it was learned that lecithin, a defi- nitely known chemical substance, has the activat- ing power, and it was, therefore, assumed that the endocomplement of er}i;hrocytes is nothing more IGO IXFECTIOX AXD IllMUyiTY Cobra-lecithid. Hemolysis by the Combined Action of Colloids. or less than lecithin. All erythrocytes contain lecithin, yet not all are equally susceptible to the action of venom in the absence of serum comple- ment ; that is to say, endocellular lecithin does not act as complement with equal readiness in all cases. In order to explain this variation it was necessary to assume that the lecithin in the cells of one animal may be more available as comple- ment because it is bound to other cell constit^^ents only in a very loose way, whereas in more resistant cells the union is of a firmer nature. The relationship between cobra amboceptors and lecithin seems to be a very definite one, for Kyes was able to obtain a union of the two without the intervention of erythrocytes. The resulting sub- stance, the cobra-lecithid of Kyes, is a completed toxin and needs no further activation. We have yet to learn of the true nature of this new cofti- pound, the discovery of which seemed to augur a more intimate chemical laiowledge of the sub- stances which are concerned in immunity. Lecithin is a colloid, and in this connection it is interesting to note that it may be used in combina- tion with still another colloid in such manner that the hemolysis which they cause is analogous to that produced by hemol^iic amboceptors and com-^ plements. Landsteiner tried the effect of col- loidal silicic acid on erythrocytes which were en- tirely freed from serum, with the result that the corpuscles were agglutinated under its influence. It developed further, however, that colloidal silicic acid not only acts as an agglutinin, but also simu- lates a hemol}i;ic amboceptor, and in the latter capacity it may be activated either by the ordinary complement of serum or b}^ lecithin. Hence, we ACTION OF 8ALT8. 161 have here an instance of the entire cytolytic action being performed by two known chemicals, which in their action appear to be analogous to ambocep- tors and complements. Yet even the action of these substances is obscure, for although the chem- ical formulae of silicic acid and lecithin are suffi- ciently well known, the explanation of their activ- ity as colloids is equally obscure with that of the albuminous substances. Another recent discovery which tends to' bring Neutralization the immune substances into closer touch with pure by saTts.**"*"* chemistry is that of Hektoen concerning the abil- ity of certain salts (calcium chlorid, barium chlorid, etc.), to combine with complement in such a way that the latter loses its activating and combining function in relation to amboceptors. This was mentioned incidentally under the sub- ject of antitoxins. The activity of the comple- ment is again restored if the inhibiting salts are precipitated by suitable chemicals. The salts are used in such dilutions that they are largely ionized, and Manwaring believes their inhibiting action is due to the formation of compounds of the posi- tive ions with the complement, resulting in such substances as Ca-complement, Ba-complement, IHlg. When the precipitating chemicals are added the ions are freed from this combination, as a re- sult of which the complement recovers its activat- ing properties. It has not as yet been determined whether variations in the salts in the fluids of the body cause changes in resistance by their action on native complements. CHAPTER XIII. Cytotoxin or Cytolysin. Theoretical Utility of Cytotoxins. CYTOTOXICS. Following the discovery of immune hemolytic serums it was a short step to experiments which involved immunization with various other tissue cells, and as a result of such work we are to-day familiar with antiserums for almost every organ of the body. Metclmikoff gave tlie name of cytotoxins to those serums which destroy cells other tlum bacteria and erythrocytes; the word cytolysin is used syn- onymously. jSTaturally a serum which destroys any cell whatsoever is cytotoxic, but according to the rather loose custom which prevails, we speak of bacteriolysans, hemolysins and other cytolysins, in- cluding among the latter serums which destroy leucocytes, the cells of the liver, Iridney and other organs. Cytotoxins are of interest, not only because they are produced in accordance with the general laws of anti-body formation, l3ut they have, in ad- dition, a certain theoretical and perhaps practical importance. Immediately on their discovery the possibility became manifest that they might be utilized in the elucidation of certain physiologic and pathologic problems. For example, by put- ting the thyroid out of function through in- jections of thyrotoxic serum it might be pos- sible to confirm, or to prove incorrect, cer- tain theories as to the role of the gland in metabolism. Or, by the selective destruction of a tissue, facts concerning its regenerative powers SPECIFICITY. 103 might be learned. The use of an antipancreatic serum might throw some light on the nature of diabetes. Therapeutic possibilities also suggested themselves. One might be able by means of artifi- cial anticytotoxic serums to counteract cy to toxins which were being formed pathologically in the body. Or, by injecting small amounts of a cyto- toxin, perhaps one could stimulate to a renewed production of the homologous cells ; small doses of a hemolytic serum might be useful in combating anemias. Or small amounts of leucotoxic serum might caiise an increase in the number of leuco- cytes, and thereby an increased resistance to infec- tion. Perhaps autocytotoxins are formed in some such manner as the following: An extraneous toxic substance causes the destruction of a few kidney cells, the constituents of the latter reach the circulation and stimulate other organs to the formation of autonephrotoxic amboceptors, which then assist in the destruction of more renal tissue, with the result that a vicious cycle is set up. In spite of so many theoretical values, the study Lack of of cytotoxic serums has not yielded the results which were anticipated, perhaps chiefly because of their lack of specificity (Pearce and others). Al- though the cells of the different organs differ wide- ly in their morphology and function, there are no doubt certain chemical constituents (receptors) which they possess in common. Of this we have experimental proof from the fact that immuniza- tion with one type of cell yields a serum which is toxic for the cells of various organs. It is difficult or impossible to injure one organ to the exclusion of all others by means of a cytotoxin. One may 'attempt to purify a C}^otoxic serum through ab- Specificity. 1(54 1XFECTI0^' AND IMMUNITY. sorption of the adventitious amboceptors by means of the corresponding cells. Inasmuch, however, as the result is a decrease in the chief amboceptors as well as of the adventitious, the desired object is not fully realized. Theoretically the cytotoxic treatment of malignant tumors offers an impor- tant field for research. But here, too, various dif- ficulties are involved, as lack of specificity of scrums and the multiplicity of cell-types which constitute different tumors. Determination Experiments with cytotoxic serums may be con- '^ActTofu ducted in vitro or in the living animal. In either ease a necessary condition for the recognition of the cytotoxic action is the presence of some dis- tinctive sign of vitality on the part of the cell, the loss of which may be taken as evidence of cell- death. Loss of motility and of proliferative power indicate the death of bacteria, and solution of hemoglobin the death of erythrocytes. Under par- ticular conditions loss of motility on the part of certain tissue cells, as spermatozoa, leucoc}i:es and ciliated epithelium, is an evidence of cell death or cell injury. The toxic action of serums on cells of fixed form is more difficult to determine, and for evidence one must rely on such points as clearing of the protoplasm (digestion?), swelling of the cell and nucleus, actual solution of the C3d:oplasm, or degenerations of the homologous organs when the serum is injected into the living animal. Technicof The tcchnic of immunization with tissue cells is Immunization, g^^^^]^^ ^q that of immunization with bacteria. In order to obtain leucocytes in abundance, artificial leucoc}i;osis is produced in the peritoneal or pleural cavity by the injection of bouillon, or lymph AMBOCEPTORS AND COMPLEMENTH. 1G5 glands, spleen or bone-marrow may bo ground up and injected. Immunization with solid organs, as liver, kidney or testicle, is easily accomplished, a necessary pre- liminary for injection being a thorough disintegra- tion of the tissue by grinding with sterile sand ; the resulting mass when suspended in salt solution passes through the injecting needle readily. Cytotoxins, like bacteriolysins and hemolysins, Amboceptors, are complex substances, in that they consist of am- and AiftTcyto^ boceptors and complements. The amboceptors to"'"*- alone are increased during immunization, the com- plement being a normal constitu.ent of the serum of the animal. The phenomena of inactivation and reactivation are observable here as in connec- tion with other cytolytic serums. Anticytotoxins are readily produced by immunization with many cytotoxins; the antiserum usually consists of anti- complement, but in some instances antiambocep- tors have been described. Simultaneously, or nearly so, Landsteiner in spermotoxin. Vienna and Metchnikoff in Paris reported the production of spermotoxic serums by immuniza- tion with spermatozoa, the natural motility of which rendered the recognition of cell death easy. The technie which Landsteiner first employed was that of the Pfeiffer experiment in that he immun- ized guinea-pigs with the spermatozoa of cattle and observed loss of motility on the part of the cells when they were injected into the peritoneal cavity of the immunized animals. Comparable with many other cytotoxins, spermotoxin kills the ho- mologous cell without causing its solution. The loss of motility i& also observed in hanging-drop preparations provided a fresh or a complemented 100 lyFECTioy axd immuxity. seriini is used. Most normal serums show a greater or less degree of toxic action for the sper- matozoa of other animals, and normal spermotox- ins like the immune consist of amboceptor and complement. Orotclmikoff claims to have pro- duced an autospermotoxin by immunizing guinea- pigs with the spermatozoa of other guinea-pigs. TVlien a spermotoxic serum is injected into the living animal it is thought that the amboceptors are taken up by the homologous cells, and this ■would seem to affect the vitality of the sperma- tozoa, inasmuch as De Leslie rendered male mice sterile for 16 to 20 days by the injection of the serum. It is of theoretical interest that castrated ani- mals will yield spermotoxin by immunization, showing that the amboceptors are not of necessity produced by the analogous tiissue of the immun- ized animal. From the fact that spermotoxic serums are hemolytic, it is assumed that certain receptors are common to erA-throc;\i:es and sperma- tozoa. Hemol}i;ic serums, on the other hand, may not be spermotoxic. There is nothing contradic- tory in this lack of reciprocal action, for those re- ceptors which are common to the two cells may not be important for the life of the spermatozoon, whereas the oppo'site condition prevails with the erythrocyte. It is certainly of interest that immunization with the plasma of ova causes the formation of spermo- toxic amboceptors, a fact which points to certain common constituents of the two cells. Antispermotoxin may be produced by immimiza- tion with spermotoxic serum (anticomplement or antiamboceptor). LEUCOTOXIC SERUM. 167 Pollowinsr technic similar to that employed by Cytotoxin T -, . • -r^ 1 i. • 1 i J. • 'O"" Ciliated Landstemer, von Dungern obtained a cytotoxic Epithelium. serum for ciliated epithelium of the trachea. The cells disintegrated in the peritoneal cavity of the immunized animal, but not in that of the normal animal. This serum also proved to be hemolytic in spite of the fact that no erythrocytes were in- cluded in the injections. That the receptors which characterize ciliated epithelium are widely distrib- uted is shown by the fact that immunization with cow's milk causes the formation of a cytolytic serum for the tracheal epithelium of the cow. Leucotoxic, lymphotoxic or lymphatotoxic Leucotoxin. serums are prepared by immunization with ex- udates which are rich in leucocytes, or with the emulsions of lymphoid organs: lymph glands, spleen, bone marrow. Metchnikoff prepared the first serum of this nature by the injection of the spleen of rats into guinea-pigs. Leucotoxic serums are toxic, not only for leucocytes, but also for red corpuscles and endothelial cells. When injected into the peritoneal cavity the endothelium is thrown off, and when given subcutaneously the capillary endothelium is attacked, with the result that blood escapes to form a large hematoma. The action of the serum on leucoc}i;es may be observed in vitro. The mononuclear cell's are often more susceptible than the polymorphonuclears, although this depends somewhat on the animals and the particular organ used for immunization. The cells lose their motilit3% the cytoplasm becomes trans- parent, and swells to form a large clear vesicle, which appears to be surrounded by a sharp, thin membrane. The cell contents may be discharged or entirely liquefied, the nucleus alone being rec- 1G8 INFECTIOX AXD IMMUNITY. Old Age. Effect of Leu- coto\ic Serum on Resistance to Infections. ognizable. Leucocytes are agghitinated by the serum. A strong lencotoxic serum may be fatal to the animal when injected into the peritoneal cavity or blood stream, the exact cause of death being obscure. ]\Ietchnikoff,, taking the view that the phenom- ena of old age depend on the destruction of vari- ous tissue cells by the mononuclear leucocytes (macrophages), expressed the hope that a lympho- toxic serum might be utilized to combat the action of these cells with the result that life would be prolonged. Wliether or not his view as to the cause of old age is correct, his plan of antagonizing it had to be abandoned because leucotoxic serums do not injure the macrophages to the exclusion of other leucoc}i;es. The injection of a leucotoxic serum into the per- itoneal cavity of a guinea-pig causes a temporary decrease in the number of leucoc}i;es, and during this period of MqDoleucocytosis the resistance of the animal to peritoneal infections with the organisms of typhoid and cholera is lowered. One may refer this effect to the destructive action of the serum on the leucocytes, by which phagocytosis is pre- vented, or, according to Wassermann, it may de- pend on the action of anticomplement which the leucotoxic serum contains. (Leucocj'tes contain complement, hence immunization with leucoc3rtes causes the formation of anticomplement.) It is probable that both factors are of influence. In the course of 24 to 48 hours after peritoneal injection of the serum, the leucocytes reaccumulate to an enormous extent. During this secondary hyper- lencocytosis resistance to peritoneal cholera or tj-phoid is increased. Some non-toxic substances. Serum. NEPHROTOXIN AND NEPHRITIS. 1G9 as bouillon, have a similar effect, and although the secondary leucocytosis is never so great as that caused by the leucotoxic serum, the protective ac- tion is equally high. It would seem that, leucoc3d;e for leucocyte, those which accumulate following the injection of leucocytoxie serum are less efficient in antibacterial action than those whose presence is caused by nontoxic substances. (Eicketts.) Hence there probably is no field for leucotoxic serum as a means of temporarily increasing resist- ance to bacterial infections. By guarded immunization Besredka obtained an antileucotoxic serum. Nephrotoxic serums have been brought into Nephrotoxic close relationship with clinical and anatomic prob- lems by a number of investigators. Some normal serums are held to be nephrotoxic inasmuch as their injection is followed by albuminuria and renal degenerations. Immune nephrotoxins have a similar but more pronounced effect, and Linde- man referred the 'death of his experiment animals to the development of a uremic condition. Of more than ordinary interest is the claim of cer- tain workers that autonephrotoxins may be formed in the body. One (Lindeman) caused a toxic nephritis in dogs by the injection of potassium- Autenephro- bichromate. The serum of this dog, although free from chromic acid, was toxic for other dogs, pro- ducing the symptoms which are caused by an im- mune nephrotoxic serum. It was supposed that the chromic acid in the fir'st dog caused disintegra- tion of renal cells and that the constituents of the latter were then taken up by nephrotoxic receptors which normally reside in the organs of the ani- mal; as a result the receptors were overproduced 170 INFECTIOy AXD IMMUMTY. and their presence became manifest when the serum was injected into other dogs. In accord- ance with this view the original toxic cause of a degenerative nepliritis would be of less conse- quence for the continuance of the condition than the formation of the nephrotoxic amboceptors ; i. e., the formation of an autonephrotoxin. Somewhat similar results were obtained by oth- ers through ligation of the renal vein or artery on one side. Constituents of cells of the isolated kid- ney were supposed to be absorbed, and as a conse- quence nephrotoxic amboceptors were produced in excess by organs of uncertain identity. To the action of the new-formed bodies were attributed the degenerative changes which were found in the opposite kidney, and the nephrotoxic properties which the serum manifeested when injected into a healthy animal of the same species. Antinephro- Accordiug to Ascoli and Figari unilateral neph- Hypertropin^ rectomy so injures the opposite kidney (overwork) that the serum of the animal becomes nephrotoxic. They state also that an animal, the serum of which contains nephrotoxin, may antagonize the latter by the production of antinephrotoxin, and suggest that spontaneous recovery from nephritis may be due to the action of such an antibody. They would account for the cardiac hypertrophy of nephritis by the action of nephrotoxic serum in causing con- traction of the peripheral vessels with consequent increase of blood pressure; and for the nervous s>Tnptoms on the basis that the serum contains a neurotoxic constituent. We liardly dare consider such far-reaching con- clusions as decisive until they have been extensively confirmed. Yet whatever mav be their real value HEPATO- AND NEUROTOXINS. 171 Neurotoxin. they serve to emphasize the possibility that those principles which are so important in relation to immunity against infectious diseases, may be equally important in relation to other pathologic conditions. Hepatotoxins have been obtained by a number Hepatotoxins. of workers, and the attempt has been made to pro- duce autohepato toxins by injecting liver tissue of the guinea-pig into animals of the same species. The success was not unqualified. Hepatotoxins when injected are reported to cause insular degen- erations of the liver ; however, the lesions may be caused, in part at least, by capillary emboli of en- dothelial cells or erythrocytes. Neurotoxic serums have been studied with some thoroughness. Whether one injects the cerebrum, cerebellum or spinal cord, the resulting serums apparently are similar; either an anticerebral or an anticerebellar serum will cause degenerations of the spinal ganglion cells. In view of their broad range of action it seems improbable that neurotoxic serums will be of service in clearing up the etiology of system degenerations of the nervou's tracts. They are usually hemolytic and hemag- glutinating and may also be endotheliotoxic and leucotoxie. Wlien mixed with emulsions of the homologous brain tissue the neurotoxic ambocep- tors are bound by the receptors of the nervous tis- sue, and the serum consequently loses its toxicity. Antineurotoxic serums have been described. Syncytdolysin is the name given to a serum which is obtained by immunization with the placenta. Certain writers (Veit and Scliolten, Charrin and Delamare) report that the injection of placentar tissue alone causes albuminuria, a consideration Cyncytiotoxin in Relation to Eclampsia. 172 IXFKCTIOX AMI IMMUXITY. \\iiieli led thorn to assume tliat the phieentar cells contain a nephrotoxic substance. Inasmuch as ]ilacentar cells or their constituents may reach the circulation during eclampsia (Schmorl) it was not a long step to suppose that the nephritis of pregnancy is due to the toxic sync}i:ial cells which are absorbed. The results which Weichardt re- ported gave some strength to the view just cited. By treating placentar tissue of rahbits with the specific cyncytiolysin the toxin supposedly was lib- erated, and the mass when injected into normal rabbits is said to have produced symptoms of an eclamptic nature. On the basis of these observa- tions the hope has been expressed that an anti- toxin for eclampsia might be prepared by immun- ization with placentar tissue. However, the con- ditions are by no means simple; any value which the destruction of circulating syncytial cells or their toxin would afford might be more than offset by the action of the hemotoxin and neurotoxin which the serum is said to contain. Wliether or not the hypothetical toxin of syncytial cells may be separated from the other cell constituents, and whether immunization with the toxin will yield an antitoxic serum are possibilities which remain for further investigation ; the results cited have not been obtained by all observers. Liepmann hopes for a serum-diagnosis of preg- nancy. If, as supposed, the blood of a pregnant woman contains syncitial cells or their products of degeneration, the serum when mixed with a specific syncytiolysin may cause a precipitate. He claims to have demonstrated the presence of placentar constituents in the circulation by this biolocjic method. TEYRO-, FA'NCREOTOXrN, ETC. 173 Thyrotoxin. Antithyroid serum is prepared by jinrniinjza- tion with ground-up thyroid tissue or with extracts of the organ. It is hemolytic, even though all the blood has been washed from the tissue which was injected. Portis immunized with the "colloid" material of the gland obtaining a hemolytic thyro- toxic serum. When injected into the living animal degenerative changes are produced in the thyroid, and some authors report the tetanic phenomena Avhich often follow surgical removal of the thyroid. In very careful work, however, Portis could not produce "the exact picture presented by thyrodec- tomized animals." Degenerative changes were foimd in various organs, as liver, spleen and kid- neys. Brown Pusey has made the interesting sugges- tion in regard to sympathetic ophthalmia that the disease may be due to the formation of autocyto- toxins which are specific for the cells of the inner surface of the ciliary body and iris. The disinte- gration products of the corresponding cells in the eye which was primarily injured would constitute the stimulus to the formation of the specific anti- bodies. The possibility is as yet a problematic one. The experimental study of cytotoxic serums for the pancreas has, up to the present time, thro"nm little light on pancreatic diseases. It stated that the serum may cause transient glycosuria, and it is said to have an antitryptic action in experiments performed in the test -glass. The results of different observers concerning the other action of antiserums for the adrenal gland are not in entire accord. Although degenerative changes may be caused in the gland when the serum is in- Sympathetic Ophthalmia. Pancreotoxin. Cytotoxins. 174 IM'ECTIOX AXD IlIilUyiTY. Toxin of Exhaustion. Concerning Autocytotoxins. "Horror Autotoxicus." jected, the action is not specific; the serum may be highly hemolytic (Abbott). Ceni claims to have demonstrated in the circula- tion of epileptics a cytotoxin which causes tlie ep- ileptic attacks, and reports the production of a specific antitoxin. Weichardt has published descriptions of a toxin which is peculiar to states of exhaustion, giving an account of the specific antitoxin which he pro- duced by immunization. Other c}^otoxins which have been prepared, as those for the pituitary body, gastric mucosa and cardiac muscle, have at the present time nothing more than general biological interest. It would seem that no question in relation to CA-totoxic serums is more important than the pos- sil^ility that autoc^-totoxins may develop and in- stitute the vicious cycle which was mentioned ear- lier. It is true that the results of some investiga- tors suggest the probability of such a process, but it would be going too far to say that its existence as an important pathologic law has been estab- lished. On the contrary, the development of auto- cytotoxins is one of the rarest of occurrences in experimental work; and Ehrlich has spoken of the inability of the body to form such antibodies as a condition of ^^lorror autotoxicus." The cells of our Iddneys and our erythrocytes certainly do degenerate, and it is quite possible that the recep- tors which are thereby liberated actually reach cytotoxic amboceptors which are situated in other organs. In the event that the process extends to this point. Ehrlich assumes that the amboceptors are of a sessile nature, that in spite of the stimula- tion to which the cells are subjected the "sessile % "HOIiROn AU'rOTOXINS." 175 amboceptors" may not be overprodiicofl aiifl lib- erated as in the case of antibodies for bacterial substances or for the cells of other species. In accordance with this explanation we are saved from intoxications of the nature in question be- cause of the sessile nature of the cytotoxic ambo- ceptors. CHAPTER XIV. PHAGOCYTOSIS. As one ma}' learn from the writings of Metchni- koff. phagocytosis, in its broad sense, exercises three distinct functions: nutritional, resorptive and protective. Phagocytosis Phagoc}i;osis, for purposes^ of nutrition, is most ofNuTntlon! highly developed in unicellular ameboid organ- isms, but is found also in animals of considerable organic differentiation. It is, perhaps, nowhere more strildng than among certain myxomycetes, which are large, naked, multinucleated, protoplas- mic masses belonging to the plant kingdom, and which possess a peculiar, slow, undulating motility. Ingestion is accomplished through protoplasmic arms (pseudopodia) which are thro "mi out to en- velop tlie object. Minute plant and animal cells, living or dead, are ingested in this manner by the myxomycetes, amebse and other unicellular organ- isms and are subsequently digested by means of intracellular ferments. The ferments which have been extracted from such cells are proteohiic since they digest gelatin and fibrin, usually in an acid but sometimes in an alkaline medium; that from amebae has been called amibodiastase. In the proc- ess of digestion a "vacuole," acid in reaction and containing the ferment, forms around the in- gested particle. -In certain phagoc^^tic unicellular organisms the protoplasm shows a degree of differ- entiation, a mouth and an anus being simulated at points where the food is most readily taken in and discharged. Instances are cited in which ameboid 0EEM0TAXI8. 177 organisms protect themselves against inimical cells by ingesting, killing, ami finally discharging or digesting the latter. The botanist, Pfeiffcr, first described the phe- nomena of negative and positive chemotaxis in re- lation to the myxomycetes. Under certain condi- tions they either are attracted toward or move from moist places. That a negative chemotaxis may be changed into a positive was shown in rela- tion to salt solutions. Wlien placed in the vicinity of or in contact with strong solutions the cell re- cedes, whereas if one passes gradually from weaker to stronger solutions the latter eventually attract rather than repel the cell. As one goes higher in the animal scale intracel- lular digestion for purposes of nutrition is con- fined to rather definite groups of cells. The intes- tinal epithelium of certain invertebrates consists of "sessile phagocytes," cells Avhich. individually or after fusion into plasmodial masses, surround and digest solid particles of food. It is said that in sponges the digestive tract is not sharply sepa- rated from the mesodermal tissue, and the cells of the latter share with the former the function of intracellular digestion. In higher invertebrates and in all vertebrates the intestinal epithelium ceases to be essentially phagocytic, digestion being accomplished rather by ferments which have been secreted hy the intestinal and related glandular epithelium. Such animals, nevertheless, possess an abundance of phagoc3'tic cells, but they are in the main mesoblastic in na- ture, and may have nothing more than a remote relationship to the nutrition of the organism. Chemotaxis. Intestinal Phagocytes. ITS INFECTION AND IMMUNITY. Macrophages Metclmikoll' divides tlie pliao-ocvtic cells of ver- and Micro- . ' ^ • phages, tebrates mto the macrophages and the micro- phages. Tlie macrophages or hirge phagocytes in- clude the large lymphocytes, endothelial cells, ameboid connective tissue cells and others which may occasionally take up foreign particles. Our polymorphonuclear leucoc}d;es are the micro- phages. In relation to immunity we are concerned chiefly with the large lymphoc5d;es (macrophages), and the polymorphonuclear leucocytes (micro- phages). Although such cells may contain many ferments, Metchnikoff recognizes but one type in Cytases. relation to their resorptive, digestive and bacteri- cidal activities. This he calls CAi:ase and distin- giiishes that of the macrophage as macrocytase and that of the microphage as microcytase. Cytase corresponds to the complement of Ehrlich. The two cells do not have identical activities, the ma- crophage being concerned specially in the resorp- tion of tissue cells and in immunity to certain chronic diseases, as tuberculosis and leprosy, whereas the microphage is the cell which is con- spicuously antimicrobic in relation to acute infec- tions. Resorption of According to Metchnikoff, the leucoc;vtes are very active in the resorption of useless or foreign cells. During the metamorphosis of certain in- vertebrates it is said that the larval tissues are englobed and digested by wandering pha- goc}i;ic cells. In involution of the uterus the muscular tissue is invaded by leuco- CA-tes which take up and digest or carry away the "retrogressive elements." Metchnikoff's concep- tion of certain atrophic processes, particularly Native Cells. A TROPni C PROCEHHEH. 179 those which are grouped among the senile atro- phies, is of interest to pathologists. In sclerotic atrophy of the ovaries the large lymphocytes in- vade the tissue, surround and destroy the ova and follicular epithelium and eventually, as fibroblasts, participate in the formation of fibrous tissue which to a degree is substituted for the original struc- ture. In old individuals or in those of failing mentality it is said that ganglionic cells are found in a greater or less degree of atrophy because of the action of certain mononuclear phagocytes (neuronophages) which are contiguous to or form a zone around the cell. The neuronophages may represent mononuclear cells from the blood or those of proliferated neurogliar tissue. The best examj)les of this condition were found in very old dogs. The chromophores of the skin, according to Metchnikoff, may be considered as chromophages. Wliether or not they are of epithelial origin, as he claims, they are said to exist normally in the hairs in a latent or inactive condition. As old age comes on, or as a result of other obscure causes, their attitude becomes an active one, and they proceed to take up and digest the normal pigments of the hairs. Hence, white hairs are the result of an autoparasitism by certain mononuclear phago- cytes. In muscular atrophy it is held that the sarcoplasm takes up the striated tissue after the manner of phagocytes. We come into closer touch with our general sub- ject of immunity when we consider the resorptive function of the phagocytes for cells which are for- eign to the host, for example, toward erythrocytes which are injected for the purpose of producing a The Whitening of Hairs. Resorption of Foreign Cells. Formation of Cytotoxins. 180 IXFECTIOy A^D IMMUNITY. liemolytic serum. Followiug such an injection into the peritoneal cavity there occurs a great accession of macropliages which ingest the erythrocytes, dis- solve the hemoglohin and eventually digest the stroma. The same phagocytes are involved in the resorption of any other foreign cells of animal ori- gin vrhich may be injected. In view of the intracel- lular lieraolysis by the leucocytes, one may suspect that the latter contain a hemolytic ferment; one which, perhaps, is analogous to the hemolysin (hemoh-tic amboceptors and complement) of serums. On this point there has been sharp dis- cussion. Metchnikoif cites observations to show that a ferment of this nature may be extracted from the lymphoid organs, that it contains a heat- susceptible constituent, and that when fresh it may be used to reactivate a heated hemolytic serum. This would indicate that the leucocytes contain cytase (complement), but it is not clear that they would also contain the fixators (ambo- ceptors). Nevertheless, the demonstration of an intraleucoc}i;ic hemolysin and a Icnowledge of the phagocytic power of the leucocytes for erythro- cytes form the basis for Metchnikoff's belief that serum-hemolysin is nothing more than intraleuco- C3i;ic hemolysin, which under proper conditions may reach the serum or plasma. By an extension of this conception it is held that all cytolysins are produced by the macrophages. Thermostabiie Korschim and Morgenroth, on the other hand, Organ^E^xTracts! ol)tained from lymphoid and various other organs, not a therraolabile hemolysin, but one which with- stands prolonged boiling — a coctostabile hemolysin which is soluble in alcohol, shows no amboceptor- CYTAHE. 181 complement composition, and is incapable of yield- ing antihemolysin by immunization. These re- sults, Metchnikoff holds, are only in apparent dis- cord with those obtained by himself and his pu- pils, and depend on the methods of extraction wliich were employed. In order to obtain the ther- molabile hemolysin uncontaminated with the ther- mostabile, the extraction must be a rapid one. If, on the other hand, it is prolonged, as Metchnikoff assumes that of Korschun and Morgenroth to have been, the intracellular ferments digest the remain- ing cell constituents, including the thermolabile hemolysin, and the thermostabile hemolysin is lib- erated or formed in the process. Believing that'cytase, under normal conditions, exists only within the leucocytes, and that its pres- ence outside these cells is artificial, Metchnikoff cites experiments similar to the following in sup- port of his views : Given a guinea-pig which has been immunized cytasean with the blood of a goose : if fresh goose corpuscles substancef are injected into the peritoneal cavity, the cells are hemolyzed in the fluid without the occurrence of phagocytosis. Two explanations of the extraleu- cocytic presence of cjrfcase and fixators, which is in- dicated by this result, are possible : first, that they are present normally and continuously in the plas- ma of the immunized animal, or, second, that they become liberated at the time the corpuscles are in- jected. According to Metchnikoff, the latter conten- tion prevails rather than the former. He recognizes phagoiysis. a phenomena which bears the name of phagol^^sis, i. e., solution, partial or complete, or phagocj'tes. Almost anv foreign substance or fluid which one IS-2 IXFKCTloy AM) IMMIXITY. Liberation of niny clioosc to ]nit iu coiitact witli leucocytes so pVa*g*'oiysi^8^. stimulates or injures them that they discharge cer- tain of their constituents. If the fixators and cytase are among the constituents which are dis- cho.rged at the time the injection is made, the extracellular hemolysis encountered in the experi- ment described above might depend on the libera- tion of these substances rather than on their nat- Preventionof ural occurrcnce in the plasma. If this be true, aao ysis. _^^^^| ^^ ^^^^ could in some way fortify the leucoc^^es against phagolysis, the plasma would remain free from hemolytic power. ]\Ietchnikoff accomplishes such fortification, i. e., prevents phagolysis, by a simple procedure, which demands nothing more than the peritoneal injection of a small quantity of bouillon or salt solution twentj^-four hours in advance of the experiment. Possibly by this means the leucocytes have been habituated to the presence of a foreign fluid, or the neAV leucocytes which accumulate possess greater resistance. What- ever the explanation, the erythrocytes which are injected at this critical time are said not to un- dergo extracellular hemolysis, but instead are en- globed and dissolved by the macrophages. These results and others of a similar nature are the basis for the belief that cytase normally is intracellular, and that it becomes extracellular only when the leucocytes are subjected to injurious influences. The fact that the serum of detibrinated or coagu- lated blood contains cytase is not in discord Avith such an opinion, for in this instance also the leu- cocytes may be injured to such a degree that cer- tain of their constituents are discharged. We are well aware that fibrin-ferment is liberated under these circumstances. NATURAL IMMUNITY. 183 It was equally desirable, if possible, to determine Fixators the relation of fixators to the leucocytes. The sit- Leucocytes.'' nation is, however, very complex, and, although Metchnikoff regards the fixators as secretion or ex- cretion products of phagocytic cells, the question is, perhaps, not definitely settled. When phagoly- sis is prevented in the manner described, the in- jected erythrocytes may well absorb fixators from the plasma and still undergo no hemolysis until en- globed by the phagocytes. It is considered that fixators in contrast to cytase may exist in the cir- culating plasma. Phagocytosis as a feature of local resistance phagocytosis against microbic invasion was considered in rela- '" '"""""'ty- tion to inflammation. We come now to speak of the relationship of the leucocytes to general states of immunity, having reference .to the condi- tions which have been designated as natural and acquired antibacterial immunity, and natural and acquired antitoxic immunity. The first expressions of Metchnikoff concerning the antimicrobic activity of phagocytes, the power of freeing the organism from "invaders of every sort," were made altogether from an a priori stand- point in an address delivered in 1883, "TJeber die Heilkraf fce des Organismus." He justified his po- sition on general grounds, having in mind the "more general phenomena of phagocytosis and the resorption of corpuscular elements," as he had observed them in various zoological studies. Shortly there came to him the opportunity of NaturaMmmun- studying an infectious disease among the Daphnia (water-flea), a small transparent crustacean. The disease was caused by a blastom3'Ces which forms ity to Bacteria. 1S4 iXFEcrioy and immunity. a long neeclle-shapod spore. After being swal- lowed by the animal the spores penetrate the in- testinal wall into the body cavity where they are snrrounded, englobed and digested by the white blood corpuscles. If this occurred with sufficient vigor all the spores were disposed of and the ani- mal recovered. Sometimes, however, the spores germinated even after they had become intracellu- lar, and when the parasitic cells reached maturity they appareiitly had the power of killing the leu- coc\i;es through the agency of a secretion peculiar to themselves. In the event that the latter proc- ess was sufficiently extensive the tissues were soon overrun with parasites and death resulted from a septicemic condition. The observations were made in. the living transparent animal. Although the example cited seemed convincing, Natural it Avas, of coursc, neccssary that observations should extend over many infectious processes be- fore phagocytosis as the cause of natural immunity could be accepted as a general fact. This has been done on rather broad lines by Metchnikoff and his pupils, and the results have served to convince them that the phagocytes are responsible for nat- ural immunity in all instances, and that the de- gree of natural immunity in a given case depends on the degree of phagocytosis which is manifested against the organism. x\s stated previously, the microphage, with its microcytase, is held responsi- ble for antibacterial immunity in most instances, although the macrophage is concerned in certain chronic infections. If an animal is susceptible to a virulent culture of anthrax, but resistant to a weak culture, the TOXINS AND CHEM0TAXI8. 185 phagocytic power is found to be greater for the weaker organism. The highly virulent culture creates a condition of negative chemotaxis, with the consequence that leucocytes are not attracted and microbic proliferation proceeds rapidly. Without going into details, studies of the follow- ing and perhaps other micro-organisms have strengthened Metchnikoff in his views: staphylo- cocci, streptococcus, pneumococcus, gonococcus, vibrio of cholera in infections of the guinea-pig, the vibrio of goose septicemia in relation to the guinea-pig, which is naturally immune, the spi- rillum of relapsing fever, tubercle bacillus, yeast cells and other fungi, and certain animal para- sites (Trypanosoma lewisii). Most important are certain conditions which create a condition of negative chemotaxis, or other- wise engage the phagoc3^es so that they refuse to take up the essential organistm. Vaillard says that all animals are immune to pure cultures of the tetanus bacillus or its spores, provided the lat- ter have been washed entirely free of toxin. The absence of toxin permits of positive chemotaxis and phagocytosis, whereas toxin when present causes negative chemotaxis, and the bacilli pro- ceed to further toxin formation. The same is held to be true in infections by some other organisms. It seems definitely established that contaminat- ing organisms (pyogenic cocci. Bacillus prodigio- sus) may greatty increase the virulence of the ba- cillus of symptomatic anthrax, Bacillus aerogenes capsulatus and the tetanus bacillus — anaerobic or- ganisms. On the one hand, the secondary bac- teria ma}^ produce more favorable conditions for Relation of Phaciocytosis to Virulence of Bacteria. Toxins as Cause of Negative Chemotaxis. Accidental Engagement of Phagocytes. 18G INFECTION AND IMMUNITY. Acquired Immunity to Bacteria. Anthrax. the growth of the anaerobes by consuming local oxygen, or, as Metclmikoff believes, they may so engage the phagocytes that the latter have no dis- position to take up the essential organism. Tliis condition may be an important one in other mixed infections, as when the streptococcus complicates diphtheria and scarlet fever. If the phagocytic poAver is an index of the de- gree of natural antibacterial immunity, is the same correspondence to be recognized when the immun- ity is acquired? To answer this question satisfac- torily it is necessary to bring phagocytosis in rela- tion to two different t5'pes of antibacterial immun- ity which it is possible to recognize. Cholera is an example of that type of antibacterial immunity in which the bactericidal power of the serum under- goes a great increase. It is stated that anthrax represents another type in which the immunity is not dependent on the bactericidal power of the seriim. Probably the same may be said of acquired immunity to the streptococcus, staphylococcus and the pneumococcus, yet it is perhaps not definitely established that the immunity in these instances is antibacterial rather than antitoxic. For the present we may, however, with Metchnikoff, con- sider that the immunity is antibacterial and that it is a cellular or phagocytic immunity. Eabbits which have been immunized against anthrax respond to subcutaneous or intraperitoneal injection of a virulent culture by concentrating so vast a number of microphages at the site of inocu- lation that the fluid becomes purulent in appear- ance. Examination shows an enormous degree of phagocytosis. When, on the other hand, non-ira- INFLUENCE OF HE RUM. 187 mune rabbits are submitted to similar inocula- tions, the fluid which accumulates locally is of a clear serous character, contains few leucocytes, and no phagocytosis is observable ; the animals die of a rapidly developing septicemia. From the results one may well suspect that the immunity is related to and perhaps coextensive with the acquired pha- gocytic power. But is the serum of no influence ? It has often Phagocytes been held that phagocytes take up bacteria only yfr'^u^elTt after the latter have been injured or killed by the Bacteria. serum or plasma. Metchnikofi: answers this objec- tion experimentally by inoculating an immune rab- bit with anthrax, withdrawing some of the exu- date at a time when phagocytosis is complete, and injecting it into a non-immune rabbit. The sec- ond animal dies. Since none but phagocytized bacilli were injected into the non-immune rabbit ( !), and since the latter succumbs to anthrax, it seems not only unnecessary, but unjustiflable, to assume that the bacteria must be attenuated by the serum before they can be taken up by the leu- -^^^ infruence oocytes. May the serum, nevertheless, have some ofserum. obscure action which may not be included under such terms as bactericidal and attenuating? It seems fairly well established that anti-anthrax serum, at least from certain animals, may exert a protective influence when injected into other ani- mals in conjunction with or in advance of the cul- ture; 3'^et Metchnikoff discredits the importance of such protection and says that "those properties of the body fluids, as the bactericidal, preventive and agglutinating, fall away into the background in such examples of immunitj^" It is the tendency 188 INFECTION AND IMMUNITY. ' of the school of Metchnikoff to refer the protective power of a serum to its faciilt}'' of stimulating the phagoc^-tes rather than to its effect on the micro- organisms. "We shall see, however, in speaking of opsonins (p. 193) that even in relation to anthrax the serum may possess a distinct property which facilitates phagoc}i;osis, not by stimulating the phagoc}i;es but by some action on the bacteria. Cholera and Concerning those diseases in which immunity fections! is characterized by a great increase of the bac- tericidal amboceptors or fixators, Metchnikoff does not disregard the existence or importance of the immune bodies, but rather seeks to show that they are a product of phagocytic activity. The con- ditions are held to be similar to those already mentioned in connection with intra vitam, hemoly- sis. That is to say, microcytase exists only in the leucoc}i;es of the immune animal under normal conditions; it escapes into the plasma, or into the serum during coagulation, only as a consequence of the phagolysis already mentioned. The phe- nomenon of Pfeiffer occurs only because the in- jected culture injures the leucocytes, resulting in the liberation of microcytase, which in conjunction with the fixators causes the solution of the vibrio. When phagolysis is prevented by a preceding in- jection of bouillon, phagocvtosis and intracellular solution of the organisms entirely supplant extra- cellular solution. Intravascular If an immune animal receives an intravascular and Phagolysis. injection of the vibrio of cholera and is sacrificed shortly, the relation of the organisms to the leu- coc)i;es may be studied in stained microscopic sec- tions of the organs (lungs). Leucocytes which FORMATION OF GYTA8E. 189 have undergone phagolysis are seen to be clumped in the pulmonary vessels and in their immediate vicinity one finds many micro-organisms which have been changed into the characteristic granules by the action of the cytase which has escaped from adjacent leucocytes. Coincident with the phe- nomenon of phagolysis, the leucocytes lose their phagocytic power; hence, no bacteria are found within the leucocytes. On the other hand, all those vibrios which are remote from the leuco- cytes have a perfectly normal appearance. Phago- lysis in the blood stream may be prevented. Just as in the peritoneal cavity, by a preceding injection of bouillon into the vessels. In this instance when the culture is injected no extracellular solution or transformation of the organisms into granules takes place, but as in the peritoneal cavity, their destruction is accomplished entirely within the microphages. Metchnikoff holds to the correct- ness of these observations and interpretations, al- though contradictory results were obtained by Pfeiffer and his pupils. As further evidence that wicrocytase is cytase does not exist normally in the plasma Metch- '"traceiiuiar. nikoff cites the condition which is found in the anterior chamber of the eye in immune animals. The vibrios continue unaffected in the aqueous humor until such a time as leucocytes wander in, when they are destroyed by phagocytosis. Hence, cytase does not exist in the aqueous humor, and if not in the aqueous humor it is surely absent from the plasma; for if present in the plasma it would reach the anterior chamber by a process of diffusion. Similar conditions prevail in edematous fluids. In another instance a portion of a vein. 190 INFECTION AND IMMUNITY. filled -with blood, was resected and centrifugated without the formation of a clot (absence of pha- golysis) ; the plasma contained no cytase. Also Gengou collected and centrifugated blood in tubes which were coated with paraffin, and thus avoided clotting; here also cytase was absent from the plasma. Increase of It would sccm, then, that two important anti- of*Phaqocy"ic bacterial factors characterize immunity to cholera and similar infections : the development of specific fixators, and a greatly increased phagocytic power on the part of the leucocytes. Metchnikoff leans to the view that bacteria, having absorbed fixators, are more readiW phagocytized, but no clear idea is given as to the change which the fixators produce. However, he would not refer the increased phago- ejtie power entirely to the influence of the fixa- tors. He believes that the leucoc}i;es of the im- mune animal have per se a higher phagocHic power than that of the normal animal. In anthrax, for example, the phagocytic power is height- ened in spite of the fact that there is no increase in specific fixators. This view, however, is op- posed by Denys and Leclef, who found that the leucocytes of the immune animal, when trans- ferred to normal serum, had no greater phago- cytic power than normal leucocytes. Fixators ]\Ietchnikoff believes that fixators, like cytase, Microph^ge! ^^*^ produced by the microphage. That the lymph- oid organs may form certain fixators seems prob- able from the observations of Pfeiffer and Marx in regard to cholera and Wassermann and Takaki in typhoid. During the process of immunization and at a time when amboceptors were absent from ANTITOXIC IMMUNITY. 191 the serum they could be demonstrated in tlie blood- forming organs (spleen, lymph glands, bone-mar- row) . MetchnikofE suggests that they may be pro- duced in these organs by the microphages which have wandered in after having englobed the micro- organisms. In contrast to cytase the fixators read- ily abandon the leucocytes which produced ihera and become a constituent of the plasma. The leucocytes have also been brought in rela- Natural tionship to antitoxic immunity and the formation [o ToxTns. of antitoxins. In experimental tetanus exudates which are rich in leucoc3^tes contain more toxin than does a similar quantity of blood. That is to say, the leucocytes have the power of absorbing toxins, and it is held that the natural immunity of the animal depends on the degree to which this power is present. The immunity of the chicken to tetanus depends not on non-susceptible nerve cells nor on the presence of natural antitoxin, but on the ' absorbing power of the leucocytes for the toxin. 'Not only do leucocytes absorb toxins, but it is held that they also are the producers of anti- toxins. As compared with the side-chain theory, it is a peculiarity of the view of Metchnikoff that antitoxin does not represent a constituent of the tissue cells, but rather the toxin itself, which has been altered by leucocytic activity in a manner as yet obscure. In passive antitoxic immunity the idea of a Passive chemical union between toxin and antitoxin does J'Jilmu'nity. not meet with general acceptance among the up- holders of the phagocytic theory. It is sometimes said that antitoxins are efficacious from the fact that they stimulate phagocytosis (absorption) of 192 INFECTION AND IMMUNITY. the toxin, the hitter then suffering disintegration in the leucoc3^tes. Sumniary. The following statements summarize the pliago- cytic theory of immunity as conceived by ]\Ietcli- nikoff : 1. Natural immuiiity to bacteria depends on and is coextensive with phagocytosis and subse- quent digestion of the microbes. Intraleucocytic destruction of the micro-organisms is accomplished by tlie C}i;ase, possibly aided by intraleucocytic fix- ators. jSTormal serum is devoid of both fixators and cytase. 2. Acquired immunity to bacteria depends on the establishment of a heightened phagocytic power as the result of immunization or infection. In disea=>es like anthrax, in which fixators are not in- creased, this new power is an. acquired property of the leucocjrtes and is independent of any in- fluence on the part of the serum. In diseases like cholera, the new fixators which are formed may render the micro-organisms more susceptible to phagocytosis, but this is probably secondary to increased function on the part of the phagocytes. Both cytase and fixator are produced by the pha- gocytic cells. In acquired active immunity to bacteria the fixators may be free in the serum and plasma, but the cytase is intracellular. In all cases cytase becomes extracellular only as the re- sult of phagolysis. 3. In passive immunity to bacteria, as when an antibacterial serum is injected for the sake of prophylaxis or cure, the serum is efficacious chiefly because it stimulates the leucocytes to increased phagocytosis. SUMMARY; OPSONINH. 193 4. Natural immunity to toxins depends on the power of the leucocytes, and perhaps the genera- tive organs, to absorb the toxin. 5. Active immunity to toxins is estal)lished througli the activity of the leucocytes, by which the toxin is probably so changed as to constitute antitoxin. 6. In passive antitoxic immunity the antitoxin presumably acts by stimulating the phagocytes to an increased absorption of the toxin. Many investigators are carrying on work in re- opsonins. gard to phagocytosis and the properties of serums from a point of vieAv wbich is entirely imbiased. From sources of this nature discoveries of recent date indicate that phagocytosis of micro-organisms by the leucocytes is impossible without the aid of some property in the serum. It seems that these substances, which tbe discoverers, Wright and Douglas, call opsonins, act directly on the bacteria, and that there is no reason to suppose that their virtue lies in a stimulation of the phagocj^tes them- selves. The facts which permit of this deduction are the following : 1. Wlien the fresh defibrinated blood of some animal is mixed with the culture of a suitable micro-organism (staphylococcus, strep- tococcus, anthrax bacillus, etc.) and placed in the thermostat for 20 or 30 minutes, stained prepara- tions of the mixture show that the polymorphonu- clear leucocytes contain a large number of the mi- crobes. 2. If, however, all the serum is washed from the blood before adding the micro-organisms, practically no bacteria are ingested. This shows the importance of the serum, but does not differ- entiate between some effect on the leucoc}i:es, on 194 IXFECTIOX AXD IMMUNITY. the one liand. or tlie bacteria, on the otlier. 3. In order to decide this point one may subject the suspension of bacteria to the action of fresli cell- free sernm. and after a contact of about 30 min- utes remove all the serum by centrifugation, and mix the "^sensitized" culture with serum-free blood; phagocytosis occurs almost to the same de- gree as when the fresh defibrinated blood, contain- ing serum, is used. These results seem to show definitely that phagocytosis depends on the power of the opsonins to affect the bacteria in some pe- culiar manner. Opsonins are very susceptible to heat, and, like complement, disappear spontane- ously from the serum in a short time. Hektoen and Ruediger, and Bulloch and Atkin have con- fi.rmed the observations of Wright and Douglas and the former have added facts of importance. It seems that opsonin has a structure like that of toxin, i. e., a haptophorous and an opsoniferous group ; -"hj heating sensitized bacteria the opson- iferous group appears tO' be destroyed, but the in- active opsonin (opsonoid) by saturating the re- ceptors of the bacteria prevents further sensitiza- tion by fresh serum" (Hektoen and Euediger). Various salt solutions neutralize the opsonins. Opsonins will be brought into still more important relationship to phagocytosis if it can be shown detinitely that they are increased as the result of immunization or infection. CHAPTER XV. THE SIDE-CHAIN THEORY OF EHRLICH AND ITS RELATION TO THE THEORY OF PHAGOCYTOSIS. In 1885, before the discovery of toxins and anti- side-thain toxins and before there was any knowledge as to piied to the real nature of immunity, Ehrlich^ published a small volume on the "Oxygen Requirements of the Body.^' Herein the belief was expressed that the assimilation of foods by cells is accomplished only after chemical union has taken place between the food substance and some constituent of cellular protoplasm. It is not the understanding that as- similation is at an end, however, when this union has occurred, for certain molecules of complex chemical nature and of great size must be split up into simpler substances before they can enter into the composition of protoplasm. Therefore, the cell constituent which combines with the nutritious molecule serves only as a link to bring the food- stuff into relation with the digestive, oxidizing or fermentative activities of the cell, Ehrlich speais of that portion of living proto- "Leistungs- plasm which represents the cellular activities as the "Leistungshern" of the cell, the center of cel- lular activity, or the central group of the proto- plasm, whereas those chemical groups which bind the food substances are called the side-chains of the " Leistungskern." The author of .the theory has made his concep- 1. Ueber das SauerstofiEbedurfnis des Organismus. kern" and Side-Chains. 190 IXFECTIOy AND IMMUNfTY. tioii more tangible through an analogy whirli was drawn with the so-called ring or nnoknis of benzol and its side-chains. The molecule of benzol, CgHg, has a definite formation in which each carbon atom is linked to two others in such a manner as to form a ring; three valences of each carbon atom are satisfied in this way, and the fourth is satisfied by atoms of hydrogen, one of which is at- tached to each carbon atom, thus : H I C / -^ H-C C-H II i H-C C-H \ II C i This ring is analogous to the "LeistuDgsl-cni" of the cell. A great variety of chemical compounds exists and very many may be produced syntheti- cally by substituting for one or more atoms of hydrogen, one or more other groups of atoms which may be ver}- simple or very complex. Tlie groups which have been substituted are called side-chains. Thus benzoic acid is formed from benzol by sub- stituting the acid radical COOH for a particular H, and the COOH in this instance is a side-chain of the ring : o c I^OH C / ^ H-C C-H II J H-C C-H C SIDE-CHAfNl^. 197 Just as the side-chains of the "Leistungslcern" may combine with food particles, so may the side- chains of the benzol ring combine with other groups of atoms and thereby assimilate the latter, so to SEiy, into the ring. To choose a simple exam- ple, the sodium of sodium hydroxid may unite with the side-chain COOH to form sodium benzoate, the hydrogen of the acid radical being replaced by the sodium, thus : o c C / -^ H-C C-H II 1 H— C C-H \ ^. C I H Presumabl}^ it is in some such manner as sodium is brought into relationship with the benzol nu- cleus, in the example cited, that the food sub- stances are brought into relationship with the ''Leistungskern" of the cell. The hypothesis of Ehrlich carries with it the Haptophores. assumption that the side-chains of a cell possess or consist of definite groups of atoms capable of unit- ing chemically with certain other definite groups of atoms in the food particles ; hence both the side- chain and the food substance have combining groups — haptophores. The side-chains of the cells Ehrlich now calls receptors, elements which we have already recognized in connection with im- munity. Inasmuch as different foods have differ- ent chemical compositions, it is likely that their binding groups are not identical; and if this be 198 lyFECTIOy AXD IMMUyiTY. true there must exist luany kinds of receptors, each of which is able to unite only with that food sub- stance Mhich has a corresponding binding group of atoms. In contrast to the condition with respect to foods, it is held that chemical substances of Imown composition, drugs and alkaloids never become in- corporated as a part of the protoplasm, that is, they do not unite with cell receptors, although the}' may affect the vitality and function of proto- plasm profoundly. Their inability to yield anti- bodies as a result of immunization is supposed to depend on this condition. Such substances, ac- cording to Ehrlich, exist in the cell in a condition of unstable salt formation with some constituent of the protoplasm, or in a state of solid solution. The following statement from a recent publica- tion by Ehrlich summarizes the nutritional aspect of the theory: "We must assume that all sub- stances which enter into the structure of proto- plasm are fixed chemically by the protoplasm. We have always distinguished between assimilable sub- stances which serve for nutrition and which enter into permanent union with the protoplasm, and those which are foreign to the body. No one be- lieves that quinin and similar substances are as- similated, that is, enter into the composition of the protoplasm. On the other hand, the food sub- stances are bound in the cells, and this union must be considered as chemical. One can not extract a sugar residuum from cells with water, but must first split it off with acids in order to set it free. But now such a chemical union, like every syn- thesis, demands the presence of two binding APPLICATION TO IMMUNITY. 199 groups of maximal chemical affinity, which are suited one to the other. The binding groups which reside in the cells and which bind food substances I designate as side-chains or receptors, while I have called those of the molecules of foodstuffs the haptophorous groups. I also assume that proto- plasm is endowed with a large series of such side- chains, which through their chemical constitution are able to bind the difEerent foodstiiffs and there- by provide the prerequisite for cellular metabol- ism." If the side-chain' theorv of nutrition is to be- sjde-chain " ... Theory Ap- come the side-cham theory of immunity it is nee- plied to essary that it undergo elaboration in order that the formation of antibodies may be adequately ex- plained. If, as Ehrlich assumes, the union of toxin with cell receptors, causes the overproduction of the latter as antitoxin, and if this union is an- alagous to that of food substances with similar re- ceptors, one may wonder that antibodies are not formed for our ordinary foods, antibodies which would be discharged from the cells and which would unite with circulating nutritious particles and thereby bring about a condition of starvation. Without entering into the intricacies of this ques- tion, it seems probable that normally a condition of ph5^siologic equilibrium exists between the food substances on the one hand and the cellular activi- ties on the other, so that the union of food with protoplasm constitutes no abnormal stimulus to the " Leistungskern" of the cell. When, however, cells are diverted from their normal metabolic function by union with toxins and other "abnormal food substances," the effect on the cell is de- 200 IXFECT/i)\ W I) I \l \IIMTY. scri])od as a coll doroet, the dofoct consisting- of tlie functional elimination of the receptor. The "Leis- tungskcrn' as the vital or regulating center of the cell repairs the defect by the formation of new re- ceptors, and in harmony with the hypothesis of Weigert produces not only enough to repair the defect, but a great excess, with the result that many are tliroAvn into the circulation. The anal- ogy of the "Leistungsl-crn" with the benzol ring can not be carried to this extent, for the latter has no power of reproducing side-chains to take the place of one which has been bound by some new group of atoms. Essential It will bc appropriate in this place to consider Ehriich's the character of the proof wliich has hoen offered **"^^" in support of the three tenets which constitute the framework of the theory of Ehrlich. Tlicse three tenets may be expressed as follows : 1. Antitox- ins counteract toxins by entering into chemical union with them ; a similar imion takes place be- tween other antibodies and their homologous sub- stances. 2. Toxins in injuring cells combine chemically with a definite constitiient of the proto- plasm, the cell receptor; other antigenous sub- stances- enter into similar union with the appro- priate receptors of cells. 3. Tlie specific antibodies of the serum are new-formed receptors identical in structure with those which, as cell constituents, had combined with the homologous antigens. First tenet : In the early days of studies on im- munity (1890-1897), the action of a toxin and the efficacy of an antitoxin could be determined only Chemical Union of Antibodies with Antigens. 2. An antigen or an antisenous siil)stanoe is one Avliich is able to cause the formation of an antibody. TOXm AND ANTITOXIN. 201 by injecting these substances into living animals, and the animal experiment naturally continues to be the means of testing the curative and prophy- lactic values of serums. So long, however, as such experiments were performed exclusively in the liv- ing animal the nature of the action of antitoxin remained to a certain extent in doubt. It re- mained uncertain wdiether antitoxin is protective because it actually destroys the toxin, because neu- tralization of a chemical nature occurs, or because in some manner it increases the resistance of the inoculated animal.- In Chapter viii, p. 78, experi- ments were cited to show that antitoxin does not destroy the toxin, and this is generally admitted to- day. There continues to be some difference of opin- ion, however, in relation to the two other possibili- ties, i. e., as to wdiether antitoxin combines chemi- cally with toxin, or is efficacious because of its stimulating power on the tissues of the animal. Behring, the discoverer of antitoxin, was from the beginning an exponent of the chemical theory, even at a time when the conceptions of Ehrlich had not been fully developed. On the other hand, certain noted investigators, especially Eoux and Buchner, and later Metchnikoff, stood for the alternative view. Following closely on Behring's great discovery, Ricmand Ehrlich studied the hemagglutinating toxin ricin, from the castor-oil bean, and by immunization with it produced a specific antitoxin, i. e., anti- ricin. Eicin is toxic to er}i:hrocytes both in the animal body and in the test-tube, and if it could be shown that antiricin protects in the test-tube by a direct effect on the toxin, it was highly prob- Antiricin. 202 INFECTION AND IMMUNITY. ChemicalNature of the Neutrali- zation of Toxins by Antitoxins- able tliat its action in the animal body wonld be of a similar nature. The resnlts left no donbt in the mind of Ehrlich that antiricin unites chemically with ricin, and the applicability of this principle in animal experiments became all the more ap- parent when it was shoT\'n that the proportion of antiricin which protects in vitro also protects in rivo. It is held that similar proof of chemical union between bacterial hemolysins, the hemolysin of venom and the leucocidin of the staphylococcus with their respective antitoxins is equally valid. Altliough the animal body can not be dispensed with in testing the action of the antitoxins of diphtheria and tetanus, certain principles of chem- ical action are found to prevail which leave no doubt in regard to the chemical neutralization of the toxins. If neutralizing proportions of diph- theria toxin and antitoxin be mixed in a test-tube and injected immediately, the serum does not af- ford absolute protection; if, however, the mixture is allowed to stand for from fifteen to twenty min- utes before injection, the protection is absolute. This alone would point to an action of the anti- toxin on the toxin, for the completion of which a certain amount of time is required. For the com- plete neutralization of tetanus toxin by its anti- toxin about forty minutes are necessary at ordinary temperatures. Then certain other chemical princi- ples described in Chapter viii, p. 79, are found to hold true: That neutralization proceeds more rapidly at higher than at lower temperatures, more rapidly in concentrated than in dilute solutions, and that it takes place in accordance with the law of multiple proportions. AMBOCEPTORS, ETC. 203 Granting, then, that neutralization of toxin by antitoxin is of a chemical nature, the first essential step in the chemical or side-chain theory is estab- lished. If antitoxin combines chemically with toxin, union must occur through combining groups which each molecale possesses. Herein lies the ex- perimental justification for assuming the existence of haptophorous groups. The situation is more difficult in regard to the Union of Aggiu- n • T -I tinin and Ambo- union of receptors of the second and third orders, ceptors with i. e., agglutinins and amboceptors with the ho- mologous receptors of bacteria and other cells. One can not titrate bacteria against agglutinin or bactericidal amboceptors so exactly as toxin can be titrated against antitoxin, for, in the first place, it is difficult to obtain at will a desired concentra- tion of bacteria and to keep it without alteration, and, in the second place, bacterial cells contain many more receptors than are necessary for their agglutination and solution. A given mass of bac- teria will take up varying quantities of agglutinin, depending on the concentration of the latter, and the same principle applies to the absorption of bactericidal and hemolytic amboceptors. As more and more agglutinin is added, the total amount absorbed increases with each addition, although the ratio of absorbed to unabsorbed agglutinin grows less continuously. The conditions which govern this phenomenon are not understood. Perhaps no condition speaks more decisively for chemical union of these bodies with cell receptors than immunization experiments which were car- ried on with cells which had been treated with a great excess of the specific antiserum. The as- J04 lyPECTIOX AXD IMMUMTY sumption was made that if one coukl force all the recc})tors of orvthrocvte:?, for example, to take \\]) the specific amboceptors, such corpuscles should lose their power to cause the formation of a hemo- l^-tic serum when injected into a suitable animal. This would follow logically, for the receptors of the corpuscles, being already bound, would not be free to unite with receptors of the immunized ani- mal. Antibodies were not formed under these cir- cumstances, from which it is concluded that the receptors of the er}i;hroc3'tes had united chemi- cally with the antibodies of the serum (Sachs). In order to completely occupy all the receptors of the vibrio of cholera Pfeiffer used 3,000,000 to 4.000,000 times the dissolving amount of the anti- cholera serum. Although the mere absorption of agglutinins and amboceptors by the homologous cells is cited in favor of the chemical hypothesis, we may bear in mind the contention of certain in- vestigators that this absorption is physical rather than chemical. Second tenet : What evidence have we that tox- ins and other antigenous substances enter into Antigens with chemical union with receptors in the cells of the Cell Receptors. . . . ^ immunized animal? It is probable that no ob- servation speaks more strongly in favor of such union than a famous experiment of "Wassermann's in which the central nervous system of guinea- pigs was ground up with tetanus toxin, the mix- ture allowed to stand for a short time and then injected into mice. The mixture was found to be non-toxic, and further experiments showed that the neutralizing power resides in the solid tissue in the emulsion. It is claimed bv Ehrlich that ChemicalNature of Union of Tox- ins and Other UNION WITH CELLS. 205 this experiment demonstrates positively that chemical union of tetanus toxin takes place with constituents of the nervous tissue. The toxin hav- ing been completely neutralized can not again be extracted from the tissue. The condition is the opposite in relation to some poisonous alkaloids, as strychnin, which it appears does not combine Avith the protoplasm firmly and may again be ex- tracted by simple methods. Von Dungern conducted very important work with the precipitins, which is interpreted as show- ing that albuminotis substances other than toxins are taken up chemically by the cells. He injected considerable quantities of a foreign serum into the veins of rabbits and studied its disappearance from the blood of the injected animal. Traces of the foreign serum could be recognized by treating the rabbit serum with a specific precipitin for the for- mer, the precipitin' having been obtained pre- viously by the immunization of other animals. The foreign serum disappeared from the circula- tion of the rabbit with some rapidity and since it could not be demonstrated in the excretions, it seemed necessary to assume that it had been bound by the cells, that is to say, by the cell receptors. Third tenet: Is there any direct experimental Proliferation proof that those constituents of cells which have been designated as cell receptors actually undergo multiplication in the cell itself as a preliminary to their discharge into the circulation in the form of antibodies? If this condition could be demon- strated in one instance, one might reasonably con- sider that it typifies a law according to Avhich all antibodies are formed. Further experiments by of Receptors. 20ti IXFECTIOX AXD IMMVSITY. von Dungern Avitli the precipitins seem to show that such intracellular overproduction actually does occur. The experiments concern the fate of ";^[ajaphlslna"' (plasma of the crawfish) wlien in- jected into the circulation of tlio ral)l)it (see above). If a single injection of the serum is given, a specific precipitin for the latter body in due time may be demonstrated in the serum of the rabbit. Eventually the precipitin disappears from the circulation by excretion or other means. At that time, when all the precipitin has disappeared, one may assume that the cells of the animal still contain an increased number of precipitin recep- tors, although the latter are no longer produced to such an extent that they are thrown into the cir- culation. If this condition exists the tissues of the animal at this time should be able to absorb a larger amount of the foreign serum, given in a sec- ond injection, and perhaps absorb it more rapidly than the tissues of an untreated rabbit. Using a specific precipitating serum in order to detect traces of the foreign serum which still remained in the blood of the injected animal, von Dungern de- termined that its tissues actually do absorb the plasma more rapidly than do the tissues of the untreated rabbit. The cells of the former have a greater absorbing power, i. e., a greater binding power for the plasma; therefore, an increased number of receptors. These examples are, perhaps, sufficient to illus- trate the principles of experimentation which have been followed in the attempt to obtain definite proof of the correctness of the essential points of the theory. The results are in entire accord with OTHER TENETS. 207 , the primary assumptions and show that the tlioory continues to serve as an explanatory basis for newly-discovered facts, and as a foundation on which new researches may be instituted. In addition to the three main principles treated other import- of above, the following points are necessarily in- of EiTrVich.**'** eluded in a summary of the views of Bhrlich, many facts of a corroborative nature having l^ecn ascer- tained in independent laboratories. 1. The recognition of different types of tissue receptors by Mdiich peculiarities in the action of the different antibodies are explained. Eeceptors of the first order, as antitoxins, anticomplements and antiamboceptors, are regarded as relatively simple bodies because no other constituent can be recog- nized than the haptophorous group by which they combine with their homologous substances. Ee- ceptors of the second order are more complicated in that they have something more than the mere binding power; usually they are able to produce some observable change in the substance with which they unite. Hence, each has a toxophorous or' a zymotoxic group in addition to the hapto- phorous, and the two groups are part of the same molecule. Toxins, agglutinins, precipitins and complements are receptors of the second order. Receptors of the third order, i. e., the bacterio- lytic, hemolytic and cytotoxic amboceptors, are still more complex in that they are, so to say, only partial antibodies, the complete body consisting of the amboceptor-complement complex. The ambo- ceptor is not an active body, but serves as an in- termediary body to connect the active substance, complement, with the cell. In the cytolytic proc- 20S IXFECTIOX A.\D IMMUyiTY. ess the amboceptor tliroiigh its cytophilous hapto- pliore first unites with tlie cell, and as a result acquires an increased affinity for complement, with AA'liich it unites through its complcmcnto- pliilous haptophore. Only after this double union is completed may complement affect the cell. From this it follows that complement in the cyto- l3i;ic process does not combine with the cell di- rectly. As previously stated, Bordet and others oppose the idea that the absorption of tliese bodies is of a chemical nature, considovinu- it railicv to he a physical process. Ehrlich has intimated liis belief tliat tissue am- boceptors play the chief role in the fixation of foods by the cells of the body. 2. The chemical theory explains the specificity which characterizes the formation and action of antibodies. Every antigen has a haptophore which is different from those of other antigens; conse- quently, it unites only with the corresponding cell receptor, and the latter w^hen overproduced and cast into the circulation retains its specific liinding power for the corresponding antigen. 3. The multitude of antibodies w'hic]i liave been obtained indicate that the cells contain a vast number of different receptors which correspond to the three types now recognized ; that is. there is a different antitoxin receptor for every kind of toxin, etc. 4. Ehrlich has limited the application of tlie term toxin to those substances of animal or plant origin, immunization with which causes tlie forma- tion of specific antitoxins. Other characteristics have been given in Chapter vii, p. G5, COMPLEXITY OF TOXINS. 209 5. Receptors of the second order, toxins, agglu- tinins, precipitins and complements, undergo a peculiar degenerative change, spontaneously or as a result of exposure to injurious agents, in wliich the toxophorous or zymotoxic group disappears or is rendered inactive. The termination -oid is af- fixed to the altered bodies, as toxoid, agglutinoid, precipitoid and complementoid, Wechsberg has described a similar degeneration of one of the hap- tophores of amboceptors, calling the product am- boceptoid. Toxoids and complementoids on im- munization cause the formation of corresponding antitoxins and anticomplements, by virtue of re- tention of their haptophorous groujDs. 6. By means of a special technic devised for studying the neutralization of toxin by antitoxin, i. e., the partial saturation method, Ehrlich found diphtheria toxin to be a very complex substance. Not all the molecules of the toxin have the same affinity for antitoxin, and according to the de- grees of their affinity have received the names of prototoxin, deuterotoxin and tritotoxin. Simi- larly, protoxoids and syntoxoids are molecules of toxoid having different affinities for antitoxin. These conditions are represented graphically by means of the "toxin spectrum" described pre- viously. 7. Ehrlich claims that the diphtheria bacillus secretes two toxins, one of which causes the acute manifestations of diphtheritic intoxication, where- as the second toxin, i. e., toxon, has a prolonged incubation period and probably causes diphtheritic paralysis. Toxon has a lower affinity for diph- theria antitoxin than the other constituents of the 210 IXFECTIOX AXD IMMUXITY. toxin solution, but is neutralized bv tbe same anti- toxin. Tbis view is strongl}^ opposed by Arrbe- nius and Madsen, wbo, working on tbe basis that the neutralization of toxin takes place according to certain laws of physical chemistry, claim that toxon is nothing more than toxin which has disso- ciated from the toxin-antitoxin molecule. 8. It is thought that the incubation period which characterizes the action of toxins represents to a large degree the time required for the action of the toxophorous group after the toxin has been bound by the cells. 9. Ehrlich stands for the multiplicity of com- plements in opposition to Bordet and others who claim the existence, of but one complement (alexin). The various complements differ in the nature of their haptophores, without regard to possible dijfferences in their zymotoxic groups. 10. Only those organs which have suitable re- ceptors may produce an antibody for a given anti- gen, i. e., only those cells which may enter into chemical combination with the antigen. It does not follow, however, that only those organs which show clinical or anatomic lesions may produce, say, an antitoxin; for other organs not so suscep- tible to the action of the toxin may still possess the suitable receptors and cast them out as anti- toxin. Causes of Dif- The various types of immunity are explainable oMmimJnity! On the basis of the side-chain theory in the follow- ing terms: 1. Natural immunity to toxins may depend on (a) a lack of suitable cell receptors, the toxin con- . sequently finding no point of attack; (h) a very TYPES OF IMMUNITY. 211 low affinity between cell receptors and toxin so .that the latter does not unite with the cells except •under special conditions (e. g., the immunity of chicken to tetanus) ; or (c) on the presence of natural antitoxins. 2. Acquired active antitoxic immunity depends on the multiplication and excretion of cell recep- tors (antitoxin) into the circulation, the new- formed bodies having the power of combining chemically with additional toxin which may be in- troduced. 3. Passive antitoxic immunity, as established by the injection of an antitoxin, depends on the abil- ity of the antitoxin, to combine chemically with the toxin and thus to divert the latter from the cells. 4. Natural immunity to bacteria depends on (a) a lack of suitable cell receptors with which the toxic bacterial constituents might combine; (h) a very low affinity between cell receptors and the toxic bacterial constituents; or (c) on the presence of natural bacteriolysins (amboceptors and com- plements). 5. Acquired active antibacterial immunity de- pends on the multiplication and excretion into the circulation of specific cell receptors (amboceptors) which have the power of uniting with complement to kill the micro-organisms which may be intro- duced. 6. Passive antibacterial immunity, as estab- lished by the injection of a bacteriolytic serum, depends on the ability of the amboceptors con- tained in the serum to unite chemically with the receptors of the micro-organism, as a result of which complement is absorbed to kill and perhaps 212 ixFEcriox AXD iMMixrry. Comparison of Theories of Fhrlich and Metchnikoff. to dissolve the Ijacteria. The (.'oniijlonient may be ])rcsent in the serum ■which is injected, or the nat- nriil complement of the individual may be utilized by the amboceptors. When one seeks to compare the theory of Eln-lii'li witli that of Metchnikoff, one finds little more in common than the general purpose of explainino: the ])henomena of immunity. Yet it is remark- able that where there is so little in common there are so few contradictions of an essential nature. The theory of Ehrlich has that degree of defi- niteness which it must have in order to be a plausi- ble chemical theory, whereas that of Metchnikoff seems more general in that it is so largely biologic and vitalistic. Each has a certain relation to nutrition. Plia;i:o- cytosis as a nutritional measure is found in lower types of animals, and accomplishes nothing further than to bring the food substance in contact "\^'ith the digestive ferments contained in the cell. Tu relation to nutrition the theory of Ehrlich begins, so to sa}'', where the phagoc}i;ic theory leaves off, involving, as it does, the method by which food substances become a part of the protoplasm. Metchnikoff, with Ehrlich, recognizes the vari- ous antiliodies which have been discovered. The former holds that all are produced by the phago- cytes without suggesting clearly a method Ijy which they may be formed. Ehrlich assumes a very precise method by which they may be formed, but designates no particular cells as their pro- ducers, stating only in a general way that an anti- body is produced only by those cells with wliich the FjHRLKJU and METCHNIKOFF. 213 antigen may combine; in some instances, the leu- cocytes may be snch cells. The theory of Metchnikoff is not concerned with the structure of toxins and the various antibodies, nor with the m.ethod by which toxins may injure the ceils, whereas Ehrlich presents delinite concep- tions on these points. Both recognize that there is more than one com- plement (cytase). Ehrlich recognizes no limit to the varieties which may exist, whereas Metehnikoff describes but two cytases, microcytase and macro- cytase. The view which Metehnikoff has expressed, tliat antitoxin is produced by some action of the phago- cytes on the toxin, is directly opposed to that of Ehrlich which, recognizes antitoxin as a product of the cell itself, They agree that amboceptors (fixators) become extracellular in the blood. Metehnikoff holds that complements (cytases) are produced only by the phagocytes and that these substances are found in the plasma or serum only as a result of injury to the phagocytes (phago- lysis). These points are not involved essentially in the theory of Ehrlich. Certain investigators who work in harmony with the side-chain theory, as well as those who represent the views of Meteh- nikoff, have extracted complement from the leuco- cytes. Some of Ehrlich's supporters believe that complement exists normally in the plasma. Metehnikoff and Ehrlich hold divergent views concerning the action of antitoxins, the former be- lieving that antitoxins stimulate the phagoc^iies to an increased absorption and consequent destruc- 214 IXFECTIOy AyO IMMUNITY. tion of the toxin, Avhereas Ehrlich claims that antitoxin neutralizes toxin by combining chemi- cally with it. According to Metchnikoff, all types of immunity depend, directly or indirectl}', on phagocytic activ- ity. Wliile the side-chain theory is not in har- mony "with such a broad assumption, it carries with it no denial of the phenomenon of phagocyto- sis nor of its importance in certain infections. From these selected considerations it is seen Compatibility ^^^^^ '*'''' ® ^^™ theories do not stand to each other in of Theories. j;]^q relation of antitheses, and in the light of pres- ent laiowledge it would seem unwarranted to cling to one view to the absolute exclusion of the other. It does not follow that because demonstrable serum properties explain immunity to one disease, or to a certain group of diseases, that recovery from all diseases miist depend on properties of the serum ; nor because phagoc^^tic activity explains recovery in certain instances that recovery from all diseases must depend on a similar activity. The conditions which exist in each disease, of course, must be recognized independently. It so happens that recovery from a certain group of di'jeases, e. g., staphylococcus, streptococcus and pneumo- coccus infections, is not accompanied by the de- velopment of conspicuous antitoxic or bactericidal properties in the serum, but they are characterized by a great increase in the number of circulating leucoc3i:es (microphages), cells of lcno\\Ti phago- c\i:ic and bactericidal power, whereas the opposite conditions are found in certain other diseases, e. g., typhoid and diphtheria. If one seeks the most apparent explanation in each case, the great leuco- OPI^ONINS. 215 cytosis would seem to be of prime importance in the first group, and the antitoxic and bactericidal power of the serum in the second. Investigations from various sources render un- opsonins, questionable the value of phagocytosis in certain infections, and of particular significance is the work concerning opsonins which was referred to in the preceding chapter. From this work it follows that even for the phagocytic destruction of bac- teria the serum contains properties which are of essential importance. This appears of all the more importance from the fact that immunization with at least some micro-organisms (streptococcus, stajohylococcus) causes an increase in opsonins or bacteriotropic substances. The accompanying illustration, with some modi- fications, is taken from "Ehrlich's Seitenketten- theorie,'' by Ludvig Aschofl;. The cell used for immunization is assumed to be a cell which will cause the formation of antitoxin, agglutinin or precipitin, and bactericidal amboceptors; the diphtheria bacillus is such an organism, consider- ing toxin as one of the receptors of the bacillus. This means that the bacillus is able to cause the overproduction of all three types of receptors. The illustration, however, is on the basis of a hypo- thetical cell (p. 216). A list of immunizing bodies, their anti-bodies, and sjmonyms for complement and amboceptor, is also appended (p. 217). IMMUNE HUBHTAyCEH. 217 List of Immunizing Bodies and Theie Antibodies. Antigens or Products of Immnnizing immuniza- substances. tion. List of Im- mune Sub- stances. Toxins. Complements Ferments. Precipitogen- o u s s ub - stances Agglutinogen- o us s ub - stances Opsinogenous substances of bacteria Cytotoxin pro- ducing sub- stances Precipitins Agglutinins Cytotoxins Hemolysins, etc. Complement Alexin Cytase Antitoxins. An ticomple- ments Antiferments Precipitins Agglutinins Opsonins Cytotoxins. . . Hemolysins Bacteriolysins Special Cyto- toxins Spermotoxin Nephrotoxin Hepatotoxin Neurotoxin Syncytioly- sin, etc. Consisting o f two bodies, i. e., comple- m e n t and amboceptor. Immunization avith Antibodies. Antiprecipitins Antiagglutinins {1) Anticytotoxins Antihemolysins, etc. Consisting either of anti- complements or antiam- boceptors ; the latter may be an antibody for the complementophilous or for the cytophilous haptophore of the ambo- ceptor. Synontms. Amboceptor Immunk'Jrper Zwischenkorper Intermediary body Substance sensibilisatrice Fixator Preparator Copula Desmon CHAPTER XVI. TEINCIPLES OF SERUM THERAPY. In the strict sense serum therapy means the in- jection of antitoxic or antibacterial serums for curative or prophykictic purposes ;■ this is passive immunization or direct serum therapy. Active immunization, in which the tissues of the individ- ual are induced to form antitoxins or antibacterial substances as a result of vaccination or protective inoculations, may be considered as indirect serum therapy. "We may, therefore, include thn latter as one of the serotherapeutic measures. Bearing in mind the significance of the terms active and passive immunization, and the fact that they may be used for curative and prophylac- tic purposes, the various procedures may be classi- fied as follows:* I. PROPHYLACTIC INJECTIONS. _ Classified- A. Active immunization, in which vaccina- therapeutic tion and protective inoculations are included, as with the organisms of typhoid, cholera and plague. Depending on the material injected, the result is the formation of antitoxins or antimicrobic sub- stances (amboceptors) ; agglutinins are formed in- cidentally. 1. Inoculation of virulent organisms, (a) In- oculation with small amounts of a virulent organ- ism, i. e., of a non-fatal dose ; used principally in experimental work. (&) Inoculation with virulent • Modified from Deutsch and Feistmantel in "Die Impfstofife und Heilsera," Leipsic. Geo. Tliieme, 1903. Measures. ACTIVE IMMUNIZATION. 219 organisms into a tissue which has some natural re- sistance. The success of vaccination against small- pox by using virus obtained directly from the dis- eased, a method which was practiced in earlier times, was probably due to the fact that the virus found unfavorable conditions for the development of virulence in the skin. In some instances im- munization is accomplished more successfully Ijy inoculation of bacteria or toxins into the blood stream, as in Kitt's method of vaccination against symptomatic anthrax and in immunization with rattlesnake venom. . 2. Injection of attenuated virus or toxin. At- tenuation may be accomplished by air and light (chicken-cholera, Pasteur) ; by cultivation at high temperatures (anthrax, Pasteur) ; by chemical agents (anthrax, Eoux; diphtheria and tetanus toxins, Behring and Eoux) ; by desiccation (rabies, Pasteur) ; by passing the virus through other animals (swine erysipelas, Pasteur). This last observation was a most instructive one; passing the bacillus through the rabbit several times in- creased its virulence for the rabbit but decreased it for swine, while passing the organism through the dove increased its virulence for swine. 3. Injection of killed organisms (anthrax, Tous- saint; swine plague, Salmon and Smith). This is the safest means of vaccinating against cholera, typhoid and plague. In the Pasteur treatment of hj^drophobia the first injection of the dried spinal cord probably contains the Irilled virus. 4. Injection of bacterial constituents (a) Bacter- ial cell plasm (Buchner's plasmin, obtained by sub- mitting micro-organisms to high pressure, and Koch's tuberculin TE) ; (&) Soluble bacterial 220 IXFECTIOX AXD IMMUXITY. products (tlie bacterial proteins, as Koch's old tuberclin and mallein ; the sohible toxins ; products of bacterial autolysis), ^\^len toxins are injected antitoxins are formed. The autolytic products of some organisms, e. g., typhoid and dysentery, cause the formation of bac- tericidal amboceptors and agglutinins, but not antitoxins. B. Passive immunization: the prophylactic in- jection of antibacterial and antitoxic serums. C. Mixed active and passive immunization: the simultaneous injection of an immune serum with the corresponding organism, which may be killed or living. The serum causes immediate, though temporary, resistance, and, in the meantime, an active, more permanent immunity develops as a consequence of the injection of the organisms. This method has been practiced with swine plague, swine erysipelas, rinderpest, and experimentally in typhoid, cholera and plague. II. CURATIVE IXJECTIONS. A. Active imnnmization. 1. Injection of killed micro-organisms in small doses with the intention of hastening antibody for- mation, as suggested by Fraenkel in the treatment of typhoid fever; value not yet demonstrated. B. Passive immunization. 1. With antitoxic serums : diphtheria, tetanus, snake bites, plague, tuberculosis (?), t3'phoid (?), streptococcus infections (?), etc. 2. "With antibacterial serums : typhoid, cholera, plague, dysentery, streptococcus (?), staphylococ- cus (?) and pneumococcus (?) infections. In general, serums to be effective must have a ANTITOXIC THERAPY. 221 certain strength. When diphtheria antitoxin was General first used j)reparations were put on the market ofiierums. which contained twenty or fewer antitoxin units per cubic centimeter, a strength which would necessitate the injection of 150 c.c. or more in or- der to introduce 3,000 units. Much of the early criticism of dijDhtheria antitoxin is traceable to the low vahie of the serums used at that time rather than to an injurious effect on the patients. If diphtheria antitoxin now contains less than 250 units per c.c. it is considered unfit for use; many serums contain 500 -or more units per c.c. Antitoxic and other serums should be free from micro-organisms and toxins. The cases of tetanus which developed in St. Louis following the injec- tion of diphtheria antitoxin will be remembered. With correct governmental supervision of the manufacture of serums, such accidents are entirely preventable.'- For the sake of simplicity we may consider the principles involved in serum therapy under the three topics of (a) antitoxins, (h) bactericidal or antibacterial serums, and (c) vaccination. (a) antitoxins. It has been sufficiently emphasized that neutral- Antitoxins. ization of toxin by antitoxin implies a chemical union between the two substances. When the two are mixed outside the body at a given temperature and at a given concentration, the rapidity and com- pleteness with which the union occurs depends only on the degree of affinity which one has for the other. There is no third substance with which one or the other may unite. In the body, however, the 1. See appendix to Chapter VII (Part I). 22-2 JXFECriOX AXD IMMUXITY. conditions are more complex; in this case two com- binations are possible for the toxin, one with the antitoxin which has been introduced and a second with the tissue cells. As an instance of the great rapidity with which toxin may unite with cells, the work of Heymans with tetanus toxin may be cited. ''Heymans found that, if all the blood were removed from an animal a few minutes after the injection of a single fatal dose of tetanus toxin and the blood of another animal substituted, still the animal died of tetanus" (Eitchie) ; that is to say, all the toxin had been bound by the cells in that brief time. Binding of Other experiments show that quantities of toxin Tissues', '^i^tl antitoxin which are neutral when mixed be- fore injection are not entirely neutral if injected separately and at difEerent points of the body. In this instance some of the toxin has had time to unite with tissue cells before it could come in con- tact with the antitoxin. Certain work by Donitz illustrates not only the rapidity with which toxin may be bound by the tissue, but also the method by which antitoxin ef- fects a cure. In relation to tetanus he found that if the toxin were injected first and the antitoxin four minutes later, a quantity of antitoxin, which was slightly in excess of the neutralizing dose, was required to prevent the development of tetanic s}Tnptoms; if he waited eight minutes, six times as much antitoxin; after sixteen minutes, twelve times as much; after one hour, twenty-four times the simple neutralizing dose was required. A few hours later no amount of antitoxin could save the animal. Similar conditions were met in the neu- tralization of diphtheria toxin by its antitoxin in CURATIVE ACTION. 223 the body. Madsen, in performing what he called "Curative Experiments in the Keagent Glass/' found that the longer tetanolysin had been in con- tact with erythrocytes^, the more antitetanolysin was required to tear away the toxin from the cor- puscles. Practical experience with diphtheria also indicates that the longer the disease lasts the more antitoxin is required for cure. The experiments just cited give us a clear con- Nature of ception as to what is meant by the curative action Actiotll of an antitoxin — an action which consists not of the neutralization of the circulating toxin, but of the wresting away from the tissue of the toxin which has been bound. Incidentally the circulat- ing toxin is neutralized, and for this step, which is essentially prophylactic in nature, the simple equivalent of antitoxin is required. But for the wresting of toxin from tissue cells not a mere equivalent of antitoxin, but a great excess, is re- quired, as shown by the experiments of Donitz and of Madsen. When diphtheria or tetanus has advanced so far that no amount of antitoxin will effect a cure, the relation of the toxin to the cells has become some- thing more than mere chemical union. Further processes of a biologic or biochemic nature have set in in which the toxin may have .become an integral part of the protoplasm, and the toxophorous group may have begun its destructive action, whatever the nature of this action may be. It is important to recognize that antitoxin can not repair an injury already done by the toxin. The repair of the injury depends on the recupera- tive power of the cells; hence, antitoxin cures by tearing from the cells, perhaps not all, but so much 224 iXFi:cTioy Axij immuxity. l\so Important Principles. Tetanus. of tlio toxin that lo. Microscopically and culturally the bacillus of Pseudodiph diphtheria can be distinguished with difficulty th^^a B««:'"'i- from a variety of other organisms which belong to the same group, and which are called pseudodiph- - theria bacilli. The latter are frequently found in diphtheritic throats, but occur also in the upper air passages and conjunctiva in the absence of all lesions. On the whole, they are non-pathogenic, but occasionallv a culture is found which causes a 24-4 lyFECTIOX AM) IMMUMTY. subcutaneous infiltration at the point of injection in an experimental animal. Hamilton cultivated one which Avas distinctly virulent for animals. Their pathogenicity, however, is altogether different from that of the diphtheria bacillus inasmuch as diphtheria antitoxin does not protect against them nor do animals which are immunized with pseudo- diphtheria bacilli become immune to the toxin of diphtheria. The Bacillus xerosis, which is thought by some to be the cause of xerosis conjunctivae, but which is also found under normal conditions, is a pseudodiphtheria bacillus. The animal experi- ment is the only positive means of differentiating the true from the pseudodiphtheria bacilli. Some consider them as diphtheria bacilli which have lost their virulence. The presence of these organisms may complicate the diagnosis of diphtheria in some cases, but there is little danger of serious error. If one found organisms resembling the bacillus of diph- theria in a membranous sore throat which was ac- companied by severe s}miptoms, there could be no wavering in the decision to use antitoxin. II. TETANUS. In 1884 Carle and Eattone demonstrated the infectiousness of tetanus by inoculating the pus from an infected wound into rabbits; 11 of the 12 inoculated rabbits died of tetanus. In 1885 the bacillus was discovered by Nicolaier, and Kitasato cultivated it artificially in 1889. Characteristics The Organism is rather long and slender (2 to 4 microns long, 0.3 to 0.5 broad), possesses many ilagella and has a small amount of motility. It stains readily with the ordinary anilin dyes and by of the Micro- orflanism. TETANUi^. 245 Gram's method. In young cultures isolated cells and threads predominate, but after a few days spore formation begins; eventually all the adult cells degenerate and the culture consists entirely of spores. The spores have a larger diameter than the bacillus; are situated at one end of the cell and give the latter the characteristic "drumstick" form. The organism is a strict anaerobe and is obtained in pure culture with some difficulty. Morphologically it is difficult to distinguish from the bacilli of malignant edema and symptomatic anthrax. Few organisms are distributed more widely and Habitat. generously than the bacillus of tetanus. It is most abundant in street dirt and in tilled ground which has been fertilized with manure. Nicolaier found it in twelve out of eighteen samples of earth. It is less abundant in timber land. Such a distribu- tion is easily accounted for, since the bacillus seems normally to be an inhabitant of the intesti- nal tract of the horse, cow and sheep, and is often found in that of man and other animals. It oc- curs on dirty clothing and readily gains access to dwellings with dust in which it may be blown and carried about. Tetanus frequently develops in gunshot wounds in which dirty clothing is carried into the tissue, and several instances of house tetanus have been noted in which a number of in- dividuals in the same dwelling have contracted the disease following injury. Particular localities may be heavily infected. In certain tropical districts a large percentage of the new born die of tetanus neonatorum, and puerperal tetanus has prevailed alarmingly in Bombay. It has been suggested that the custom of bleaching the linen on the 246 INFECTION AND IMMUNITY. ground may be responsible for the prevalence of tlie disease in these localities, but from the fact that it has decreased under aseptic practices the general lack of surgical precautions is probably of greater importance. Tetanus has resulted from the injection of impure gelatin for hemostatic purposes. The bacillus has been found in sea water. The ability of the bacillus to proliferate outside the animal body has not been determined. Some observers liold that it exists as a vegetative organ- ism only in the intestinal tract of animals, but the possibility of proliferation in soil is by no means excluded, particularly since it is so often found in association with organisms which are known to favor its growth. When incrusted in solid ma- terial and accompanied by suitable saprophytes it may readily find the anaerobic conditions which are demanded for germination of the spores. Resistance. The sporcs are very resistant. In one instance they remained virulent for eleven years "on a splin- ter of wood. They may be killed in six days by direct sunlight. In comparison with non-spore- forming organisms they are very resistant to anti- septics. Kitasato found that they were killed in five minutes by steam, in fifteen hours by a 5 per cent, carbolic acid, in two hours by 5 per cent, carbolic acid to which 0.5 per cent, of hydro- chloric acid was added, in three hours by 1/1000 corrosive sublimate and in thirty minutes by the same solution to which 0.5 per cent, hydrochloric acid had been added. Tetanus is conspicuously a wound infection and that it develops so frequently from wounds which are contaminated with earth is readilv understood TETANUS. 247 from the distribution of the organisms as cited infection Atria , /^ • T ■ 1 ii'j 1 i> and Conditions above. Considering, however, the great number ol which Favor such wounds and the prevalence of the bacillus, " *«^t">"- the rarity of the disease is remarkable. In expla- nation of this fact investigations have shown that the organism is not a vigorous parasite, that it demands special conditions for its development in the tissues. According to Vaillard and Rouget, the spores when washed free of toxin do not cause tetanus, but rather are taken up and destroyed by leucocytes. The bacillus, furthermore, is a strict anaerobe, Anaerobic demanding for its development a wound from li^wounds. which the air is largely excluded. It is well known that penetrating wounds in which infected ma- terial is carried beneath the fasciae, as the rusty nail wounds, also those accompanied by deep lac- erations, as wounds inflicted with blank cartridges, or those in which dirt and micro-organisms have been ground into the tissues, as in crushing inju- ries, are prone to be followed by tetanus. Under such conditions the bacillus lies deeply imbedded in the tissues and remote from the air. Of equal importance is the presence of foreign mhibitionof matter and particularly of other micro-organisms, •'•'agocytosis. Relatively superficial wounds in which there is laceration of the tissue with consequent necrosis, as in wounds by toy pistols, even the paper-cap pistol, are well adapted for the development of tetanus if the germs were on the skin at the time of injury. Kecrotic tissue favors the proliferation of the tetanus bacilli in two ways. In the first place it seals up the wound to a certain extent, and thus provides the requisite anaerobic condi- tion ; in the second place it would seem to prevent Infections, 248 IXFECTION AND IMMUNITY. phagocytosis of the bacilli in some obscure way. It has been suggested that the strong, cheraotactic relation which exists between necrotic material and leucocytes causes the latter to take up the dead tissue rather than the bacilli. That innocent for- eign material may favor the development of teta- nus in the presence of the microbes was shown by Vaillard and Rouget: tetanus would develop in the presence of an artificially produced hematoma or a subcutaneous fracture while in the absence of such predisposing factors the bacilli were taken up by phagocytes. Mixed Saproplniic organisms and the pus-producing cocci which are usually found in wounds contami- nated with earth appear to favor the development of tetanus. This may be explained to some extent by their ability to increase the virulence of the tetanus bacillus, a condition which is noted in cul- tures. In the wound they may engage the leuco- cvtes in phagocytosis and prevent ingestion of the tetanus l3acilli. As aerobic organisms they may facilitate development of the bacilli by consuming local oxygen. Our great harvest of tetanus following Fourth of July injuries is closely associated in the first place with the warm, dry season in which the bacilli are more readily disseminated with dust, and in the second place with the nature of the wound and mixed infections, as described above. Occasionally tetanus follows the simplest wounds, which may have healed entirely before symptoms develop. In "idiopathic tetanus" and in the so-called "tetanus rheumaticus," which fol- lows exposure to cold, the infection atria are un- known. In the latter instance a latent infection, TETANUS. 249 which is stirred into activity by the reduction of resistance which often follows exposure^, may be present; avirulent tetanus bacilli (?) were culti- vated from the lungs of one such patient. The oc- casional occurrence of tetanus following diphthe- ria and typhoid suggests that infection may take place through wounds of mucous surfaces. Neither the bacillus nor its toxins penetrate the unbroken skin or mucous membranes, and the alimentary tract is further protected by the ability of the gas- tric and pancreatic juices to digest the toxin. The incubation period varies from two or three Period of days to several weeks. In the statistics of Eose 20 "*^" ^*'**"' per cent, of the cases showed symptoms in the first week, 45 per cent, in the second, and about 30 per cent, in the third or fourth weeks. The shorter the incubation period the more fatal the disease. In the statistics cited the mortality with short in- cubation was 91 per cent.; when the incubation ■ period was moderate it was 81.3 per cent., and when prolonged, 52.9 per cent. The nearer the infection atrium is to the central nervous system the shorter is the incubation period; 'Tiead teta- nus" develops quickly. The pathogenic properties of the tetanus bacil- Pathogenesis. lus reside in its soluble toxins, of which two, teta- nospasmin and tetanolysin, are loiown. The char- acteristic nervous phenomena of the infection de- pend on the action of the former, whereas the lat- ter, a hemolytic toxin, is of minor importance. As in diphtheria, a systemic distribution of the bacilli is not necessary for the development of the dis- ease, the toxin being produced by the organisms in the woimd, whence it is carried to the nervous tissue by way of the lymphatics. Particularly in 250 INFECTION AND IMMUNITY. . mixed infections tetanus bacilli may be carried to neighboring lymphatic glands and eventually reach the circulation; pure cultures have been ob- tained from the lieart's blood in experimental work. The blood, on account of its content in oxygen, is thought to be unfavorable for the growth of the organism. Just before death the toxin has been demon- strated in the blood of man by injecting some of the serum into mice. Its excretion in the urine is questionable. Tetanus produces no characteristic anatomic changes, although degenerative lesions in the ganglionic cells occur. Death usually occurs from asphyxia caused b)'' contractions of the dia- phragm, or muscles of the glottis, or from cardiac failure. In some instances the blood has been found more or less laked because of the action of the tetanolysin. Tetanospasmin. Tetanus toxin (tetanospasmin) has a very strong affinity for the nervous tissue of susceptible animals. This may be demonstrated in test-tube experiments in which the toxin is mixed with an emulsion of the nervous tissue; the nervous tissue neutralizes the toxin more or less completely, as determined by subsequent inoculations of the mix- ture (Wasserman's experiment). It is held by certain authorities that the toxin attacks only the nervous tissue in man; in some of the lower ani- mals, however, various organs, especially the liver, have an affinity for the toxin. The method by which tetanus toxin reaches the central nervous system has been the subject of much speculation and experimentation. Eecent observations by jMarie and ]\Iorax and by Eansom and Meyer show with a great degree of probabil- . TETANUS. 251 ity that it is absorbed by the end organs of the motor nerves and from there passes to the gang- lionic cells through the axis cylinders. This ab- sorption takes place very quickly; when the toxin is given intravenously it disappears from the blood in the course of minutes. It has been found in the nerves within an hour and a half after subcutane- ous injection. Its further transmission centrally occupies more time and, indeed, the investigators mentioned explain the rather long incubation period of the disease on the basis of the time re- quired for this transmission. The brief incuba- tion period in "head tetanus," accordingly, would depend on the short distance the toxin is obliged to travel to reach the ganglionic cells. Although the toxin appears not to be taken up varieties of by the sensory nerves, a painful form of the dis- Tetanus. ease, tetanus dolorosa (Meyer), may be pro- duced experimentally by injecting the toxin into the posterior roots of the spinal nerves. Eoux caused "cerebral tetanus" by introducing the toxin into the cerebral tissue; the condition is charac- terized by absence of contractures. "Local teta- nus," in which the muscles in the vicinity of infec- tion or inoculation are involved in contractures, is the first symptom of tetanus in experiment ani- mals; it rarely occurs in man except in head teta- nus. The phenomenon depends on the fact that the toxin, being transmitted through the motor nerves, reaches first the ganglionic cells which cor- respond to the infected area. According to ]\Ietchnikoif, the only natural im- immunity munity which man possesses to tetanus is leuco- '" *"' cytic and this may be sufficient to protect under favorable conditions. The observations of Vaillard 252 IXFECTION AXD IMMUXITY. and Eoiiget (cited above) support this claim. Sus- ceptibility depends not onlj- on the presence of suitable receptors in the nervous tissue, but also on the degree of affinity which exists between tliese receptors and the toxin. In man and some animals this affinity is very great, whereas in fowls it is weak and an enormous amount of toxin is re- quired to cause tetanus. A further proof of this weak affinity in non-susceptible animals rests in the fact that the toxin when injected into the blood remains unabsorbed for a long time, whereas in susceptible animals it disappears very quickly. Ac- quired immunity depends on the presence of anti- toxin in the circulation. Prophylactic Tctanus antitoxin is a thorough prophylactic. Antitoxin. This fact has been heralded so extensively in re- cent years that there can be little excuse for ignor- ance on the part of any physician. At the same time, the returns from the "Fourth" show that the principle is not yet deeply imbedded in the medical mind. It is quite certain that a large percentage of these fatalities could be prevented by two injec- tions of antitetanic serum, one at the time of in- jury and a second from five to eight days later. An epidemic of puerperal tetanus in an obstetric ward in Prague was checked by prophylactic injec- tions of the antitoxin. In a certain section of France 4,000 horses, with injuries commonly fol- lowed by tetanus, received antitoxin and none de- veloped the disease. No degree of efficacy on the part of the anti- toxin, however, justifies disregard of the surgical care which the wound demands. From the facts cited it is clear that thorough and frequent disin- fection of the wound, free drainage, the removal TETANUS. 253 of all foreign and necrotic material, and the ac- cess of air are measures of eminent importance. Punctured wounds should be opened up. Anti- toxin, preferably as a powder, may be used in the wound, and the serum infiltrated into the adjacent tissue. The principles which apparently underly the ill curative Vaiue success of the antitoxin as a curative agent were ** Anntoxm. treated of in Chapter XVI, Part I. Its adminis- tration as early as possible after symptoms have appeared is demanded. After symptoms have ex- isted for more than thirty hours Behring main- tains that there is no hope of cure by the subcuta- neous route. Inasmuch as forty hours or more are required for complete absorption from the subcuta- neous tissue, intravascular injection of at least the first dose would seem to be indicated. Yet by neither of these methods is the most essential end accomplished, for the antitoxin does not reach the nerves nor can it be recognized in the cerebrospinal fluid in conspicuous quantities. The most that such injections accomplish is the neutralization of the circulating toxin, that which is not yet on its way to the central nervous system through the mo- tor nerves. It is, of course, important to neutral- ize the circulating toxin and it must be done quick- ly, for in the course of a few hours the fatal quan- tity of toxin may have been absorbed; "a dose of antitoxin which would save in the morning may be without effect in the evening." At the same time it is of greater immediate im- Method of portance to neutralize that which has already en- Antitoxin. tared the peripheral nerves, and if possible to tear away some of the toxin already bound by the gang- lionic cells. To accomplish this object, or to at- 254 IXFI-JCTJOy AXD IMML MTV. tempt it, special procedures are demanded. "We may then consider the antitoxic treatment as fol- lows : First: The neutralization oL" the toxin which has already been absorbed by the peripheral nerves and spinal cord at a point as near the vital centers as possible. This involves surgical exposure of the large nerves of the part as near the trunk as possi- ble and their infiltration with antitoxin (Ransom and Meyer), and in desperate cases the infiltra- tion of the antitoxin in the spinal cord in the vicinity of the medullary centers. From five to fifteen minims may be injected into the nerve trunks at a sitting, and the operation may be re- peated on subsequent days; the needle should be partially withdrawn and reinserted in different di- rections during the injection. Eogers recommends tying loose ligatures around the nerves after the operation so that they may be readily drawn up and identified for further injections. In order to reach the medulla the intracerebral method of Roux or that of Rogers may be utilized. Kocher has devised a technic for the intracerebral injec- tions. Anterior to the parieto-frontal suture and to one side of the median line the scalp is pre- pared, and a hole drilled through the skin and skull, having its direction toward the foramen magnum. By means of a long needle, the ventri- cle is penetrated and the serum, after injection, finds its way to the fourth ventricle to the imper- iled respiratory and cardiac centers; 10 c.c. may be injected. Rogers seeks to accomplish the same end by a different technic. He introduces the needle between the sixth and seventh cervical ver- tebrae, punctures the cord deeply, and injects from TJ^TANUH. 255 20 to 30 minims at a sitting. Although there is danger of intraspinal hemorrhage in the proce- dure, no ill effects were noted. It has been recom- mended also that the cerebrospinal fluid be with- drawn by means of lumbar puncture and substi- tuted by antitoxin. Some physicians who have "iised this method report favorable results. Second : The neutralization of all toxin which, is not yet bound by the nervous tissue or absorl)ed by the motor nerves. This demands the infiltra- tion of the wound and surrounding tissue with the antitoxin, and injection of a sufficient amount of the serum into the circulation in order that circu- lating toxin may be neutralized. The intraneural, intraspinal or intracerebral injections should . al- ways be supplemented by subcutaneous or intra- vascular injections. The first dose should be given intravenously, whereas subsequent injections may be given subcutaneously. The injections should always be repeated. Unfortunately, tetanus antitoxin is not stand- standardiza- ardized by American manufacturers and dosage toxin! can not be controlled with any accuracy. Although standardization can not be accomplished with the same degree of accuracy as in the case of diphthe- ria antitoxin, its approximate value can be deter- mined (within 5 or 6 per cent.), which is suffi- cient for practical purposes. The antitetanic serums of Behring, Tizzoni and the Pasteur Insti- tute are all standardized, but on somewhat differ- ent bases. Behring advises the administration of 20 units of his serum for prophylactic purposes, and 100 units as the "simple" curative dose when given soon after the development of symptoms. N'ot less than 10 c.c. of American serum should Bacillus Botulinus. Infected Meats. 250 IXFKCTWX AXD IMMUXITY. be givcu for prophylaxis, and the dose should be repeated. No definite limits can be given as to the amount which may reasonably be given for cura- tive purposes. Ten cubic centimeters given intra- venously at once, and an equal amount subcutane- ously on subsequent days, would seem to be suffi- cient to neutralize the unbound toxin if the serum' has reasonable strength. Standardized serums cer- tainly are to be preferred. x^gglutination has no practical significanc'e for diagnostic purposes. An agglutinating poAver has been noted in the serum on the eighth day. Ag- glutinins may be produced by immunizing animals (rabbits) either with the bacilli or the toxin. In the latter case the formation of the agglutinin is due to the presence of agglutinogenic receptors in the toxin solution. HI. BOTULISM. Botulism is a peculiar form of meat poisoning in which the nervous system is involved princi- pally. From twenty-four to thirty-six hours after the poisonous meat is eaten salivation, ptosis, dila- tation of the pupils and paralysis of the ocular muscles develop and death from bulbar paralysis occurs rapidly in from 25 to 30 per cent, of the cases. In the event of recovery, convalescence may extend over weeks or months. The disease occurs especially in some European districts in which improperly preserved or raw meats are eaten. The term ichthyosismus is ap- . plied to a similar or identical disease which is caused in Russia by salted fish. In 1895 von Ermengem investigated a ham which had caused 50 cases of botulism, and isolated from it an anae- robic, spore-forming bacillus, which produces a BOTULISM. 257 soluble toxin capable of causing the entire symp- tom-complex of the disease.^ The organism pos- sesses flagellge, has limited motility, grows only in alkaline media, and in contrast to most pathogenic organisms prefers a relatively low temperature (18-25° C). It is probably on account of its physiologic activity at such temperatures that it is able to produce its toxin in meats which have been kept in a cool place. It is found in decom- posed ham and various sausages (Leberwurst and- Blutwurst), and probably gains access to the meat after the animal has been killed. Von Ermeji- gem investigated two hams from the same animal. One was under anaerobic conditions being covered with brine, while the other was exposed to air; only the former was toxic. The organisms may be absent from the superficial portion of the meat, but abundant in the deep portion. The spores are relatively susceptible to heat, being destroyed by a temperature of 80° C. for one hour. Aside from its occurrence in meat, nothing is known of the li le history of the bacillus. The disease is caused by the toxin which has al- Toxin. ready been produced in the meat and not by the activity of the organism after it has reached the alimentary tract (v. Ermengem). If an extract of the meat is made with water and the bacteria removed from the latter by filtration, the fluid shows characteristic toxicity for animals. This experiment may be used for determining the pres- ence of botulism toxin in suspected meat. The guinea-pig is the most susceptible animal. 1. other pathogenic organisms, especially B. enteritidis and B. coli communis, and recently the paratyphoid bacil- lus, have been found in poisonous meats. The term botulism formerly was applied to various forms of meat poisoning. 258 INFECTION AND IMMUNITY. According to v. Ermengem, the bacillus does not proliferate in the body, nor does it produce toxin vigorously at body temperature; hence, he consid- ers it to be a strict salprophyte — a pathogenic sap- rophyte. The toxin is taken up by the circulation j'roni the alimentary tract and is not destroyed by the gastric and pancreatic juices, differing in this re- spect from the toxins of diphtheria and t»tanus. It is prepared artificially by growing the organism anaerobically in suitable bouillon and subsequently . sterilizing the fluid by filtration. Like the other soluble bacterial toxins, it is susceptible to the ac- tion of air and light, and is destroyed by n ti'in- perature of from 60 to 70° C. Pathogenesis. That the toxin has a special affinity for the nerv- ous tissues is evident from the symptoms of the disease; histologically, the ganglionic cells show degeneration in fatal cases. Further evidence of a strong affinity between the toxin and nervous tissue lies in the ability of the latter to neutralize the toxin in the test-glass. The toxin, however, ap- pears not to be so selective in its action on the nervous tissue as the toxin of tetanus, for in bot- ulism degenerations of the glandular organs, and of the vascular endothelium with consequent hem- orrhages are characteristic anatomic findings. Man appears to be very susceptible to the intoxica- tion, whereas dogs, rats, and cats are relatively im- mune. The toxin is pathogenic by suljcutaneous or intravascular injection. Acording to v. Erfnengem, the bacilli when in- oculated subcutaneously do not proliferate, but are taken up by the phagocytes immediately or after thev have been carried to other organs. Animals and Antitoxin. PYOCYANJWS. 2.'5!) which have recovered from infection or which have been immunized acquire rather strong immunity to subsequent inoculations^, the immunity being antitoxic. The prophylactic measures consist in the avoid- Prophylaxis, ance of poorly preserved and improperly cooked meats, especially sausages. Botulism would seem to be very rare in this country where raw meats are not used extensively. The antitoxin (Kempner) has proved of some value in animal experiments, but its commercial preparation has not been warranted on account of the rarity of the disease. IV. BACILLUS PYOCYAlSrEUS. For a long time it was thought that the "bacillus Pathogenic of blue pus" Avas of no importance as an infectious agent for man, although its pathogenicity for ani- mals had been recognized experimentally. It is found with some frequency in the blood and or- gans of man at autopsy, when death has resulted from some other infection or chronic disease, and in such instances it is supposed that a so-called "agonal invasion" by the organism has occurred. During recent years, however, several cases of pri- mary pyocyaneus septicemia have been observed, the bacillus having been obtained from the blood in pure cultures during life or from the blood and organs shortly after death. It has been found as the sole organism in meningitis and vegetative en- docarditis. Some of the cases indicate, however, that a previous lowering of resistance, as that caused by tuberculosis and syphilis, is important for general invasion by the bacillus. It has been found several times in suppurative processes in the middle ear, and would seem to be either the cause 260 IXFECTION AND IMMUNITY. or a strong adjuvant in some cases of severe enter- itis, especially in cliildern. In systemic infec- tions, the sjTQiptoms are typlioidal in character, with high temperature, diarrhea and a tendency to the formation of hemorrhages in the skin and internal organs. Its Manifold The BacUlus pyocyaneus is widely distributed Activities. l ,j .j j and that it causes sq few infections is probably due to its low pathogenic power. It is an organism of manifold activities. It produces a substance, pyo- cyanin, which, when exposed to the air, assumes a bluish tint, and on which the color of the pus de- pends; pyocyanin is soluble in chloroform., from which it may be precipitated in crystalline form. I'nder proper conditions the organism also forms Ferments, a fluorcscent pigment. It produces a strong pep- tonizing ferment, coagulates milk, and in old cultures an autolytic ferment is found which di- gests many of the bacilli. As stated in a pre^^ous chapter, Emmerich and Lowe have identified a bacteriolytic ferment, pyocyanase, which dissolves the anthrax bacillus and other organisms. The ferment natiu-e of this substance is in some doubt, inasmuch as it resists the boiling temperature. Dietrich thinks its action is due to the production of osmotic changes. Old cultures contain a hemo- lytic agent (pyocyanolysin) of an alkaline nature, which resists boiling and is not a true toxin, since Endotoxin, immunization with it does not yield an antitoxin (Jordan). In addition to the products mentioned, the organism secretes a true soluble toxin for which.it is possible to obtain an antitoxin, and possesses, furthermore, an endotoxin for whicli an antitoxin can not be obtained. The soluble toxin of Bacillus yyacyaneus is not PYOCYANEUS. 261 produced in large amounts. It differs from the other soluble toxins in its resistance to heat, with- standing a temperature of 100° C. for five min- utes. It produces the symptoms which are char- acteristic of infection with the living organism, the principal anatomic changes being parenchyma- tous degenerations and ecchymoses, the latter sup- posedly being due to degenerative changes in the endothelium of the vessels. By immunizing with young cultures grown on y^ntito^ic and an agar surface a serum which is purely bacterid- ggp^^s*^'**^' dal is obtained. On the other hand, if an older toxin-containing bouillon culture be used, the serum is both bactericidal and antitoxic. The serum which is purely bactericidal has no power of neutralizing the toxin. The toxin solution con- tains not only the true toxin, but also quantities of endotoxin which were liberated as the dead bacilli were dissolved. Inasmuch as the antitoxin neutralizes only the true toxin, leaving the endo- toxin unbound, the toxicity of the filtrate can not be destroyed entirely by antitoxin, a condition which is brought out clearly when the attempt is made to neutralize a multiple of the simple fatal dose by the corresponding amount of antitoxin. In such multiples a fatal amount of endotoxin is present. Although a strong antitoxin may be ob- tained, it would appear to be of little practical importance because of the rarity of infections by the bacillus. Infection in man has caused the formation of Agglutination. agglutinin in several instances, but it has been absent in others. An agglutinating serum is read- ily produced by artificial immunization. The Toxin. Pathogenesis. 2G2 IXFJX'TIOy AXD I.UMUXITY. V. OTHER SOLUBLE BACTERLVL TOXINS. Soluble toxins, of perhaps secondary impor- tance, which are produced by the staphylococcus and streptococcus, will be considered in the sections dealing Avith these organisms. It seems probable that they do not represent tlie essential toxic agents of the cocci, but rather that the toxicity of the latter depends chiefly on the action of endo- toxins. B. INTOXICATIOX BY SOLUBLE PLAXT TOXIXS. I. HAY FEVER. Dunbar separated from the pollen of various grains a toxin which is able to precipitate typical attacks of hay fever in those who are susceptible, having first demonstrated that the crude pollens cause the disease. The pollen from the following are said to contain the toxin : Eye, barley, wheat, maize (corn), dog's tail, couch-grass, millet, rice and some others. The so-called autumn-catarrh which is common in America may be due to a slightly different toxin coming from the golden- rod, rag-weed, and perhaps other autumnal flower- ing grains. The toxin usually is associated with certain starch-like granules which are contained in the pollen, but it occurs also in pollens which do not contain these granules. It may be extracted with water or salt solution, is precipitated by alcohol, resists the boiling temperature, and is of an al- buminous nature. When the crude pollen reaches the conjunctiva, nasal or bronchial mucous membranes, the toxin is dissolved out by the secretions and absorbed by the lymphatics. When applied to the conjunctiva HAY FEVER. 203 it causes swelling, redness and laclirymation. It is carried by the tears to the nose and here causes excessive secretion, swelling of the mucous mem- brane and sneezing. It may become distributed systemically as a result of absorption from the free surfaces and cause the asthmatic attacks and general symptoms which are seen in the intoxica- tion. "When injected subcutaneously into the arm both the asthmatic attacks and coryza-like sjmip- toms were produced. Dunbar's antitoxic serum (poUantin) is ob- Antitoxic Serum tained by immunizing horses with the toxin. It seems to be of undoubted value in a certain per- centage of cases, but fails unaccountably at times. It is, perhaps, most effective when used in the prodromal stage, the attacks being thereby pre- vented. Its failure in certain instances may be due in part to the inefficacy of the antitoxin against the toxins of certain pollens. Again, in certain individuals the affinity of the toxin for the tissues may be unusually great so that a more vigorous use of the remedy is demanded. Llibbart and Prausnitz published statistics of 285 cases, of which 65 were autumnal. In ordi- nary hay-fever the serum gave positive results in 57 per cent., partially positive in 32 per cent, and negative results in 11 per cent, of the cases. In autumnal catarrh, 70 per cent, were positive, 19 per cent, partially positive, and 11 per cent, nega- tive. The small bottles of antitoxin are accompanied by a pipette with which from one to several drops may be instilled into the eye or the nose. 2G4 IM'IJCTION AXD IMMUNITY. The serum does not cure permaneutly and one who is susceptible should carry a vial for imme- diate use during the ha3'-fever season. II. OTHER PLANT TOXINS. Eicin. from the seeds of Ricintis coDununis; abrin, from Ahrus precatorius; crotin from the seeds of Croton tiglium; and robin, from the leaves and bark of the locust tree (Rohinia pseudoacacia) are chiefly of experimental interest. They are similar in their action, are very toxic to animals, jDroducing both local and general changes with fatal termination when given in sufficient doses; they have pronounced agglutinating action on the erjiihrocj'tes of most animals, and in some in- stances are slightly hemolytic. By guarded im- munization antitoxins may be obtained for them. Robert gave the name of plialUn to a toxic sub- stance which may be extracted from poisonous mushrooms, particularly the "Deadly Amanite" (Amanita phalloides). In some countries many deaths are caused by eating this variety: Russia, Germam% Italy, France, Japan (Ford). Phallin is very toxic for animals and is strongly hemolytic for many bloods. By immunization Ford has re- cently obtained an antitoxin Avhich neutralizes the hemoMic action of the poison, and which in a dose of 0.5 c.c. protects rabbits against five fatal doses of the toxin. The toxin is an aqueous extract of the dried plants. C. INTOXICATION BY SOLUBLE ANIMAL TOXINS. I. POISONING BY SNAKE BITES. The poison apparatus of snakes consists of a se- cretory gland on each side which communicates with a tubular fang by means of a duct. In the f SNAKE VENOM. 265 passive state the fangs are directed backward on Toxic _ the roof of the mouth, but when the animal strikes their points are made to project forward and the poison is forced through the canals by muscular compression of the sac. The venom is a glandular secretion. The venoms of different snakes vary a great deal in their toxic properties. The most impor- tant constituents are those which attack the nerv- ous system (neurotoxin), the blood corpuscles (hemolysins and hemagglutinins) and the endo- thelium of the blood vessels, causing hemorrhages (hemorrhagin, an endotheliotoxin). The three are independent. The neurotoxin causes death by paralysis of the cardiac and respiratory centers. The hemolysin appears to be of less importance as a cause of death. The venoms of the cobra, water-moccasin, da- variations in boia and some poisonous sea-snakes are essentially tiesand'cr''" neurotoxic, although they have strong dissolving powers for the erythrocytes of some animals. In studying the hemolytic powers of the venoms of cobra, copperhead and rattlesnake, Elexner and Noguchi found cobra venom to be the most hemo- lytic and that of the rattlesnake the least. They attribute the toxicity of rattlesnake poison chiefly to the action of hemorrhagin. The same authors studied the action of different venoms on the cells of various animals and by absorption experiments found independent cytotoxins for the testis, liver, kidney and blood. ISFot only was there a distinct cytotoxin for each organ of an animal, but also for the same organ of different animals, results which speak for a remarkable complexity of totoxins. % 2GG lyPECTIOX AXD IMMUXITY. • venom. Certain venoms contain a leucocytic toxin. Ferments. That venoms contain proteolytic ferments is sliown by their ability to digest gelatin and fibrin. This power may be related to the softening of the mnseles which has been noted clinically in cases of poisoning. The rapid decomposition of the body wliich follows death by snake-poisoning is asso- ciated with a decrease in the bactericidal power of the blood, which, according to Flexner and No- guchi depends on fixation of the complement by the venom. Amboceptors The hcmolvsin and neurotoxin, and perhaps and Comple- ,-, t i •" ^ • j. e i j. ment. otlicr cvtolvsins 01 venom, consist ot amboceptors which in themselves are non-toxic; they become toxic only through the aid of complements which are present in the body of the poisoned animal. In this instance, complement which usually is a source of protection becomes a source of danger to the animal possessing it. Not only does ordinary serum-complement serve for activation, but Kyes discovered that cells (er3'throcytes) may contain another kind of complement, an "endocomple- ment," which activates the amboceptors after the latter have combined with the cells. Flexner and ZSToguchi found that this also was the case with the neurotoxic amboceptors. The ability of lecithin to activate the hemolytic amboceptors of cobra venom and the preparation of cobra-lecithid (Kyes) were described in Part I, Chapter XII. pages 158-160. In the preparation of cobra-lecithid the neurotoxin is separated from the hemolysin, the former remaining in solution, whereas the latter settles as a precipitate in com- bination with the lecithin. Immunization with SNAKE VENOM. 267 the neurotoxin isolated in this way causes the for- mation of a specific antineurotoxin (Elliot). The neurotoxin may also be abstracted from the venom by treating the latter with the nervous tissue of a susceptible animal (Flexner and Noguchi). The hemolysin is distinct from the hemagglu- tinin and the latter may be eliminated by heating the venom to from 75° to 80° C. In the action of venom on erythrocytes agglutination precedes he- molysis. The toxins may be converted into toxoids by Toxoidsand heat or treatment with chemicals. Immunization with toxoids causes the formation of antitoxins. Eadium is said to destroy the toxicity of venom (Physalix). The antivenin of Calmette is obtained by im- munizing horses with a mixture of venoms (80 per cent, cobra, 20 per cent, viperine venom), which are attenuated before injection. Six months are required to produce a strong serum. The claim of Calmette that his serum is effective against all snake-venoms is erroneous. It neutralizes those venoms the toxicity of which depends largely on neurotoxins and hemolysins, but has little influ- ence on rattlesnake poison, the essential toxin of which is hemorrhagin. Antivenin for the rattle- snake and water-moccasin may be prepared by im- •munization with the corresponding venoms which have been attenuated by weak acids. Noguchi has produced serum of such strength that it promises to be of practical value in the treatment of rattle- snake bites. As indicated previously, the action of venom is preceded by no aj)preciable incubation period; hence, an antitoxin to be effective must be admin- 26S INFECTION AND IMMUNITl'. istcred not later tlian a few hours after the bite has occurred. Noguchi found in relation to anti- venin for the rattlesnake that the antitoxin neces- sary to save was quadrupled three hours after in- travenous injection of two fatal doses of venom. Fortunately the venom is less toxic when intro- duced subcutaneously. II. OTHER ZOOTOXINS. Phrjmolysin, which is present in the blood and skin of certain toads, has been studied especially by Proscher. It is a thermolabile, hemol3rtic toxin for which an antitoxin can l)c o1)tained by immuni- zation. Arachnolj'^sin, obtained from the bodies of cer- tain spiders, is a hemolytic toxin, which by immun- ization yields a specific antitoxin. A poison, with properties resembling those of snake venom, may be obtained from the caudal segment of the scorpion. Antitoxin is produced by immunization. Ichthyotoxin, a name given to the toxic proper- ties of eel serum, is composed of a neurotoxic and a hemotoxic constituent. From the poisonous glands of certain fish {Tracliinus draco) a highly toxic, thermolabile substance is obtainable, for which an antitoxin can be prepared by the immunization of rabbits. GEOUP II. Acute infectious diseases caused by bacteria which do not secrete strong soluble toxins in cul- ture media, but which contain endotoxins (toxic protoplasm). Infection or immunization causes immunity of considerable or prolonged duration. In active immunity the serums agglutinate the corresponding organisms and are protective for other animalS;,* but have little or no curative power. The formation of antitoxins is not defi- nitely established. In most instances vaccination has been accomplished. Clinically there is leuco- cytosis in some instances and hypoleucocytosis in others (typhoid and Malta fever). A. The serum in acquired immunity is bactericidal. I. TYPHOID FEVEK. Eberth first saw Bacillus typhosus in micro- scopic preparations of the mesenteric lymph gland? and spleen of a typhoid corpse, in 1880. Koch also observed it at about the same time, and stained it in the intestinal wall, spleen, liver and kidney. It was obtained in pure culture by Gaffky in 1884. The organism is rod-shaped, 0.5 to 0.8 by from 1 to 3 microns in dimensions, with nothing char- acteristic in its morphology. It possesses from ten to twelve flagellffi situated at the end and on the sides and is actively motile under suitable condi- tions. It forms no spores and is readily cultivated on many media. The bacillus is one of the rather numerous "in- * This has not been established in regard to Malta fever. 270 JXFIJCTWX AMP IMMUyiTY. . testinal group" of organisms, certain members of which are so simihir that they can be differentiated only by means of special culture manipulations, animal experiments, or the agglutinating and bac- tericidal action of specific immune serums.^ Distribution of The Organism has been cultivated from earth the Bacillus. ^^^ iufcctcd Water, and from the feces, urine, blood, rose-spots and the various organs of typhoid patients. In many instances in which an epidemic has certainly been caused by an infected water sup- ply attempts to cultivate the bacillus from the water have failed. The organisms may not have been included in the samples which were analyzed, or, what is equally probable in certain instances, they have died out in the water by the time the disease was so widespread as to be considered epi- demic. Its occurrence in nature depends on the distribution of the infected excretions of the dis- viabijity and oascd. The viability and virulence of the bacillus in water, earth, etc., vary Avith the nature of its surroundings. It has been found to live for periods of from 3 to 4 weeks to 2 or 3 months in water, from 3 to 4 months in milk, from 3 to 5 months in surface water, and from 11 to 16 months in sterilized earth; 100 days in ice, from 12 to 30 days in oysters, from 50 to 80 days when dried on clothing, for 3 months in typhoid feces, for 96 days in the dead body of an experiment animal. "When in water or moist earth which contain many saprophytes its life is short- ened. It survives drying for many months, al- 1. Of this group the baciUus of dysentery, paratyphoid baciUus, BaciUus entcriiidin of Giirtner, colon bacillus and Bacilhts alcalifjenes, in addition to the typhoid bacillus, are the most important because of their similar morphologic and cultural properties and the pathogenicity of certain of them. TYPIIOUJ FKVER. 271 Typhoid Epidemics. thougli direct sunligbt kills in the course of a few hours. The typhoid bacillus secretes no soluble toxin, Endotoxin but contains an endotoxin which may be obtained in solution by the autolytic digestion of cultures, by extracting ground-up bacilli or by squeezing out the plasma under high pressure. Up to the pres- ent time, immunization with none of these prepa- rations has resulted in the production of an anti- toxic serum of accepted value. Typhoid fever may become epidemic either through a contaminated water supply or by contact infection. "^^Hien due to infected water there is something characteristic about the explosive-like suddenness with Avhich dozens or even hundreds are stricken within a short period. The water of streams, small lakes or reservoirs may become in- fected from an ill-constructed out-house, or from discharges which have been thrown on the ground in their vicinity. TjqDhoid stools thrown on the ground adjacent to wells have caused miniature epidemics. Fruit, vegetables and milk cans may be infected by washing them with contaminated water, and it is supposed that the disease may be acquired from oysters Avhich have lain in water contaminated with sewage. By whatever means an epidemic is set in motion, primarily, it is usually aggravated and prolonged by the occurrence of contact infections (indirect contact). The hands of the nurse, physician, or others who come in contact with the patient be- come contaminated from the stools, urine, soiled linen or skin of the patient, and the organisms subsequently are transferred to food, drinking water, or in other accidental ways reach the mouth. IXFECTIOX A.yD niMUXITY The Infection Atrium. importance. Dust or feces and drop or the sputum of Incubation Period Each new case is a fresh focus from Avhich infec- tion may be carried to others, and the clumces of milk and food infection become greater as the cases multiply. AA^ien the discharges are not dis- infected or are improperly disposed of, soil or house infection may occur and the possibility of transmission by germ-laden dust becomes of infection from dried iirine infection from urine, water, the patient are theoretical- 1}^ possible, but would seem to be of minor sig- nificance. That flies may carry the organisms from open vaults or cesspools and deposit them on food or in drinking Avater has been appreciated in relation to epidemics in military camps. Typhoid bacilli have been cultivated from flies which were taken from the vicinity of infected material. The micro-organisms gain access to the body through the lymphoid tissue of the intestinal tract (Peyer's patches and the solitary follicles). The occurrence of primary infection of the lungs through inhalation of infected dust is possible, but has not been definitely proved. In this instance typhoid bacillemia might occur either with or without intestinal infection. In the latter case it would seem essential that some local lesion exist in the lungs or elsewhere from which organisms could constantly be supplied to the blood. Neufeld doubts the ability of the typhoid bacillus to pro- liferate in the blood, because of the strong bacteri- cidal power of the latter, and considers that infec- tion takes place through the intestines even in cases of "tA-phoid without intestinal lesions.'^ The incubation period is subject to considerable variations. In a series of cases in which the date Localization of the Bacilli. ryPHOID FEVER. 273 of exposure was known, 62 per cent, showed symp- toms in from 20 to 25 days, 2 per cent, in from 14 to 20 days, and 3 per cent, later than 30 days. Following the development of intestinal lesions, the bacilli reach the circulation by way of the lym- phatics, and through the action of the bactericidal constituents of the blood (amboceptor-complement complex and possibly leucocytes) they are killed and dissolved in large quantities. It is now gen- erally believed that only through the disintegra- tion of the bacterial cells are their toxic constitu- ents thrown into solution in the body, a condition which is necessary in order that the tissues be in- jured. Infection of the blood stream with living organisms, in the early stages of the disease and preceding relapses, occurs in a large percentage of the cases. It is possible to establish the diagnosis of Diagnosis by typhoid fever by cultivating the bacilli from the blood, even before the serum has developed suffi- cient agglutinating power to give a positive Widal reaction. A small flask of bouillon is inoculated with from 1 to 5 c.c. of blood, drawn from the median vein of the arm, and after twenty-four hours of incubation a small portion of it is plated out. Colonies which devlop on the plates may be identified by the usual bacteriologic methods, or the agglutination test may be performed with a known antityphoid serum. After from the tenth to the fourteenth day the organisms can rarely be cultivated from the blood; the bactericidal sub- stances of the blood may have so increased by this time that circulating bacilli are killed rapidly. In from one-fourth to one-third of the cases, in the third week, or during convalescence, the bacilli Blood Cultures. 274 i\fj:cti()\ 1 \/> iMMi \rry. ' appear in large niiinbers in tlie urine, in \vhieh tliev may persist for many weeks. According to Kanjajelf, they are discharged into the urine from metastatic foci in the kidneys. Many of th.e symptoms, complications and se- quelcB of typhoid fever, as the rose-spots, enlarged spleen, bone lesions, and in some instances nervous lesions and pneumonia, depend on the distribution of the bacilli. This is in contrast to the conditions in diphtheria and tetanus, in which the distribu- tion of the bacilli is of little significance for the involvement of particular organs. The anatomic changes and clinical symptoms suggest that the lymphoid tissue and central nervous system have a special affinity for the toxic constituents of the typhoid bacilli. Endothelial Tlic greatest changes take place in the organs Hyperplasia, ^lymphoid) wliich Contain the bacilli most con- stantly and in the greatest numbers. It is here that the toxic substance may be j^resent in greatest concentration, as a consequence of the continual salution of the organisms. Mallory doscrilics an enormous hyperplasia of the endothelial cells, es- pecially those of the lymphatic structures. The cells are phagocj'tic, and especially in the lymphoid tissue of the intestines and in the mesenteric lymph glands, englobe and destroy the lymphoid cells on a large scale. It seems probable that the endothelial proliferation which has been described is due to the rather mild but prolonged action of the dissolved toxic constituents of the typhoid ba- cillus; the condition is that of an inflammatory hyperplasia. It has been suggested that the hypo- leu cocytosis of typhoid fever is due to the destruc- tion of the lymphocytes in the lymphoid organs by the endothelial phagocytes. TYPJIOrn FEVER. 275 Mixed Infections. The granular and fatty (J cgon orations of the parenchymatous organs do not differ from those seen in many acute infections. The conditions in the intestinal tract would seem to favor mixed infections, especially hy the colon bacillus and streptococcus, and the primary infection probably decreases the resistance to sec- ondary invasion. The role of the colon bacillus in typhoid fever is perhaps not definitely established, although it has been found in the circulation, in abscesses, and in the urine in cases of cystitis ac- companying the disease. The typhoid and colon bacilli grow well together. A mixed general in- fection with the streptococcus causes a grave sep- tic condition characterized by an irregular tem- perature curve. This condition may be discovered by blood cultures. It is thought that the strepto- coccus does not increase the toxicity of the typhoid bacillus, the result being rather a summation of the intoxication of the two infections. Post- typhoidal suppurations are often due to the strep- tococcus and in many of the metastatic complica- tions (parotitis, pleurisy, peritonitis, meningitis, otitis media) streptococci and staphylococci have been found. Pneiimococcus pneumonia not infre- quently complicates typhoid fever. A combined infection of t^'phoid and malaria is said to occur in the tropics; the complication is grave. T3q3hoid and diphtheria may occur together, and typhoid may be superimposed on acute tuberculosis. The period of greatest susceptibility to typhoid immunity and is found from the fifteenth to the ' twenty-fifth susceptibility. years. The resistance of infants and children is not satisfactorily explained. A certain amount of resistance inherited from the mother may persist 276 INFECTION AND IMMUNITT. for some j'ears after birth. It is known that anti- bodies ma)^ pass from the mother to the fetus through the phicenta. In very early life the tissues may respond more energetically to incipient in- fection by the rapid formation of typhoid anti- bodies, or the phagocytic cells may be more active. The conditions which render older people less sus- ceptible are no better understood. A' loss of suit- able receptors may have occurred so that the toxic constituents of the bacilli find no anchorage in the body, or the affinity between the receptors and the toxic constituents may have become less. The in- dividual during the course of years may have been gradually immunized by the entrance of non- pathogenic quantities of the bacilli into the cir- culation. That resistance to typhoid infection is decreased by low nutrition and overwork is a long- known fact. Natural and A large amouut of protection is afforded by the munity. hvdrochloric acid of the gastric juice, and it is reasonable to believe that suppression or an insuf- ficient amount of hydrochloric acid may favor the passage of living bacilli to the intestines. Normal human serum is rather strongly bactericidal for the typhoid bacillus, and the leucocytes ingest and destroy it. Metchnikoff ascribes natural immun- ity to the action of the microphages. Duration of The immunity which follows an attack of immuniTy*! typhoid fcver is generally of long duration, but second attacks occur with some frequency. It has been noted that limited communities which have experienced an epidemic may remain relatively free from the disease over a period of some years, although neighboring districts are attacked. All the susceptible persons having had the disease, a TYPHOID FEVER. 277 state of temporary regional immunity is created. Acquired immunity is characterized by an increase of the bactericidal amboceptors, agglutinins and typhoid precipitins in the serum. It is com- monly believed that recovery is due to the increase of the bactericidal power of the body fluids, which becomes most marked during the later period of the disease or during convalescence. It seems cer- tain, however, that the new resistance persists be- yond the time when the bactericidal power of the serum has returned to normal, which may take place in from one to several years. The bacteri- cidal power sinks rapidly during and following convalescence. However, the general principle is well established that, although the antibodies may have disappeared entirely, they are reformed more readily as a consequence of an old infection (Neis- .ser and Shiga). The tissue cells have, so to say, been trained, and are stimulated by a few micro- organisms to produce such a quantity of bacteri- cidal amboceptors that the incipient infection is ■overcome. It is, of course, understood that the amboceptors require the aid of complement in kill- ing the micro-organisms. A second attack of typhoid fever usually is mild. • Metchnikoff does not deny that the amboceptors (fixators) play an important part in acquired im- munity, but claims that the new resistance de- pends chiefly on an increase in the phagoc}i;ic power of the microphages (polymorphonuclear leu- cocytes). ■ This is not clear from the clinical standpoint because of the hypoleucocytosis which is somewhat characteristic of typhoid — a hypoleu- cocytosis caused chiefly by a disappearance of the microphages. It has been suggested that our con- Leucocytes. 27S IXFECTIOX AXD IMMUyiTY. elusions as to hypoloiu-ocvtosis arc based on ex- amination of the poriphoval blood, whereas the mesenteric vessels may show hyperleucocytosis. Mallory, however, found a striking absence of microphages even in tlie intestinal vessels. Con- cerning a theory that the liypcrplasia of the lym- phoid organs serves as a substitute for the hyper- leucoc3i;osis, we may recall the findings of Mallory that this hyperplasia is chiefly one of endothelial cells. The importance of these endothelial cells for the destruction of typhoid bacilli needs further investigation. Prophylaxis. Prophylaxis should begin with the thorough disinfection of the stools and urine of typhoid pa- tients, and this should be continued until they no longer contain typhoid bacilli. It is not good hygiene to discharge a patient until bacteriologic examination of stools and urine show them to be free from the organisms. It would be difficult to carry out this rigid precaution under all condi- tions, but at all events the stools and urine may be disinfected for a reasonable period, say through- out convalescence. There is no sufficient reason for the neglect of the bacteriologic examination in hospital practice. There is a growing sentiment that typhoid patients in hospitals should be iso- lated in wards or rooms in which there is a fixed routine for the disposal of infectious materials — urine, stools and sputum. Soiled linen, the bath water of typhoid patients, the remnants of food and drink, and the eating utensils should be dis- infected before removal from the room. jSTurses or attendants should not eat or drink in typhoid rooms. TYI'IIOIIJ J'/'JVKJC. 279 Serum Therapy and Vaccina- tion. The value of hexamethylenamine in causing the Hexamethyi disappearance of bacilli from the urine is now well ^"■•«""^- known, and the advisability of using the drug as a routine measure for public safety is worthy of consideration. The room should be kept free from flies and eventually it should be disinfected, pref- erably by formalin. During an epidemic, in case the water supply of a community is susceptible to contamination ,all water used for drinking, wash- ing of vegetables and eating utensils, should be boiled, and that used for general cleaning may be otherwise disinfected. The possibility of dust in- fection of a house should not be disregarded. There are two methods of specific prophylaxis against typhoid: 1, the injection of antityphoid immune serum; 2, preventive inoculation with killed cultures of the bacilli. Antityphoid serum confers a fairly strong and immediate immunity which, however, is of short duration, because of the rapid elimination of the serum. Its use as a general preventive, therefore, is not advocated. AVright has been influential in showing the util- ity of protective inoculations against t3'phoid. His first experimental work was j)nblished in 1896. Since that time the inoculations have been carried on extensively in British regiments in India and South Africa. The occurrence of typhoid among the inoculated was one-half that among the unin- oculated, and the inoculations reduced the mor- tality of the disease by one-half. The protection, so far as known, lasts for two or more 3^ears, al- though in some instances infection has occurred in from three to six months after vaccination. The methods of preparation of the vaccine are elaborate in order to insure sterility and standard- Wright's Method and Results. The Vaccine. 280 IXFECTIOX AXD IMMUXITY. ■ ization. Cultures of the baeillus are gro^ni in bouillon for from twenty-four to forty-eight hours, and then sterilized at GO C. The contents of several flasks are mixed in order to obtain a uniform distribution of organisms, and standard- ization is then accomplished by a convenient meth- od of estimating the number of bacilli in a cubic centimeter of the vaccine. The purity of the vac- cine is insured by bacteriologic tests, and for pres- ervation carbolic acid or lysol is added. Effects. AYriglit has abandoned his original method of giving a single injection and now recommends two moderate doses, which are given from eight to fourteen days apart. The first dose includes a quantity of vaccine which contains from 750,000,- 000 to 1,000,000,000 of bacilli, the second 1,500,- 000.000 to 2,000,000,000. Wright finds that "the inoculation of these quanta induces an ample elaboration of antitropic substances (antibodies) without producing any severe constitutional reac- tion." The inoculations increase the bactericidal and agglutinating powers of the serum and it is concluded that an increased resistance to typhoid intoxication is established because the second in- jection causes milder symptoms than the first. The phagocytic power of the leucocytes is raised, because of an increase in the "opsonic antitropins" (Part I, Chapter XIV). The curve of the anti- bodies is like that usually obtained by active im- munization with bacteria, toxins or other sub- stances. Immediately following the inoculation there is a decrease even of normal antibodies. This "negative phase" lasts for from one to several days and corresponds to a period of increased suscepti- bility. It is quickly followed by a positive phase Reactions. TYPHOID FEVER. 281 in which the antibodies and, correspondingly, the resistance increase rapidly. When very small doses are administered the positive phase may be recognized after twenty-four hours (Wright). Large doses cause a prolonged negative phase and are to be avoided. Following injection, "the local symptoms first Local make themselves felt after an interval of two or three hours. The effects then seen are the develop- ment of a red blush and more or less serous exuda- tion at the site of inoculation, followed by some lymphangitis along the lymphatics which lead, ac- cording as the vaccine has been inoculated above or below the middle line of the trunk, in the direc- tion of the glands of the axillas or of the groin. . . . Even severe inflammation has never led on to suppuration.'' The exudate is somewhat hem- orrhagic, and the pain moderate to severe, but not of long duration. With the technic as recom- mended at present, "the constitutional symptoms General are limited to some headache and to two or three hours of real malaise. . . . The next day his temperature comes down to normal, and he feels comparatively well except in respect to pain at the seat of inoculation." The adoption of antityphoid inoculation or vac- conditions for ,. n , . T,. ,1 Vaccination. emation under certain conditions appears to be warranted. Typhoid never has been a world pest; hence, the occasion for universal vaccination does not exist, but in the presence of epidemics so fre- quently seen in American cities it will be impos- sible to avoid the consideration of vaccination as a means of protecting the uninfected. The question is a pertinent one also for those cities in which typhoid is so extensive as to be called endemic. 282 lMi:VTIOX AXD IMMVXITY. Mixed Actjve It has bcoii suggostccl that the ''negative phase" and Passive , •! i i ■"" p ^ • xi , .„ Immunization, descnoeil abovc IS a source ot danger m the pres- ence of an epidemic. The phase is so short, how- ever, tliat tlic danger is minimal and it seems probabk' that the practice of mixed active and passive immunization woukl eliminate it entirely. This is accomplished by the combined injection of antit3'^phoid serum and vaccine. The serum as- sures a positive phase from the start, and before this has subsided, that induced by the vaccine is established. When specific serum is mixed with the vaccine the local reaction is said to be less severe. The products of autodigestion of typhoid cul- tures have been suggested as suitable vaccine (Neisser and Shiga). The local reaction is said to be mild, and the body reacts by the formation of bactericidal amboceptors and agglutinins. Bactericidal serums obtained by the immuniza- tion of horses with typhoid bacilli have not shown distinct curative properties. Chantemesse im- munizes horses with a typhoid "toxin" which is prepared by growing the organism in a liquid cul- ture which contains an emulsion of splenic tissue. One cubic centimeter of this toxin will kill a guinea-pig, a dose which in comparison with other bacterial toxins is very weak. Chantemesse has used his antitoxic serum in the treatment of more than 500 cases, reporting a mortality of about 6 per cent., whereas that among untreated patients was from 10 per cent, to 12 per cent. Although these figures indicate some value for the serum it has had little trial outside of France. McFadyan and Eowland immunize horses with extracts of typhoid bacilli, which have been ground Serum Therapy. TYFJIOW FEVER. 283 up while they were kept in a brittle state by the temperature of liquid air. Although antitoxic and bactericidal properties are claimed for the serum, there is no conclusive evidence that it differs from a bactericidal serum prepared in the ordinary way. Jez produces a high degree of immunity in rab- Preparation bits by artificial immunization with the typhoid bacillus, then prepares an extract from the spleen, bone marrow, brain, etc., of the immunized ani- mals. The extract is administered by mouth. Jez justifies this method, from the fact that the l}Tn- phoid organs have been shown to form typhoid antibodies (Wasserman). From the clinic of Eichorst and some others favoral)le reports con- cerning the remedy have been published. It has had no extensive use. The preparation is made by the Serum Institute of Berne (Switzerland) and is expensive. The suggestion made by Fraenkel, that typhoid patients be treated by subcutaneous injections of small quantities of killed typhoid bacilli in order to hasten the formation of antibodies has been kept alive through the "typhoin" of Petruschky, but is yet without much practical trial. Of a simi- lar nature is the suggestion of Richardson, that the filtrates of typhoid cultures be injected. The principles and technic of the agglutination Agglutination test were described in Part I. The serum commonly becomes agglutinating on from the seventh to the tenth day, rarely as early as the second or third, and as late as from the twentieth to the fortieth day. The power is highest during convalescence, when it may agglutinate in dilu- tions as high as 1/5,000 or higher, and from that time sinks gradually. An agglutinating 284 INFECTIOX AND IMMUNITY. • power of 1/1()0 has often been found at eight' months, and of 1/50 after from seven and one-half to eleven years; but the latter duration is not the rule. In performing the test a scrum dilution of not less than 1 to -iO, or 1 to 50 should be observed as previously set forth. The following sources of error are to be borne in mind: Typhoid fever occasionally runs its course without the formation of agglutinins; the reaction may mysteriously be absent one day to recur a few days later, a condition which indicates the importance of repeated tests; rather high ag- glutinating power for the typhoid bacillus occa- sionally develops in other infections, as pneumo- nia, meningitis, icterus, Weil's disease, etc. ; the possibility of group agglutination, for the positive elimination of which control tests with related or- ganisms may be demanded. In case negative results are obtained in a sus- picious case, the reactions should be tried with the paratyphoid bacilli. The test of the bactericidal powers of the serum has been recommended as a substitute for the ag- glutination reaction, but the technic is so much more complicated that the method will probably not come into general use. For diagnosis previous to the formation of ag- glutinins, blood cultures should be made as de- scribed in a preceding paragraph. II. PARATYPHOID FEVER. Paratyphoid In 1900 Schottmliller cultivated from the blood colon" Bacilli, of fivc "typhoid" patients organisms which differ from the typhoid bacillus in that they attack dex- trose with gas formation and are not agglutinated conspicuously by antityphoid serum. Since that PARATYPHOID. 285 time many similar cases have been reported and two types of the paratyphoid bacillus have been recognized (SchottmilUer). Group B causes first an acid reaction in milk which changes to a per- manently alkaline reaction in about ten days, whereas Group A causes permanent acidity (Kay- ser). They resemble the typhoid bacillus morpho- logically, but culturally are more closely related to to Bacillus enteritidis. Organisms which have previously been described as "paracolon" bacilli (Widal, Gwyn) do not differ from those which are now called paratyphoid bacilli, and the infections caused by them resembled the recorded cases of paratyphoid fever. The term "paracolon" should no longer be applied to them. Paratyphoid fever occurs sporadically or in epi- Epidemiology. demic form, and bears a close resemblance to mild typhoid-like epidemics which have been noted from time to time, and which, presumably, are caused by eating poisonous meats. One such epidemic of 600 cases was caused in Switzerland in 1878 by the meat of a sick calf; the mortality was 1 per cent. A still older epidemic (1839) is cited, like- wise caused by meat. In both instances the infec- tion eventually was carried from person to person by contact. A recent outbreak in Kiel, proved to be paratyphoid, is assumed by Fischer to have been caused by infected meat, on account of the peculiar distribution of the cases among the patrons of a particular market. Kurth also attributed a small epidemic to either uncooked meat or milk. Fischer mentions 50 cases in East Holstein which probably were infected by the milk of two cows. Shortly after the epidemic began the cows died and para- typhoid bacilli were cultivated from the muscles. iM'EcTiox A\n fMMrxrrr. Characteristics of the Disease. Excretion, Re- sistance and Distribution. spleen, liver and intestines. De Feyl'er eites an in- stance iu wliieh the disease apparently was trans- mitted through the water of a stream in whieh the clothing of the first patients had heen washed. In another instance, a regimental infection was traced to the discharges of a single soldier, the water sup- ply having become contaminated through a defec- tive water closet. Paratyphoid, like typhoid fever, is accompanied by an enlarged spleen and many rose spots. Al- though severe symptoms may be present for a time, the course of the disease usually is mild and the mortality is low. The incubation period approxi- mates that of typhoid. In the few cases which have come to autopsy the intestinal lesions have varied from a mild ileocolitis with an intact mu- cous surface to a condition of superficial ulcera- tion. The involvement of Peyer's patches and the solitary follicles which is so characteristic of ty- phoid is absent, although these structures may be moderately swollen. The mesenteric lymph glands are not markedly involved and there is little pro- liferation of the lymphoid or endothelial cells (Wells and Scott). The disease has no specific anatomic lesion. The organisms are found in the blood and vari- ous organs, in the rose spots, urine and feces of the patients. Practically nothing is Imown of the oc- currence of the bacilli outside the body. Because of their presence in the stools and urine of the pa- tients, the methods of dissemination and infection doubtless are similar to those concerned in typhoid. The bacillus is said to have a marked resistance to heat, withstanding 60° C. for 30 minutes and not all cells hems: killed durina- one liouv at PARATYrilOID. 287 this temperature. This may explain the fact that the virus is not alwa_ys killed by cooking the meat. The organism probably has a wide distribution because of the occurrence of the infection in vari- ous parts of the world. The toxicity of the bacilli depends on the exist- ence of a fixed endotoxin; a soluble toxin is not produced. The principles of prophylaxis against typhoid also apply to paratyphoid fever, with the addition that in the latter disease the possibility of meat in- fection must be kept in mind. The serums of patients and immunized animals acquire bactericidal and agglutinating powers for the organism. There is no serum therapy for the infection, nor has the occasion arisen to attempt vaccination. Serum from a paratyphoid patient may aggluti- Agglutination nate the homologous bacillus in a dilution of cultures. 1/1000 or 1/2000 or more (E. H. Ptuediger), whereas the typhoid bacillus is agglutinated only in low dilutions by the same serum. How- ever, bacillus A and bacillus B are not identical in their agglutinable properties; in this respect it is stated that the latter is more closely re- lated to the typhoid bacillus than the former. The agglutination test is said to have a higher diagnostic value than the Gruber-AVidal reaction in typhoid, a stronger agglutinating power being developed in the serum of the patient. JsTever- theless, the formation of coagglutinins may render the test confusing if proper serum dilution is not practiced. Conclusions should not be attempted until the test has been performed with both strains of the paratyphoid bacillus and with the tj^phoid 288 IXFECTIOy AXD IMMUXITY. ■ bacillus. As iu typhoid, early diagnosis may be best accomplished by bacteriologic examination of the blood. III. ACUTE EPIDEMIC DYSENTERY. In addition to amoebic dysenter}^ we have be- come familiar with an acute dysenteric infection which appears epidemically in both tropical and temperate climates, and prevails especially in the summer months. Such epidemics occur extensively in Japan, where the mortality may be 24 per cent. ; in the Philippines, United States, Germany and other European countries. In industrial settle- ments in Germany the mortality is about 10 per cent. (Kruse). The incubation period may be as short as two or three days. In mild cases the pa- tient may recover in from four to eight days, whereas severe cases last from two to four weeks, and may terminate fatally. Occasionally the in- fection lasts suflBciently long to be considered chronic. Two Types In 1898, Shiga, basing his conclusions on posi- of Bacilli. |.-^g results with the agglutination test and on the constant presence of the organism in the stools of the infected, identified as the cause of the disease, in Japan, a microbe which is Icno^Ti as Bacillus dysenterm (Shiga). Flexner, in 1900, made simi- lar observations on epidemic dysentery in Manila, and his organisms, or one of them, differing slight- ly from that of Shiga, is called Bacillus dysentcrioe (Flexner), or the Flexner-Harris bacillus, Harris being the name of a patient from whom this typical strain was cultivated. Kruse (1901) found both the Shiga and Flexner types in Germany, needlessly giving the name of "pseudodysentory" bacilli to the latter. In this countrv similar organ- ACUTE DYSENTERY. 289 isms liave been found as the caiise of institutional summer dysentery by Vedder and Duval, of summer diar- Diarrheas. rheas of infants by Duval and Bassett, and by Wol- stein. It is the belief of Vedder and Duval that acute dysentery, the world over, "whether sporadic, institutional or epidemic, is caused by the dysen- tery bacillus." We must note, however, that the organism is not found in all cases of clinical dys- entery, even by skilled bacteriologists. "Clinically,, 24 of our 97 cases in which the dysentery bacilli were found did not differ from the cases of ileocoli- tis in which the dysentery bacilli were not found.'" (Weaver and others.) It seems certain, neverthe- less, that Bacillus dysenterice is the most impor- tant cause of acute dysentery. It rarely occurs in the stools of healthy individuals. The organisms of Shiga and Flexner differ in their actions on sugars (i. e., in their acid-forming powers) and in their agglutinability ; the "Flex- ner" type is the stronger acid-former. An artificial- ly produced immune serum which is specific for one organism has rather higher agglutinating and bac- tericidal powers for the corresponding type, but low for the other. In this country the "Flexner" bacillus is much more common than that of "Shiga," but here and abroad both types are met, and sometimes in the same individual. Several other organisms have been cultivated from dysen- teric patients, but the variations from these two types are slight. All are certainly very closely re- lated. The organism is somewhat thicker than the ty- characteristics phoid bacillus, but probably is non-motile, al- " * ^ ^^^' '" though Vedder and Duval, in opposition to others (Lentz), claim to have demonstrated flagella. It 200 IXFJJCTIOX A\D IMMUXITY. often shows a polyinorphoiis appearance in cul- tures, but forms no spores. It is Gram-negative. It lives for from 12 to 17 days when dried (Pfuhl) ; direct sunlight kills it in 30 minutes, 1 per cent, carbolic acid in 30 minutes, 5 per cent, carbolic acid plus corrosive sublimate (1/2000) almost instantaneously. It is thought that it may live over winter and cause fresh outbreaks in the spring (Kruse). Distribution Thc bacillus is fouud only in the stools of the in the Body. ■ n , j • ,r. , , . infected, m the mucous or muco-hemorrhagie por- tions of which it exists almost in pure culture, few colon bacilli being in the immediate vicinity; it has not been found in the blood or iirine. In fatal cases, Shiga found it only in the intestinal ulcers and swollen lymphoid structures and in the mesen- teric lymph glands. Flexner mentions its occur- rence in the liver. The organism, if it reaches the circulation at all, either does so in small quantities, or is rapidly destroyed by the blood. The infection resembles cholera, but differs from typhoid and paratyphoid in this respect. An observation by Markwald (cited by Lentz) indicates, however, that the bacilli may reach the circulation. A woman sick with dysentery gave birth to a child, which died within a few hours. Dysenteric changes were found in the intestines, and the bacillus of dysentery was cultivated from the diphtheritic de- posits on the intestines, from the meconium and from the heart's blood. The organisms must have reached the child through the placenta from the circulation of the mother. Lesions. The intestinal lesions vary from a simple in- flammatory hyperemia to rather extensive superfi- cial necrosis (diphtheritic inflammation), which ACUTE DYSENTERY. 291 rarely extends below the submucosa. Such foci are said to be the most marked in the descending colon and sigmoid where mechanical injury is more likely to occur. The necrotic areas separate by sloughing, leaving superficial ulcers. The lym- phoid follicles ai'e swollen and infiltrated with polymorphonuclear leucocytes, which also accumu- late in the dilated lymph spaces of the intestinal wall. The ileum is so commonly involved that the condition is called an ileocolitis. Conspicuous changes are not found, in the mesenteric glands or spleen. The liver and kidneys commonly show parenchymatous degenerations. The dysentery bacillus is highly toxic. Subcu- Toxicity of taneous injections of killed cultures produce in man a more profound reaction than the organism of either cholera or typhoid. Ordinary laboratory animals are so susceptible that they are immunized with difficulty; the horse is less susceptible. The toxicity of the organism apparently depends on an intracellular toxin (an endotoxin) rather than on a soluble toxin. When living or killed cultures are submitted to autodigestion in salt solution (Conradi, Msser and Shiga), or when bouillon cultures are allowed to grow for 30 days, the liquids are found to be toxic after the organisms are removed. In both instances this toxicity prob- ably depends on the liberation of endotoxins. The question as to whether the bacillus in the intes- tines produces a soluble toxin which is absorbed by the lymphatics, is undetermined. It seems more probable that the conditions are analogous to those of cholera, intoxication resulting from the libera- tion of endotoxins by the solvent action of the tis- sue fluids or cells on the bacilli. Dysenteric symp- 292 IXFECTIOX AXD IMMUyiTY. • toiiis arc not producod in animals by feeding the organisms. Dissemination TliG stools of the patient are the only known and Infection, j^q^^j.^.^ ^f ^]^q organism and it continues to be ex- creted during convalescence. Latent or chronic cases are a source of danger to a community. Al- thougli the conditions outside the body are not favorable for the growth of the organism, it may remain living and virulent for several months. The methods of infection appear identical with those seen in typhoid. Water infection seems certain, and indirect transmission is acomplished by con- tact with the discharges. The best examples of contact infection are found in institutional epi- demics. Prophylaxis The first esscutial for prophylaxis is correct di- *"*' tibli^ity! agnosis, for which the agglutination test and bac- teriologic examination of the stools are essential. Disinfection and other precaiitions should be prac- ticed as rigidly as in tjqDhoid. The patient should not be discharged until the stools are free fi'om • dysentery bacilli. Poorly nourished individuals are particularly susceptible to infection, and among them the mor- tality is high. The disease is most common among young children, old people, and those who are con- fined in institutions. The conditions in Japan, however, where from June to December of one year nearly 90,000 were attacked, and in Germany, where severe epidemics occur in industrial com- munities, indicate that susceptibility is quite gen- eral. Digestive disturbances and enteritis from other causes are said to be predisposing factors. The normal serums of man and animals have vei-y little l)actoricidal power for dysentery bacilli. ACUTE DYFiENTERY. 293 The subject of acquired immunity to dysentery immunity. is hardly on a satisfactory basis. The serum of convalescents shows a distinct bactericidal power for the organism, and there is good reason to be- lieve that the acquired immunity persists for some time after the disappearance of the bactericidal am- boceptors, an event which takes place rather early. As in typhoid, animals which through immuniza- tion have once been stimulated to produce anti- bodies, form them much more readily on the occa- sion of a subsequent inoculation. This acquired facility in producing antibodies may be a factor in acquired immunity. By immunizing horses, serums of rather high protective power have been obtained. Kruse prepared a serum of which 1/80000 gram would save a guinea-]3ig from a dose of the bacilli which killed a control in 20 hours. It is assumed that the protective power of this serum is due to its bactericidal action. The anti- toxic serum which Eosenthal prepared, by immun- izing with 30 days' old bouillon cultures, protected not only against the toxin, but also against the bacilli ; and conversely an antibacterial serum pro- tected against the toxin (cited by Lentz). Such results leave us very much in doubt as to the exist- ence of a true antitoxic serum. The value of protective inoculations is not well vaccination established. Shiga at one time practiced mixed Therapy!™ active and passive immunization (bacilli plus im- mune serum) on 10,000 individuals. This did not decrease the number of infections, although a lower mortality resulted. Shiga claims that the thera- peutic use of his serum reduces the mortality to one- third that of the untreated. The serum of Kruse, and also that of Eosenthal, are said to be cura- 294 IXFECTIOX AND IMMUNITY. . tive; the discharges rapidly decrease in number and the course of the disease is shortened. In the hands of the Eockefeller Institute, antidysentery serum proved of no distinct value. Agglutination. The agglutination reaction with the serum of patients shows great variability. It is sometimes absent in spite of the presence of bacilli in the stools, and often disappears rapidly during con- valescence (in two weeks occasionally). It is rarely as high as in typhoid. In infantile diarrheas ag- glutinins appear at about the end of the first week of illness (Duval and Bassett). Evidently mild cases in which the course of the disease is from four to eight days may not be recognized by means of the agglutination reaction before the period of convalescence. In chronic cases the agglutinating power may persist for three or four months. No reaction was obtained with the typhoid bacillus. Kruse considers the reaction diagnostic when it occurs in a dilution of 1/50 ; Pfuhl, 1/30. Strong co-agglutinins for other organisms, i. e., above 1/50, have not been observed (Lentz). The tests should always be performed with both the "Shiga" and "Flexner" types, as the two have not identical agglutinable properties, and either organism may be the cause in a given instance. The absence of the reaction does not exclude a dysenteric infec- tion positively. Bacteriologic examination of the stools is important, often necessar}', for early diag- nosis. IV. MEAT POISONING BY BACILLUS ENTERITIDIS. Botulism as a special form of meat poison- ing and the occasional production of paratyphoid by infected meats, have been mentioned. In addition to these, more or less extensive epidemics^ BACILLUS ENTERITIDIB. 295 supposed to be due to ptomains which were found in putrid meat, have occurred not infrequently. It is now well established that most epidemics of this character are caused by pathogenic Ijacteria which are present in the meat, whereas putrid de- composition of the latter is an unessential incident. Gartner, in 1888, had the opportunity of study- Bacillus ing an epidemic caused by the meat of a cow which tntentidis. had been slaughtered in extremity. The symptoms differed from those of botulism or paratyphoid, as described below. He obtained from the muscle and spleen of the cow, and from the spleen of a man who had been fatally poisoned, an organism which has since been loiOAvn as Bacillus enteritidis ( Gart- ner). The same bacillus, or organisms which re- semble it closely, have been obtained repeatedly during similar epidemics, both from the suspected meat and from the organs in fatal cases (intes- tines, blood, spleen, etc.). Drigalski, from a com- parative study of several strains which had been obtained from different sources, concluded that all are members of a closely related group of or- ganisms, the group of Bacillus enteritidis. His conclusions were based on cultural properties and agglutination tests. The typical organism is a short rod, often ovoid in shape, possesses from four to twelve long flag- ella and has moderate motility. It ferments vari- ous sugars and is not stained by Gram's method. Variations among individual strains need not be discussed here. According to v. Ermengem, and also Drigalski, Pathogenicity. its pathogenicity depends on the elaboration of a soluble but heat-resistant toxin. Bouillon cul- tures twelve days old, in which the bacteria have 290 IXFECTIOX AXD IMMUXITY. been killed by heat, also similar cultures from which the bacteria have been removed by filtration, are toxic for mice and guinea-pigs (Drigalski). It is noteworthy, however, that relatively large quan- tities of the bouillon were necessary to kill guinea- pigs (4.0 c.c.) which is in contrast to the toxins of diphtheria and tetanus. The rapidity with which sj-mptoms develop following the ingestion of in- fected meat is a further indication of the exist- ence of this soluble toxin, which, it would seem, is formed in considerable quantities in the meat. Symptoms occasionally develop so quickly as to suggest some strong metallic poisoning. With- in a few hours vomiting, violent diarrhea and colicky pains set in, followed by more or less collapse, weakness, headache and not imcom- monly by erythematous, urticarial or herpetic eruptions. Fever is absent or inconspicuous. The mortality is not high, from 2 to 5 per cent. ; convalescence is said to be slow. ISTephritis and catarrhal pneumonia have been noted as sequelae. Autopsy shows the anatomic changes of an acute gastroenteritis, sometimes of hemorrhagic charac- ter, with swollen Pe5'er's patches; the large intes- tine is not greatl)'" involved. The spleen may be swollen and the kidneys degenerated. The ana- tomic findings are not specific. Sources of It has been shown in numerous instances that the cattle or horses (Drigalski) which furnished the meat were sick with an intestinal or general infection with Bacillus enteritidis before they were slaughtered. "In a very large number of cases it can be demonstrated that the animals from which the meat was taken had been slaughtered in ex- tromitv or had died recentlv. and, indeed, that Infection. BACILLUS ENTERITIDL^. 297 they had (in certain instances) died hefore they could be slaughtered. Most often they suffer from septic inflammatory processes or from traumatic, puerperal or other sorts of septicemia, or from other ill-defined pathologic conditions which are accompanied by symptoms of enteritis or intestinal or pulmonary inflammations." (v. Ermengem.) Subsequent infection of the meat by Bacillus en- teritidis, i. e., after slaughtering, has not been noted. The organism occurs in the blood and various Growth in organs of infected animals and man. Poisoning ^ ^ ' most commonly arises when the meat has been kept for several days, which usually is the case by the time it is made into some form of sausage. In the meantime the bacilli have proliferated and ad- ditional toxin has been produced. In at least one instance a certain number of patients who ate the meat while it was fresh suffered moderate or no intoxication, whereas those who ate it several days later became violently ill. In an epidemic caused by horse meat Drigalski found that "only those persons suffered from intoxication who ate the meat after it had lain for eight days or more." The micro-organism is very resistant to heat Toxin in and the temperature which is attained in ordinary cooking may not be sufficient to kill the bacteria which are remote from the surface. Even in the event that the meat has been thoroughly sterilized, the heat-resistant toxin may be present in suffi- cient quantity to cause the intoxication. N'ot much is Imown concerning the distribution of Bacillus enteritidis. v. Ermengem suspects that it may be a factor in poisoning by oysters and fish, but this remains undetermined. 298 IXFECTIOX AXD IMMUNITY. Agglutinins. The blood acquires specific agglutinins during the course of infection. Even eight days after the beginning of sjonptoms agglutination may be ob- tained in dilutions varying from 1/200 to 1/4000. The agglutinins disappear very rapidly. Working with artificially prepared immune serum, Drigal- ski determined the existence of coagglutinins for typhoid and paratyphoid bacilli. AYe should bear in mind the likelihood that meats poisoned with Bacillus enterltidis, as well as by paratyphoid bacilli, may be encountered in America, as well as in foreign countries. V. BACILLUS COLI COMMUNIS. Bacillus coll communis. Bacterium coli com- mune, or the colon bacillus, is the type of a large group of organisms the members of which show individual differences, but possess certain domi- nant features in common. The typical colon bacil- lus ferments various sugars, with the production of gas, is a strong acid producer and curdles milk. It is flagellated, has moderate motility and does not stain with Gram's method. One type or another is the normal inhabitant of the intestinal tract of many animals, and, although the organisms are widely disseminated in nature, their occurrence is related directly or indirectly to the distribution of feces. Resistance. Its Optimum temperature for growth is 37° C, and above 46° C. it does not proliferate. It is killed at a temperature of from 60° to 61° C. in from five to fifteen minutes; it is not killed by such low temperatures as from — 20° to — 24° C. It resists absolute desiccation for periods var3dng from a few days to several months (different ob- servers). Direct sunlight kills 99 jDer cent, of the COLON BACILLUS. 299 germs in two hours (Billings and Peckham), and they are very susceptible to ordinary antiseptics. The normal serums of many animals are bacterici- dal for the colon bacillus. Escherich;, a noted authority on this organism, lays down the principle that that strain which may be cultivated from the feces of the nursing child should be considered as the typical Bacterium coli commune, maintaining that a constant type of or- ganism is found under these conditions. It is said to occur here in relatively pure culture. Within a very short time after birth the organ- Distribution in ism is found in the intestines of infants, and its **'® "destines. method of entrance has been the subject of much discussion. In view of its ready dissemination it is not difficult to conceive of many circumstances which favor its entrance. Having once reached the intestines, it finds there its optimum conditions for growth. The small intestines in man are rather free from colon bacilli and other organisms as well. This, perhaps, is due, to some extent, to the alkalinity of the medium and to the rather rapid flow of the intestinal contents at this point. The colon bacillus reaches its maximum develop- ment in the large intestine, where, in fact, the whole bacterial flora of the intestines is most con- centrated. In view of the fact that the colon bacillus is a Normal normal inhabitant of the intestines, the conception has occurred to many that it may be of distinct value to the economy, either because of the action it has on certain foods (splitting of carbohy- drates), or because in some obscure way it in- fluences favorably the assimilation of foods, or in that it antagonizes other bacteria of distinct patho- 300 INFECTION AND IMMUNITY. genie powers wliicli also exist normally in the in- testines or reaeh them through accident. This is not the place to consider these questions in detail, and the}' are on none too definite a basis. It may. be stated, however, that the colon bacillus and an- other closely related organism. Bacillus lactis aero- gencs, distinctly antagonize the action of certain proteol}i;ic bacteria which appear to be associated with the putrid decomposition of milk and other proteid-containing foods. Bacteria of the latter type exist in the intestines. Unsterilized milk has a natural resistance to putrid decomposition, and sterilized milk which contains the colon bacillus or Bacillus lactis aerogenes has a similar resistance. These two bacteria flourish in the presence of car- bohydrates, which they decompose with the liberal formation of acids, and through these acids they "limit intestinal putrefaction and influence (fa- vorably) pathologic processes which are caused or maintained by the existing "^alkaline fermenta- tion' " (Escherich and Pfaundler). That the or- ganisms in question antagonize the action of putre- factive bacteria has been shown in test-tube experi- ments (Hirschler). Pathogenicity. Since the time that Emmerich upheld the colon bacillus (or a colon-like microbe) as the cause of Asiatic cholera (1885), opinion as to the patho- genic powers of the organism has undergone many fluctuations. Following Koch's demonstra- tion of the vibrio of cholera as the etiologic factor in cholera, the colon bacillus was, so to say, re- pressed as a pathologic agent. Later, and especially in France, great significance was again attached to it. The condition still shows a great deal of chaos, although, on account of more refined technic and the elimination of other organisms, as the dysen- COLOIi BACILLUS. 301 tery and paratyphoid bacilli and Bacillus enteriti- dis, from the colon group proper, we are, perhaps, ^on the way to a more satisfactory understanding of the pathogenicity of this organism. Although certain authors hold at the present time that the colon bacilli which normally inhabit the intes- tines are devoid of virulence, such a radical posi- tion is open to question. Avirulent strains have often been encountered, however. As harmless as the colon bacillus appears to be virulence when confined in the intact intestines, its viru- lence for animals, although low, has been demon- strated in many instances. A bouillon culture of the average bacillus which has grown for from one to two days, and when freshly cultivated from the stools, causes the death of a 300 to 400 gram guinea-pig in two or three days, when given intra- peritoneally in a dose of from 2 to 3 c.c. Subcu- taneous inoculations, the feeding of cultures, their introduction into the bladder and biliary passages induce inflammatory jarocesses. It is stated (Escherich) that whether the cultures are intro- duced into the skin, peritoneum or vessels, symp- toms of severe gastroenteritis are produced, not unlike Asiatic cholera. This fact doubtless in- fluenced Emmerich in considering the organism as the cause of cholera. The general symptoms are those of an acute febrile intoxication. The organism is most pathogenic when freshly cultivated, and soon loses its virulence after re- peated transplantations. As in the case of some other bacteria, virulence may be re-established by "passage" through suitable animals. The cultivation of the colon bacillus from the blood and organs of man at autopsy has not the 302 IXFECTIOX A\D IMMUNITY. viruieoce significance Avhich Avas once attached to it. It has been recognized that the colon bacillus in particu- lar, and less commonly other intestinal organisms,, may enter the circulation a short time before death, at a time when resistance is very low, and may obtain the general distribution which is so often encountered at autops}'; this is the so-called "ago- nal invasion," which may occur without much re- gard to the primary cause of death. The condi- tions which favor agonal invasion remain, to a large extent, obscure. Distinct defects of the in- testinal mucosa probabl}'' are not essential, al- though this view has its representatives. In states of low vitality in which resistance to infection is decreased (disappearance of complement!), the or- ganisms find conditions favorable to proliferation when they have once reached the circulation. In spite of the low virulence of the colon bacillus, it commonly has a certain amount of toxicity and it may often be of significance even as an agonal in- fection. Postmortem invasion of adjacent structures, as the gall bladder and liver through the biliary pas- sages, and of the peritoneum through the intesti- nal wall, also occurs. True It has been shown that the colon bacillus occa- sionally causes the following conditions : Suppura- tive cholecystitis which may extend to the liver, peritonitis, septicemia, meningitis, cystitis, pyeli- tis and ascending suppurative nephritis, and ab- scesses in various organs, including suppurative processes in the middle ear. In one or more in- stances it has been thought that it caused vegeta- tive endocarditis. Probably colon infections of the gall bladder do not occur in the absence of biliary Infections. COLON BACILLUH. 303 stasis. Orflinarily eases of peritonitis in wiiicli the colon bacillus is encountered also show the presence of other pathogenic organisms, as strepto- cocci or staphylococci; this is always the case in perforation peritonitis. Doubtless wrong conclu- sions have been drawn in many instances as to the bacteriology of peritonitis from the fact that the colon bacillus readily overgrows many other bac- teria in culture media. Escherich attributes great importance to this or- cystitis. ganism as the cause of cystitis, especially in chil- dren, and states that it is probably the most com- mon cause of cystitis, pyelitis and ascending sup- purative nephritis. In 58 of 60 cases of cystitis in children the colon bacillus was found either alone or in mixed cultures. An increased agglutinating power of the patient's serum for the organism cul- tivated from the urine is noted in these cases. Great interest attaches to the colon bacillus in Diarrheas, relation to enterocolitis and dysenteric diseases. Escherich speaks of an enteritis follicularis, or colitis contagiosa, or colicolitis, epidemics of which have been noted at different times. A number of these epidemics occurred before the identification of the dysentery bacillus, and certain of them ma}' have been true dysenteric infections. Neverthe- less, dysentery bacilli are not found in all cases of enterocolitis, and the probability that genuine cases of colon enteritis occur can not as yet be neg- lected. A specific colon toxin has not been obtained. Immunization with the colon bacillus causes the formation of bactericidal amboceptors and agglu- tinins. Xot all strains of the colon bacillus are identical 304 IXFECTIO^' AND IMMUNITY. Aqgtutinaiion. in tlioir aiXglutinoiieiiic ivei'ptors. A serum whirli agglutinates one colon strain does not necessarily agglutinate all strains. The reaction, according to Paltaul' and others, is largely an individual one. The serum of a patient with a colon infection will agglutinate the strain causing the disease, but may not ailect other strains. Hence, for diagnostic purposes, the test must be performed with the cul- ture which has been obtained from the patient. Pfaundler says in reference to colicolitis that if other colon infections can be excluded, and if the serum of the patient gives the agglutination reac- tion in a dilution of 1 to 50 with the bacillus which has been cultivated from the stools, colon infection is indicated (Paltauf). VI. CHOLERA. In 1883 Koch discovered the Vibrio cholera and cultivated it from the stools of cholera patients. The organism may be cultivated from the stools of the patients invariably, and is never found in other diseases nor in normal stools, except in the case of non-susceptible persons who may be encountered during an epidemic. The latter are a source of danger as "cholera carriers." Characteristics Tvpicallv the cliolera vibrio is about 1.5 microns oftheortian- ^^^^ ^^^^ onc-fourth as broad. The cells of young cultures have the so-called comma shape which has given the organism the name of the comma bacil- lus. The form in reality is that of a segment of a spiral. AVhen two cells are attached end to end an S-shape may be produced, and long spirals are made up of many cells which are joined at the ends. In old cultures the cells may assume the form of thick rods or even appear coccus-like. Tlie vild'io possesses a single long flngclluni. Avliicli is sit- CHOLERA. 305 iiatcd at the end. Altliongh two, four and six fiag- ella have been described, KoUe states tliat such or- ganisms are vibrios of another nature. In the character and rapidity of their movement, as seen in a hanging-drop, Koch compares them to a swarm of mosquitoes. Old cultures may lose their motility to a large extent. The cholera vibrio does not form spores, although certain involution forms simulate them. It stains readily with the ordinary anilin dyes and is Gram negative. The comma bacillus grows readily in alkaline cultivation culture media with characteristic appearances ; it stools. * is an obligate aerobe under artificial conditions, in spite of the fact that it flourishes in the intes- tines. The optimum temperature lies between 30° and 40° C. A very simple method of obtaining the organism in pure culture from the stools was dis- covered by Koch. In tubes of peptone bouillon which have been inoculated with the feces of a patient, the vibrio proliferates rapidly and within a few hours exists in almost pure culture at the surface of the liquid. Isolated colonies are ob- tained by transferring a small amount of the sur- face fluid to tubes of liquefied gelatin, then plating the latter. The colonies appear in a few hours as identification. small translucent points from which pure cultures are made on a suitable medium. For more positive identification agglutination tests are performed with anticholera serum. The Eoyal Institute for Infectious Diseases (Berlin) keeps on hand a dried serum of known strength (1-10,000) for this pur- pose. The tests being made with high dilutions, coagglutinins for other vibrios are practically elim- inated. To the agglutination test may be added the "Pfeiffer experiment," in which the protective 306 INFECTIOX I \ 7> IMMUNITY. ' power of an anticholera serum is determined wlien guinea-pigs are infected intraperitoneally with the suspected culture. If the serum shows a protective power against this organism which approximates that sliown against a Icnown cholera vibrio, or, if the organisms are dissolved, the diagnosis of chol- era is justified. In performing such experiments the serum is mixed with the culture before injec- tion. Resistance. The resistance of the cholera vibrio is very low. It dies in about two hours when dried (Koch) and on this account dust infection is thought not to occur. It is killed instantly by the boiling tem- perature, and in five minutes at 80° C. It is ex- tremely susceptible to carbolic acid (killed by 1 per cent, in five minutes), corrosive sublimate (1 to 2,000,000 or 3,000,000 in from five to ten min- utes), and to acids. Calcium chlorid is an effi- cient disinfectant when thoroughly mixed with the stools. The micro-organism lives in distilled water not longer than twenty-four hours, in ordinary water for several days to several weeks, and in one instance it was cultivated from the water of an aquarium after several months. Its life is short in the presence of putrefactive bacteria and rapidly- growing saprophytes, dying in sewer water in from twenty-four to thirty hours (Koch). Because of the large overgrowth of other organisms, the vibrio can rarely be cultivated from the stools later than from one to three days after death. Its life in and on foods depends on the reaction (alkalinity is favorable), and on the presence or absence of moisture. It lives longer in sterilized milk (ten days) than in that which contains other micro-or- ganisms. CHOLERA. 307 Infection develops in the small intestines fol- infection lowing ingestion of the organisms. Infection by Dissemination. way of the lungs or through wounds does not take place. In the patient the living vibrio occurs only in the intestines^ and it is excreted only with the feces. So far as known^ it has no normal habitat outside the body, although a stream or other water supply may contain the vibrio over a long period through constant reinfection of the water. This can only occur, directly or indirectly, through the stools of patients. The washing of soiled linen or bathing in water which is used for drinking and other household purposes have caused outbreaks of cholera. The water supply of a city may be in- fected by the discharges of patients who are con- fined to a ship. Convalescents may retain virulent organisms in their stools for forty-eight days (Kolle), and, as stated, healthy persons who are insusceptible to cholera and who have resided in an infected district may carry virulent vibrios in their intestines. These conditions have contrib- uted to the futility which, to a large degree, has met attempts to limit the extension of cholera by quarantine measures. Cholera extends from coun- try to country along the lines of travel. In some instances it has been possible to trace the origin of widespread epidemics to the delta of the G-anges, a region in which the disease is endemic. Pilgrims from India carry the infection to Mecca, and pil- grims from Eg3^pt carry it to their native land on their return from Mecca. Either from Egypt, or through Arabia, Asia Minor and Southern Eussia or Turkey, cholera has, with more or less rapidity, extended to Western Europe. The development of rapid transit has increased the rapidity with which Epidemics. 308 IXFECTION AND IMMUNITY. cholera ma}- extend. From Europe the disease has been carried to various ports of the western conti- nent, Canada, the West Indies and southern ports of the United States, from wliich extension has oc- curred to different sections. Of six widespread epidemics of the past one hundred years, tliree liave involved thft United States, reaching consid- erable proportions. The means of introduction is not always apparent. As in typhoid, two types of epidemics arc known, the two often being associated: First, that caused by water infection, and, second, that in which the disease spreads by direct and indirect contact. The explosive character of an epidemic caused by in- fection of a water supply is much more striking than in the case of typhoid fever. In large cities hundreds, or thousands, may be striken within a day. The brief incubation period, from twelve to twent3'-four hours, contributes to the acuteness of the outbreak. The distribution of a "water- borne" epidemic corresponds with the distribution of the infected water. A remarkable occurrence il- lustrating this point was noted in the epidemic which attacked Hamburg in 1892. In certain streets in which the residents of the two sides ob- tained their water supply from different sources, one of which was infected, cholera was limited to that side which was supplied with infected water. Only irregular cases due to contact infection oc- curred on the opposite side of the street. Epidemics which are due solely to contact infec- tion develop slowly and irregularly. A common incident is the successive involvement of the mem- bers of a family, whereas others in the immediate neighborhood are unaffected. Water-borne epi- CHOLHRA. 309 demies are invariably complicated by tbe occur- rence of contact infection. Tlie methods of con- tact infection are not different from those men- tioned under typhoid fever. Food or milk which has been infected by contaminated water or by other means may cause the development of isolated groups or cases. Animals do not contract cholera under natural Susceptibility conditions. By rendering the gastric contents of guinea-pigs alkaline and introducing cultures into the stomach through a tube, Koch induced a chol- era-like process from which the animals died with- in from twenty-four to thirty-six hours ; an intra- peritoneal injection of opium, to quiet peristalsis, seemed to be necessary for the success of the ex- periment. Similar results were obtained in very young rabbits by feeding cultures to them (Issaeff and Kolle, Metchnikoff). Guinea-pigs withstand the subcutaneous inoculation of moderate amounts, but are very susceptible to intraperitoneal inocula- tion. Intravenous injections are exceedingly toxic for rabbits, and a fatal cholera-like condition with localization of the organisms in the intestines and intestinal mucosa has been produced in this way (Thomas). The essential poison of the cholera vibrio is in- Endotoxin. tracellular, and becomes free only after solution of the bacterial cells. Cultures which are killed care- fully as by chloroform vapor (Pfeiffer) are highly toxic, although the fluid alone is non-toxic. The filtrates of young cultures have little or no poison- ous action. The toxicity of older filtrates is due partly to the solution of the bacteria with conse- quent liberation of endotoxin, and perhaps also to secondary disintegration products which have a the Intestines. 310 IXFECTIOX A\D IMMUNITY. certain toxicity. Tlie soluble toxin of Metclini- koff, Eoiix, and Taurclli-Salimbeui is a dissolved endotoxin and not a secretion of the living cells, according to Kolle. Conditions in Kocli considcrs that cholera is an acute infec- tious process of the intestinal epithelium, whereas the general condition is one of acute intoxication. It is assumed that the condition in the intestines corresponds to that in the culture media, i. e., that here, too, no true soluble toxin, comparable with that of diphtheria or tetanus, is secreted, but that the toxin which eventually reaches the circulation is that which is liberated from the bacteria after the latter have been dissolved by the bacteriolysin of the plasma, or perhaps by the leucoc}i;es. Doubt- less a great deal of endotoxin is liberated in the in- testinal canal, but it is Koch's conception (cited by Kolle) that the primary intoxication comes from those organisms which have penetrated be- tween and beneath the ei^ithelial cells and here have undergone solution. One effect of the toxin in this situation is to cause desquamation of the intestinal epithelium, as a consequence of which rapid absorption of the toxin from the intestinal canal takes place through the denuded surface. This theory supposes that the toxin is not readily absorbed through the intact epithelium. The liv- ing vibrio has never been cultivated from the blood. The changes in the intestines depend on the duration of the infection. In cases which prove fatal within a few hours the mucosa shows only moderate general reddening, which is intensified at the borders of Peyer's patches and the solitary follicles. The intestinal contents are of a rather C HOLE It A. 311 clear fluid nature in which are suspended flakes of mucus and epithelium; the fluid may be tinged with blood. With a longer duration the destructive processes in the mucosa become more intense, and consist largely of desquamation of the superficial epithelium and intense congestion of the denuded submucosa. In the more prolonged cases, "chol- era-typhoid," the mucosa, especially above the ileo- cecal valve, may show diphtheritic necrosis. The serous surface of the intestines is injected. The rational prophylaxis founded by Koch, on Prophylaxis. a knowledge of the biologic characteristics of the comma bacillus, has proved of great efficiency. The essential points are the following: 1. Imme- diate bacteriologic examination of the stools in suspicious cases. 2. Absolute isolation of patients, in a hospital whenever possible. 3. Thorough dis- infection of the stools, linen, room and all articles with which the patient has been in contact, includ- ing water-closets and privies. 4. Continued iso- lation during convalescence until the stools are free from vibrios. 5. Eepeated bacteriologic ex- amination of the stools of those who have been in contact with cholera patients until their freedom from vibrios is assured. 6. Frequent examination of the water supply at different points in order to detect the occurrence of water infection. 7. In case water infection exists, exclusion of the water from all domestic uses, and the institution of means to rid the water of infection. This may be done in the case of infected wells, but in the case of large systems reconstruction may be necessary for future protection. Water for household use should be boiled. Kolle compares the conditions in Germany and Eussia during the epidemic of 312 iXFKcrioy A\n iMMrxiiy. ISy.V^-i. In Gennaiiy, where Koeirs prineiples of prophylaxis were rigidly observed, about 10,000 cases occurred, 9.000 of which were confined to Hamburg, whereas in Eussia, where precautions were not enforced strictly or generally, 800,000 cases developed during the same period. Vaccination. Protective inoculation has shown itself to be of distinct value for prophylaxis. Ferran, a Span- iard, first practiced vaccination on a large scale in 1884, although little definite knowledge of the value of the procedure resulted from his Avork. He is supposed to have used impure cultures. Hafi'- kine introduced protective inoculation on a large scale in India, and up to 1895 had inoculated 40,- 000 persons. Following Pasteur's method with anthrax, he used two vaccines. Vaccine 1 was a culture which had been attenuated by prolonged growth at 39° C. Vaccine 2, which was adminis- tered five days later, was a virulent culture. The living organisms were used in both vaccines and the injections were given subcutaneously. The local and general symptoms w^ere mild. Instead of living cultures Kolle has proposed the use of virulent cultures which have been killed by expo- sure to a temperature of 58° C. for one hour. The vaccine is preserved by the addition of 0.5 per cent, phenol. In the Japanese epidemic of 1902 this method was used on an extensive scale. The incidence of disease among the uninoculated was 13 per cent., among the inoculated 0.06 per cent. ; the mortality among the uninoculated was 10 per cent., among the inoculated only 0.02 per cent. The disease, when it occurred in the inoculated, was of a mild type. A single injection of from 2 to 4 mg. of a killed agar growth was given sub- CIIOLJ'JJiA. ■ 313 cutaneously (cited by Kolle). Strong has pro- posed the use of the products of autolysis of the cholera vibrio as a vaccinating substance, a method founded on the observations of Neisser and Shiga in relation to typhoid, and of Conradi and Drigal- ski in relation to dysentery. The local and general symptoms are said to be of a mild type. The method has had no practical trial. From what was said above in connection with ^^"(i^^l^^ the so-called cholera carriers, it is evident that not susceptibility. all are equally susceptible to infection with chol- era. In the few instances in which infection has been attempted deliberately, some contracted the . disease, at least one case ending fatally, whereas in others either a mild infection or none at all took place. The conditions on which such cases of in- dividual immunity depend are not known conclu- sively, although it is often intimated in a general way that a strong bactericidal power of the body fluids, or a high phagocytic power on the part of leucocytes, is responsible for it. The gastric juice, on account of its acidity, offers a barrier to the passage of living vibrios into the small intes- tines, and this is particularly true of cholera. It is nevertheless evident that the barrier in many instances is not a serious one. A number of cases are recorded in which investigators while working with cultures have become infected with cholera, the cases running typical courses which sometimes ended fatally (Pfeiffer, Pfuhl and others). Or- ganisms which are ingested with water may pass rapidly to the intestines without being affected by the acid of the stomach, or when taken with food they may be buried in the latter and hence not come in contact with tlie gastric secretion. It 314 INFECTIOy AyO IMMUyiTY. • seems probable that tlie intestinal epithelium has a certain resistance to invasion which is most mani- fest in the case of those who do not become in- fected in spite of the presence of the organisms in their intestines. Natural immunity appears to be one which is directed against the bacteria rather than against the endotoxin, proliferation of the organisms in the intestinal epithelium being pre- vented. Poorly nourished individuals, the very young and the very old are particularly suscepti- ble. Other gastrointestinal disorders, in the pres- ence of an epidemic, predispose to infection. De- fects in the intestinal epithelium, or a decreased resistance of the latter ( ! ) , may afford favorable conditions for invasion. Acquired Activc immunity, as that which results from in- fection or from protective inoculation, is charac- terized by the appearance of bactericidal ambocep- tors, agglutinins and specific ])recipitin8 in the serum. It is now widely believed that acquired im- munity depends on the presence of the bactericidal amboceptors in the circulation and body fluids, al- though Metchnikoff holds, on the other hand, that it depends largely on an increased phagocytic power on the part of the leucocytes. According to Pfeiffer and Marx, the antibodies are produced in the blood-forming organs. An attack of cholera confers immunity of prolonged duration, although it is not always absolute. Passive immunity is readily induced in animals by the injection of anticholera serum. As in other instances, it is of short duration. Doubtless the same condition may 'be induced in man. Besredka has proposed mixed active and passive immuniza- tion for iiTotc-tivc inoculation, usinc" kill('(l bac- PLAGUE. 315 teria which have been saturated with the specific amboceptors. Serum therapy has been no more successful in serum cholera than in typhoid fever. The antitoxic Agglutination. serum of Eoux and others has had no practical trial, x^ccording to Achard and Bensaude, the serum of cholera patients, on the third or fourth day of the disease, agglutinates the cholera vibrio. However, they used the serum in dilutions of 1-20, and in this strength even normal human serum may be agglutinating (PfeifEer and Kolle, cited by Paltauf). Convalescents even after seven months may show an agglutinating power of from 1/100 to 1/120. The bacteriologic examination of the stools is the most reliable means of early diagnosis (see above). VII. PLAGUE. Plague was known in the second and third cen- turies. In the sixth century it ravaged the Eoman empire and destroyed half the population in the eastern provinces. Under the name of the 'Tjlack death" it swept over Europe in 1347-50 with a sacrifice of one-fourth of the inhabitants — about 25,000,000. During the fifteenth and sixteenth centuries many epidemics prevailed in various parts of Europe, and the disease seemed to have fastened itself on that part of the world. However, the pneumonic form of the disease, the most con- tagious, gradually became less common, or the vir- ulence of the infection diminished, and this, 'with the institution of quarantine regulations, decreased the prevalence of the plague during and following the seventeenth century. ISTevertheless, there have been occasional outbreaks in Eastern Europe since 31G L\Fi:cT10.\ AM) IMMUNITY. ■ that time. Following the recrudescenee of plague iu Hongkong in 1893 and in other places later, the disease has been subjected to scientific study, its cause has been discovered, and the importance of rigid quarantine measures at seaports in pre- venting its universal extension has been proved. Characteristics j^ ^j^g Hongkong epidemic of 1893-4 Kitasato qanism. -^i^^ Yersin, working independently, discovered the bacilhis of plague, Bacillus pestis. The organism is minute (1.5 to 1.75 by 0.5 to 0.7 microns), and typically is of long oval shape. The frequent oc- currence of short oval cells (coccus form), longer rods and distorted, swollen, vacuole-like cells (in- volution or degeneration forms) signifies a liigli degree of pleomorphism which is characteristic. The longer the disease has lasted, or, on the other hand, the older the culture, the more numerous are the atypical forms. In bouillon long chains de- velop. It is non-motile, has no flagella aiid forms no spores. A capsule may be demonstrated by ap- propriate technic. It does not stain by Gram's method, and with methylene blue, carbol fuchsin, etc., the ends stain more densely than the central portion (polar staining). Because of its general • properties it is placed in a group with a number of bacteria which cause hemorrhagic septicemias in various animals — the "hemorrhagic septicemia group." There occurs in bouillon the so-called "stalac- tite" growth, in which visible processes extend from the surface toward the bottom, where they meet other processes which extend toAvard the sur- face ("stalagmites"). These formations utilize as their starting points the side of the fla>k or dro])S of butter or oil which are placed on the surface. Cer- PLAGUE. 317 tain other organisms grow in a similar manner. It is said to be a characteristic feature of the plague bacilli that many involution forms appear on agar which contains 3 per cent, of sodium chlorid. The optimum temperature for growth is from 25° to 30° C, which is somewhat lower than that for most pathogenic organisms. It grows rather slowly even under the best conditions. In mixed cultures it is overgrown by saprophytic or- ganisms (e. g., colon bacillus). The plaffue bacillus may live for from four to viability and seven days in the putrefying organs of man or ani- mals. Its virulence may be retained in the cadaver of a rat for two months (Bandi and Stagnitta- Balistreri). During this time the organisms pene- trate all the tissues of the body, even growing through the skin. It may live in the pus of a bubo for twenty days when unmixed with other organisms (Albrecht and Gohn) ; in the sputum from plague pneumonia for ten days; in various foods, as milk, potatoes, for one to three weeks; in water from five to twenty days, depending on the number of saprophytes which are present; in earth from two weeks to three months, depending on the quantity of organic matter and other organisms. In all these instances the higher the temperature, i. e., above 30° C, and the more numerous the saprophytic organisms, the shorter is the life of • the plague bacillus. In winter, when contaminat- ing saprophytes grow less rapidly, the plague bacil- lus lives longer. Its resistance to desiccation, sun- light and disinfecting agents is rather low, par- ticularly when the surrounding temperature is above 30° C. In temperatures of from 29° to 31° C, when thoroughly dried, it rarely lives longer 3 IS I.XFECTIOy AM) IMMUNITY. than from six to seven days, whereas at lower tem- peratures, 16° to 20° C, cultures may he ohtained after from one to several weeks, depending on the material which contains the organisms. It lives longer in woolen and cotton threads (clothing) than when isolated as in dust; hence, dust infection is improhahle (Dieudonne). In sputum (plague pneumonia) and purulent exudates in which the hacilli become incrusted to a degree, life may per- sist for from three to four weeks. Sunlight kills tliem in from two to six hours, depending on the temperature and the proximity of the organisms to the surface. Although cultures for the purpose of vaccination have been killed at a temperature of G5° C. for one hour, precautions to insure an even distribution of the heat are necessary to render cer- tain the death of all organisms. A temperature of 100° C. kills them at once, and 80° C. in from five to ten minutes (moist heat) . They are very resis- tant to cold, remaining alive at a temperature of — 20° C. for several weeks, even when repeatedly thawed out during this time, and they even prolif- erate slowly at from 4° to 7° C. virulence Cultures of the plague bacillus retain their viru- lence over a long period when kept in a cool dark place and wdien not allowed to dry. However, they often loose in virulence unaccountably. The nature of the toxic substance is as yet obscure. A concentrated soluble toxin has never been obtained in cultures. Filtrates of young cultures show lit- tle or no toxicity, whereas in older cultures the fluid becomes more or less toxic (liberation of en- dotoxin?). Lustig and Galeotti extract cultures with 0.75 to 1 per cent, potassium hydroxid, from which they precipitate a toxic substance with ace- and Toxins. PLAGUE. 319 tic or hydrochloric acid. Markl found the cell bodies to be very toxic after eight weeks' growth at room temperature, provided the organisms were killed by chloroform rather than by heat; killing by heat destroys the toxic substance largely. He believes some metabolic product of the organism is the chief toxic constituent, claiming at the same time the presence of a certain amount of soluble toxin. The plague bacillus is exceedingly virulent for virulence rats, guinea-pigs and monkeys; somewhat less f*"" ^""''ais. virulent for mice and adult rabbits ; other animals, cats, dogs, swine, cows, horses, sheep, goats, may be infected artificially, although they commonly re- cover even after large doses. Eats and guinea- pigs may be infected by subcutaneous, intraperito- neal and intravascular injections, by the feeding of infected material or by placing it on the nasal mu- cous membrane or in the conjunctival sac, and by inhalation experiments, the last method commonly resulting in plague pneumonia. Guinea-pigs and young rabbits die of plague septicemia in from four to five days when cultures or material con- taining the organisms (sputum, feces, organs from plague cases), are rubbed into the shaven or even unshaven skin (Albrecht and Gohn). This experi- ment is of value for detecting virulent plague ba- cilli and separating them from contaminating or- ganisms. Following inoculation into a cutaneous or mucous s^irface a local reaction of varying in- tensity develops in which the subcutaneous tissue becomes edematous or even hemorrhagic, in a num- ber of hours the regional lymph glands become swollen and hemorrhagic, and in from two to five days the animals die of plague septicemia. Cul- 320 lyPECTIOy AND IMMUNITY. , tures of low virulence not infrequently cause a chronic infection which is characterized by the for- mation of large granulomatous nodules on the sur- face of the liver and spleen and in the omentum. Such foci contain many plague bacilli, and the death of the animal results in a few weeks from intoxication or from general infection. Although rabbits are much less susceptible than rats or guinea-pigs, young animals succumb to cutaneous inoculation. Endemic Dicudonne cites four foci in which plague is Plague. . ^ . known to be endemic at the present time : One is in China (province of Yiinnan), from which the Hongkong epidemic originated; a second in the Himalayas, which led to the outbreak in Bombay; a third in a mountainous region south of Mecca, and a fourth was found by Koch and Zupitza in British East Africa near the source of the White Plague The opinion is held by many that plague is pri- marily a disease of the rat and that certain regions remain pest-infected because of this fact. Eats, in certain districts, suffer from a chronic form of the disease, and it is possible that the organism at times acquires increased virulence, as a conse- quence of which the infection becomes widespread and rapidly fatal among these animals. It is prob- able that the chief method of transmission from rat to rat is through the eating of plague cadavers. The possibility of transmission from one animal to another by means of fleas is upheld by some. The blood which fleas suck from infected rats fre- quently contains bacilli, but transmission to other rats by the bites of fleas is still disputed. The means by w^hich the disease extends from in Rats. PLAGUE. 321 rat to man are not definitely determined. This much is known, however: First, that the bacilli are excreted in the urine and feces of infected ani- mals, and, second, that the disease attacks those Houses. especially who live in dark, damp, filthy quarters in which rats are numerous. Europeans who live under hygenic conditions in plague-infected dis- tricts rarely contract the disease. A great mor- tality among the rats not uncommonly precedes an outbreak of plague in man. The existence of "plague houses" may depend on the prevalence of the disease among the rats which infest the houses. On the other hand, the organisms excreted by a plague patient through the sputum, urine or feces, find, in the conditions described above, surround- ings which favor their prolonged life; hence, the occurrence of subsequent infection in the same house in many instances may be traceable to a pre- vious case. The theory has been advanced also that fleas Ffeas. may be an important means of transferring plague from rats to man. This is objected to on the ground that every animal has its peculiar flea and that the flea of the rat will not bite man. Never- theless, it may alight on the skin of man tem- porarily and there discharge bacillus-laden excre- tions. Flies, in a like manner, may distribute the bacilli from rats or the infected excretions of man. When plague invades a new country it commonly makes its first appearance in coast cities. Pre- - sumably this is accomplished through infected rats which may board a ship during its stay in a pest- ridden harbor, and which subsequently escape at the new port. Epidemics of plague lack the explosive-like sud- 322 IXFECTIOy AXD IMMUNITY. Epidemics. Infection Atria. donncss in their development which characterizes cliolera and, to a certain extent, typlioid and dys- entery. The cases occur in y neuralgia and inflammation of the scrotum and epididymis" (Scheuhe). It occurs especially in the summer months. Basset-Smith found the serum in practically all stages of the disease and in convalescence to have little or no bactericidal power for the coccus. Nor- mal serum appeared to be more bactericidal than that of the patients, although such an action was often missed in normal serum. Wright says that normal human serum is devoid of bactericidal power for the organism. Basset-Smith also con- cluded that the phagocytic power of the patient's leucocytes is less than in the case of normal leuco- cytes. According to Wright, the, organism "is em- inently sensible to the opsonic action of the nor- mal serum," under the influence of which it is taken up in large numbers by the leucocytes. Agglutination by the serums of patients takes place in dilutions varying from 1-300 to 1-2000 or even as high as 1-GOOO. Agglutinins develop fairly early in the course of the infection, and the test is of great diagnostic importance. Bacilhts meUtensis, discovered by Bruce (1887) in the spleen of patients who had died of the dis- ease, is a minute organism, slightly oval in shape. According to Gordon, it possesses one flagellum, rarely two or four, and is slightly motile. The l)aeilius is found in pure cultures in the spleen, MALTA FEVER. 335 which is greatly cnlargecl. Its growth in culture media is very slow. It is thought that infected water may be one means of transmission of the disease. Laboratory infections have occurred through small wounds. The disease is not transmitted from person to per- son. Up to the present time the monkey is the only animal known to be susceptible to artificial infec- tion, although the organism may have a low degree of virulence for rabbits and guinea-pigs (Durham). One attack confers immunity, which may disap- pear, however, after some time (Hughes). An immune serum which was prepared by Wright is said to influence favorably the course of the disease. GROUP III. Acute infectious diseases in which acquired im- munity of prolonged duration is not established. In some instances soluble toxins are produced which are of unknown importance in infection (staphylococcus, streptococcus). Some of the or- ganisms contain rather strong endotoxins (pneu- mococcus, gonococcus), whereas in others a reason- able basis for their infectiousness is not at hand. In some instances immunization causes increased resistance to infection (staphylococcus, streptococ- cus), whereas this property has not been fully demonstrated in others.* The serums of immun- ized animals may or may not be protective for other animals. Those organisms which cause sys- temic infection give rise to clinical leucocytosis " (except influenza). Local inflammations are ac- companied by the accumulation of polymorphonu- clear leucocytes. I. PNEUMOCOCCUS INFECTIONS — PNEUMONIA. Organisms No onc Organism is the exclusive cause of any Pneum'lfnia^ ouc t}^e of pncumonia, except perhaps the viruses of syphilis and tuberculosis. Any microbe which causes pneumonia can also set up infla;mmations in other organs. The following may cause acute pulmonitis: Diplococcus pneumonice. Streptococ- cus pyogenes. Staphylococcus pyogenes^ bacillus of Friedlander (B. pneumonice) , B. infiuenzce, B. pes- tis, B. dipMher'm, B. typhosus, B. coli communis, ♦ This point is diflScult of determination when an organ- ism has little or no pathogenicity for animals (influenza, gonococcus, bacillus of Ducrey, etc.). PNEUMOCOCGUS. 337 and Micrococcus catarrhalis. The organisms of tuberculosis, actinomycosis, the virus of syphilis and some other infections cause chronic inflamma- tions of the lungs. Some of these organisms have already been considered and others will be dis- cussed later, in their relation to pneumonia, with- out, however, entering into details as to the vari- ous types of the disease. The Diplococcus pneu- Dipiococcus monice is the commonest cause of lobar pneumonia. Pneumoniae. It produces lobular pneumonia not infrequently, and has been found as the only organism in acute interstitial pneumonia (Weichselbaum). Friedlander (1882) found that capsulated cocci were present constantly in the exudate of pneumo- nia. Such cocci in all probability represented the organism which at present is known as the diplo- coccus of pneumonia, yet the cultures which he ob- tained somewhat later showed the characteristics of the organism now loiown as the bacillus of Friedlander. Fraenkel, in 1884, obtained the first- named coccus in pure culture, and his investiga- tions, together with those of Weichselbaum and many others, eventually established the independ- ence of the tAvo organisms. The typical pneumococcus is slightly elongated, Typical and and both in the tissues and in culture media it suams."^*' grows in pairs. Typically, also, the pair possesses a capsule which is present constantly in the tissues and may be obtained on certain culture media (milk and serum). It is non-motile, non-flagel- lated, forms no spores and stains by Gram's meth- od. Rather scant growth occurs on the ordinary culture media in the form of small colonies which resemble those of the streptococcus, and unless spe- cial media are used it usually can not be carried 338 INFECTIOy AXn IMMIXITY. Confusion with Streptococcus. Resistance. through many generations. When grown in si)n- tiim, or on a medium wliicli contains ascitic fluid, the hlood or serum of man or some favorable ani- nuil, its virulence may be preserved for some time. By growth at 39° C. virulence is lost rapidly. Strains which are atypical in one of several ways are encountered. They may show low virulence, may grow well at ordinary temperatures (the typi- cal organism not doing so), may produce long chains in liquid media, or may grow without a capsule. Eecently the danger of confusing tlie pneumo- coccus with the streptococcus has received renewed attention, and newer methods of differentiation render it extremely probable that such confusion has occurred in the past. An important differen- tial method is that of cultivation on agar plates which contain blood (Schottmiiller) ; the strepto- coccus produces a clear zone of liemolyzed corpus- cles about its colonies, whereas the colonies of the pneumococcus present a greenish color and produce no hemolysis. In using this test Euediger found a surprising number of pneumococci in normal throats, whereas previous work had shown them to be much less common than streptococci. In spite of the poor viability of the organism on ordinary culture media, it is fairly resistant to desiccation and sunlight, especially when imbedded in sputum. It is possible that the surrounding spu- tum is protective and that the well-formed capsule which the coccus possesses as a parasite, increases its resistance. Wlien dried and powdered it is much less resistant, being killed by direct sunlight in about an hour. Like other bacteria, it resists dif- fuse sunlight better than direct, and in the former PNEUMOCOCCUS. 339 may live for as long as fifty-five days in a drietl state (Bordoni-Uffreduzzi, cited by Weichsel- baum). It has very little resistance to heat, being killed by a temperature of 53° C. for ten minutes. No characteristic soluble toxin has been obtained, Toxic . ' Properties. although more or less poisonous substances, some of them of a chemical nature, have been described. Presumably the toxic properties reside in an endo- toxin. The pneumotoxin of F. and Gr. Klemperer was prepared by precipitation with alcohol. The pneumococcus is a pyogenic organism and causes exudates which are rich in fibrin. Occasionally serous rather than purulent exudates are produced. Its toxic action is directed toward various organs, and it is doubtful if any of the tissues of the body are non-susceptible. Some strains are supposed to be more neurotoxic than others. The susceptibility of animals varies greatly. Eabbits and mice are extremely susceptible and are used as test animals for the identification of the organism. Other laboratory animals have greater resistance, and the pigeon and chicken are almost absolutely immune. In susceptible animals a rap- idly fatal coccemia or more or less extensive local lesions are produced, depending on the virulence of the culture, the seat of inoculation and the suscep- tibility of the animal. In rabbits lobar pneumonia has been produced by inoculation into the pleura, trachea, blood stream or subcutaneous tissue. The pneumococcus is present in the nose, mouth pccu and pharynx of a large percentage of individuals. It is encountered more frequently in crowded cities than in country districts. It persists for weeks and months in the mouths of convalescents from pneumonia, and it reaches the mouths of those Susceptibility of Animals. rrence in the Body the Lungs. 340 IXFECTION AND IMMUNITY. who are in the vicinity oi' pncunionics. It is found frequently in the conjunctiva and occasionally in the deeper air passages. That it may reach the stomach and intestines with the sputum is appar- ent, and it has been found there as the cause of diphtheritic enteritis, a condition wliich may be followed by pncumococcus peritonitis or general infection. Entrance into The luugs are infcctcd by inhalation of the cocci. Suspended in droplets of saliva or mucus, or adherent to foreign particles, they may be car- ried fairly deeply into the bronchial tubes. That they ever reach the alveoli by this means alone is questioned by many. Two factors would seem to prevent their being carried to the alveoli by cur- rents of inspired air : First, foreign bodies or in- fected droplets are likely to strike and adhere to the walls of the respiratory passages before they have traversed a great length, and from this situa- tion may again be carried out by the action of the ciliated epithelium or coughing; tlie tortuous pas- sages of the nose and its hairs and moist surfaces arrest many micro-organisms. Second, the velocity of the inspired air is greatly reduced or is nil by the time the particles might have reached the alveoli, a condition which renders their arrest all the more probable. Nevertheless, pneumococci do reach the alveoli, and by some it is supposed that even in health they are carried there more or less constantly and are as constantly destroyed. Occa- sionally they have been found in the parenchyma- tons tissue of the lungs of individuals who have died of other than pneumococcal infections or of non-infectious diseases. In order to show that micro-organisms may be carried into the paren- PNEUMOVOCCUS. 341 genous In- fection. chyma by inspiration Nenninger allowed animals to inhale a spray containing Micrococcus prodigio- sus, and killing the animals after one-half hour, was able to cultivate the coccus from the base of the lungs where only alveoli and the finest bron- chial branches were present (cited by Weichsel- baum) . Various other agencies have been suggested l)y '-^^^^^^^"o""* which the cocci may be carried to the parenchyma- tous tissue. For example, during the forced res- piratory efEorts which accompany coughing they may be carried from the bronchial branches into the alveoli. Or the organisms having reached the bronchi, may be carried through the walls of the latter, perhaps by the leucocytes, and reach the alveoli directly through the lymph channels or after having caused infection in 'the peribronchial lymph glands. Others express the opinion that pneumonia follows blood infection in many or most instances, i. e., that the infection is hemato- genous, the cocci having reached the blood in some obscure manner. That the infection may be hema- togenous is shown by the occasional occurrence of pneumonia secondary to pneumococcus infection in other parts of the body. Knowing the fairly constant presence of pneu- mococci in the upper respiratory passages in the normal individual, it seems certain that some un- usual condition must arise to precipitate infection of the pulmonary tissue. Concerning the nature of these conditions, we have little but theories. They may rest either with the microbe or the in- dividual, or with both. The pneumococci which are normally on the mucous surfaces may undergo an increase in virulence, or more virulent organ- Conditions for Infection. Decrease of Resistance. 342 IMJJCTWX A.\D IMMLNITY. isms from the outer world, or from pneumonic pa- tients, may be inhaled. The latter condition is an important one in relation to the contagiousness of pneumonia and the development of epidemics. Park and Williams found a larger percentage of virulent organisms in the sputum of pneumonics than in that of normal persons. It is possible that the pneumococcus in being passed from one patient to another undergoes an increase in virulence, sim- ilar to the increase which may be obtained by pass- ing bacteria through animals. On the other hand, it is very probable that es- sential changes take place in the individual, changes which in some may cause the lowered re- sistance which is so often referred to as a condition for infection. Exposure to cold has long been known as an important predisposing factor, al- though we continue in ignorance of its precise effects. Animals are more susceptible to pneumo- coccus infection after artificial reduction of the body temperature. It is possible that a lowered body temperature may decrease antibacterial ac- tivities; that the activity of the bactericidal fer- ments of the plasma or of the leucocytes may be suppressed, or phagocytosis may be inhibited so that organisms which reach the bronchi and peri- bronchial lymphatic structures are allowed to pro- liferate. It is probable that in health the leuco- cytes continuously pass through the bronchial and alveolar walls where they may englobe foreign par- ticles (coal dust) or bacteria, and leucoc3^tes are present on the mucous membranes of the mouth cavity. Following exposure and the reduction of the body temperature, or following the prolonged inspiration of cold air. the activity of the phago- PNEUMOCOOCUS. 343 Other Predis- posing Factors. cytes may be inhibited so that cocci which reach these surfaces are not ingested and continue to proliferate, or the same conditions may decrease the exudation of tlie leucocytes from the vessels. It is possible also that the activity of the ciliated epithelium is reduced similarly so that the cocci are not so readily carried to the exterior. Extreme exposure is not always followed by pneumonia, however, and not all cases of pneumo- nia are preceded by exposure; many other condi- tions may predispose to infection, as a lowered resistance due to alcoholism, other infections or to non-infectious processes. That certain local con- ditions may favor infection is indicated by the fre- quency with which individuals with chronic tuber- culosis of the lungs die of pneumococcus pneumo- nia, and the development of the disease in areas of hypostatic congestion. Age is of influence. "To the sixth year the predisposition to .pneumonia is marked; it diminishes to the fifteenth year, but then for each subsequent decade it increases" (Osier). The cause of these variations is not known, although the rise in later years may be associated with increased exposure. The conditions which predispose to infection are now the subject of active study in many labora- tories, and the commission which the New York Department of Health has established for the study of acute respiratory diseases has already made im- portant observations as to the prevalence and viru- lence of pneumococci. Many observers have found pneumococci in the complications, blood in a large percentage of the cases, and recent work by Eosenow indicates that the blood is prob- ably infected in all cases at some stage of the dis- 344 INFECTION AND IMMUNITY. ease. This being the case, the i'requeuey with which pneumococcus infections occur in other organs as complications of pneumonia is readily understood. Pleuritis is present almost constantly, pericarditis frequently, and the peritoneal cavity is invaded not infrequently by way of the diaphragm, with general peritonitis as the occasional result. In pneumo- coccus pleuritis tlie exudate is frequently of a serous character. Endocarditis, meningitis and arthritis are frequent complications. Conjunctivi- tis, otitis media, cutaneous or subcutaneous infec- tions, intramuscular abscesses and osteomyelitis may develop. The kidneys and liver usually show acute degenerations. Diplococcus pneumonia occurs as a complication in typhoid, diphtheria, tuberculosis, influenza, ery- sipelas and other infections, the organism of the primary infection also being found in the lungs. Not infrequently staphylococci,, streptococci, Mi- crococcus catarrliaUs, or the bacillus of Friedland- er, are found with the pneumococcus, the latter being the predominating organism. Eecent work from Phipps' Institute (Flick, Ravenell and Er- win) suggests that the pneumococcus ma}^ be an exciting cause of pulmonary hemorrhage in the tuberculous. Prophylaxis. Prophylactic measures are largely of an individ- ual character. One should not come in contact un- necessarily with those suffering from pneumonia. The susceptible should be guarded against expos- ure; pneumonia should be considered as a conta- gious disease, the cases isolated as sucli, the sputum disinfected, and rooms cleaned with moist antisep- tics rather than by dusting and sweeping; the sick room should be flooded with sunlight, and the PNEUMOGOCOUS. 345 mouths of convalescents disinfected. Expectora- tion in public places should be limited. To what extent the dust-laden atmosphere which prevails in most of our large cities is a factor in causing pneumonia is unknown. Vaccination is not yet an established procedure. It is probable that the susceptibility of man immunity and varies greatly. Under equal conditions of expos- susceptibility. ure not all contract pneumonia, and an individual who eventually contracts the disease may have undergone many similar exposures previously. Klemperer introduced a culture of the pneumococ- cus which was virulent for rabbits imder his skin without suffering more than temporary disturb- ance. Eecovery seems to indicate an acquired immun- Recovery. ity or resistance which is by no means permanent, and often is of very short duration. One may have as many as eight or ten attacks of pneumonia, the intervals between attacks being from three to five years on the average (Griswolle). What the re- covery or acquired resistance depends on is un- known. The marked leucocytosis of pneumonia, and the known phagocytic power of the leucocytes for the diplococcus, suggest strongly the impor- tance of the leucocytes for recovery. The serums of convalescents and of immune animals show no increased bactericidal power for the organism, nor are they strikingly antitoxic. Beginning with Fraenkel (1886), many have serum shown the possibility of increasing the resistance and'opsonins of susceptible animals to the pneumococcus by in- jecting first dead or avirulent and then virulent cultures ; in this way the subjects can be made to withstand many multiples of the minimum fatal Phagocytosis. 340 IXFECTWX AM) IMMUNITY. dose. Culture filtrates and precipitates (the pucu- motoxin of F. and G. Klemperer) have been used for similar purposes. The serum of immune ani- mals, and in some instances of convalescents, has been found to have a protective effect when in- jected into other animals, and by some a curative effect is claimed when the serum is given shortly after infection. Mennes made the interesting ob- servation that "normal leucocytes only become phagocytic toward pneumococci when they are lying in the serum of an animal immunized against this bacterium" (Muir and Eitchie). This action may have been due to the effect of the opsonins which Wright and Douglass have shown to be essential for the phagocytosis of pneumococci. According to iSTeufeld and Eimpau, autipneumococcus serum is not bactericidal, but through the influence of bacteriotropic substances (opsonins ? ) which it contains renders the cocci more susceptible to phagocytosis.^ Likewise, Park and Williams found antipneumococcus serum from the sheep to be protective for mice and to stimulate phagocytosis. The correspondence between bacteriotropic action and protective power was variable, however, so that it did not appear certain that the protective power of the serum was due entirely to its influence on phagocytosis. We are, of course, not sure that events in the animal body correspond Avith those in the test-glass. Some of the serums Avhich have been prepared ^"una^Fdn! ^^^^^ been used therapeutically in man. The re- sults have not been sufficiently satisfactory to put 1. This bacteriotropic substance, according to Neufeld, differs from tlie opsonin of Wriglit in that it is not de- stroyed by low degrees of heat. Serum Therapy PNEUMOCOCaUS. 347 them on a good basis, althougli some favorable re- ports have been given. The serum of Eoemer, which is best known at the present time, is obtained by immunizing dif- ferent kinds of animals with several strains of pneumococci. The receptor apparatus of different strains probably differ; hence, a serum obtained by immunization with several strains probably would be effective against a large variety of pneu- mococci. Furthermore, since different animals may respond to immunization with a given organ- ism by the formation of amboceptors with different complementophilous haptophores, a theoretical ad- vantage is to be gained by mixing immune serums from several animals. The amboceptors of one or more of the serums may be susceptible to activa- tion by the complement of the patient's body, whereas if only one serum were used the chance of such activation would be decreased. Passler, in summing up the results obtained in the treatment of 24 cases with this serum, finds the course of the disease shortened, the temperature reduced and a tendency to limit the extension of the disease to other parts of the lungs. The serum of pneumonic patients shows an in- creased agglutinating power for the pneumococcus. The maximum is reached at or near the time of crisis, but rarely has a higher value than 1 to 50 to 1 to 60 (Neufeld, Eosenow). It disappears quickly after recovery. In immunized animals the agglutinating power may be pushed to much higher limits. Not all strains yield -agglutinins equally, and not all are agglutinated equally by the same serum. According to Collins, pneumococci fall into different groups, depending on their agglu- Serum of Roemer. Agglutination. 348 IM'EVnoX AXD niilUNITY. finable properties; the same author detenniued the presence of group agglutinins in an immune serum. Neufeld states that avirulent strains were not agglutinated by the serum of pneumonic pa- tients. OTHER INFECTIONS BY THE PNEUMOCOCCUS. Complicating infections b}^ the pneumococcus during the course of pneumonia were mentioned above. They may occur by way of the lymph channels, as in pleuritis, pericarditis and peritoni- tis (through the diaphragm), by continuous exten- sion, as in infection of the bronchi, nose and, per- haps, the middle ear, or as metastatic infections following the invasion of the blood stream by the organisms. It is undoubtedly in the last named manner that meningitis, endocarditis, arthritis, muscular and subcutaneous abscesses arise. Mode of Other infections by the pneumococcus occur in- dependent of the existence of pneumonia. Such conditions are alveolar abscesses, conjunctivitis, dachryocystitis, serpent ulcer of the cornea, in- flammation of the middle ear, meningitis, enteri- tis, rarely peritonitis, and pneumococcus septice- mia which may be complicated by infection in vari- ous organs. The eye is exposed to infection from without and the ear from the pharynx. Primary jjneumococcus meningitis occurs both sporadically and epidemically, although the meningococcus is a more frequent cause. The organisms may gain entrance through the middle ear or nose, or through the circulation from a primary focus in another organ, perhaps an undiscovered focus. Pre- ceding and during meningitis the nose is not in- frequently the scat of pneumococcus rhinitis, and Infection. STREPTOCOCCUS. 349 the organisms may bo carried from the nose to tlie meninges by way of the lymph channels. The blood may be infected secondarily. Pneumococcus meningitis is almost invariably fatal. The organ- ism causes chronic meningitis less frequently than the meningococcus. Infection of the peritoneum may follow an intestinal infection ; a pure pneumo- coccus infection of the peritoneum in the absence of pneumonia is extremely rare. Pneumococcus infections of the eye, ear, intestines and perito- neum are likely to be accompanied by other or- ganisms. Pneumococcus conjunctivitis occurs in epidemic form and the same precautions should be taken to limit it as for the limitation of influenza con- junctivitis. Serpent ulcer of the eye, a progressive phage- denic process in the cornea, has the pneumococcus as its essential cause, although other organisms may be present. Eoemer treats the condition with an antipneumococcus serum and claims that he is able to arrest the process if the treatment is begun sufficiently early. The serum is injected beneath the conjunctiva. II. STREPTOCOCCI. When wound infections, cases of septicemia and Discovery of pyemia were first studied bacteriologically, various Pyoaemc coccf, names were applied to certain cocci which were found. Such were the Microsporon septicum of Klebs and the Coccobaderia septica of Billroth and others. Pasteur recognized such organisms and cultivated them at an early date, but Ogsten, in 1880 to 1884, using the newly-devised technic of Koch, was the first to recognize two sorts of 350 IXFECTIOX AND IMMUNITY. pyogenic cocci, to which he gave the names of strep- tococci and staphylococci. The former grew in tlie form of chains and the hitter in chisters. In 1883 Felileisen obtained the streptococcus in pure cult- ures from cases of erysipelas. Rosenbach deter- mined more exactly the significance of streptococci in wound infections and septicemia, and gave to the organism the name of Streptococcus pyogenes. Morphology. The typical streptococcus is a spherical or spheroidal cell, about one micron in diameter, which grows in the form of chains of varying length. Division takes place in one direction only. Variations in form, such as diplococcus-like cells in pairs or chains, or elongated cells resem- l)ling bacilli, represent accidental stages or anoma- lies in division. Streptococci commonly appear as diplococci in the blood and tissues of the infected. Unusually large cells may be involution forms. The difficulty of distinguishing the pneumococcus from the streptococcus has been mentioned. At one time it was thought that streptococci could be separated into those which grew in long chains (S. long us) and those which produce short chains (S.hrevis). Although these names are still used for convenience, they are not well grounded, since the length of the chains is not an inherent prop- erty; one form may be changed into the other by appropriate methods of cultivation. Similarly the S. erysipelatis of Eehleisen is not a specific or- ganism for erysipelas, since strains from other sources are able to cause experimental erysipelas in man. Streptococci growing in short chains may be cultivated from the normal mouth cavity and they are usually of low virulence for animals. On the other hand, *S^. longus is more often obtained STREPTOCOCCUS. 351 from wound infections, septicemia and malignant tonsillitis. Capsulated strains of high virulence are occasionally found in the body. Ordinarily, however, streptococci are not surrounded by a cap- sule. The Streptococcus mucosus capsulatus may be a pneumococcus. Although streptococci are de- scribed which do not stain by Gram's method, those with which we are concerned invariably react posi- tively. Streptococci are never motile, possess no flagellse and form no spores. Streptococci grow better in a neutral or slightly cultivation. alkaline medium than in one of acid reaction, but virulence is lost rapidly. They may be cultivated indefinitely in media which contain serum or ascitic fluid, but even here virulence disappears gradually; frequent transplantation is necessary. In bouillon those strains which produce short chains or grow as diplococci cause a diffuse cloud- ing of the medium, whereas those growing in long chains sink to the bottom, leaving a clear overly- ing fluid. Streptococci demand little oxygen, all are facultative anaerobes and some are said to be obligate anaerobes; obligate anaerobes may be cul- tivated from the vagina and intestines. The optimum temperature for growth is 37° C. When dried, streptococci live for from ten days to several weeks; they are destroyed more quickly in the presence of sunlight. Susceptibility to antiseptics depends on the nature of the medium in which they are suspended or imbedded. When unprotected by bouillon or other fluid they are killed in a few seconds by 1/1000 corrosive sub- limate and 3 per cent, carbolic acid (Fehleisen) ; when in bouillon, by 1/1500 corrosive sublimate and by 1/200 carbolic acid in fifteen minutes. Ly- Resistance. 352 lyFECTION AXD IMMUNITY. ing on a mucous surface, where they are imbedded in mucus or tissue fluids, they are protected against antiseptics to some extent. They are fairly resistant to heat, being destroyed by a temperature of 70° to 75° C. in one hour (v. Lingelslieim). Virulence. Strcptococci vdiy widcly in their pathogenicity. Cultures which are entirely non-pathogenic for animals are frequently cultivated from nature and from man. As a rule, however, the long chains obtained from pathological processes in man are pathogenic for rabbits and mice. Their virulence is very labile, and by passage through suitable ani- mals (rabbit, mouse) it may be pushed to a very high point; in doing this, however, the original virulence of the culture undergoes modifications. For example, Marmorek so increased the virulence of one strain that the milliardth part of a c.c. was fatal for rabbits, but it had lost its pathogenicity for man, as shown by inoculations into carcino- matous patients. Hence the pathogenicity of cul- tures for animals is not a good index of their viru- lence for man. Those which produce long chains in bouillon are more pathogenic than those form- ing short chains (v. Lingelsheim). Eabbits and mice are the most susceptible ani- mals. The rat, guinea-pig and cat, and larger ani- mals, as the horse, goat and sheep, are less sus- ceptible. A bouillon culture of which .01 to 1.0 c.c. will kill a mouse or rabbit in from one to four days is considered of high to moderate virulence. Virulent cultures cause systemic infection, regard- less of the method of inoculation. Less virulent cultures produce changes which are more localized in character and which may heal : abscesses, areas of necrosis and erysipelatous inflammations. STREPTOCOCCUS. 353 The properties on which the virulence of strepto- Endotoxin. cocci depends are little understood. The conflict of opinion concerning many points probably de- pends on the use of different strains of the organ- ism in experimental work. The amount of endo- toxin which virulent strains contain is subject to great variations. Aronson found practically none in the killed cells of a very virulent strain. It. seems probable that the endotoxin is rather sus- ceptible to heat, since cultures which are killed by mild methods, as by chloroform, are more toxic than those whicli are killed by heat. The filtrates of old bouillon cultures are more or less toxic. A strong "toxin" was prepared by Marmorek by growing a virulent strain in a mixture of serum and bouillon for three months and filtering the culture. More recently he uses a medium contain- ing glycocol and leucin. Toxic precipitates from fluid cultures have also been obtained. Bouillon filtrates of virulent cultures after two to fourteen days of growth have low toxicity (Aronson). Besredka, and later Gr. P. Euediger, showed that streptocoiysin virulent streptococci produce a hemolytic toxin Toxin!*"^***^^*"^ when gro\\Ti in various heated serums. Euediger proved that this hemolysin (streptocoiysin) is a true toxin, possessing a haptophorous and toxo- phorous structure. This discovery has an im- portant bearing on the fact that the blood in fatal streptococcus infections, especially in rabbits, is often more or less laked. Streptocoiysin is de- stroyed by a temperature of 70° C. in two hours, by peptic digestion, deteriorates rapidly at ordi- nary temperatures, and is non-dialysable. Certain normal serums contain antistreptocolysin (Eue- diger). Another significant discovery by Eue- 'Soi IXFECTIOy AXD IMMUXITY. diger is that virulent strains, when grown in soruni and ascitic fluid, produce a substance -\vhieli kills leucocytes and inhibits phagocytosis. This may explain the failure of leucocytes to take up virulent organisms, whereas non-virulent strains are readily phagocytized. Lingelsheim states that strains cul- tivated from subacute or chronic processes produce •more soluble toxin (nature unknown) tlian highly virulent strains. Not all toxic fdtrates contain streptocolysin, the hemolysin being independent of other toxic constituents (Simon). Lingelsheim concludes that the infectiousness of streptococci is not explained by the toxic properties which have been demonstrated. He lays stress on their resist- ance to the bactericidal activities of the tissues and tissue fluids. It is safe to say that up to the ])res- ent time the essential toxin of the streptococcus has not been demonstrated. Pathologic Streptococci are the frequent cause of wound in- Processes fections, the most common cause of lymphangitis and dift'use inflammations of the subcutaneous and intermuscular connective tissues (cellulitis), endo- metritis and puerperal septicemia, endocarditis and tonsillitis, are often the exciting organisms in pneumonia (lobular, usually), bronchitis, meningitis, inflammations of the serous surfaces (pericardium, pleura, peritoneum joints), enteritis and suppurative processes in the middle ear. They are the exclusive cause of erysipelas, which occurs naturally, and serious attempts have been made to show tliat they arc etiologic factors in scarlet fever and rheumatic fever. The streptococcus is the most common organism found in the lesions of impetigo contagiosa, although it may be mixed with other bacteria, especially tlio staphylococcus. STREPTOCOCCUS. 355 Occurring as mixed infections in pneumonia, tu- berculosiS; scarlet fever, enteritis and other proc- esses, they cause grave and often fatal complica- tions. Xot all streptococci are able to cause erysipelas. Erysipelas. and a streptococcus cultivated from a case of ery- sipelas is not able to cause the disease in all indi- viduals. Furthermore, cultures obtained from other sources (phlegmon) may produce the dis- ease. (Koch and Petruschky.) Koch produced an erysipelatous inflammation with a staphylococ- cus. It has been suggested that streptococci which cause erysipelas, rather than some other process, do so because of some peculiarity in their virulence or in the resistance of the individual, or perhaps both. Another suggestion is that this type of in- fection depends on some peculiaritj^ in the skin and subcutaneous tissue of the susceptible. The conditions are obscure. The infection atrium is not always known. In facial erysipelas entrance probably is gained through the mucous membrane of the nose in many instances. Erysipelas is a wound infection in most or all instances, although the atrium often escapes observation. The cocci lie principally in the hniiph spaces and interspaces of the connective tissue. They are rarely to be cultivated from the scales or the fluid of blisters, but may be obtained from skin which is excised from the border of the inflamed area. (Fehleisen.) They probably are not excreted through the un- broken skin. Erysipelas is an inflammation of the superficial Lymphangitis. honphatics of the skin, while in hTnphangitis the deeper lymphatics are involved. Thrombosis of the lymphatic vessels, congestion of the adjacent 3.")*! IXFJX'TIOX AM) /.!/ 1/r.\ 77'1'. blood vessols, cau.-ini;' I'cddciU'd ^^l•(■nks ;uid local lu'inolysis (?). arc disliimuishing local I'caturos. Metastases occur to adjacent lyinpli glands and the infection niav become general. Jn this process, as well as in wound infections, thrombosis of the ailjaccut vessels mav occur, \\liicli may be the first step in the production of pyemia with multiple points of infection. Cellulitis may also be caused by the staphyloeoecus alone or infection with the lat- ter may be superimposed on a ])rimary streptococ- cus cellulitis. Pneumonia. Pneumonia |)i"oduc-i'd by the streptococcus may either be primary or secondary to infection in other parts of the body. Characteristically, it re- send)les the lobular type in the occurrence of multiple foci, which present a smooth surface on section and are very rich in cells. It occurs less frequently as the cause of lobar consolidation, and very frequently as a mixed infection in pneumo- nias caused by the pneumococcus and other organ- isms. Streptococcus infection of the lungs in pul- monary tuberculosis is a serious and frequent com- plication of the latter disease. It produces a septic condition, involves adjacent healthy tissue, and its role in causing consolidation and liquefaction of the tissues predisposes of hemorrhages. In cultures the streptococcus is said to inhibit the growth of the tubercle bacillus, and it has occasionally been noted that the tuberculous, after suffering a strep- tococcus infection (erysipelas), show an improved condition ! Meningitis. Primary streptococcus meningitis is rare or of doubtful occurrence. It frequently is secondary to otitis media, and has been noted following ton- HTRHI'TOCOaCUH. 357 Vagina and Uterus. sillitis, facial erysipelas, pneumonia, endocarditis and as part of a pyemic process. Streptococci are perhaps the most important Enteritis, cause of enteritis in children, the inflammation often being membranous and accompanied by desquamation of the epithelium and by hemor- rhages. It is not infrequently followed by peri- tonitis and septicemia. Virulent organisms prob- ably reach the intestines through milk in many instances. Escherich found streptococci in nearly every sample of milk which he examined. Digest- ive disturbances due to other causes predispose to infection. The organisms are nearly always pres- ent in the intestines of the adult, but cause en- teritis less frequently than in children. The normal vagina does not offer a good cul- ture medium for patliogenic bacteria, although streptococci are occasionally found there. They occur more frequently in those who have borne children. The vagina tends to purify itself me- chanically and by the acid nature of its secretions. If the secretion for any reason becomes alkaline, as in catarrhal conditions, or if it contains blood and serum, which provide a good culture medium, virulent streptococci proliferate. Infection takes place through denuded surfaces and tears ; endome- tritis, metritis, parametritis, salpingitis, peri- tonitis and sepsis may follow. Thrombosis of the blood vessels may be followed by the development ■of pneumonic foci. Streptococci are probably always present on the Upper Respira- tonsils, the mucous membrane of the mouth, very frequently in the sputum and not infrequently on the mucous membrane of the anterior -nares. Pre- sumably they proliferate under inflammatory con- 358 IXFIJCTIOX A\D IMMUNITY. ditioiis from wliatover c-auso, finding in tlie serum and plasma wliich exude a medium favorable for growth and the development of virulence. Thej^ are of great significance in severe local inflamma- tions, as in diphtiieria and scarlatina, and when general resistance is lowered, as in typhoid, typhus, variola, measles, etc. Lingelsheim characterizes their relation to diphtiieria as follows: they injure the tissues locally, penetrate beneatli the uiciu- brane into the tissues and take part in the forma- tion of the membrane; they increase the virulence of the diphtheria bacillus; alone, or in conjunction mth the diphtheria bacillus, they may invade the lungs, causing bronchopneumonia, or enter tlie circulation and injure various organs, but particu- larly the kidneys. Their method of entering the lungs from the upper respiratory passages probably is similar to that involved in pneumococcus infec- tion. Furthermore, having obtained a footing in the pharynx, for example, they may reach the bronchi and perhaps the alveoli by extension along the surface. Streptococci are usually the essential organisms in follicular tonsillitis, are frequently found in alveolar abscesses, but in both instances may be mixed with other organisms, especially the staphy- lococcus and pneumococcus. Streptococci in tlie throat may appear in diplococcus form in fresh preparations. Beginning primarily in the nose, tonsils or pharynx, streptococcus infection may extend to the adjacent sinuses, the middle ear, meninges, or through the tonsils may cause sys- temic infection with endocarditis as a frequent complication. Tlie endocarditis caused by streptococci usually HTREPTOVOCCUH. 359 Rheumatic Fever. is vegetative in character, but may be ulcerative, Endocarditis. and may result in metastatic foci of infection (e. g., septic infarcts). Infarcts from strepto- coccus endocarditis are not always infected, how- ever. Not infrequently the vegetations contain staphylococci as well as streptococci. Since 1867, when Salisbury described a fungus which he called Zymo host's translucens,TsxQiiy micro- organisms have l^een described and cultivated from the joints, blood, endocarditic and pericarditic lesions and from the tonsils in acute articular rheumatism. Among them were the "Monadinen" of Klebs (1875), short bacilli by Wilson (1885) and others, staphylococci and streptococci by Weichselbaum (1885) and by many others, and an anaerobic bacillus resembling that of anthrax by Achalme (1890). Streptococci have been found more frequently than other organisms. The ba- cillus of Achalme acquired considerable prominence at one time, being found in rheumatism in a num- ber of cases, but it has been found since in other conditions, and normally, and Achalme himself gave up his original claims for its etiologic significance. The organism, possibly, is identical with B. aerogenes capsulatus of Welch (Harris). Many of the observations are of little value, since the cultures were made postmortem, when contami- nations and agonal invasions by other organisms could not be excluded. The conditions were very confusing, however, since the injection of pure cultures occasionally produced arthritis, peri- carditis and endocarditis in animals. This was the case with a short anaerobic bacillus or diplo- bacillus cultivated by Thiroloix, and by Triboulet, Coyon and Zadoc (1897). 300 INFECTION AND nfMUNITY. In 1897-98 Triboulet and C'ovon cultivated from the blood of tive cases of rheumatic fever a di])lo- coceus, pure cultures of which caused arthritis, endocarditi:^. etc.. in rabbits. Similar oliservatinns liave been niadr by Wcst|ibal. W'asscniiaiiii ami ^[alkoir, Poynton and Paine, i^eaton and Walker and others, and the possibility of producing lesions characteristic of rheumatic fever by the inocula- tion of pure cultures into rabbits lias been well es- tablished. Although the organism was called a diplococcus by the discoverers, it can not be dis- tinguished from the ordinary streptococcus pyo- genes by cultural tests. These discoveries do not, however, put this particular streptococcus on a satisfactory l^asis as the cause of the disease, since streptococci liom various sources are able to cause experimental arthritis in rabbits (Cole, Harris). It seems that virulent streptococci from whatever source have a predilection for serous surfaces. This is apparent from the frequency witli which the joints, endocardium, etc., are involved in strepto- coccus septicemia in man. The view of Singer and of Menzer that "acute rheumatism is simply one of" the many manifestations of streptococcus invasion" (Harris), finds some justification in the streptococcus tonsillitis witli which the dis- ease iisually begins, the recovery of streptococci from the lesions and the production of these lesions in rabl)its by the injection of pure cultures. The fact remains, liowever, that streptococci can not always be cultivated from the lesions of rheumatic fever; hence it is possible that the organism may exist as a mixed infection with more or less con- stancy, and that the real cause is as yet unknown fpiiiiiip). STREPTOCOCGU^. 361 Relation of Streptococci to The theory that scarlet fever is of streptococcus etiology has been held particularly by Babes, ScarTetTever. Klein, Moser, Gordan and Baginsky and Sommer- feld. Some have held that streptococci isolated from the disease show distinctive properties and deserve the name of Streptococcus scarlatina' . This, however, is not agreed to by most bacteriologists, the organisms not differing from streptococci ob- tained from various sources. The organisms are not found constantly in the erythematous eruption. Virulent streptococci are found on the tonsils almost invariably in scarlet fever. In 65 per cent, of the cases a membrane is formed (Ranke), and this is often due to the streptococcus, which is sometimes, however, associated with diphtheritic infection. The frequency with which streptococci invade the blood during scarlet fever is related to the severity of the disease. Occasionally they are found in mild cases, which run a short, uncompli- cated course, but "more frequently in severe and protracted cases, in which there also may develop local complications and clinical signs of general infection, such as joint inflammations" (Hek- toen). Baginsky and Sommerfeld found strepto- cocci in the blood and organs of each of eighty- two fatal cases. Hektoen states, however, that streptococcemia is not necessarily present in fatal cases. At the present time there is not sufficient ground for considering streptococci as the specific agent in scarlet fever, although they are undoubtedly the cause of the most frequent and serious complica- tions. The mortality of the disease probably is greatly raised by mixed infections with the strepto- coccus. 3G2 IM'EOriON AND IMMUNITY. Beneficial lafluences. Effect on Sarcoma. Streptoeofcus filtrates or cultures may cause de- generative changes in the spinal cord (Honien and Laitineu). Certain strains of streptococci are said to exer- eise a curative eU'eel in experimental anthrax. Emmerich and di Mattei found that by intra- venous injection of the cocci rabbits could be saved from an anthrax infection which otherwise would prove fatal in forty-eight hours. This result can not always be obtained, and it may be that only certain strains have this etfect (Zagari, cited by Lingelsheim). It is noted occasionally that lupus improves or actually heals following an attack of erysipelas. A reputed effect of a similar nature in tuberculosis of the lungs was mentioned above. The rather old observation that an attack of erysipelas often causes a decrease in the size of malignant tumors, especially sarcomas, received some confirmation from the experimental work of Fehleisen. With the hope of reproducing erysipe- las with pure cultures, Fehleisen had inoculated streptococci into those suffering from such tumors. Among six patients so inoculated, a decrease in the size of the tumor was noted in five. Killed cul- tures were tried without effect. Coley's mixture of killed cultures of the streptococcus and Bacillus jyrodigiosus received rather extensive trial as a substitute for living cultures of the streptococcus, and in many instances improvement and even cures have been reported. Others have had no favorable results. Senn used the preparation in twelve cases of inoperable sarcoma "with negative results." The Bacillus prodigiosus is supposed in some way to increase the efficacy of the strepto- m'RFJ'TOVOVCUH. 363 COCCUS toxin; it contains a toxic protein. These toxins seem to have no influence on carcinomas. Concerning the natural susceptibility and im- yjJ^5J"jj^j"j"*' munity of man to infections with the streptococcus little is known. It seems probable that the un- impaired mucous surface resists invasion by the organisms which occur constantly in the mouth cavity; the physical protection of the intact sur face, the rapid desquamation of epithelium, the rapid excretion with the saliva, the inhibiting in- fluence of the saliva on the proliferation of bac- teria and the destruction of bacteria by the leuco- cytes which constantly appear on the mucous sur- face are probably important factors in this local resistance. Congestion of these surfaces, espe- cially the tonsils, from any cause, as from ex- posure, or the occurrence of some other infection, as may be the case in scarlet fever, may lower the local protective powers. And, as stated, the serum and plasma which exude in simple (?) catarrhal conditions or other inflammations, provide a me- dium which favors the growth and development of virulence by streptococci. Concerning the conditions which, in the body, antagonize infection, we are largely in the dark. It has been impossible to demonstrate antitoxic and bactericidal substances in the normal serum of man. Streptococci grow freely in fresh normal serum which contains no leucocytes. (Weaver and G. F. Euediger.) Phagocytosis of streptococci first came under the observation of Metchnikoff, who in 1887 noted it as a striking occurrence in erysipelas. Only the microphages took up the cocci. The marked lucocytosis which is noted clinically suggests, but of course does not prove, that the 364 INFECTIOX AM> / 1/ l/r.\77')'. leucocytes tako an active pari in llic destruction of the cocci. Hxperiuiental Avork showing such a relationship is not lacking, however. Bordet con- cluded that all the protection which guinea-pigs and rabbits show against streptococci is due to the phagocytes. In actual infection streptococci have often been found within the leucocytes of the blood and inflammatory exudates. (G. F. Rue- digcr.) Xon-virulent or weakly virulent strains are phagocytized more readily than the virulent in experimental work. Ruediger also demonstrated conclusively that the streptococci taken up by poly- morphonuclear leucocytes may be killed by the lat- ter. Hence the evidence in favor of a protective role by the leucocytes is more than presumptive. Ruediger suggests the importance of the leuco- cytic toxin of the streptococcus for the develop- ment of infection. It may either kill the leuco- cytes or cause negative chemotaxis, and under these conditions proliferation of the cocci nuiy proceed. Acquired The streptococcus usually is classed with those organisms, infection with which does not cause the development of lasting imijiunity. A certain amount of immunity probably is established, how- ever. This is suggested by the results of Fehlei- sen, who could not always cause second attacks of erysipelas by tlie inoculation of pure cultures into the susceptible. It is also suggested by the ease with which relatively high resistance can be produced in animals by brief immunization. A streptococcus infection of the horse which occurs naturally ("Druse") is said to produce immunity which lasts for a year or two. One may immunize animals cithci- witli toxic filtrates or with killed and liviim' cultures. The Immunity. STREl'TOCOCCUii. 305 filtrates are inueli less effective in producing iin- immunization T • j^i 1 1 01 Animals. mnnity than the hacterial cells, and m the hands of nianv ]io innmmity Avliatever could be estab- lished. A number of dili'erent principles liave been fol- lowed in immunizing with cultures. It seems that virulent strains cause a higher degree of immunity and a serum of higher protective power for other animals than strains of low virulence. On this account Marmorek, and also i\.ronson, immunize horses with streptococci, the virulence of which has been pushed to a very high point by passing them through rabbits. Strong resistance is induced by this method, and the immune serum, particularly that of Aronson, shows distinct protective power for other animals. Such serums, however, have the highest protective power against the particu- lar strain which was used for immunization, al- though the serum of Aronson is not devoid of pro- tective powers against other pathogenic strains. Concerning the serum of Marmorek there are di- vergent opinions. In the hands of Marmorek it is highly protective in animal experiments; others have found it without value. The method of Mar- morek and of Aronson rests not only on the basis MuiUplicity that strains of the highest virulence will give the «f streptococci. strongest serums, but also on the assumption of the unity of all pathogenic streptococci. If all are alike in their biologic and pathogenic proper- . ties, a serum which protects against one should protect against all. As pointed out, there is at present not sufficient ground for considering the streptococci of erysipelas, scarlet fever, rheuma- tism, sepsis, etc., as independent species. By cul- tivation and passage it is possible to so modify any 30G INFECTIOX .1\7> IMMIMTY. one of them that it is imlisi iimuisliiililc from the others, on the basis of iiioi|)hologv and patho- genicity. On the other liand they are not all itlentical in some very iiii|i(M-tant properties. For example, not all strains prixliiee hemolysin to the same degree, and they differ greatly in their sus- ceptibility to the action of an agghitinating serum. We have also to remember that pathogenicity for animals is not a reliable index of patliogenicity for man. From these confusing conditions we can only regard the question of unity or multiplicity of streptococci as an open one. \vl)icli may ho tlo- cided by future investigations. Univalent and The scrums of Marmorck and Aronson are uni- Serums. \alent serums, a single strain being used for im- munization. Certain investigators. l)elieving in the multiplicity of streptococci, utilize several strains in immunization. The serum of Denys is obtained by immunizing with several strains the virulence of which has been artificially increased. Such a serum would, theoretically, have a wider range of action than a univalent serum ; it is poly- valent. Having in mind the fact that passing a cul- ture through rabbits increases tlic virulence of the organism for the rabbit, l)ut alters its virulence for the original host (man), Tavel, Moser and Menzer prepare serums on a dilTerent basis. Tavel employs several strains of streptococci cul- tivated from pathological processes in man, avoid- ing such alterations in virulence as would be caused by passing the cultures through animals. On the assumption that scarlet fever is a streptococcus disease, j\Ioser immunizes horses with strains (about twenty) which are cultivated from cases of scarlet fever. In a similar manner, Menzer, STREJ'TOfJOC'CUH. 36i Protection. supposing that rlieiiiDatic fever is a streptococcus infection, immunizes with a number of strains cul- tivated from the tonsils of cases of rheumatism. Both Moser and Menzer avoid passage in order to retain the original biologic properties of the cul- tures. In animal experiments, some of these serums, serum and particularly that of Aronson, have exhibited strong protective powers. Aronson's serum in doses of 0.0004 to 0.0005 c.c. protects a mouse against ten fatal doses of the streptococcus given twenty-four hours later than the serum. A serum of which 0.01 c.c. protects against a dose known to be fatal is considered of normal strength. The present serum, then, is of tAventy- to twenty-five- fold value. In some instances animals can be saved when the serum is used some hours after infection, but this period is a brief one. Statements concerning the value of antistrepto- serum coccus serums in treating human infections are very conflicting. The serum of Marmorek has been given more general trial than any other, and the results have not been satisfactory. Favorable effects, such as the lowering of temperature and improvement in the general condition, have been reported, but the serum possesses no distinct cura- tive power in established infections. Koch and Petruschky deny that it has a prophylactic power in experimental erysipelas. Escherich, by using the serum of Moser, and Baginsla^ by using that of Aronson, observed a shortening of the course, a reduction of the fever and general improvement in cases of scarlet fever. Moser claims that it re- duces the mortality of the disease. The use of anti streptococcus serum in the treatment of scarlet Therapy. Scarlet Fever. 308 IM'KCnoX AM) niMi.MTY. ' rover doi's luit roiiiinit oiu' to tlio streptococcus etiology of tlie ilisease, Inil i-;itlu'r to the impor- tance of streptococcus coni})lications ; lu'iuc, if the (hinder of these complications can he rediu'cd hy antistreptococcus serum its use is justilied. It renuiins for future work to demonstrate to our satisfaction that it has such value. What has lieeii said eoiireniinii' the t I'cat iiient of Rheumatism, scarlet fcvcr with the serums of Moser and Aron- son also a))])lies to the treatment of rheumatism w ith the seniiii of ]\Ienzer. Favorable reports have- appeared conc-erning its value, l)ut a sufficient mass, of experience has not accumulated to permit of satisfactory judiiment. "80 much appears from, observations in uuin that the different streptococcus^ serums are harmless" (Dieudonne). As nearly as can be learned at present, anti- Properties strcptococcus scrum is protective (and cura- erum, ^j^.^ ( ?) ) bccausc of its ability to stimulate phago- cytosis, rather than l)ecause of serum antitoxins or bacteriolysins. This was indicated by the ob- servations of Bordet in animal experiments, in which marked phagocytosis of streptococci took place in the peritoneal cavity of immunized ani- mals, but verv little in normal animals. A sinii- Stimulation of , i-i- ' i t ■ n ± j ^ Phagocytosis. I'Av condition was iiotcd HI tlic tcst-glass experi- ments of Denys and van der Yelde. A mixture of normal rabbit serum and leucocytes showed very little phagocytosis of streptococci, whereas the addition .of antistreptococcus serum caused active phagocytosis, w^ith death of the cocci. The presence of a definite substance in the serum which stimulated phagocytosis was conceived by van der Yelde and also by Lingelsheim. It was heat-re- sistant (62° to 65° C), and was not destroyed STREPTOCOCCUS. 369 by dilute acids and alkalies (cited byLingelsheim). Hence its resistance is greater than the opsonins of Wright and Douglass, but perhaps not greater than the bacteriotropic substances of ISTeufeld. It is probable that some of these substances are heat- resistant and others heat-susceptiljle. The agglutinability of streptococci from differ- Agoiutination. ent sources, and even from the same source, varies a great deal. Also the normal serums of man and animals have a variable agglutinating power for different strains of streptococci. By immunization with a given strain the agglutinating power is in- creased, but not uniformly for all strains. Com- monly the strain used for immunization is agglu- tinated more strongly than heterologous strains, the latter sometimes undergoing no agglutination whatever. These variations do not depend on dis- coverable differences in the cocci or the diseases which they produce. A given antistreptococcus serum does not agglutinate equally all streptococci from cases of scarlet fever (Weaver). Also strep- tococci vary greatly in their ability to stimulate to the formation of agglutinins. On the whole those which produce long chains are more suscep- tible to agglutination and yield stronger serums than those with short chains. (Aronson, Tavel, V. Lingelsheim. ) By passage the agglutinating properties undergo rather complex changes. The organism then produces a stronger agglutinating serum and is agglutinated more readily by this serum than the same strain which liad not been passed through animals. If passage is discon- tinued it reverts to its former condition. The variations are such that the agglutination 37U l\ri:cTI()\ AM) I M Ml MTV. vractioii is of little or no \;iliu' in (litVcrcmiatiiig tliUVront tyju's of strt'ptofoc-ii. As to tlu' c-linii-al value of tlu' Icsi lor \\\v di-.x^j;- nosis of srarU't iVviT, the i-oucliisidus of Weaver may be cited : 1. Of streptococci cultivated ri'om eases of sear- latiua, some are agglutinated In almost all sear- latinal sera, but at dilutions varying from 1/GO to 1/4000; others are agglutinated by the same sera with less constancy and at lo\v(.'i- dilutions, and many are not agglutinated at all. 2. Streptococci cultivated from cases of scar- latina arc agglutinated by sera from cases of lobar pneumonia and erysipelas at about the same dilu- tions as by scarlatinal sera, and in the case of ery- sipelas even at higher dilutions. 3. The same appears to be true of typhoid fever serum, so far as limited tests indicate, and to al- most the same extent of puerperal-fever serum. 4. The agglutination reaction between the streptococci cultivated from cases of scarlatina and the serum from cases of scarlet fever is in no way specific, and can not be of any value as a means of diagnosis. By growing streptococci on a medium which contains serum (serum bouillon), they form fewer and shorter chains and are better suited for ag- glutination tests. III. STAniYLOCOCCI. Staph5dococci are spherical cells from 0.7 to 0.9 microns in diameter, typically, and l)y light stain- ing are often seen to consist of two hemispheres, which are separated by a delicate cleft. In pus they are found in small gi'oups of two to nine or ,rrM'if)ij>('0(jcus. 371 Ferments. ten, ocasioiially as (lijjiocoeci. tetrads or very short chains. They are luxuriant growers on nearly all media Cultivation and which are suitable for bacteria, preferring, how- erties. ever, a slightly alkaline reaction. Growth is best in the jDresence of oxygen, but proliferation occurs in its absence. Sputum, serum and ascitic fluid are favorable media, and in the last two the cocci may be agglutinated. An alkaline reaction is pro- duced in litmus milk, and the casein is precipitated and partly digested. The production of a proteo- lytic ferment is shown by liquefaction of gelatin and the formation of a clear zone about the colo- nies when grown in plates which contain coagulat- ed serum (Loeb, cited by ISTeisser and Lipstein). Albumen is changed into peptone. Loeb distin- guishes between a ferment which liquefies gelatin (gelatinase, a "collolytic'- ferment), and one which digests albumen (tr3'ptic ferment). Gelatinase is present in staphylococcus filtrates and normal serums are rich in antibodies for it. A fat-splitting ferment (lab ferment) is also present in the filtrates. The fact that the pus which is produced in staphylococcus infection does not coagulate may be due to the action of the proteolytic ferment, which digests the fibrinogen. Van der Velde had noted in 1894 that "staphy- lotoxin" (staphylococcus filtrates) cause hemoly- sis. Neisser and Wechsberg, in 1901, by growing the organisms in bouillon of suitable alkalinity, obtained hemolytic filtrates, giving the name of staph3dolysin to the hemol3^tic principle. The hemo- lytic action of the staphylococcus is readily seen in cultures on blood-agar plates; a zone of hemo- Ivsis forms about the colonies. Ervthrocvtes of the Staphylolysin. 372 IXFECTIOX AM) IMMUNITY. rabbit, when placed in bouillon cultures, undergo hemol3-sis. Stapliylotoxin also produces hemolysis in the living body. The maximum production of staphylolysin occurs after a growth of nine to fourteen days in alkaline bouillon, and nearly all pathogenic strains yield it. wlietlicr aureus, albus or citreus. It is not formed by non-patho- genic strains. The toxin is destroyed by exposure to a temperature of 56° C. for twenty minutes. A specific antitoxin is present in many normal serums and may be increased by immunization with the toxin or the living organisms. Leucocidin. In 1894 van der Velde found in the pleural exudates caused by inoculation with killed cultures of the staphylococcus a substance which is toxic for leucocytes, causing them to swell and the nuclei to disappear. This substance is called leucocidin. It is also produced in culture media, but the ability to form it is not so widely distributed as in the case of the hemolysin. Leucocidin is a true toxin, like the hemolysin; most normal serums contain antileucocidin, and the latter is increased by im- munization with the toxin.* The suggestion is a natural one that leucocidin may be a factor in combating phagocytosis in infections with the etaphylococcus. Neisser and Wechsberg de- vised a "bioscopic method" of determining the cytocidal action of the toxin. Living leucocytes, like other living cells, have the power of decoloriz- ing methylene blue when oxygen is excluded. The destructive action of the toxin on the leucocytes is indicated by the failure of this reduction when the toxin is mixed with the cells. * Leucocidin and staphylolysin will not yield antitoxins when their activity has been destroyed by heat. staphylococcus'^. 373 Old culture filtrates (two to three weeks) show Toxic a rather high degree of toxicity for animals, pro- ducing extensive degeneration of the convoluted tubules in the kidney, a degeneration which is somewhat selective; hemorrhages into the in- testinal mucosa; degeneration of the ganglionic cells, and fever. According to Levaditi, a mast- cell leucocytosis develops. The nature of the fever- producing substance is unknown. The toxicity of filtrates is said to be destroyed by a temperature of 56° C. Cultures of the staphylococcus killed by heat Endotoxinf?) show little toxicity, hence the question of the ex- istence of an endotoxin is on no better basis than in relation to the streptococcus. It is possible that the heat required to kill the organisms destroys the endotoxin as well, as the soluble toxins mentioned above. The virulence of the organisms has no direct relationship to the hemolysin or leucocidin, or the toxicity of the filtrates. Very pathogenic strains may produce a filtrate of little or no toxicity. It seems then that the essential patho- genic agent of the organism is unlcnown; as in the case of the streptococcus, its infectiousness may depend on its ability to resist the antibacterial ac- tivities of the body (phagocytosis, , bacterioly- sis (?) ), which, of course, is a very indefinite assumption. Wliat part the leucocidin plays in this resistance is not definitely known. The many varieties of the staphjdococcus are differentiated on the basis of pathogenicity, pig- ment formation, liquefaction or ndn-liquefaction of gelatin, and other cultural properties. The alhus differs from the aureus only in its inability to form pigment, and it can not be made to ac- quire this property. Pigment is formed most Varieties of Staphylo- coccus. 374 /\ri:'"ri()\ i \ /; /i/ i/rv/v r. abundantly on potato, whereas little is rornied on blootl serum. Other ])ignient-rorniing varieties are: .S*. cereus fiarus. S. pi/ogencs citreus, S. scar- laliitii.'< and Micrococcus lirinaio'dcs. The 0° C. for one-half hour kills many strains when suspended in bouillon. They are not killed by re- peated freezing and thawing, and are very resist- ant to desijccation. When in the form of fine dust they die in twenty-eight days (Kirstein). Resist- ance to the action of sunlight is variable; some strains are killed in from three to five hours. Staphylococci have fairly high resistance to anti- septics; when dried, corrosive sublimate (1/1000) kills them in two to three hours, and when im- bedded in pus thirteen to sixteen hours are re- quired (Ottaviano). Methyl alcohol, tincture of green soap and methyl violet are relatively good disinfectants. "Methyl violet in a dilution of 8TAPHYL0C0CCUH. 375 1/10,000 kills them in five to fifteen minutes (Stilling). Formalin readily hinders develop- ment, but its bactericidal power is low. It is difficult or impossible to sterilize wounds infected with the staphylococcus by means of antiseptics. Staphylococci are very widely distributed in na- ture and are to be found constantly in the super- ficial layers of the epidermis (*S^. epidermidis al- hus). In infections the staphylococcus attracts large Leucotacticand numbers of leucocytes, and the pus does not coagu- substances. late. The substance which attracts leucocytes is heat-resistant, since killed cultures will cause abscesses. In all but the most superficial lesions a characteristic result of infection is that of cell necrosis and the liquefaction of tissues. IsTeisser and Lipstein state that the necrotizing substance is a soluble toxin, since culture filtrates cause marked necrosis of the internal organs when in- jected (liver, heart, kidney). "Hence in staphylo- mycosis we can distinguish two active substances (von Lingelsheim), the leucotactic substance in the bodies of the cocci and the more important soluble staph3dotoxin which exercises not only a local but also a general toxic action on the body" (Xeisser and Lipstein). Davidson produced amyloid degeneration in rabbits and mice by the injection of living cultures. This was confirmed by Lubarsch, who found the condition most readily produced in the chicken and with more difficulty in the mouse, rabbit and dog. It rarely results if suppuration is avoided. Killed cultures may be used. Eabbits and mice are the most susceptible ani- mals. The susceptibility of man is much greater. Amytoid Degeneration. JM'ECTIOX AM) fMUUMTY Susceptibility of Animals. Infections n Man. Skin. The orgauisins are most virulent for rabbits when injected intra venously, and a variety of lesions may result, as abscesses in various parts of the body (especially the kidney, heart and muscles), arthritis, endocarditis, etc. They are less patho- genic when injected into the pleural or peritoneal cavities. Eabbits are rarely to be infected by the feeding of cultures. In experimental infections degi'nerations of the axis cylinders in the white and gray matter, and of ganglionic cells, have been noted. The virulence of staphylococci is subject to great variations, and it may be increased by passage. In passing a culture through the rabbit eight times, Lingelsheini reduced the fatal dose for rabbits from 5 c.c. to 1/100 c.c, but a corre- sponding increase in virulence for the mouse and guinea-pig did not occur. Virulence for animals is not a reliable index of virulence for man. The staphylococcus is the most common pus producer in man. The most frequent infections are those of the skin, the organisms gaining en- trance through the hair follicles rather than through the sweat ducts (Unna), resulting in such conditions as acne pustules, abscess of the skin and subcutaneous tissue, furuncles and carbun- cles. They are found almost constantly in the lesions of impetigo and often in pure culture. They have been much vaunted as a cause of eczema and they may be important as a secondary agent in this condition. The ordinary eczema prob- ably is not parasitic in its cause, however (Sabou- raud), and ISTeisser and Lipstein dispute the claim of Bender and others that eczema produced by staphylococcus fdtrates is due to products of the microbe. This conclusion was Justified, since the STAPHYLOCOCCUS. 377 Mucous Surfaces. same results were obtained witli pure IjouiUon of similar alkalinity, the property eould not l)e d(;- stroyed by heat, and antistaphylococcus serum was not able to prevent the dermatitis. Furuncles may be produced by rubbing virulent cultures into the skin, and abscesses by the injection of minute amounts. The staphylococcus causes purulent or seropurulent conjunctivitis rather infrequently. Primary infections of cavities which communicate with the surface, as the antrum of Highmore, the middle ear, nose, bronchi, lungs and tuberculous cavities, are not uncommon, and mixed infections with the staphylococcus in these localities is the rule, regardless of the primary cause. Infection of the mucous surfaces is less common than of the skin, however. It rarely causes aphthous inflam- mations, anginas, pneumonia, enteritis and cys- titis when unmixed with other organisms. Staphylococcus septicemia of great virulence oc- Septicemia, casionally follows primary infection in other parts of the body, as wound infections, tonsillitis, puer- peral infection (rare) and the so-called malignant carbuncles of the uj)per lip. In such instances a thrombophlebitis may be the means by which the organisms are poured into the circulation in large numbers. Inflammations of the serous surfaces, as the pleura, peritoneum and endocardium, are rarely primary, but follow systemic infection; the endocarditis usually is ulcerative and leads to metastatic foci of infection. Staphylococci have a particular afiinity for the bony tissues, especially the bone marrow and the periosteum ; they are the most common agent in the production of osteomye- litis and cause the so-called periostitis albuminosa. It is thought that they may persist in bone lesions Serous Surfaces and Bones. 37S /.V/-'7;('77(>\ I \ /' nnil MTV. Tor a period of years and later start up a I'resli |)r(H-c'ss. Tliev involve tlie joints less frequently, Imt have liiH'u lnund. iircsiiiiialil y as secondary ai,^ents. in acute rheumatism, and as tlie primary cause in pyemic abscesses of the joints. They are found occasionally in abscesses of ihc iiiaininary and parotid glands, liver, lungs, and in [jyorrhea MUed alveolaris (rare). The cultivation of staphvlococei Infections. ^ ' '■ • in a pure state from the tissues does not of neces- sity indicate that they are the essential organism in the process (smallpox, rlicumatisin. etc.). Pre- vious infections by many organisms, and likewise traumas, predispose to localization of the staphy- lococcus, and any infections process in the skin is I lively to be invaded by these organisms secondarily. Leucocytes lufections witli the staphylococcus are charac- 'il!!i**"I*' terized bv both local and general leucocvtosis, the Immunity. ~ local leucocytosis being a part of the suppurative process. As stated above, the staphylococcus con- tains a thermostabile constituent, Avhich exerts a ])ositive cliemotatic effect on the leucocytes. Al- though it is possible to consider the accumulation of the leucocytes merely as the expression of this affinity, it has been shown with sufficient clearness that polymorphonuclear leucocytes are able to in- gest living staphylococci and kill them.* They may be found within the leucocytes in both natural and experimental infections. When injected into the pleural or peritoneal cavity oL' the guinea-pig phagocytosis is well begun within one-half bonr and reaches its height in four to five hours. Bactericidal Experiments which were begun l)y van d<'r A elde ^cocyteJ a*n"d in 1894 demonstrate the bactericidal action of lou- Leucocytic Exudates. * Phagoc.vtosis of staphylococci was first oljserved b.v Kircli in 1889. n n i ii mune serum is given than that airorded by the ■ experiments of Proscher, Avho injected guinea- pigs, rabbits and mice with normal and immune serums and followed this 2-1 hours later with in- oculation of the cocci into the peritoneal cavity. Thirty minutes after injection of the cocci the exudate in all animals showed an enormous leuco- cytosis. At first they were chiefly mononuclears, but later gave place to polynuclears. In the ani- mals which had received the immune serum, mas- sive phagocytosis had occurred, and in the course of an hour verv few cocci were extracellular. On STAPHYLOCOCCUS?. 381 the other liand, practically no phagocytosis had taken place in the animals which had received the normal serum (cited by JSTeisser). Virulent staphylococci were taken up less readily than avirulent. Such results suggest that the protective power of the serum is due to its ability to stimulate phagocytosis, and this in turn depends on the increased quantity of bacteriotropic substances formed in the serum as the result of immunization (Wright and others). In the hands of Wright, vaccination with killed Vaccination. cultures of the staphylococcus has been very suc- cessful in the cure of obstinate cases of acne, fur- unculosis and sycosis barbae. Bouillon cultures are grown for three weeks and. then killed by ex- posure to a temperature of 60° C. for an hour. In order to control dosage, the vaccine is standardized by estimating the number of bacilli in each cubic centimeter. This is done by mixing equal quanti- ties of the vaccine with normal blood, and, after staining a preparation on a slide, determining the ratio of cocci to erythrocytes. There being about 5,000,000 erythrocytes to the cubic millimeter In normal blood, the number of cocci is readily reck- oned from the ratio which was found. From 2,500 millions to 7,500 millions of cocci may be given in an injection. The quantity to be used is determined by the effect which an injection has on the opsonic content of the patient's serum. If a suitable dose has been given, there occurs a short negative phase in which the opsonins are decreased in quantity, and this is followed by a rather pro- longed positive phase when they undergo an in- crease. If too large a dose is given, the negative phase is exaggerated and prolonged. In many in- 382 !Xri:CTl(>\ A\l> l]nil MTV. "Opsonic stances it has been noted that iiuprovoinent and '"****■' recovery go liand in liand witli an ineroase in the opsonins. The quantity of opsonins present in a serum is expressed by an "opsonic index."* Agglutination. q^hp normal scrums of man and many animals nniy agglutinate the staphylococcns. l)ut witli no constancy. In one instance human serum ag- glutinated in a dilution of 1-100 (Kraus and Low), and normal goat serum in a dilution of 1-50 to 1-100 (Amberger, cited by Xeisser). The serums from cases of staphylococcus infection (e. g., osteomyelitis) and of highly immunized an- imals undergo an increase in the quantity of ag- glutinins. The agglutination usually is strongest for the homologous strain, and if other strains are agglutinated equally it signifies a close relation- ship to the homologous strain. From the fact that only pathogenic strains pro- duce liemolysin and leucocidin, Neisser and * To obtain the opsonic index human leucocytes, oli- tained from deflhrinated blood, are washed free of serum, and equal parts are added to two e(|ual jiortions of an emul- sion of the staphylococcus. One portion of the emulsion has previously been treated with the serum of the patient for about twenty minutes, and the other portion with normal human serum. The opsonins of the two serums combine with the cocci, rendering them susceptible to phagocytosis (sensitization). After the leucocytes have been in contact with the sensitized cocci for fifteen to thirty minutes, films of the two mixtures are stained with the Romanowsky or a similar stain, which colors both the cells and the cocci. The average number of cocci in say fifty leucocytes on each slide is determined. The average phagocytosis in the pa- tient's serum divided by that in the normal serum gives the opsonic index. For example, if the former showed an average of 10 cocci to each leucocyte and the latter an average of 5, the index is 2. The degree to which the op- sonic index can be raised by the immunization varies. In one instance it was increased from .S to I.Ci : in another case which reacted less vigorously it was raised from .87 to .95. MI(JU()(HW(J(JS (JATAURIIMjIH. .'i8:j Wechsberg- considered them specifically difteront from non-pat] logenic strains. This view is borne out by the results obtained with the agglutination test. Serums obtained by immunization with pathogenic strains have a much higher aggluti- nating power for these strains than for non-patho- genic varieties, and the converse is also true. There are, however, many variations in the agglutinabil- ity of the members in each group, a fact which in- dicates variations in the receptor complex of the different strains. It has been suggested that a polyvalent serum obtained by immunization with a sufficient variety of pathogenic strains will be efficient in difEerentiating the latter from non- pathogenic varieties by means of the agglutina- tion test. Wright, noting an increase in the agglutinating power when patients are treated by his method, considers that this increase is an index of the im- munity which is established. IV. MICROCOCCUS CATARRHALIS. For some years diplococci resembling the gono- coccus and the meningococcus morphologically and in staining reactions have been found in the spu- tum by a number of observers, and to this coccus Pfeiffer gave the name of Micrococcus catarrlialis. It is frequently found in the respiratory passages in influenza-like infections and other inflamma- tory conditions, and occasionally in lobular pneu- monia. It may be associated with the influenza bacillus or the pneumococcus. Among 140 cases of diseases of the respiratory passages Gohn and H. Pfeiffer found it eighty-one times, and M. ISTeisser demonstrated it in sixteen cases of whooping- 384 lyFECTION AND IMMUNITY. . lougli. in one ol' measles and scarlet fever, and in two of diplitlieria. It loses signiiicance in relation to these diseases, however, since Jiindell found it frequently in the mucus of the normal trachea, and Weichselbaum cultivated it frequentl}^ from the healthy nasal fossse. According to Gohn, Pfeiffer and Sederl, "The Micrococcus catarrhaUs, ■\^^thout the association of other microbes, is able to cause bronchitis and pneumonia with the clini- cal type of pneumonia due to the pneumococcus. The symptoms caused by the Micrococcus catarrh- alt^ do not form a clinical type. They resemble infections by the pneumococcus or the bacillus of Pfeiffer (Influenza)" (cited by Bezancon and de Jong). Others are not so positive concerning the pathogenic properties of the organism. Its etio- logic role is not yet well established. It has little pathogenicity for animals, although peritoneal and pleural infection is possible in guinea-pigs. It differs from the gonococcus and meningococ- cus in certain cultural characters. Y. GONORKHEA AND OTHER INFECTIONS WITH THE GONOCOCCUS. Tha A. Neisser discovered the gonococcus in 1879, Gonococcus. cultivated it in 1884, and demonstrated its specific relation to gonorrhea by the inoculation of pure cultures into the human urethra. It is a diplo- coccus, young pairs having a figure-of-eight con- tour, whereas older pairs show a typical biscuit or coffee-bean shape. The organism is non-motile, has no flagella and forms no spores. It can be cultivated only on media which contain serum, ascitic or a similar fluid. Its failure to stain by Gram's method is of great diagnostic importance GOWOCOCCUS. 385 in the examination of urethral discharges; other organisms resembling the gonococcus are found in the urethra and vagina with great rarity. The reaction loses its differential value in the examina- tion of secretions of the nose, mouth, and, to some extent, of the conjunctiva, where the meningococ- cus and the Micrococcus catarrhaUs may be en- countered. In the purulent stage of a gonorrheal infection phagocytosis, the cocci are found almost entirely within the leu- cocytes, whereas in earlier stages, . when the dis- charge is slight and of a mucous character, and also during convalescence, when the secretion again becomes mucous, they are largely extracel- lular. They are never within the nuclei. The process is one of active phagocytosis in which the cocci play a passive role. They occur not only on the surface of the epithelium, but penetrate be- tween and beneath the epithelial cells, and even into the adjacent connective tissue. In culture media growth is slow and scant, and Cuitivatjon cultures rarely live longer than one or two weeks, unless they are transplanted to suitable fresh media. On the latter they may be carried through many generations without losing their virulence. When dried they die very quickly, but may live for some hours on linen (towels) or the skin, and for twenty-four hours in warm water. They are very susceptible to temperatures above 42° to 43° C. and show very little resistance to antiseptics, par- ticularly the silver salts. The gonococcus secretes no soluble toxin, but contains an endotoxin or toxic "protein^' which causes local and general symptoms in both man and animals. Dead cultures produce an inflamma- and Resistance. Toxicity and Virulence. Susceptible Tissues. 380 l\ri:CTf<)\ A\l> IMMIXITY. tor}' exudate in the peritoneal cavity of guinea- pigs and mice, resulting in death if the dose is sufficiently large, and when injected into the urethra of man a temporary inflammation results. An actual infection of any sort can not be pro- duced in animals; the cocci are killed without be- ing permitted to proliferate. The endotoxin (gon- otoxin) is fairly resistant to heat, being destroyed only after prolonged exposure to a temperature of 100° C. In man the mucous membranes and endothelial .surfaces are more susceptible to infection than other tissues. The urethra of male and female at all ages, the conjunctiva in the new-born, the vagina, nterus and tubes are probably the most susceptible. Less susceptible are the vagina in older women, especially those who have borne chil- dren; the bladder, and in adults the conjunctiva. It is remarkable that there are so few cases of gonorrlieal ophthalmia in adults, considering the opportunities for infection. Infection of the mouth, nose and tear sacs is extremely rare. Ex- tension from the urethra to adjacent structures takes place either by way of the surfaces, as in involvement of the prostate, epididymis, glands of Bartholin, uterus, tubes, ovaries, peritoneum, blad- der and kidneys, or by way of the lymphatics as in infections of the periurethral tissue or cellular tis- sue of the pelvis. Usually infections of the bladder and kidney, and not infrequently of the prostate. Fallopian tubes and j^elvic tissue are of a mixed character (staphylococcus, streptococcus), but not necessarily so. Arthritis, tendovaginitis, endocar- ditis, which usually is vegetative but may be ulcer- ative, are the more common metastatic complica- (joxoaoccuH. 387 tions. Less frequent are pericarditis, pleuritis, subcutaneous abscesses and iritis. As to whether the cutaneous phenomena sometimes seen are due to metastases or are of purely toxic origin seems to be undetermined. The blood stream may be in- fected by way of the lymphatics or local blood vessels (gonorrheal thrombosis). The influence of the enormous phagocytosis of the cocci on the course of gonorrhea is unknown. Since the ingested cocci usually have a typical form and stain well, it would seem that they resist the action of the leucocytic ferments. Likewise the nuclei of the leucocytes usually stain well, hence there is no evidence of a marked toxicity of the cocci for these cells. The mechanical im- prisonment of the organisms by the leucocytes may be of influence in localizing the infection. During the course of gonorrhea "there takes urethral place a pronounced metaplasia of the epithelium in which the cylindrical cells are changed into a more cuboidal and even pavement form." Follow- ing this change the gonococci are limited to the surface of the altered epithelium and penetrate more deeply only in the vicinity of the glands and crypts. "Eventually the gonorrheal process is limited to such isolated points and the gonorrhea thereby enters into a chronic stage" (observations of Finger, cited by Neisser and Scholtz). The conditions which cause the subsidence of chronic acute gonorrhea and allow it to persist as a chronic infection have been the subject of much specula- tion, unproductive for the most part. It is not due to a decrease in the virulence of the cocci since their original infectiousness is retained for others : nor does the local resistance of the mucous 388 IM'KCTIOX A.\n IM.MUXITY. Immunity. uiouibraue reach a high point, since reinfection, or better "'superinfection" is possible at any time. A man suffering from clironic gonorrhea and liaving infected his M'ife, may again be infected by his wife when the gonorrhea of the latter has become subacute or chronic. It has been suggested that the condition in chronic gonorrhea may be one of "mutual habituation between the mucous membrane and the gonococcus," i. e., a habituation between this particular mucous membrane and this particular gonococcus. Because of prolonged existence under unvarying conditions, the growth energy of the organism may have become less, whereas, if it is placed in a slightly different me- dium (transference to another individual), its growth energy (ability to proliferate), becomes augmented, and reinfection of the original host Avith the same strain becomes possible. It has often been noted that subsequent attacks run a milder course than the primary infection, but susceptibility is always present. Mendez, Calvino, and also de Christmas have immunized with the coccus or toxic substances prepared from it. By growing the organism in serum bouillon de Christmas prepared a toxin, the toxicity of which was tested by intracerebral injections in the guinea-pig. Immunization of the guinea-pig resulted in a serum with antitoxic properties. Corroborative work has not been pub- lished. VI. EPIDEMIC CEREBROSPINAL MENINGITIS. ^Cau^^na -^cute inflammation of the meninges may be Meningitis, caused by a number of micro-organisms: Micro- coccus meningitidis, also called the Diplococcus MENINOOCOCGUS. 389 intracellular is meningitidis, or briefl_y the men- ingococcus; Diplococcus pneumonia;; Streptococ- cus pyogenes; Staphylococcus pyogenes; Bacillus influenza; Bacillus pneumoniw ; Bacillus iypli,o- sus; Bacillus coli communis; Bacillus mallei; Ba- cillus pestis. The first two of this number, the meningococcus and the pneumococcus, in addition to causing sporadic cases, also produce more or less extensive epidemics of so-called primary men- ingitis. That the pneumococcus may also cause meningitis secondary to pneumococcus infections in other parts of the body has been mentioned. Also the meningitis caused by the other pyogenic cocci usually is secondary to some other suppura- tive focus, often the middle ear; that caused by the organisms of typhoid, glanders, plague and influenza occurs during the course of the diseases •caused by the corresponding micro-organisms. Previous to 1887 diplococci resembling the pneu- Micrococcus „^ -, -, . Meningitidis. mococcus had been found m the exudate m cases of cerebrospinal meningitis by Foa and Bordoni- Uffreduzzi, by Fraenkel and others. Weichsel- baum made similar observations during the same y^ear, and in addition described six cases in which a diplococcus of another nature was present in pure cultures. To the latter he gave the name of Diplococcus intracellularis meningitidis. Exten- sive observations by others, both in Europe and America (Councilman, Mallory and Wright, and others), revealed the presence of the last-named organism in many instances, and showed that it is the most common cause of epidemic cerebrospinal meningitis. The meningococcus resembles the gonococcus closely in that it is usually found in biscuit-shaped 390 LM'KrTlOX A\D IMMIMTY. Resistance. Virulence; Endotoxin. Infection Atria, pairs, nearly always witliin pus cells, and does not stain by Gram's method (Weichsclbaum). It is properly to be called a micrococcus since it divides in two transverse directions (Albrccht and Gohn) ; tetrads, small groups and short chains are some- times seen. However, it forms no striking chains, is non-motile and produces no spores. Growth m«i.y be obtained on some of the ordinary media (glycerin agar), in which the organism differs from the gonococcus, but a medium which contains blood or serum is much more favorable. It is an obligate aerobe, grows best at the body tempera- ture and virulence is soon lost under artificial conditions. It produces a membrane on meat broth with clouding of the medium. Viability is retained only for a few days at room temperature. When dried on paper and exposed to the sunlight it lives no longer than twenty-four hours, in a dark room seventy-two hours (Councilman. ]\ralIory and Wright). It is killed by a temperature of 65° C. for thirty minutes (Albrecht and Gohn). The meningococcus has little virulence for ani- mals. When injected in sufficient quantity into the peritoneal or pleural cavity of white mice death results in from twenty-four to forty-eight hours, but not when given subcutaneously. Men- ingitis may be produced by subdural injections, but the disease does not resemble the epidemic meningitis of man. So far as is known at the present time the organism does not produce a soluble toxin, but possesses rather an endotoxin. Although the disease is usually spoken of as a primary meningitis, there is reason to believe that it is secondary to an acute rhinitis or acute in- MENINGOCOCCUS. 391 flammation of the accessory sinuses or middle ear, in many instances. From these places the coccus may readily reach the meninges by way of the lymphatic channels. It has been found repeatedly in the noses of those who were associated with cases of the disease; in such cases an acute rhi- nitis may be present without the subsequent de- velopment of meningitis. Clinical histories show that the infection commonly is preceded by acute rhinitis. The inflammation in the meninges is always cerebrospinal in its distribution and is characterized by a purulent or fibrino-purulent exudate in which the diplococci are present in varying quantities. Diagnosis may often be estab- lished clinically by the microscopic or cultural examination of the cerebrospinal fluid which is removed by lumbar puncture. Acute encephalitis, acute bronchitis, lobar pneu- complications monia and acute arthritis have been observed as f„"fertions, complications, in which organisms resembling the meningococcus' have been found in a number of instances. An accompanying bronchitis, lobar or lobular pneumonia may be caused by mixed infec- tion with other organisms (pneumococcus, strepto- coccus, staphylococcus). Since it would be diffi- cult to explain some of these complications except on the basis of metastasis, it seems very probable that the organism reaches the blood stream. Micro- cocci resembling the meningococcus have been found in acute bronchitis, rhinitis, lobular pneu- monia and conjunctivitis, in the absence of cere- bral involvement, and it is possible that it may be the cause of independent inflammations in these tissues. Weichselbaum, however, is inclined to doubt the identity' of such organisms with the 392 IXFECTIOX AND IMMUXITY. Transmission and Contag- iousness. Susceptibility and Immunity. meningococcus. Particular!}' in cases of bronchi- tis and lobular pneumonia the coccus may be con- fused with the Micrococcus catarrhalis of Pfeitl'er, with which it is identical morphologically. The extent to "vvliich the meningococcus is a normal iuhal)itant of the nasal mucous membrane is unknown. Since the organism seems to be excreted chiefly or only with the nasal discharges, the latter prob- ably are important for transmission of the infec- tion. Because of the low resistance of the organ- ism to desiccation and light, transmission prob- ably is a fairly direct one. This is suggested also by the occasional occurrence of epidemics in insti- tutions. Contagiousness is of a rather low order ; this is indicated by the distribution of the 111 cases observed by Councilman, j\[allory and Wright in Boston^ the city being somewhat dif- fusely infected with very little tendency of the dis- ease to occur in groups of individuals or in several members of a family. The desirability of avoiding contact with the infected is evident; special prophylactic meas- ures are not known. In the presence of an epi- demic the treatment of rhinitis with local antisep- tics would suggest itself. Children and young people are particularly su^;- ccptible to both epidemic and sporadic infections Avitli the meningococcus. Exposure incident to the cold and variable weather of the winter and spring, in which seasons the disease prevails, may be in- fluential in lowering resistance. Second attacks are rare. Councilman, Mallory and Wright col- lecting only five such examples from the literature. Lipierre immunized animals with cultures and m FLU EN Z A. 393 with a toxin, the hitter being a glycerin extract of old cultures. Their resistance to infection was said to be increased, and the serum of highly im- munized animals was antitoxic, preventive and curative for other animals. Corroborative work is lacking. According to Davisj the serum in cases of epidemic meningitis shows an increased bactericidal power for the coccus on the thirteenth day of the disease; the agglutinins which develop probably persist for some time, but are little above the normal after two and one-half years.^ Fairly strong agglutinins may be obtained by the im- munization of rabbits (Jager and Albrecht and Gohn). VII. INFLUENZA. Influenza occurs sporadically and in epidemics of greater or less proportions. Its extreme con- tagiousness is shown by the striking rapidity with which it spread over the whole civilized world in the epidemic of 1889 and 1890, leaving behind it 1. The conclusions of Dr. Davis are as follows : In five leases of epidemic cerebrospinal meningitis, the meniugococcus (Weichselbaum type), was obtained in every case from the cerebrospinal fluid, and in one case from the nose and sputum by cultures. In the other four cases Gram-negative diplococci suggestive of either meningococcus or Micrococcus catarrhalis were seen in smears, but were not recovered in cultures. Agglutination of meningococcus by the serum of patients with meningitis occurs in a dilution of 1-5 or higher. The meningococcus grows in some deflbrinated normal bloods, but not in others, there being thus an interesting individual variation. In the blood of three meningitis cases it did not grow. Normal human serum is distinctly bactericidal toward the meningococcus. This property is increased in sera of meningitis cases, and is diminished, but not entirely de- stroyed by heating to 60 C. for thirty minutes. Cerebro- spinal fluid acts in much the same way as heated serum. The opsonin content of the blood does not appear to be altered during the course of' epidemic meningitis. Normal cerebrospinal fluid does not contain opsonin for meningococci. — Jour, of Infectious Diseases, 1905, vol. ii. 394 IXFECTIOy AND IMMUNITY. Bacillus Influenz*. Symbiosis. Pseudo- Influenza Bacilli. a trail oi: lesser epidemics which have prevailed up to tlie present time. During the epidemic just cited a number of or- ganisms were erroneously described as the cause of the disease. In 1892, however, Pfeiffer discovered a minute bacillus which he found constantly and in large numbers in the sputum of influenza pa- tients only. Tlic observations of Pfeiffer have been confirmed by a large number of investigators, and the organism, Bacillus influenza', is now ac- cepted as the cause of the disease. It is one of the smallest of bacteria (0.2 or 0.3 by 0.5 microns), is non-motile and forms no spores. A medium con- taining blood or hemoglobin is essential for its artificial cultivation, and even under the best con- ditions it grows meagerly and slowly. A number of bloods, but particularly those of man and the dove, favor its growth. It is a strong aerobe. The organism is best stained by a dilute solution of carbol fuchsin (1 to 10), and, like the plague bacillus, exhibits polar staining, i. e., the ends stain more deeply than the central portion. ^\lien the staphylococcus and some other organ- isms are grown in mixed culture with the influ- enza bacillus, the latter is stimulated to a more vigorous growth. According to Jacobsohn, killed cultures of the streptococcus greatly increase the virulence of the influenza bacillus when the mix- ture is injected into animals. Pfeiffer designates as pseudoinfluenza bacilli a number of influenza-like organisms w^hich have been found in man and animals. They have the morphology of the influenza bacillus, are a little larger, and also prefer a medium which contains hemoglobin, but since some of them occur in ani- INFLUENZA. 395 mals which are known not to be susceptible to in- fluenza, it is concluded that they can not be identi- cal with the influenza bacillus. The influenza-like bacillus which Jochmann and Krause consider as the cause of whooping-cough, may be mentioned in this connection. The resistance of the bacillus to desiccation, Resistance ane Virulence. sunlight and unfavorable temperatures is very low. It dies in from twenty-four to thirty-six hours at room temperature, when contained in sputum, and lives for about thirty-two hours in hydrant water (Pfeifler). It is not highly virulent for experi- ment animals, although a condition said to resem- ble influenza has been produced in monkeys b}' placing pure cultures on the nasal mucous mem- brane. Fatal infections may be produced by intra- venous inoculation of the bacillus into monkeys and rabbits, and killed cultures produce a fatal intoxication in rabbits. Virulent cultures in suffi- cient quantity produce fatal peritonitis in guinea- pigs. Since the bacilli seem" not to proliferate when fatal quantities are injected intravenously into rabbits, and since fatal intoxication, without the occurrence of bacteriemia, may take place when a tracheal infection is induced in the ape (Pfeiffer), it is concluded that the toxic phenom- ena of influenza are due to the absorption of bac- terial toxins from the mucous surfaces. A soluble toxin has not been obtained in culture media. The organism is a facultative pus producer. So far as is known the influenza bacillus is ex- Distribution creted only with the secretions of infected surfaces, i. e., from the upper respiratory passages, con- junctiva, ear, etc. The belief, commonly held, that the influenza bacillus does not enter the cir- 396 I M' EC T I OX AND IMMIWITY. culation probably is erroneous. That metastatic * infection is possible, by way of the lymph or blood channels, is shown by the occurrence of influenza meningitis, and, rarely, of influenza peritonitis (Hill and Fisch). According to Jehle, the influ- enza bacillus invades the blood very frequently in some of the acute exanthemata. It was found in the blood in 22 out of 48 cases of scarlet fever, in 15 of 23 cases of measles, and in 5 of 9 cases of varicella (cited by Hektoen). Hence, these dis- eases would seem to create conditions favorable for invasion by this bacillus. When the bacilli reach the blood they probably are killed quickly. It is probable that the ordinary nervous phenomena of the disease are due to intoxication rather than to actual infection of the nervous structures. As to whether the symptoms of so-called intestinal in- fluenza are due to an invasion of the intestines by the bacilli or to a specialized action of circu- lating toxin seems not to have been definitely set- tled. There certainly is abundant opportunity for infection of the intestines in cases of bronchial influenza. In the bronchitis of influenza the or- ganisms are found in large numbers in the smaller Ijronchial tubes, both free and within leucocytes, hence, in searching for the bacilli clinically it should be certain that the sputum examined repre- sents the bronchial exudate. In influenza pneu- monia, which usually is of the lobular type, the bacilli, mixed with pus cells and contained in them, are found in large numbers in the alveoli. Pure cultures of the bacillus have been obtained from cases of .conjunctivitis, and they occur not infrequently in middle-ear complications which develop during tlic course of the disease. Influ- Infections. INFLUENZA. 397 cnza conjunctivitis sometimes occurs in epidemic form, particularly in institutions and schools. Pneumonic foci which develop during influenza Mi^ed frequently show the pneumococcus, and sometimes the streptococcus or the bacillus of Friedlander in addition to the influenza bacillus, and similar mixed infections occur in pleurisy and in middle- ear disease. Influenza may be superimposed on other infections; individuals suffering from pul- monary tuberculosis are particularly susceptible to influenza, and in them the prognosis is unfavor- able. The disease is transmitted directly from man to Transmis- n 1 • n • • 11 p • siofit Infec- man and, chieny, it is supposed, by means of m- tion Atria fected droplets of sputum which are expelled in yiaxis. coughing and sneezing. Obviously kissing affords opportunity for infection. Infection by indirect contact is of less importance because of the rapid death of the bacillus after it leaves the body, but living germs may well be disseminated by soiled handkerchiefs or other contaminated linen. Dust infection possibly is of minor consequence. Chronic influenza in which the bacilli may persist in the bronchi for weeks, and cause recurrent acute at- tacks, is of importance for the maintenance of an epidemic. In tuberculous cavities the bacilli may flourish for long periods. Primary infection takes place in the upper res- piratory passages, and the disease extends readily from one surface to another, as from the nose to the pulmonary tissue. Infection of the ear usually is a complication of pharyngeal or pulmonary in- fection. Occasionally an influenza conjunctivitis is found without other localization. "Primarj** infection of other organs, as the brain and perito- 398 i\ri:cri(i\ \\i> immcmty. neuni, are inetastalic-, altlioiiuli tlic urigiiuil focus or atrium may not be observed. Little or nothing can be done in the way of general prophylaxis. Washing of the nose and mouth with antiseptics during an epidemic may reasonably lu' prartii-od. luii wiili wliai success is uncertain. The aged and those of low vitality should avoid exposure to infection^, for in them the severer complications^ such as pneumonia, are more likely to occur. When influenza conjuncti- vitis appears epidemically in schools, the latter should be closed or the infected children excluded. Immunity, Sus- Although little or nothing is known concerning ceptibilitv and » . t ■ 4. • Recurrences, the possibility of a natural immunity m man, ex- perience teaches that he is, on the whole, very sus- ceptible. The belief expressed b}^ some that nurs- ing children are less susceptible tlian older people seems to have some foundation, although it is well Ivnown that they are not entirely immune. Influ- enza is sometimes cited as an infection in which one attack creates a predisposition for a second, but the truth of this is doubted by many who have had extensive experience with the disease. Wutz- dorff, in a study of the epidemic which prevailed in Germany during 1891-92, finds in the small number of cases, the irregularity of their distribu- tion, and comparative exemption of rather large districts, reasons for believing that one attack con- fers a degree of acquired immunity ; that is to say, the population had been so thoroughly infected (durchgeseucht) during the preceding year or two that comparatively few remained who were sus- ceptible, although the disease itself appeared to be more malignant than in the previous year (cited from Beck). However, the occurrence of second CHANCROID. 399 Properties. attacks shortly after the first, and of repeated in- fections in some individuals indicate that acquired immunity is of short duration. The aged, those of low vitality, and those with pulmonary tuber- culosis, have low resistance to infection. Although Delius and Kolle Avere able to produce seru a slight increase in the resistance of guinea-pigs by the intraperitoneal injection of cultures, noth- ing like a well-marked immunity was obtained; nor did the serum of immune animals or convales- cent man show increased protective power for other animals. Slatineano, however, obtained serum of some protective value for guinea-pigs, by the immunization of rabbits and guinea-pigs, but it had no curative effect. The results of Can- tani were similar, and both observers noted the de- velopment of bactericidal power, as determined by the Pfeiffer reaction, and of agglutinins. At the present time there seems little to hope from vac- cination. There is said to be some increase in agglutinins in man as a consequence of infection. The agglu- tinating power of the serum of an immunized ani- mal may be as high as 1 to 500 (Cantani). VIII. SOFT CHANCRE. The independence of soft chancre and syphilis, and the infectiousness of the former by inoculation with the purulent secretions of the ulcers, were established long ago. Rollet found that filtered" pus lost its infectiousness. A large number of observers had found bacteria Bacillus of one kind or another in the pus and in stained o^oucrey. sections of the walls of the ulcers, and probably some of them (e. g., Unna), had seen the bacillus 400 lyFECTIOX AXD IMMVXITY. wliich Ducrcv described (188i)) and later culti- vated, ami which is now proved to be the cause of tlie disease. The bacillus is very small (0.4x1.5 microns), is non-motile and shows polar staining. It resembles tlie plague bacillus in form, but is somewhat smaller, and does not show the exten- sive involution forms of the latter. In the ulcer it lies singly, in small groups, or more characteris- tically in the form of bands, made up of two or more parallel chains, which infiltrate the wall of the ulcer. Large numbers are often found in the pohTnorphonuclear leucocytes of the pus, par- ticularly at an early stage of the lesion (Kroeft- ing). Great difficulty was encountered in culti- vating the bacillus, and Ducrey's first success was obtained with a medium w^hich contained human skin. It has since been cultivated on agar which contains the blood or serum of man, rabbit or dog. Himmel attempted to cultivate it in the fresh defibrinated blood of the guinea-pig, but was unsuccessful because the bacilli were phago- cytized by the leucocytes (Babes). An. ulcer resembling that of soft chancre may be produced in the ape, and also in the cat, by the inoculation of pure cultures. Didey reinoculated man, successfully, from the ulcers of the cat. When living cultures are injected into the guinea- pig (peritoneal cavity, subcutaneous tissue, dura mater), the bacilli are quickly taken up by leuco- cytes and digested (Himmel). Himmel reports having so decreased the resistance of guinea-pigs by peritoneal injections of lactic acid that they became susceptible to infection. After two or three passages the culture became so virulent that CAP8ULATED BACILLI. 401 fatal bacteriemia was caused without previously lowering the resistance of the animals. In man the infection is transmitted to the in- guinal lymph glands, but never becomes general. One attack in man does not confer lasting im- munity. SiDontaneous recovery occurs, but its cause is not known. Inasmuch as the bacilli are found within leucocytes, phagocytosis may be a factor in recovery. The readiness with which the autoinoculation of adjacent skin takes place, even after the disease has existed for some time, sug- gests that general immunity is not established. IX. BACILLUS OF FKIEDLANDER AND OTPIER MEM- BEES OF THE CAPSULE-FORMING GROUP. The bacillus of Friedlander, or Bacillus pneu- capsuiated moniwj, is the type of a rather large group of bac- ^^"^'"'• teria, called the Friedlander group, or the group of Bacillus mucosus capsulatus. In addition to the ability to produce a mucus-like capsule or en- velop, they have in general the following charac- teristics (Abel) : short, plump rods, varying in their proportions, having no motion, no flagella, no spore formation, and not staining by Gram's method. They form mucus-like masses in cul- tures, do not liquefy gelatin and are facultative anaerobes. They are widely distributed in nature, vary from innocuousness to extreme pathogenicity for animals, are rarely found in the mouth, nose and bronchi normally (bacillus of Friedlander), one type being a normal inhabitant of the intes- tines, especially in children (B. laciis aerogenes). Perkins has been able to classify the members of this group on the basis of their fermenting powers for lactose and saccharose. He found their viru- 402 INFECTION AND IMMUNITY. Pneumonia Caused by Friedlander's Bacillus. Rhinoscleroma and Ozena. lence for anilnal!^, iniiiuinizatidii and agglutination tests, too variable to serve as bases for classifica- tion. In man three members of the group — they may be the same organism or variations of a type — are of interest from the standpoint of infection : Bacillus of Friedlander, the bacillus of rhinoscle- roma and the ozena baeilhis. In 129 cases of acute inflammation of the lungs, Weichselbaum found the bacillus of pneumonia nine times, twice with streptococci and once with the diplococcus of pneumonia. The organism causes lobular pneumonia more frequently than lobar. The homogeneous non-granular surface, and the large amount of fluid of a viscid or mu- cous consistence, are characteristic anatomic feat- ures. The alveoli contain massive numbers of the bacilli. The bacillus of Friedlander is found also as the cause of pyelitis, cystitis, pyelonephritis, serous or purulent pericarditis, pleuritis and meningitis, which may be accompanied by brain abscesses. Meningitis when produced by this or- ganism usually or always is secondary to infection in other parts of the hody by the same organism (middle ear and accessory sinuses of the nose). An organism of the Friedlander type is found with few exceptions in the tissues in rhinoscle- roma, and by many is considered as the cause of the condition. A similar organism is found con- stantly in the secretions and crusts in ozena. Antiserums of distinct power have not been ob- tained for members of the group. Prolonged im- munization with pome strains yields an agglutinat- ing serum of low value. The agglutination re- action is of no value for identification of the dif- ferent members of the group, nor for clinical diagnosis. RELAPSING FEVER. 403 X. RELAPSING FEVER. ■ In 1868 Obermeier discovered in the blood of The Parasite. patients suffering from relapsing fever, "very fine threads exhibiting motility'^ ; these "threads" have since been known as the Spiroclieta ohermeieri.* and are recognized as the cause of the disease. They are very thin (about 1 micron), from 10 to 40 microns in length, and of spiral form. Three types of motion are described : a screw-like, a for- ward and backward movement and a lateral bend- ing. They are found only in the blood and blood- forming organs. They disappear from the blood with remarkable rapidity at the time of crisis, al- though they may be found in the spleen one or two days later. The organism has not been grown artificially, but it may be kept alive for a number of days in the blood or serum of patients. As the micro-or- ganisms die agglomerations are formed and they undergo granular changes. The organism is not found in Nature, and. Transmission since it occurs only in the blood of the sick, it has long been assumed that infection can be accom- plished only by the inoculation of infected blood. * This organism is sometimes called a spirillum, incor- rectly. The spirillaceoe, Migula's third family under the Order of Eubacteria, comprises organisms with these char- acteristics : "Cells which are twisted screw-fashion or repre- sent a segment of a spiral. Division takes place only in one direction of space after the cell has elongated." The dif- ference between spirillum and spirochseta is shown by the following : "3. Genus : Spirillum. Cells rigid, with polar tufts, for the most part bent in the form of a half-circle, as organs of locomotion. 4. Genus : Spirochseta. Cells with snake-like bending, organs of locomotion unknown." Although Migula classes this organism with the bacteria, there is some ground for considering it protozoon in nature. 404 IXl'ECTIOy SyO IMMUNITY. The parasites have been demonstrated repeatedly in bedbugs wliieh are found on the mattresses of the sickbed, and monkeys liave been infected by inocuhiting them with the blood found in the bodies of these insects, and by the bites of the lat- ter (Tictin). It is said that they may remain alive in bedbugs for as long as thirty days. It is not altogether excluded that other vermin also transmit the disease. The spirocheta does not appear in any of the ex- cretions, unless they happen to be of a bloody character. Certain monkeys, those belonging to the slender- nosed family (Catarrliince), may be infected by injecting the blood of patients, provided the blood used is taken during the paroxysm, i. e., at a time when the microbes are Imown to be in the blood. ]\Ionkeys do not contract the disease under natural conditions. Other . animals are not susceptible. The incubation period in man usually is from five to seven days, and in monkeys from one and one- half to four days. Cloudy swelling of the paren- chymatous organs, ecchymoses and infarcts of the sjileen and kidneys are found in fatal cases. Prophylaxis consists in isolation of the patient, cleanliness, and the destruction of vermin, espe- cially bedbugs. Eelapsing fever occurs in various races of man, and so far as Imown none are immune. Osier states that in the United States the disease has not been seen since 1869, when it was epidemic in ISTew York and Philadelphia. The natural immunity of other animals is referred either to phagocytosis or to normal bacteriolysins, but the conditions probably are not thoroughly understood. RELAPSING FEVEIt. 405 As stated above, a remarkable feature in the Phaciotytosis course of the disease is the rapidity with which the lysins. micro-organisms disappear from the blood at the time of the crisis. MetchnikofE refers this to phagocytosis by the microphages, which undergo a progressive increase during the paroxysm and decrease after the crisis. Very little phagocytosis appears to take place in the circulating blood, but in the spleen many spirochetse are found within polymorphoneuclear leucocytes. Tictin also found them in the parenchymatous cells of the kidney, liver and lungs. Phagocytosis is most marked at or near the time of the crisis. According to Metchni- koff, relapse or reinfection is accomplished ^by spirochet^e Avhich again invade the body from the spleen. Eussian observers have studied the development of a specific bactericidal power in the serum of the sick and in animals which were immunized by the injection of infected blood from man. Inasmuch as the organism can not be cultivated, bactericidal tests must be performed with the organisms as they occur in the blood or serum of the patients, and Gabritschewsky has devised a technic for this procedure. A drop of serum from an immune animal or a Technic. convalescent patient is mixed on a slide with a drop of serum which contains the spirocheta, the latter serum being taken from a patient during an attack. The preparation is sealed under a cover- glass and examined at intervals, and the death of the organisms is determined by their loss of mo- tility. It is said that the bactericidal power of human blood following infection, and that of im- munized animals, is increased. 40G IM'KCTWX A'SD IMMUNITY. Active In view of the facts that three or more relapses sive Immunity, may occur and that reinfection is possible at a later period, it seems probable that man does not readily acquire immunity to the infection, al- though second and third relapses are said to be lighter than the first. Monkeys which have been artilicially infected several times acquire some resistance to the disease. The view of Metch- nikoff that the spleen is essentially involved in recovery and immunity seems to have been dis- proved l)y the experiments of Tictin, who found that splenectomy had no influence on recovery or the development of immunity. The serum of convalescents affords a certain de- gree of protection to the monkey ( Gabritschew- sky) . Loventhal utilized the serum of immunized horses in the treatment of the disease in man, and reported a decrease in the number and severity of relapses. The action of the serum has been re- ferred both to its content in bactericidal antibodies, and to its ability to stimulate phagocytosis. Melkich states that agglutinins are formed and that they appear on from tlie third to the fifth day of the disease. A rapidly fatal disease of geese, spirocheta septi- cemia, or spirillosis of geese, is caused by an or- ganism which resembles the spirocheta of OIkt- meier, and a similar infection has been noted in chickens in Brazil and in cattle in the Transvaal. GEOUP IV. Infectious diseases which usually are chronic, but may run acute courses. They are characterized by marked local tissue changes, which exert a lim- iting influence on the processes, and include the infectious granulomata, excepting syphilis. Infec- tion produces little or no immunity. In some in- stances the prolonged immunization of animals in- duces increased resistance to infection (tuberculo- sis) ; in other instances this has not been deter- mined, or is difficult of determination because of the non-susceptibility of experiment animals to the corresponding infections. The serums of im- munized animals, in so far as this subject has been investigated, show little or no protective or cura- tive power. I. TUBEKCULOSIS. Klemke, in 1843, but more particularly Ville- min, in 1865, demonstrated the infectiousness of tuberculosis by animal experiments, and these re- sults were substantiated later by such investigators as Klebs, Chauveau, Baumgarten and Conheim. Baumgarten first saw the tubercle bacillus in sec- tions of tuberculous material from which the tis- sue cells had been dissolved by potassium hydroxid, and at almost the same, time Koch succeeded in demonstrating its presence in all tuberculous lesions by a special staining method. He eventu- ally obtained the organism in pure cultures with which he again produced tiiberculosis in experi- ment animals. The tubercle bacillus is an obligate aerobic para- site, has the form of a slender, non-flagellated rod. 408 IXFECTIOy AMJ IMMUMTY. Characteristics of the Bacillus. Staining Properties. often sliglitly curved, from 2 to 4 microns long and from 0.3 to 0.5 microns broad. In stained and even in unstained specimens, when properly treated, a number of spherical, oval or elongated clear spaces can be seen which Koch at one time thought to be spores. They are now considered cither as vacuoles, or as representing some form of degeneration or reserve nutritious material. Spore formation is uncertain. The organism is sup- posed to possess a membrane which may be re- sponsible for its strong resistance against heat and desiccation. Feinberg speaks of a nucleus ( ?) which may be demonstrated by a modified Romanowsky stain. The organism shows many variations in its morphology under different conditions. It often exists in isolated clumps, either in cultures or in tissues, and may be excreted as such in the urine. In certain cultures and sometimes in animal tis- sues it grows in the form of longer or shorter branching threads, in this respect resembling acti- nomyces. This last occurrence has led a number of authorities to class the tubercle bacillus as a streptothrix, while others would give it an inter- mediate position between true l)acteria (schizomy- cetes) and the streptothrix (a hyphomyces). Oval or spherical degeneration forms, the capsules or corpuscles of Schron, are found in advanced tuber- culosis of the lymph glands and other organs in which there is a great deal of necrosi?. The tubercle bacillus is one of a group of organ- isms Avhich are said to be "acid fast" in their staining properties. When stained with the carbol fuchsin of Ziehl and subjected to the action of mineral acids in dilute solutions the fuchsin is not removed.. After counterstaining with methylene TUBEJWULOHfS. 409 blue, the tubercle bacilli appear red, whereas other organisms, not "acid fast," are stained with the methylene blue. It is not diflicult to recognize the bacilli in sections of tissue when the proper technic is used, although the search is at times a laborious one. In old processes the organism often can not be recognized, and recourse to animal inoculation may be necessary in order to demonstrate the ex- istence of tuberculosis. It is ordinarily a difficult task to obtain the Cultivation. tubercle bacillus in pure culture, the technic of which we need not consider. Even under the best conditions growth is very slow, and may not be recognizable to the naked eye for from six to ten days. Coagulated serum of the cow to which has been added from 2 to 4 per cent, glycerin is the most favorable culture medium. Good growth oc- curs also in glycerin agar, in glycerin bouillon and on potatoes. The optimum temperature is 37° C; growth does not occur above 42° C. nor below 30° C. When a small amount of culture is planted on the surface of glycerin bouillon it proliferates slowly to form a heavy membrane. In time this growth sinks from its own weight and a new mem- brane forms. This process continues until large masses have accumulated at the bottom of the flask. In its resistance to desiccation the tubercle ba- Resistance. cillus is exceeded only by spore-forming organisms ; it lives approximately for three months in dried sputum which appears to form a protective coat- ing about it. Direct sunlight destroys it in a few hours at the most, whereas diffuse light kills it only after from five to seven days (Koch). It is said that the guinea-pig when exposed to sunlight 410 lyFKCTIOX AXD IMMUXITY. ■ witlistaiuls luborculosis for a longer time than one which is kept in tlie dark. Eoeutgen rays are bac- tericidal for tlie organism, killing it in about one hour (Rieder). Under moist heat a temperature of 55° C. kills it in from four to six hours, 60° C. in one hour, 70° C. in from ten to twenty minutes, 80° C. in five minutes, from 90° to 95° C. in from one to two minutes. When embedded in sputum it is more resistant, five minutes being required to kill it at the boiling temperature. Corrosive sub- limate is not a good disinfectant in this case, inas- much as it produces an albuminous precipitate around the organism which prevents penetration of the sublimate. Five per cent, carbolic acid added to equal parts of sputum kills the bacillus in twenty-four hours. Formalin vapor is a good dis- infectant for dr}', but not for moist sputum. Iodo- form is not a good disinfectant, in spite of its bene- ficial influence on the infectious process. The re- sistance of the bacillus to gastric digestion lias an important bearing on the occurrence of infection in the intestinal tract. The gastric juice of the dog, in one instance, failed to kill the bacillus after six hours' exposure, although it had the power of prohibiting proliferation. Virulence. The bacillus of liuman tuberculosis, although fairl}' constant in its virulence, may be attenuated by various means. Its prolonged existence in putrid sputum decreases its virulence and a similar de- crease occurs on potato, in old cultures or in those w^hicli contain iodoform, boracic acid and some other substances. Inoculation with such cultures produces a chronic form of tuberculosis in animals which may heal. In other instances cultures which have grown on artificial media for many years re- tained their original virulence. TUBERCULOmB. 411 The organism contains about 90 per cent, of water. One-fourth of a dried bacterial mass may be extracted as a wax-like or fat-like substance by a mixture of alcohol and ether. The acid-fast staining property of the bacillus depends on this substance. The remaining portion of the mass, consisting largely of proteins, which may be ex- trated by dilute alkalies, contains a toxic nucleo- albumin. Cellulose, representing a portion of the capsular substance, is also found in the residue. Killed cultures when given subcutaneouslv pro- Toxic , . , ° . . 1 Products. duce necrosis, abscesses, caseation, marasmus, ana a subnormal temperature. Wlien given to rabbits and guinea-j^igs intravenously they cause rapid emaciation and death in from a few days to a few weeks. By beginning with very minute doses, how- ever, the animals may be gradually habituated to intoxication by the dead bacilli and eventually withstand large doses. The same holds true of the various toxic substances, including tuberculin, which may be extracted from cultures. The pro- teins and alkaline extracts cause abscesses when given subcutaneously. The fever -producing sub- stance which is present in the preparations men- tioned below is one of the metabolic products of the bacillus, rather than a constituent of the bac- terial cell (Koch). This substance is 100 times as toxic for tuberculous animals as for healthy and causes an increase in the eosinophiles of the blood. • In addition to the fever-producing substance, Maragliano and others recognize as a constituent of the bacillus a heat susceptible "toxalbumin'^ (destroyed at 100° C.) which reduces temperature. Hammerschlag speaks of a toxin which in animals causes fatal convulsions. The toxic products of the 412 IXrECTIOX A\D TMMTXITY. - tubercle bacillus show their greatest toxicity when injected into tlie brain, and this method of injec- tion has been suggested for the standardization of tuberculin. lubercuiin. Of the toxic preparations of the bacillus the greatest interest attaches to tuberculin which Koch, in 1891, announced as an agent which could be used for the specific diagnosis of tuberculosis and which, when properly administered, had cer- tain curative effects. Its ^preparation is simple. Cultures are allowed to grow for four weeks in peptone bouillon which coiitains 5 per cent, of glycerin. At the end of this time the organisms are killed by exposure to a temperature of 100° C. for one hour (Marx). The fluid is reduced to one- tenth its original volume by evaporation under a vacuum at a low temperature and the bacterial cells are eventually removed by filtration. The percentage of glycerin which is present in the final preparation acts as a preservative, but 0.5 per cent, carbolic acid may be added in addition. The active substance in tuberculin may be precipitated by 66 per cent, alcohol; its chemical nature re- mains imlvuown.. "ta,"^^"tr;| In addition to the "old tuberculin,"' which has just been described, Koch has made several other preparations having similar properties, the use of ■which has been proposed for diagnostic and cura- *tive purposes and for convenience in carrying out the agglutination reaction. One of these, "TA," is an alkaline preparation which is made by ex- tracting cultures with 1/10 normal sodium hy- droxid solution. Its value as a diagnostic was equal to or exceeded that of tuberculin because of the longer duration of the reaction. In view of TUBERCULOHIH. 413 the fact, however, that it contained undissolved cells, whicli caused the formation of abscesses at the point of injection, its use was not encouraged. For purposes of immunization Koch prepared a fluid which contained all the bacterial constituents and which at the same time is readily absorbed without abscess formation. For its preparation dried masses of the organism are ground up in an agate mortar; after suspension in distilled water and centrifugation, the emulsion consists of two layers. The overlying opalescent whitish fluid was designated as "TO" {Tuberculin-Ohers). After removal of the fluid from the precipitate the lat- ter was again dried and ground, suspended in water and centrifugated as before, and the process .repeated until none of the sediment remained. The different fractions of fluid, except the "TO," were combined to constitute "TE" {Tuberculin-Rest) , which is really an emiilsion of minute fragments of cells. It is readily absorbed and does not cause the formation of abscesses. This is commonly called Koch's "new tuberculin." Still another preparation which Koch has recently devised for active immunization and for convenience in per- forming the agglutination test consists of dried and ground iip bacilli which are suspended in equal parts of glycerin and water, NeutuhercuUn Koch (Bazillenemusion) . Preparations which in many respects are analo- other gous to those of Koch have been made by different investigators; the tuberculocidin of Klebs, the tu- berculins of de Schweinitz and Porset and that of Denys, the two toxins of tuberculins of Maragliano, which he utilizes for the preparation of antitoxic serums, the oxytuberculin of Herschfelder, the 414 INI'IJCTIOX AM> IMMl'MTY. Standard- ization. Dissemination. '"TD" aud the "TDR" of Behring- and the tubercu- loplasmin of Buchner. Marmorek claims to have obtained the true toxin of the tubercle bacillus by iiTowing young, vigorous cultures on a complicated medium, denying that tuberculin represents the true toxin of the organism. Tuberculin can not be standardised with accur- acy. Because of the extraordinary susceptibility of tuberculous animals to tuberculin, Koch decided to estimate its value by the quantity required to kill such animals. From 0.5 to 1 c.c. of tuberculin, when injected into a healthy guinea-pig, causes neither a local nor a general reaction, whereas from 0.1 to 0.15 c.c. kills a tuberculous guinea- pig in from twentj'-four to forty-eight hours. For standardization von Lingelsheim recommends in- tracerebral injection into healthy guinea-pigs, be- cause of the extreme toxicity of tuberculin when introduced into the central nervous system; only 1/180 as much tuberculin was required to cause death by intracerebral injections as compared with subcutaneous or intraperitoneal. Behring bases the value of tuberculin on its toxicity for healthy guinea-pigs and in his terms the expression "1 c.cm. = 1,000 M." means that one gram of the toxin is fatal to 1,000 grams of guinea-pig tissue. His "TD" has a value of 1,250 M., and ''TDR," 12,500 M. The tubercle bacillus undergoes no proliferation outside the body and its occurrence in nature de- pends on the distribution of the infected excre- tions, particularly the sputum, of man. Hence it is found most abundantly in the rooms and homes of patients and in tuberculous wards of hospitals. Reception of sputum on the handkerchief of the TUBERCTJLOHIH. 415 patient, where it subsequently dries, and its dis- charge on the floor in public places, where it quick- ly becomes pulverized, as in street cars, are condi- tions which favor dissemination and the infection of others. In unconfined. places which are exposed to the action of light and sun, as the streets and sidewalks, the danger is less on account of the shorter life of the organism under these conditions and the greater volume of surrounding air. The calculation of Heller that a tuberculous patient may excrete 7,200,000,000 of bacilli in a day sug- gests the number which may lurk in a single mis- placed portion of sputum. Sputum which is Jcept moist is not a source of particular danger, inas- much as ordinary currents of air do not dissipate it in the form of infected drops. Droplets of spu- tum which are expelled by coughing contribute greatly to the infected dust which surrounds a pr ■ tient. Large quantities of bacilli are often excreted i:i the feces in intestinal tuberculosis and in the urine in genitourinary tuberculosis, or in general miliary tuberculosis with localization of the process in the urinary organs. The pus from tuberculous ab- scesses commonly is infectious. Great interest attaches to the possibility of infec- tion of man by the milk and meat of tuberculous cattle. Previous to 1901, through the work of Smith and others, the opinion had been gaining ground that the bacilli of human and bovine tuber- culosis are not identical. It was not always possi- ble to produce tuberculosis in cattle by feeding them or causing them to inhale tuberculous spu- tum or pure cultures which were highly infectious for other experiment animals, although bacilli of Dried Sputum Bovine and Human Tuberculosis. 41G INFECTION AND IMMUNITY. bovine origin invariably cansod the disease in cattle when administered in a similar manner. It seemed then that the two bacilli are not identical in their pathogenic powers. Koch having performed such experiments without being able to infect cattle with bacilli of human origin expressed his belief that the converse also is true, i. e.,that the bovine ba- cillus is not pathogenic for man. Perhaps the strongest argumeiit in favor of this view is the circumstance that primary tuberculosis of the ines- tines and mesenteric glands is very rare in chil- dren, who drink a good deal of milk, in spite of the great prevalence of tuberculous cows. ]\[any protests folloAved the announcement of Koch's views, and in a short time a number of investiga- tors showed, first', that it is possible in some cases to produce tuberculosis in cattle with tuberculous material from man, and, second, that infection of man with tlie bovine bacillus is possible. Un- questionable proof of the latter consists in the de- velopment of localized tuberculosis in those who have performed autopsies on tuberculous cattle (Kavanel and others). These occurrences, of course, do not prove the identity of the two organ- isms, for there is still abundant reason to believe that the two bacilli are most pathogenic for their respective, natural hosts, and much less pathogenic for the alternative hosts. Theobald Smith has pointed out that many experiments in which the pathogenicity of the human bacillus for cattle was investigated by the feeding of tuberculous sputum must be repeated, inasmuch as it was not deter- mined in advance whether the organism contained in the sputum was of the human or bovine type. Xaturally, absolute conclusions as to the patho- TUBERCULOSIS. 417 genicity of the human bacillus for cattle could not be drawn with this fact undetermined. In some cases the combined sputum from many patients has, been fed to cattle, and, since both human and bovine bacilli may have been administered, the re- sults are valueless in relation to the point under discussion. In each instance the organism should be obtained in pure culture, its identity as a human or bovine bacillus determined and the experiment performed with such pure cultures. The following points serve to distinguish the bovine bacillus from the human: First, the bovine bacillus is shorter Differences in than the human; second, when first cultivated it grows feebly in media in which the human bacil- lus flourishes; third, it has a higher virulence for rabbits and guinea-pigs, and, fourth, it produces more extensive lesions in cattle. To these Smith has added a fifth point, which he has found to be distinctive in a large number of cultures. In bouillon which contains 5 per cent, of glycerin and which is 2 per cent, acid to phenol phthalein the bovine bacillus produces a neutral or faintly alka- line reaction in from three to several weeks,, whereas the human bacilhis, after causing tempo- rary alkalinity, produces a terminal acidity of from 0.5 to 1.5 per cent. On the basis of this test and other points the bacilli of two cases of mesen- teric tuberculosis in man were recognized as bo- vine in type. In view of the fact that infection of man with the bovine bacillus has been shown to be possible, we are still justified in considering the meat and especially the milk of tuberculous cattle as the probable sources of infection in a limited number of cases. Comparatively few cases of undoubted congeni- 418 INFECTION AND I}rMUNITT. Congenital ttil tuborculosis liavc becii observed, and in such Tuberculosis. n • cases the mothers are usually in an advanced stage of the disease. It is probable that the organisms reach the fetus following metastatic invasion of the placenta. In a number of cases in which the uiother had advanced tuberculosis tlie organs and blood of the fetus (stillborn or dying soon after birth), contained very many bacilli, although his- tologic lesions had not as yet been produced. Warthin and Cowie suggest that the tissue? of the fetus may possess considerable immunity in such cases. Baumgarten is a strong believer in the pos- sibility that tubercle bacilli may pass to the fetus during pregnancy and, remaining latent m some of the. tissues (lymph glands) for a long period, cause active tuberculosis later in life. Others who are less radical still admit that we should consider this as a possibility (Warthin and Cowie, Har- bitz). Infection Pulmonary tuberculosis is by far the most com- mon form of the disease in man, and without doubt this is due to inhalation of the dried and pulver- ized sputum of tuberculous patients. Drop infec- tion may well occur in the case of those who are in intimate contact with the sick. In kissing, direct infection from mouth to mouth is a dangerous jjossibility. The reason for the inception of pulmonary tu- berculosis in the apex in so many cases is not clear- ly recognized, although it is often referred to the relative immobility of this tissue, which renders excretion more difficult and affords improper aeration. These conditions not only allow the or- ganisms to accumulate and to proliferate, but the insufficient oxygenation probably causes a low tis- TUBERCULOSIS. 419 sue resistance. The suggestion which has been made that apical tuberculosis if the result of ex- tension of the disease from the cervical glands does not correspond with the condition seen in tubercu- losis of adults in whom the cervical adenitis is commonly wanting. The ^'anatomic tubercle" is a primary infection of the skin ; lupus vulgaris, it is supposed, may be either a primary infection or secondary to tubercu- losis in some other organ; ulcerative tuberculosis is usually a secondary lesion, often occurring by direct extension from tuberculous lymph glands. Tuberculosis of the nose is uncommon. Infection of the tonsils is not infrequent and probably is a common cause of secondary tuberculosis of the cer- vical lymph glands. Primary infection of the pharynx sometimes occurs and large, coarse granu- lations of this surface have been proved in some cases to be of a tuberculous nature. Tuberculosis of the pharynx and larynx, however, most often arises from infection with tuberculous sputum. In the process of dust infection of the lungs, and also by other means, many organisms lodge on the mucous membranes of the nose, mouth, pharjTix, trachea and larger bronchi, but usually without producing a tuberculous infection. On account of the movement of the ciliated epithelium, tortuos- ity of the nasal channels, excretion of the bacilli with mucus, the conditions at these points are not favorable for infection. Tuberculous ulcers of the esophagus and stom- ach are very rare, as is primary tuberculosis of the intestines. Secondary tuberculosis of the intes- tines usually is caused by the infected sputum 420 INFECTION AND IMMUNITY. which tlie patient swallows. Primary infection of the genital organs may arise from direct contact. That tubercle bacilli have often been found on the hands and finger nails of the sick as well as on those who are intimately associated with them is a significant fact in relation to the possibility of in- fection by direct contact. Metastases. From a given focus tubercle bacilli extend to other structures in several ways. On more or less theoretical grounds one speaks of "extension by growth^' of the organism into contiguous tissues. The commonest method of extension, however, is that of metastasis by way of the lymph channels. When bacilli penetrate a surface, with or without the formation of a lesion at the point of entrance, as in the mouth cavity, intestinal canal, or bron- chial surface, they are carried to the lymph glands of the region in which the tuberculous process is instituted. As in plague, the infection atrium at times is indicated by the set of glands which is in- volved. In certain localities the secondary invasion of other structures takes place directly without the intermediate involvement of lymph glands, as in tuberculous meningitis caused by extension from the middle ear, and tuberculous peritonitis or peri- carditis by extension from the pleura. A^ery fre- quently tuberculosis of the lymph glands and other tissues heals spontaneously, as described below. In case such healing does not occur, metastases con- tinue from one lymph gland to another and to new sets of glands until the larger lymph channels are reached, as a consequence of which extensive re- gional or general tuberculosis results. Accidental localization of a focus often causes a wide depart- ure from the slow development Just described. Not TUBERCULOSIH. 421 infrequently tuberculosis in a lymph gland, which is contiguous to a large lymph channel, as the tho- racic duct, invades the wall of the latter, the sur- face softens from caseation or liquefaction and the contents, impregnated with coimtless bacilli, are gradually thrown into the circulation. Miliary tuberculosis, first of the lungs and then of other tissues, through the arterial circulation, follows such an accident. A similar course with variations ill localization, follows invasion of the walls of branches of the pulmonary artery or vein. Eup- ture of a focus into a bronchus is followed by re- gional or more extensive dissemination of the ba- cilli throughout the lungs by respiratory forces. A sloAver eccentric extension is seen, particularly in the lungs, in which smaller and larger areas of consolidation occur. By means of short lymphatic metastases into contiguous territory new foci are instituted, which eventually fuse with the original lesion. It is suggested and generally believed that bacilli may be carried longer or shorter distances by wandering phagocytic cells. When tuberculosis once involves a surface like that of the pleura, peri- toneum, pericardium or pelvis of the kidney, the whole surface frequently becomes involved in thickly studded miliary tubercles. It is probable that a great deal of dissemination is accomplished by the movements of the fluids and the surfaces of these cavities. In other instances, as in the ure- ters. Fallopian tubes and spermatic cords, exten- sion seems to occur in the submucous tissue by means of the lymphatics. The autopsy often dis- closes that tuberculosis which appeared to be "pri- mary^' in such organs as bones, suprarenal glands, and meninges was preceded by an old process in a 422 IXFKCTIOX AM> niMUMTY. l3-inph gland from wliirli metastases occurred to the tissues in question. The Tubercle Certain auatoiuic conditions produced in tuber- "■e chlnqM! culosis wliicli are associated with recovery from the disease, or the contrary, may be referred to. The tubercle, the histologic unit of the tuberculous process, is produced as follows, according to the interpretations of Baumgarten: When a bacillus reaches a lymph gland, for example, it multiplies slowly and, partly through its presence as a foreign body, but particularly through its toxic secretions, injures the surrounding connective tissue and en- dothelial cells to a certain degree. Under some circumstances, especially in the parenchymatous organs and lymph glands, this injury may be so gTeat as to cause the death of the adjacent cells (focal necrosis). When it is of a lower order the connective tissue and endothelial cells respond to the stimulus by dividing raitotically and eventu- ally accumulate in large numbers within a limited area surrounding the micro-organisms. Not only the endothelial cells of the lymph spaces, but also those of the adjacent blood vessels, take part in the proliferation, many of the vessels being obliter- ated in consequence. ISTot infrequently bacilli are ingested by the new cells, although the ability of the latter to destroy the organisms is not clearly established. Metchnikoff saj^s that tubercle bacilli may remain intracellular for many months and, although not killed, the pathogenicity is decreased or destroyed. The new cells are of polygonal shape, are fairly rich in cytoplasm, contain large vesicular nuclei and are termed "epitheloid" cells. Certain of the epitheloid cells, usually those in . the center of the tubercle, where the bacilli are TUBERCULOSIS. 423 most numerous, undergo atypical proliferation in that repeated nuclear division takes place without corresponding division of the cytoplasm. This process results in the formation of the multinu- clear giant cell vi'hich is so characteristic of the well-developed tubercle, although not distinctive of the disease. According to Weigert, the failure of complete cell division is due to injury to the cyto- plasm (partial necrosis) by the bacteria which the cell contains. Metchnikoff and others take a dif- ferent view of the formation of giant cells, con- sidering that they represent individual epitheloid cells which have fused to form a multinuclear mass. Still more remote from the center of the tuber- cle, that is, surrounding the epitheloid cells, wan- dering lymphoid and plasmal cells accumulate. Certain retrogressive changes, especially necrosis and caseation, characterize the further history of the tubercle, although these changes do not occur equally early nor with equal intensity in all cases. Necrosis begins in the center of the lesion, and the view is often expressed that the formation of the giant cell is the first indication of the retrogressive change. Cell degenerations, however, with karyor- rhexis may occur before giant cells have formed. With the death of the central tissue there occurs sooner or later the death of many of the bacilli in this portion of the tubercle. The progressive for- mation of new tissue continues in the periphery as the degenerative changes take place toward the center; the tubercle enlarges, both epitheloid and the surrounding hanphoid cells increase corre- spondingty, and new giant cells form at the periph- ery of the necrotic center, only to be included in Giant Cells. Retrogressive Changes. 424 iXFEcrrox .wn ntMUxiTY Formation of . Fibrous Tissue. Caseation, Cal- cification and Liquefaction. General and Secondary Disturbances. the degenerated area as the latter extends. In favorable cases, in Avhicli the virulence of the or- ganism is low or the resistance of the individual strong, the tuberculous area is eventuall}^ sur- rounded b}' adult fibrous tissue which in a sense accomplishes the isolation of- the infected area. Without question such a capsule of scar tissue is an obstacle to the extension of the tuberculous proc- ess, whether it surrounds a nodule in a lymph gland, a cold abscess or a tuberculous sinus. Further steps in the healing consist of caseation of the entire area, its partial or complete substitution by connective tissue (tuberculous scar), or partial impregnation with lime salts (calcification). Not infrequently the caseous portion of a nodule under- goes liquefaction, which some have referred to the action of proteolytic ferments. The contents of such foci finally become sterile. In the event that healing of this nature does not occur, the infection is transmitted to other organs as described above. The temperature, loss of weight, fever, increased cardiac action, and arteriosclerosis which are seen in tuberculosis indicate that the products of the bacillus have a profound effect on the functions of the body, and produce great disturbances in meta- bolism, although they seem to have no marked se- lective action for particular tissues. Many disturb- ances are secondary to changes produced in partic- ular organs and are not referable to specific ac- tion of the toxins, such as those which are conse- quent on poor oxygenation in pulmonary tuberculo- sis, and the amyloid degeneration which follows prolonged suppurative tuberculosis. Mixed infection, especially with the streptococ- cus, plays a very important part in the course of TUBERCULOSIS. 425 pulmonary tuberculosis, especially in the caseous and cavernous forms. Staphylococci, B. pyocya- netis, various diplococci, the pneumococcus, bacil- lus of Friedlander, diphtheria and pseudo-diph- theria bacilli, and the influenza bacillus are also found as secondary organisms in pulmonary tuber- culosis. Some of them invade the surrounding healthy tissue, cause lobular consolidations, and in this way probably prepare a favorable soil for further extension of the tuberculous process. They doubtless hasten the liquefaction of caseated tissue, a step in the formation of abscesses. The high and irregular fever often seen in advanced tuberculosis is commonly septic in its cause, and a terminal streptococcus septicemia is not infrequent. It is evident that mixed infections may complicate at- tempts at serum therapy. The essential principles in the prevention of tuberculosis consist of, first, the early recognition of the disease, so that the patient may be properly treated and cured, if possible, with the result that a new center of contagion is avoided; second, the rendering of well-developed cases harmless by suit- able isolation and proper disposal of infected ex- cretions; third, the disinfection of the rooms, clothing, linen and surroundings of tuberculous patients. A fourth point, the prohibition of mar- riage among the tuberculous, is one of great con- sequence, although we have little ground to hope for its realization. A fifth point, not 5'et fully established, is the possibility of universal vaccina- tion against the disease. The collection of infected sputum in properly constructed water-proof paper boxes, which, with their contents, should be burned daily, is the safest Mixed Infections. Principles of Prophylaxis. 426 INFECTION AND IMMUNITY. Disposal method of disposing of this material, and the most effective means of preventing infection of the pa- tient's surroundings. Metallic, glass or earthen- ^vare sputum-cups containing 5 per cent, carbolic acid are serviceable, but must be subjected to fre- quent cleansing. When sputum is coltected on a handkerchief the latter should be boiled within twelve hours and not allowed to dry ; that the hands of the patient are likely to be contaminated from the handkerchief is evident. In coughing, the handkerchief should be held to the mouth to catch droplets of sputum and saliva Avhieh are expelled. The ordinances and rules which prohibit expecto- ration in street cars and other public places should be enforced. When bacilli are discharged in the urine and feces or in the pus of tuberculous ab- scesses and sinuses, these secretions should be dis- infected by suitable means (chlorid of lime). Healthy persons should come in contact with the tuberculous as little as possible, and the eating utensils of the latter should be used by no one else. Disinfection. T]io floor of a rooui whicli is inhabited by a tuber- culous person should always be moistened before it is swept, in order to avoid stirring up the dust. After the death or removal of a patient, the entire surface of the room and all its contents should be thoroughly disinfected by appropriate means. The proper disinfection of the premises which werp once occupied by a consumptive should be a legal requirement. Just as similar procedures are de- manded in the case of smallpox and some other contagious diseases. The special hospital in which the indigent tuber- culous may be properly cared for and isolated has TUBERCULOSIS. 427 been a powerful factor in causing the decrease of tuberculosis which has been noted in many coun- tries. The removal of a patient to such an institu- tion means the elimination of an infected focus from the community. Cold-blooded animals (fish, amphibians, rep- tiles), and most birds are not highly susceptible to tuberculosis, although special varieties of the ba- cillus cause the disease in certain of them under natural conditions. When tubercle bacilli are in- jected into the circulation of birds, they may re- main in the blood and organs for months, produc- ing little or no tissue change, although they retain their virulence for other animals (guinea-pigs). No animal exceeds the guinea-pig in its susceptibil- ity to this disease. Goats and sheep are fairly re- sistant, and the same is probably true of the horse, although its artificial infection is not difficult. That different varieties of a species may vary in their susceptibility is illustrated by the field mouse, which is highly susceptible, and the white mouse, which is relatively immune. Although similar variations may exist among different races of men, they are not readily demonstrated. The high sus- ceptibility which appears to exist among certain races, as the negro, may be explained in part by un- hygienic methods of living, in which safeguards against infection are not taken. The discovery of healed or healing tuberculous foci in 70 to 90 per cent, of all autopsies, in con- trast to the 15 to 20 per cent, of deaths from tuber- culosis, shows that susceptibility and immunity are subject to marked individual variations. The ability of an individual to overcome a tuberculous infection is referred in a vague way to an unusual Susceptibility, and Immunitir. Racial and Individual Variations. 428 INFECTION AND IMMUNITY. • resistance on his part; his defensive powers are said to he strong. Although -we remain to a large extent in the dark concerning these defensive powers, they seem to rest chiefly in the ability of the tissues to destroy the bacilli; that is, the re- sistance is antibacterial. Many bacilli may be de- stroyed by leucocytes or endothelial cells before they are able to cause tissue changes. It was stated previously that healing in many instances depends on isolation of the focus by epithelioid, lymphoid and plasma cells, and by connective tissue. On general grounds we may assume that a tissue reac- tion of this nature takes place with greater vigor and rapidity in a strong, healthy person than in one of lower vitalit3^ Aside from the qucj^tion of individual resistance, recovery or progressive infec- tion may depend on the smaller or larger amount of bacilli which gained entrance to the body, as well as on their virulence. Experiments show that susceptible animals recover from minute doses, whereas they succumb to somewhat larger doses of bacilli. Predisposing Yarious external influences increase susceptibil- inftuences. ^^^ ^^^ resistance. Tuberculosis is to no small de- gree a disease of the poor, who so frequently live in an undernourished condition, in crowded, dirty rooms, with little sunlight and fresh air. The disease is more common in the cit}' than in the country, where an outdoor life is the rule. Alco- holism, diabetes, measles, scarlatina, whooping cough often, and influenza not infrequently, are precursors of tuberculosis. Conditions which favor anemia, as pulmonary stenosis (rare), predispose to pulmonary tuberculosis, whereas insufficiency of the left heart, accompanied by congestion of the TUBERCULOSIS. 429 lungs, is not often associated with the disease, al- though it has no influence in preventing infection in other organs. Tuberculosis is more frequent during the first two or three years of life, when children are so commonly confined, than from the third to the fifteenth year, when they live in the open air so largely. From the fifteenth year to middle life or later the disease increases in fre- quency because of greater exposure to infection. Physicians who are familiar with tuberculosis in Scandinavian countries and in America comment on the extent to which tuberculosis develops among Scandinavians after they come to this country. Nothing is commoner than the occurrence of -Hereditary several successive cases of phthisis in the members tendency." of a family, and the expression, heard on all sides, that "tuberculosis is in the family," indicates the general belief that a family tendency may be trans- mitted from generation to generation. During recent years, however, closer analysis of the condi- tions has led many to doubt the existence or, at any rate, the importance of family tendency or inher- ited predisposition, and to refer the frequent oc- currence of tuberculosis in a family to the greater exposure to infection which is occasioned by close contact with a pre-existing case. Cornet, who has made a close statistical study of tuberculosis, dis- credits entirely the hypothesis of hereditary pre- disposition, and Cornet and Meyer refer to the "hahitus plitMsicus," which we are disposed to look on as an objective evidence of hereditary ten- dency, as a result rather than a cause of pulmonary tuberculosis. It is fair to say that the development of tuberculosis in several members of a family is not prima facie evidence of the existence of a 430 INFECTION AX I) IMMUyiTY. family predisposition lor the disease. Wiierc there are tubercle bacilli there is likel}^ to be tuberculosis, and the occurrence of the infection in one fur- nishes the prerequisite, that is. bacilli, for the de- velopment of the disease in other members of the family. It is probable that the verdict of family tendency has often been pronounced erroneously. At the present time, however, Ave may not be justi- fied in considering the subject a closed chapter. Concerning It is the commonly accepted opinion that recov- immunity. ery from tuberculosis does not confer immunity to subsequent attacks. Cornet and Meyer suggest as an explanation of this condition that the local le- sion is so strictly isolated that a sufficient amount of toxin does not escape into the circulation to cause a general reaction, hence the formation of an- titoxin or other antibodies is impossible. This ex- planation seems inadequate, however, when we re- member the strong antitoxic immunity which de- velops in tetanus and diphtheria in spite of the lo- calization oi the bacteria. The results of artificial immunization, in which iinlimited amounts of toxic material or bacilli may be injected without the formation of satisfactory antitoxins, seem to indicate that the toxic constituents of the tubercle bacillus lack the power of causing the formation of a strong antitoxin. In opposition to the prevailing opinion, certain observers find ground for the belief that recovery from local tuberculosis of the lymph glands, skin or bones, actually does render the patients immune to pulmonary consumption (]\Iaragliano and others). In early experiments Koch noted that when tuber- cle bacilli were injected subcutaneously into guinea-pigs which were suffering from general tu- TUBERCULOSIS. 431 berculosis, the subcutaneous inoculation remained as a local infection and not infrequently healed after sloughing. The general infection would seem to have increased local resistance. Although other investigators failed to duplicate the observation of Koch, this result is said to have suggested to him the idea of active immunization as a cure for tu- berculosis, a method subsequently practiced by treatment with the various tuberculins. In the United States, Trudeau and de Schwein- Active itz, and in Europe, Koch, Behring. Maragliano '"""""'"»'»"• and Baumgarten, with, their followers, have prac- ticed assiduously the artificial immunization of animals Avith the tubercle bacillus or various prep- arations from the organism, with the hope of pro- ducing active immunity to the disease. Some of the procedures, especially those of Koch, have been transferred to man as curative measures. In addi- tion to active immunization of man, Maragliano especially has prepared an antituberculosis serum, to which he assigns antitoxic and bactericidal properties, and which he and others claim to have used with good results in the treatment of tuber- culosis. Marmorek also prepares an "antitoxic" serum. It has been shown that active immunization may so increase the resistance of various domestic animals (guinea-pig, sheep, rabbit, dog, calf, cow, etc.), that they withstand doses of bacilli which are invariably fatal for control animals. When the bactel-ial cells are used for immunization it is customary to begin treatment either with killed bacilli, or with living cultures which are naturally of low virulence, or the virulence of which has been lost by prolonged artificial cultivation. Eelatively 432 INFECTION AND IMMUNITY. ■ avinilcnt strains as those cultivated from fish, turtle or fowls, have been utilized for the first in- jections. As immunization progresses one of two processes may be followed : either the quantity in- jected ma}^ be increased gradually, as when killed or avirulcnt bacilli are used, or the immunization having been begun Avith avirulent living cultures those of higher virulence may be substituted later. In any case immunization is difficult and slow, and many animals may be lost from cachexia or from tuberculosis which develops from hasty pro- gression in dosage. The subcutaneous injection of intact cells has the disadvantage that local ab- scesses frequently develop, and to avoid this the intravenous injection of smaller doses has been practiced in some instances. For active immuniza- tion the "new tuberculin" of Koch containing all the cellular constituents in a finely divided form has the advantages that it may be given subcu- taneously without abscess formation and is ab- sorbed with some rapidity. An animal or person immunized with TK is immune to all the constitu- ents of the bacillus. The condition produced by active immunization is one of increased resistance rather than of absolute immunity; large doses of bacilli may cause infection. The nature of the new resistance is not satisfactorily established. Tuberculin Inasmucli as tubcrculin is used not only for in Diagnosis. -, . • i i i >> i ■ • diagnosis but also for curative purposes m man (active immunization), and since the principles of action are similar in both instances, the use of tuberculin may be considered at this point. A healthy man is not susceptible to moderate doses, but a tuberculous man is even more susceptible to the toxin than the tuberculous guinela-pig. TVBERCULOHIH. 433 since 0.001 c.c. oL'tcn causes an intense reaction, E. Weigert classifies the disturbances which tuber- culin may produce in the tuberculous as thermal, circulatory, respiratory, digestive, nervous and vasomotor, and secretory. Necrosis may be pro- duced at the point of injection. In so far as the di- agnostic use of tuberculin is concerned, we are in- terested chiefly in the thermal disturbances, which are accompanied by chills, malaise and muscular pains. Following injection of a suitable quantity, a period of incubation of from eight to fourteen hours follows, and at the end of this time the temperature rises progressively for two or more hours and may reach a maximum of from 40° to 41° C; after remaining at this point for from two to six hours, it recedes rapidty. In addition to this general reaction, the toxin causes conges- tion, redness and swelling at the site of the tuber- culous lesions, i. e., the foci become surrounded by an inflammatory reaction. This is seetn most readily in the tubercles of lupus vulgaris, and in the lungs declares itself by an increase in rales and expectoration, caused by the exudation ac- companying the inflammatory reaction. For diagnostic purposes the technic of adminis- tration is as follows: It must first be assuredi that the patient has no continued fever by noting the temperature every two hours for several days. One milligram of tuberculin is injected subcu- taneousty, this amount being obtained by suitable' dilution of the original solution. If no tempera- ture is produced by this amount, 5 or 10 mg. may be given in a second injection after an interval of two or three days. When the quantity is determined which causes a rise in temperature of one-half 434 IXFKCTIOX AXO /.I/ l/C'-Y/'/T. degree C. or more, tlie dose is to bo repenti'd after the temperature produced by the first injeelioii has subsided. Two positive reactions should be con- sidered necessary- for the diagnosis of tuberculo- sis. One who, after injection of 10 mg. on two different occasions, gives no reaction is to be con- sidered free from the disease (Marx). Limitations in Experience has taught certain limitations to the of Tuberculin, diagnostic value of tuberculin: 1. The test can not be applied to febrile cases inasmuch as the l^re-existing fever could not be separated from that which the tuberculin might produce. 2. Cases of advanced tuberculosis frequently fail to give the reaction. The tissues of such patients have be- come resistant to the poison. 3. It is said that tuberculin frequently causes a similar reaction in those suffering from lepros}', actinomycosis and svphilis. Cornet and Meyer suggest that the phenomenon as it occurs in leprosy and actinomy- cosis is to be considered in the nature of a "group reaction" in view of the close relationship of the tubercle bacillus to actinomycee and Bacillus leprcB It does not always occur in syphilis, and in posi- tive cases a latent tuberculosis may be responsible for the reaction. By a number of writers the facts just stated are taken to indicate that the reaction is not of specific character; that it may often be ob- tained in the tuberculous by the injection of ap- parently indifferent substances as trypsin, peptone (albumose), sodium cinnimate and the "mycopro- teins" of other bacteria provides additional sup- port to this view. On the other hand, since rela- tively large amounts of these indifferent sub- stances are required to produce the reaction, where- as minute amounts of tuberculin suffice, others TUBERCULOSIS. 435 hold that the specificity of the latter substance may be maintained. Early tuberculosis reacts to tuberculin in the most typical manner. On account of the fact that latent or healing cases may respond to the test, its positive outcome gives no indication of the serious- ness of the patient's condition, which is a practical question of some importance. The fear that tuberculin, in producing an in- Danger f?) fiammatory reaction around tuberculous areas, Tuberculin. may cause a dissemination of the bacilli, has acted strongly in preventing the use of the toxin for both diagnostic and therapeutic purposes. On a priori grounds, such an event would seem to be a possibility, for, with the inflammation, the vessels surrounding the tubercles become congested, new leucocytes accumulate and there is an extravasation of fluid. Since during the subsidence of the in- flammation a certain number of leucocytes may again leave the area and as the extravasated fluid returns to the circulation, bacilli may be carried to other tissues by them. Contrary to such reasoning, however, the observations of Koch and his follow- ers in animal experiments and in the diagnostic and therapeutic use of tuberculin in man, lead them to say that tuberculin when properly ad- ministered never causes an aggravation or exten- sion of the disease. Similar conclusions were reached by Trudeau, Baldwdn and Kinghorn in animal experiments in which, "as in previous ob- servations, a favorable absorptive influence was noted on the diseased focus." Bearing in mind the limitations mentioned above, and the possibil- ity of the reaction being induced by leprosy, acti- nomycosis and syphilis ( ?), the statement of Osier 430 IXl-ECTWN A\n IMMUXITY. may bo quototl that "iu obscure internal lesions, in joint cases and in suspected tuberculosis of the kidneys the use of tuberculin gives most valuable information"' Tuberculin The Original unfavorable results "which were ob- tained in the therapeutic administration of tuber- culin are referred by Ivoch, Petruschky and others to improper selection of cases. Those in a febrile condition and those in whom destruction of tissue is advanced are not suited for the treatment, and in them little or nothing is to be hoped from the administration of tuberculin. Its curative value is supposed to depend on the local inflammatory reac- tion which it causes around tuberculous foci, and perhaps also on the necrosis Avhich Koch claims is caused in the tubercles themselves. It must be the object during the whole course of treatment to ad- minister the toxin in such doses that a moderate or minimum local reaction occurs. Larger amounts which would cause febrile reactions and eventually render the patient resistant to tuberculin and thus preclude the local changes are to be avoided. It is customary to begin with 1/10 to 1/20 milligram and gradually to increase the amount injected. If fever is caused by a particular dose, larger amounts are not to be given until fever ceases to follow this dose. By the time a dosage of 50 milli- grams is reached, which may require many months, the patient usually has lost the power of reacting and the injections are to be interrupted until he again becomes sensitive to the toxin (from tliree to six montlis), after Avhich treatment should be resumed. Cure is recognized when the patient has lost permanently the power to react, his condition then being identical with that of the healthy man. TUBERCULOBIH. 437 ISTimierous German writers on the basis of practi- cal experience assign an unquestionable curative power to tuberculin when administered as de- scribed. Its use has not extended widely. The principles on wdiich the action of tuberculin depend are hypothetical. Marmorek says that the fever and local changes are due to a special toxin (the true toxin), which the bacillus secretes under the stimulation of the tuberculin. Ehrlich sup- poses that cells adjacent to the tubercles have been injured moderately by the tuberculin which is pro- duced in situ, and that as a consequence of this injury such cells are particularly susceptible to the additional tuberculin which is injected, and react to the stimulus by proliferation (Marx). In ac- cordance with this conception the fever also in some obscure way is related to the local reaction. Investigations are needed to clear up this point. In -active immunization with TE, in which the Treatment with solid constituents of the bacilli are injected rather lub^rcuiin^.*^' than the toxic tuberculin, the cure is supposed to depend on the development of immune bodies rather than on local tissue changes. Koch pub- lished favorable results from its use, but reports from other sources were less satisfactory. Koch's Neuiuherculin (BaziUenemidsion) is used in a similar manner. Koch proposes to use the agglu- tinating power of the patient's serum as an index of the immunity caused by the injection. The for- mation of agglutinins perhaps indicates in a gen- eral way the ability of the patient to form anti- bodies, but from the well-known fact that the ag- glutinating power does not go hand in hand with the protective power of serum in relation to many infections, this method of estimatins: the degree 438 iyri:cTio\ axd immvxity. •of iinmunity does not rest ou a good basis. The aggluiination reaction is carried on with the emul- sion which is used for immunization. Treatment in man is begun by the injection of 0.0025 mg. of solid substance and the amount is increased rap- idly every day or two until a reaction occurs with a temperature of from 1.5° to 2° C. After a pause of a week the injections are begun again and event- ually a dose of 20 nig. may be given. During treatment the agglutinating power of the patient's serum is tested frequently, and if it is not suffi- ciently high intravenous injection of the fluid por- tion of the emulsion may be practiced. The agglu- tinating power may go as high as from 1 to 25 to 1 to 150, rarely 1 to 200 or 300. With both TR and the last preparation animals may be successfully immuni/^ed against tul)ercu- losis. Serum of Maragliauo publishes the following conclusions. ^'1. that it is possible to produce a specific (serum) therapy for tuberculosis; 2, that it is possible to immunize the animal organism against tuberculo- sis as is done in other infectious diseases, and that there is good reason for hope for an antitubercu- losis vaccination for man." He recognizes bacteri- cidal, antitoxic and agglutinating properties of the serum as nornuil defensive powers of the body, and says that these powers are increased as the result of immunization. The bactericidal power of the serum is determined by its ability to inhibit the growth of cultures of the tubercle bacillus; its antitoxic power by its ability to neutralize a test poison which is olitained from cultures by macerat- ing them in hot water; and its agglutinating power, is tested with tlie homogeneous cultures of Maragliano. TUBERCULOHIH. 439 Courmont and Aiioing. For the immunization of animals a soluble toxin prepared by the filtration of young cultures, and also the intracellular toxins •which are extracted by Avatcr from killed virulent bacilli, are injected. By using both substances, antitoxic and other antiljodies arc said to be formed. The unusual claim is made by Maragliano that his antituberculosis serum is effective in the treat- ment of human tuberculosis not only because of its own properties, but because it causi3s the tissues to form additional antibodies. It is difficult to take the latter claim seriously, since it is not in accord with the laws of anti-body formation as we under- stand them at the present time. However, favor- able reports of the value of the serum have been published principally from Italian sources. It is claimed that the serum manifests its curative pow- ers and causes an increase in specific antibodies when given per os. Maragliano also advocates a method of mixed Mixed immun- active and passive immunization in man, in which vacdnat?on. a cubic centimeter of serum is given subcuta- neously every second day for twenty days; for a second period the same quantity of serum is given, but supplemented by increasing amounts of the toxic extract of bacilli ; and for a third period the toxic extract is injected in increasing doses during from three to four months. The same authority thinks it may be possible to vaccinate against tuberculosis by a single subcuta- neous injection of a vaccine (killed bacilli?). He states that in both man and animals antibodies are formed in the serum following the vaccination, and that in animals their resistance to infections with 440 INFECTION AND IMMUNITY. Serum of Marmorek. Immunization by Milk. living bacilli is increased. ]\Iarmorck asserts that killed tubercle bacilli which have been treated with his antitoxic serum are readily absorbed from the subcutaneous tissue, and proposes the use of such bacilli as a vaccine. As stated above, Marmorek discredits tuberculin as the specific toxin of the bacillus. His "true'' toxin is prepared by growing young and virulent bacilli ('"primitive" bacilli) in a medium which contains leucotpxic serum, liver extract, glycerin and bouillon. The leucotoxic serum is prepared by immunizing calves with the leucocytes of guinea-pigs. Theoretical considerations which we need not detail suggested the use of this medium. The cultures are filtered after a few days of growth and the formation of tuberculin is avoided as much as possible. The immunization of horses with this filtered toxin yields the antitoxic serum of Mar- morek. Conflicting reports concerning its value are published from French sources. Schwartz an- nounces the complete cure of a case of tuberculosis of the larynx, and another of virulent tuberculosis of the conjunctiva and cornea by the exclusive use of Marmorek's serum. Both Maragliano and Behring aflSrm that the immunizing subst-ances are excreted in the milk of cows which have been strongly immunized against tuberculosis, and both have suggested that the use of such milk by infants may render them more re- sistant to tuberculosis. The agglutination reaction has been suggested by Courmont and Arloing and others as a means of diagnosis in tuberculosis. Others who criticise this idea affirm that agglutinins are not developed suf- ficiently in tuberculosis to render the test of TUBERCULOBIH. 441 value, and that tlic scrum of normal man may l>e as liiglily agglutinating as that of the tuberculous. In view of the fact that the tubercle bacillus grow? in coherent masses in ordinary cultures special manipulations are necessary to render it suitable for the agglutination reaction. Courmont and Ar- loing prepare a homogeneous culture by first grow- ing the organism on a certain potato medium and .then in glycerin bouillon, which is frequently shaken. The cells are said to be well isolated after this procedure. Koch uses his emulsion of pow- dered bacilli for the test. The serum of man or animals as a result of immunization may reach an agglutinating power of 1 to 2,000 exceptionally (Maragliano). APPENDIX. TUBERCULOSIS AND PSEUDOTUBERCULOSIS IN ANIMALS. Certain differences between the bacilli of human and Bovine bovine tuberculosis were mentioned in the preceding Tuberculosis. section. In cattle the disease shows a characteristic tendency to remain localized in one organ or group of organs over a long period. It is a nodular disease as in man, but differs from human tuberculosis in that no- dules often grow to large size, may be imbedded in and sharply differentiated from surrounding healthy tissue, and not infrequently involve serous surfaces, forming large masses of firm sessile or pedunculated tumors. The nodules frequently are fibrovis from the beginning, undergo early and extensive calcification and rarely soften. We are not to understand, however, that miliary tuberculosis does not occur in cattle. Although the process in the lungs is usually of a fibrous and large nodular nature, rapid dissemination with formation of many miliary tubercles may cause the picture of acute tuberculous consolidation in a certain number of cases. According to the statistics of Ostertag, based on 43,000 cases of bovine tuberculosis, localization is as follows: Lungs, 75 per cent.; plevira and peritoneum, 50 per cent. ; peribronchial glands, 60 per cent. : spleen, 40 per cent. In more or less generalized cases the lungs are in- volved in 100 per cent, of the cases; serous membranes, 44-2 IXFJJCTIOX A.\D niMUMTY. 90 per cent.; liver, So per eent.j digestive tract, 00 per cent.; spleen, 50 per cent.; kidneys, ."50 per cent.; mouth cavity, 5 per cent. In cows the uterus, in general infec- tion, is involved in 05 per cent, of the cases, the udders in from 5 to 10 per cent., and the ovaries in 5 i)er cent. It seems tliat the lungs are tlie most connnon infection atrium, and transmission probably is accomplished chief- ly through the secretions of the respiratory passages. In the udders the process may at first be one of miliary tuberculosis, but a large amount of tibrous tissue forms in time, numy acini are transformed into retention cysts, in which tubercle bacilli, free or intracellular, may be present in large numbers. Aside from anatomic changes and clinical symptoms, diagnosis depends on the tuberculin reaction, and, in relation to the udder, the demonstration of bacilli in the milk by staining methods or inoculation into guinea- pigs. The tuberculin reaction in cattle is similar to that in man and is subject to the same general limitations, but is used extensively with the most satisfactory results. The complete elimination of tuberculosis from herds of cattle is possible, by using tuberculin as a diagnostic test, the slaughtering of infected animals, and the dis- infection of stalls. Tuberculosis among sheep and goats is rare. It occurs occasionally in tlie liorse, hog and dog, and with more frequency in the cat. Avian ^^ form of tuberculosis is very common in the chicken, Tuberculosis, and attacks also the pheasant, dove and turkey. The duck and goose are exempt from it. Altliough the or- ganism resembles that of human tuberculosis in size, staining properties and other general characteristics, differentiation is accomplished by means of the follow- ing points: 1. The avian bacillus shows a greater tend- ency to pleomorphinism as shown by club-shaped forms, unstained vacuoles, "spore-like" bodies, and branching threads. 2. It has a greater affinity for aqueous anilin dyes. 3. Growth takes place in artificial media more rapidly and on solid surfaces is characterized by its moist appearance and mucus-like consistence in contrast to the dry, warty, brittle growth of the human bacillus. 4. The optimum temperature for gi'owth (from 40° to 45" C. ) is several degrees higher than that of the mamma- lian organism. 5. Its pathogenicity for guinea-pigs is less and for rabbits greater than that of the human and bovine bacilli. Their difference in pathogenicity is further shown by the difficulty which is met in trying to l'Si:iJD<)TUHi:h'(JUL(),ShS. 44:i infect fowls with the human bacillus. By varying tlie conditions of cultivation and by animal passage the two may be made to resemble each other very closely, al- though the permanent transformation of the human into the avian, or vice versa, has not been accomplished. The disease attacks especially the intestines, mesen- tery and liver, in which are found hard, yellowish-white nodules, often rich in lime salts, and varying in size from that of a pea to that of a walnut. These condi- tions suggest the intestines as the infection atrium. The foci are rich in bacilli and histologically show the es- sential characteristics of tuberculosis. '^Bacillus tuberculosis fiscium" is the name given to an acid-fast organism resembling the tubercle bacillus which was cultivated from an inflammatory tumor in the abdominal wall of a carp. It grows well at low tem- peratures, the optimum being 25° C, is found in large numbers in the lesions within giant cells, and is dis- tinctly pathogenic for frogs. Certain authors state that the human bacillus when inoculated into the frog under- goes changes in its cultural and pathogenic characteris- tics, eventually resembling the organism cultivated from fish. Similar bacilli have been cultivated from a form of tuberculosis in the turtle (Friedman), and Blindsch- leiche — ^blind worm ( Moeller ) . OTHER OEGANISMS RESEMBLING THE TUBERCLE BACILLUS. Certain other organisms of low pathogenicity resemble the tubercle bacillus in their acid-fast properties, their ability to grow in the form of branching threads, and to produce tubercular or nodular infections of a local na- ture in animals. They may be placed in a group which includes the tubercle bacillus. C. Fraenkel, also Neufeld, recognize in smegna two acid-fast bacilli, -calling one "tuberculoid" because of its morphologic resemblance to the tubercle bacillus, and the other "diphtheroid" since it shows the pleomorphism of the diphtheria bacillus. One of these organisms may be identical with the "syphilis bacillus" (?) of Lustgarten. Smegma bacilli are most numerous beneath the prepuce in man and about the clitoris and \ailva in women. Their chief significance lies in the danger that they may be mistaken for tubercle bacilli in suspected cases of genitourinary tuberculosis. Smegma bacilli may readily enter the urethra in women and be carried into the blad- der during catheterization or cystoscopic examination. In man the danger of bacteriologie error may be elimin- Tuberculosis of Fish, Etc. Smegma Bacil- lus and the Ba- cillus of Lust- garten. 444 INFECTION AND IMMUNITY. ateil largely by doansing tlif glans and carefully irrigat- ing the urethra. Urine which is then passed is not likely to contain smegma bacilli (Young and C'hurchman). „ .... . "Milk bacilli'" and "butter bacilli" are acid-fast or- Milk, Butter ganisms resembling the tubercle bacillus moriihologi- and Grass, cally. In injecting milk into guinea-pigs as a test for tuberculous contamination, Petri occasionally noted, as a consequence, a thick membranous growth which en- cased the liver and spleen and bound the coils of intes- tines together. The omentum was thickened, and this structure and the mesenteric lymph glands contained nodules. In pure culture the organism is pathogenic for guinea-pigs only when given in large doses, and may kill the animals in several weeks with the anatomic changes noted above. Its virulence is increased by the simul- taneous injection of butter. It is not pathogenic for man (Herbert). Moeller cultivated organisms resembling the tubercle bacillus from timothy (timothy bacillus), from manure, and a third (grass bacillus II) from the dust of a manger. The last is marked with great pleomorphism, thread formation and motility in young cultures. The leprosy bacillus and the B. of Lustgarten which resemble the tubercle bacillus will be considered later. PSEUDOTUBERCULOSIS IN ANIMALS. Although some of the organisms described above are often called pseudotubercle bacilli, the term pseudo- tuberculosis is now applied somewhat specifically to a nodular disease occurring in rats, mice and sheep (and perhaps in other domesticated animals), and in which organisms differing from the tubercle bacillus in stain- ing and culture properties, morphology and pathogenic- ity, are found. The clinical course and anatomic changes are similar in the three animals mentioned, al- though the organisms are different. The lymph glands near the infection atrium become enlarged chielly by a cellular infiltrate rather than extensive proliferation of fibrous tissue. The nodules undergo a soft caseation very early and rarely show calcification. The infection finds its way to other sets of lymph glands and may be- come more or less generalized with the formation of smaller and larger sized nodules. Rats and Pseudotuberculosis of rodents, occurring spontaneous- Mice. ]y jn rats, guinea-pigs, rabbits and cats, is caused by an organism of considerable pathogenicity, and may occur in epidemic form in laboratory animals. Chickens also may contract the disease. Intraperitoneal inoculations LEPROHY. 445 in guinea-pigs are fatal in a few days. Spontaneous in- fection takes place through the intestinal tract, and re- gional organs show the principal changes. The liver and spleen contain many nodules which may be as large as a hazelnut, and which are frequently caseated in the cen- ter. The organism is called BaciUus pseudotuberculosis rodentium or Streptoiacillus pseudotuberculosis dor. The disease in mice is caused by a diphtheria-like or- ganism called Bacillus pseudotuberculosis murium and is pathogenic especially for the gray mouse. A similar infection in sheep is of more importance and sheep. occurs with some frequency. It is called pseudotubercu- losis ovis, and the bacillus has a corresponding name. The organism is supposed to gain entrance through wounds in the feet and legs, following which the adja- cent lymph glands become involved, and the infection may be transferred to the lungs and other organs through the lymphatic circulation. The lesions are nodular, of varying size, usually surrounded by a fibrous capsule, and are either semipurulent or undergo early caseation. They- may be found in all the visceral or- gans. An organism resembling that cultivated from the sheep has occasionally been found in nodular conditions in cattle. II. LEPKOSY. Leprosy existed in Egy]3t in prehistoric times course of and extended to another land only when inter- "tension. course was established between the two countries. It reached Greece at about 345 B. C, Italy in the first century before Christ, and from the latter country extended to Germany, France and Spain. Crusaders returning from the Orient also brought back the disease in later times and eventually all Europe was infected. Leprosy is known to have existed in Great Britain in the tenth century, and from that country it was carried to Iceland and Greenland. From Germany it extended to the Scandinavian countries, and from the latter to Finland and Russia. It also reached Russia from the South and East, and in the South it was at 44(; lXFi:CTl()\ AXn rMMUXITY. one time called the Crimean disease. The West Indie*; and South America probably were infected from Spain, and through these channels tiie disease was carried to the southern states. The leprosy of the western states seems to have been imported by Norwegian immigrants chiefly. In 1902 the T'nited States leprosy commission found 278 cases in this country. One hundred and eighty-six of these individuals probably contracted the disease in this country. 120 were born in foreign coun- tries and 14:5 were native l.)()iii. The disease also extended around tlie glolie in the opposite direc- tion, reaching China, Japan and the East Indian islands from India. The Sandwich Islands be- came infected in the nineteenth century. The contagiousness of the disease appears to have been recognized at a very early period. In 636 A. D. leprosy houses were instituted in Italy and other countries, and the practice of segregat- ing lepers soon became general. The hospitals were called Lazarus houses in middle Europe and St. George houses in Scandinavian countries. Pipin and Charles the Great declared marriage be- tween lepers illegal. The rapid disappearance of leprosy in middle Europe during the sixteenth century is ascrilied largely to the segregation of the patients. Bacillus of In 1872 Hansen announced that small rods, Leprosy, ggj^^g^jj^gg intracellular and sometimes free, were to be found constantly in teased preparations of leprous tissue. These rods, leprosy bacilli, are now imiversally recognized as the cause of the disease, and in 1879 they were stained by Neisser and a vear later l)v Hansen. The orofanisin ii? non- LKI'ROHY. 447 motile, has about the dimensions of the tiiberclo bacillus, the same staining reactions, and fre- quently shows a beaded appearance (degeneration forms (?) ). It is said to take up dyes more readily than the tubercle bacillus, but the difference is not so great as to be distinctive. It stains by Grain's method. Success in cultivating the bacillus has been re- ported a number of times, but the researches of others have failed to confirm these successes. Up to the present time it is probable that the organism has not been made to grow in artificial media. The resemblance of the bacillus to other acid-fast organ- isms, which are not pathogenic for animals, and the non-susceptibility of experiment animals to leprosy, are conditions which render very difficult the identification of a culture as that of the leprosy bacillus. Nicolli is said to have produced leprous nodules in monkeys by inoculating them with dis- eased tissue. So far as known the organism has no natural Dissemination. existence outside the human body, and it is dis- seminated only by the secretions of the diseased. It is discharged chiefly through the secretions of the nose and the upper respiratory passages, the surfaces of which are so commonly the seat of lep- rous ulcers, and also through ulcerating lesions of the skin. Expectoration, sneezing and coughing have approximately the same significance for the dissemination of leprosy bacilli as of tubercle ba- cilli. However, the organisms which are found in the sputum and nasal secretions appear to be largely degenerated, a condition which may lessen the infectiousness of these substances. Transmission.' Infection Atria. 44S IXFECTION AXD IMMUXITY. The infoetiousuess of the leprosy bacillus is of a low character. "Epidemiologic experience teaches that infection occurs only through intimate and prolonged association with the diseased, in which doubtless uucleanliuess plays a very important role"' (Gotschlich). A leprous husband eventually infects his wife, and the children of lepers com- monly develop the disease early in life. The high percentage of leprosy which is noted among the laundresses of infected localities indicates that the disease may also be transmitted by indirect contact. Gotschlich throws some doubt on the importance of dust infection since so many of the bacilli found in sputum appear to be degenerated. Nothing is known of the resistance and viability of the organ- ism outside the body. On account of the early appearance and almost constant occurrence of leprous lesions in the nasal passages Strieker believes that the latter constitute the chief infection atrium; of this Hansen is not positive. JSTasal ulcers may be present in latent or apparently healed cases. Kolle cites a case show- ing extensive involvement of the spleen and liver in which the intestinal tract was considered the in- fection atrium. In some instances in which the disease is first noted in the feet, the organisms are supposed to gain entrance with infected soil through abrasions in the skin. According to Cor- nil and Babes, infection may take place through the hair follicles and sebaceous glands. The theory of Jonathan Hutchinson that leprosy may be con- tracted through eating diseased fish, or that the lat- ter in some way may render individuals susceptible to infection is not now credited. Hereditary acquisition of the disease is of doubtful occur- LEPROSY. 449 rence, altlioiigh the bacilli have been found in ova (Babes) and commonly are present in enormous numbers in the testicles. Hansen states, however, that he has never found them in the female gen- erative organs. The presence of large masses of bacilli in leprous tissues is a characteristic of the disease. To a large extent they are intracellular and they are often grouped in such a way as to resemble bundles of cigars. Hansen believes that the bacillus is essen- tially an intracellular parasite, and that it becomes extracellular only as a result of degeneration and disintegration of infected cells. Unna, on the other hand, considers their location in lymph spaces as most characteristic. They appear to be carried to distant parts through the lymphatics. Certain large vacuolated cells, the lepra cells of Virehow, the glohi of Hansen, which are filled to bursting with the leprosy bacilli, are characteristic of the disease. Unna and others consider these bodies as zooglear masses rather than as intracel- lular accumulations, and Kanthack interprets them as bacillary thrombi in the lymphatic vessels. The nodules, or lepromas, consist of granulation tissue, containing many roimd and epithelioid cells, lepra cells and occasional multinuclear giant cells. In cutaneous macules columns of round cells surround the blood vessels, there is some proliferation of epithelioid cells, but . relatively few bacilli. The bacilli are most numerous in the nodular lesions. They are found in the Glissonian tissue of the liver, in the pulp and follicles of the spleen, in the glom- eruli and interstitial tissue of the kidneys when these organs are involved, in the nerves in both the nodular and maculoanesthetic forms of the Location of Bacilli. 450 IXFECTIOX AXD IMMUNITY. disease, and iu the vascular endothelium. They have been demonstrated often in the ganglionic cells of the posterior root ganglia. Their occur- rence in these cells leads MetchnikofT to say that the latter have phagocytic properties. Endotoxin (?) In yiew of the chronic course of leprosy and the absence of signs of intoxication over considerable periods, it seems probable that the bacillus secretes little or no soluble toxin. From time to time, how- ever, patients with tubercular leprosy develop fever, which may persist for weeks or months and event- ually terminate in death. During such attacks the nodules not infrequently enlarge, become soft and later disappear. Lie conceives that such periods represent massive infection of the blood with the bacilli, and that at this time the latter imdcrgo extensive disintegration and liberate en- docellular toxins to which the toxic phenomena are due. It is a remarkable fact that intercurrent in- fections, as measles and smallpox, and the adminis- tration of potassium iodid, cause a similar enlarge- ment, softening and final disappearance of leprous nodules, accompanied by marked degenerative changes in the bacilli. Hansen is of the opinion that the fever induced by these conditions has an actual curative effect, although its influence is not readily anal5^zed. He quotes the opinion of Dan- ielssen that potassium iodid may be used to deter- mine the cure of leprosy, which would be indicated by absence of a febrile reaction. General confidence is not felt in the "leprolin" which Rost prepared from his cultures of the lep- rosy bacillus (?). His cultures are said to have ^"amf Means ^^^®^ mixtures of micro-organisms. of Defense. Bccausc of the failure to cultivate the leprosy LEPJtOHY. 451 bacillus^ experimental work with the serum and cells of man and animals, by which conclusions as to the defensive powers of the body might be drawn, can not be carried out. It seems probable that all men are susceptible to leprosy under the proper conditions. Sauton states that children of from 4 to 5 years are particularly liable to infec- tion. Other conditions which may increase sus- ceptibility are of a conjectural nature. It is pos- sible that leprosy predisposes to tuberculous infec- tion (?). The condition in leprosy seems to be that of an organism of low virulence against which the body possesses no decisive protective agency. The reac- tions for the most part are of a local nature, involv- ing the proliferation of connective tissue and hlood vessels, and the accumulation of lymphocytes. That phagocytosis by macrophages (lymphocytes, con- nective tissue, endothelial and ganglionic cells) is a factor which antagonizes the proliferation of the bacilli is suggested by the large number of bacilli which are found in these cells. The principles of prophylaxis may be illustrated Prophylaxis. by citing the practices in Norway. Originally all lepers were confined to institutions. At the present time, however, only indigent lepers and those who can not be suitably cared for at home are required to enter an asylum, where they live under the best hygienic conditions. Other patients are allowed to remain at home, with the understanding that they sleep alone and, if possible, have separate rooms, that their clothing, linen and eating utensils be used by no one else, and that proper precautions be taken in the washing of linen. Dressings and bandages must be burned. Under these regulations 452 lyFECTION .l.YD IMMUNITY. the number of lepers in Norway has decreased from 2.8:0 in 1S5G to 577 in 1900. Banishmont to tlie Ishiud of ]\Iolokai is practiced in the Sandwich Is- hmds. Segregation of lepers should be brought about in this country. Carasquilla attempted the production of an anti- leprosy serum by immunizing liorses with the Idood of leprous patients. Although a few favorable re- ports concerning its effects appeared it has not proved of value in the hands of others. III. GLANDERS (FARCY). Occurrence of Under natural conditions the horse is the chief t e isease. ^^j^gj-gp from glanders or farcy, the former name being applied to the disease as it occurs in the nose, the latter when in the skin. These names are relics of the time when the two forms of the disease were not recognized as having a common etiology. In either locality the disease may be acute or chronic, and in the horse about 90 per cent, of the cases are chronic. The ass is occasionally infected, and in this animal, as well as in man, an acute general infection (bacillemia) frequently develops, in ad- dition to the cutaneous and nasal lesions which characterize the disease. Fortunately, glanders in man is rare. Cows and rats are immune, or nearly so ; the sheep, goat and dog have fairly high resis- tance, although they may be infected artificially; the dog and rabbit are moderately susceptible, and for the guinea-pig and members of the cat family (tiger, lion and leopard), the bacillus is very vir- ulent. Infection of the last named animals has been noted in menageries as the result of feeding them with the meat of a horse which had died of glanders. The acute infection usually is fatal, and Mallei. GLANDERS. 453 complete recovery from the chronic form of the dis- ease is infrequent. Something less tlian 50 per cent, of the chronic infections in man terminate in recovery. The specific microbe^ Bacillus mallei, discovered Bacillus in 1882 by Loeffler and Schiitz,' is an aerobic or- ganism which has approximately the morphology and size of the tul)ercle bacillus, but lacks the acid- fast property of the latter. It stains with anilin dyes, especially carbol fuchsin, but not by Gram's method. With weak staining it shows a granular structure. It grows well on ordinary culture media, showing a characteristic appearance on potato. In unfavorable media it may produce threads, while under more favorable conditions coccus-like forms are seen. Marked involution forms occur on media containing 3 per cent, of sodium chlorid (Wherry). The optimum temperature for growth is from 30° to 40° C. The bacillus is only moderately susceptible to Resistance and sunlight, by which it is killed in about twentj^-four hours. It withstands freezing, lives for two or three weeks in a dried condition at room tempera- ture, and is killed by a temperature of from 56° to 60° C. in from ten minutes to one and one-half hours, depending on the amount and character of the medium in which it lies. Its resistance to the ordinary disinfectants (corrosive sublimate, car- bolic acid, etc.), is not high. Milk of- lime and solutions of calcium chlorid are suitable for the dis- infection of stalls. In culture media the organism secretes no soluble toxin, but it contains an endo- toxin which probably is one of the constituents in the various preparations of mallein. The method bv which the mallein of Eoux and Endotoxin. 4o4 INFECTION AND IMMUNITY. Preparation XoL'urd is pivpurcd is idoiilifal uilh that used in the preparation oi' the old tuberculin. A virulent strain of the glanders bacillus is allowed to grow for some time (from two weeks to two or three months), in bouillon which contains from 4 to 5 per cent, of glycerin, the culture is tlien sterilized by heat and the bacteria removed by filtration. The toxin is not destroyed by high temperature. Other preparations, also called mallein, are made by extracting ground-up bacilli with a solution of gh'cerin and water (Helman, Kalning), or with water alone (Kalning and others) ; by killing a liquid culture of the bacillus (Bromberg) ; or by precipitating bouillon filtrates with absolute alco- hol (de Schweinitz and Kilbourne), or with am- monium sulphate or magnesium sulphate. The dry powders "morvin" and "dried mallein" are prepared by one or another of these precipitation methods. Distribution Glandcrs bacilli are found only in the tissues and secretions of diseased animals, and the nasal discharges of the latter are the chief means of con- taminating feed, water and stables through which the disease usually is carried to other animals. The glanders bacillus does not readily penetrate the intact skin and mucous membranes, although occasionally it may gain entrance through the hair follicles or sweat ducts. In the presence of even slight defects in these surfaces, as those caused in the mouth or nostrils of horses by hay or other food, infection readily occurs. According to No- card, invasion takes place commonly through the gastrointestinal tract following the ingestion of in- fected feed or water. Although involvement of the intestines and adjacent tissues frequently results, of Bacilli and Infection Atria. GLANDER8. 455 the organisms may become generalized, causing the disease in the nose, skin or other organs, without the establishment of foci in the intestines. In man infection occurs chiefly through abra- sions in the skin, and perhaps also through the nose, to which the bacilli have been carried by soiled fingers or other means. Several cases of acute glanders, ending fatally, have occurred in laboratory workers as the result of accidental in- oculation. There appears to be little danger to man in eating the meat of horses in which the dis- ease was localized, provided the meat has been well cooked. Such meat was fed to soldiers in one in- stance with no ill results. Variations in the course of the disease and in the Tissue intensity of the pathologic changes in different cases probably depend on variations in the resist- ance of the host and in the virulence of the para- site. In acute general infections in man, follow- ing an incubation period of from two to five days, during which the point of inoculation becomes vio- lently inflamed, a severe febrile condition develops, which is accompanied by general pains, swollen joints, a macular eruption, and often muscular and subcutaneous abscesses. In a short time nodules and indurated cords, made up of a leucocytic exu- date, edematous fluid and proliferating connective tissue cells, form in the subcutaneous lymphatic channels, and mark the progress of the infection toward the lymph glands. The nodules, and also the cords, commonly undergo softening, and ab- scesses form and rupture through the skin. Nod- ules similar to those in the skin develop in various organs of the body; in the nose they break down and constitute ulcers. In chronic infections the Protective Processes. 45G INFECTION AND IMMUNITY. lesions are of the saiuc nature, although they evolve more slowly and tend to remain limited to particu- lar regions. Xasal, i)haryngeal. tracheal or pulmon- ary glanders are forms of the disease which are en- countered in the horse. Connective tissue develop- ment is more marked in chronic than in acute glanders, although the peculiar liquefaction, sup- puration and ulceration oL' the lesions occur in tiie former as well as in the latter. Moderate Icucocy- tosis is found in the blood (12000-14000). The nature of the pathologic changes found in glanders, the frequent chronic and the progressive course of the disease, and the fact that infection does not confer distinct immunity, are conditions whicli ally glanders very closely to tuberculosis, pseudo-tuberculosis and leprosy. The essential lesion is the "infectious granuloma," and it is prob- able that the new connective tissue which is formed is to no small extent a factor in limiting the exten- sion of the infection. jSTodules of glanders fre- quently are isolated by the surrounding reaction, the centers caseate and the contents eventually are discharged through the skin; cicatrization and healing in many lesions follow evacuation. Phago- cytosis of the bacilli by the epithelioid cells and leu- cocytes in the nodules is said to be rather extensive. According to I^ocard, there is no such thing as an acquired immunity to glanders; chronic glanders may at any time become acute. The cause of the natural immunity of cattle and some other animals seems not to have been determined. Treatment of glanders with immune serums has ""waHein! not been successful. Such treatment has been at- tempted with serum prepared by immunization witli mallein (Semmer), and with the serum of Serum Therapy GLANDERS. 457 diseased animals (Plell and Toeper). The value of mallein in the diagnosis of glanders or farcy is similar to that of tuberculin in tuberculosis. Al- though it causes a rise in the temperature of nor- mal animals when given in considerable doses, the reaction produced in infected animals is so much more intense, and occurs with such smaller doses, that it is generally considered as specific in nature. Some doubt, however, has been thrown on the spe- cificity of the reaction from the facts reported by various observers that toxic substances Irom other organisms, as tuberculin and preparations from the pneumobacillus of Friedlander, Bacillus pyocijaneus, etc., cause similar phenomena in ani- mals suffering from glanders. Wladimiroff asserts, however, that the reactions caused by these sub- stances differ from that of mallein. For diagnosis a dose must be used which causes no reaction in a normal animal, and this varies with different preparations. The typical reaction has two essential components : 1, A rise in tem- perature which begins in from six to twelve hours after the injection, reaches its maximum (from 40° to 42° C.) in from six to eight hours later, where it remains for a few hours, then gradually sinks, only to recur on the second day ; 3, an edematous and inflammatory tumor at the point of injection, which begins in from six to eight hours, and runs its course in from three to eight days, ending in resorption (Wladimiroff). Veterinarians gener- ally agree that mallein is a valuable diagnostic agent. Mallein also has been used in the treatment of glanders, but with rather doubtful results. Bacteriologic diagnosis is accomplished by culti- vating the bacilli from the abscess or secretions and 458 IXFECTIOX AND IMMUyiTY. testing the virulence of the culture b}' animal ex- periments (guinea-pig). Agfliutination. Xonual horse scrum aggluiinatcs the glanders bacillus in dilutions of from 1/500 to 1/700, that of the diseased animal in a strength of from 1/1600 to 1/2000. In some instances, however, infection causes no increase in the agglutinating power of the serum. Agglutinins are said to be formed more readily in man tlum in animals. IV. RHINOSCLEROMA. (See page 402.) V. ACTINOMYCOSIS. Actinomycosis is a chronic infectious disease of man and animals, the lesions of which present, characteristically, a central mass of purulent and necrotic material containing colonies of "ray fungi," about or through which is disposed an abundant growth of granulation or fibrous tissue. In young or rapidly progressing lesions the amount of purulent material is large, while in older lesions well formed connective tissue is more conspicuous. The disease prevails especially among cattle, al- though it is met occasionally in the horse, hog, sheep, dog, cat and other animals ; man is infected not infrequently. Although fungous threads had been found in diseases resembling actinomj^cosis in 1845 and later, Bollinger, in 1877, gave the first accurate de- scription of the disease in cattle, and in 1878 J. Israel described it as a new disease in man. A short time later Ponfick demonstrated the identity of bovine and human actinomycosis. The specific organism, Actinomyces hovis et • ACTINOMYCOSIS. 459 hominis, on culture media consists of a mass of del- The runKis. icate threads which exhibit "true branching" and which^ to a certain extent, segment to form "spores." The radially arranged groups of cells which occur as macroscopic granules in the pus of the actinomycotic abscesses, and which give to the organism the name of the "ray fungus," are essen- tially a manifestation of parasitic existence, although colonies developing on media which contain serum or ascitic fluid may show a degree of "club" formation (Wright). . Each granule represents a colony of organisms the members of which possess club-shaped extremi- ties, and in the center of the mass and extending from it are many of the delicate threads found in cultures of the organism. It grows on various culture media, often as a mold, and stains by Gram's method. The actinomyces is an organism of considerable Resistance. resistance. Cultures remain alive for one year or more when in a dried condition and the spores in one instance germinated after having been pre- served for six years. A temperature of 80° C. for fifteen minvites kills the spores (Berard and Nicolas) . When suspended in bouillon, spores are killed in fifteen hours by direct sunlight, but when thoroughly dried, approximately ten days' expos- ure produced no injury. Attempts to place the actinomyces in a botanic system have resulted in many differences of opin- ion. By some investigators they are considered as an independent family midwa}^ between the hy- phomycetes and the schizomycetes (bacteria), oth- ers place them under the hyphomycetes in the group 4G0 IXFECTION AXD I Mil UN ITT. Artificial Infection. Transmission and Infection Atria. of the streptothrix. while still others consider them as pleomorphous bacteria, placing them in the group cladothrix. Petruschky recognizes acti- nomvces. strejitothrix, cladothrix and leptothrix as genera in the family trichomyces, the latter belong- ing to the order hyphomyces. Biological variations which have been encountered have led to the rec- ognition of several species of actinomyces, among which are a number of non-pathogenic forms. Wright limits the term actinomyces to those strains which produce colonies of club-shaped organisms in animal tissues. Many attempts have been made to transmit actinomycosis to animals by inoculating them with tiie diseased tissues of animals and man, and with pure cultures obtained from these tissues. Al- though a number of experimenters have reported positive results, the attempts usually have been fruitless. Probably Wright has been more success- ful than others in producing actinomycotic lesions in rabbits and guinea-pigs by the inoculation of pure cultures. Colonies of club-shaped organisms developed with considerable uniformity. In many instances the infection remains localized, not caus- ing the progressive and destructive changes which actinom5^cosis produces when it occurs naturally. The organism has been found on grains, straws and other kinds of feed, with which it may be im- planted in the soft parts of the mouth (gums, tongue), or in carious teeth. Transmission to man by eating the meat of actinomycotic cattle has not been noted. In man the disease is primary in the internal organs (lungs, intestines, liver, brain, etc.) in a large percentage of the cases, whereas "lumpy jaw" is rare. The disease extends locally ACTINOMYCOSIS. 40 1 by the gradual involvement of adjacent ti^^sues, which in time become occupied by sinuses, ab- scesses and masses of connective tissue. Numerous "spores" and bacillus-like cells, having their source in the fungous threads, abound in the vicinity of a colony. The occurrence of such forms in leuco- cytes and other large mononuclear cells has led some to the vievs^ that the micro-organisms may be carried to neighboring tissues or to distant parts as cell inclusions. In cattle the disease usu- ally is more chronic than in man, more fibrous tis- sue is formed and metastases in internal organs are less frequent. In man the lesions are more purulent in character, large abscesses sometimes form as in the liver, and metastases in visceral or- gans are more common. Cases of general acti- nomycosis are occasionally met with in both cattle and man. Little can be said in the way of prophylaxis Prophyiaxi*. against actinomycosis. Knowing the part that in- fected grains, straws, etc., play in instituting in- fection, the practice of biting or chewing grains or of using straws as toothpicks, evidently is one which affords opportunity for infection. The pres- ence of carious teeth has often been suggested as a predisposing condition for infection. Practically nothing is known concerning the de- gree to which susceptibility to actinomycosis pre- vails, and the question of immunity to the disease remains unexplored. The inability to reproduce the infection in animals at will renders a satisfac- tory study of these questions very difficult. The presence of large numbers of pol5'morphonuclear leucocytes in the vicinity of the organisms sug- gests, but does not prove, that they may have some Immunity and Susceptibility. 462 IXFECTIOX AXD IMMUMTl. infhieuce in combating the infection. Surely the abundant mass of connective tissue which develops about the abscesses and sinuses aids in confining the process to a definite region. That the iodid of potassium has a c ma live influ- ence on some cases of actinom3'cosis seems to have been well demonstrated. The principles by which it produces its effects are nnknown. VI. MADURA FOOT. Mycetoma. j\Iycctoma, or Madura foot, resembles actinomy- cosis in the formation of abscesses, sinuses and granulation tissue, but it shows a peculiar predilec- tion for the foot, which probal^ly is explained by the greater exposure of this part to infection. This disease differs from actinomycosis in that the course is more chronic and it is never accompanied by generalized infection. The bones are not in- volved so frequently as in actinomycosis. Granules similar to those of actinomycosis are found in the cells, which, however, do not assume the pro- nounced club shape seen in colonies of the ray fun- gus. Two varieties of the disease are known, one in which the granules are brown or black, and an- other in which they are white or yellowish; the latter is encountered much more frequently than the former. Pure cultures of the organism, which is called Streptothrix madurce (Vincent), were first ob- tained by Vincent in 1894, and have been studied by a number of observers since that time. It bears a close resemblance to the actinomyces and by some is considered a variety of this organism. Differ- ences between the black and white varieties are not OIDIOMYCOaiii. 463 clearly set forth. Tlie disease occurs in southern Asiatic countries, in northern Africa, and in the United States (rare). VII. INFECTIONS BY STREPTOTHRIX, CLADOTHRIX AND LEPTOTIIRIX. Cultures of streptothrix, differing from the streptothrix ,. 1 , ^ L • -\ e i-\ -\ Infections. actmomyces, have been obtained irom the lungs in a number of instances and in various countries. They have been found in such lesions as broncho- pneumonia, or more extensive consolidation of the lungs, and in cases of empyema. In other instances organisms which have been classed, some as strep- tothrix, others as cladothrix, have been cultivated from processes which resembled actinomycosis. Nocard considers a streptothrix as the cause of farcin du tceuf (farcy of cattle), a disease encoun- tered especially in the countries of southern Eu- rope, and similar organisms have been cultivated from suppurating or granulomatous foci in other animals. Leptotlirix huccalis, a thread-like organism which does not form branches and, hence, is not an actinomyces nor a streptothrix, is frequently found as a saprophytic organism in the mouth cavity, and a similar fungus, Leptothrix vaginalis, has been encountered in the vagina. Although organisms of this type are relatively harmless, they have occa- sionally been found in diseased conditions of the tonsils and pharynx. VIII. OIDIOMYCOSIS. In 1894 Gilchrist described a skin disease, which has since been known as blastomycetic dermatitis, or blastomycosis or oidiomycosis of the skin. From a second case he cultivated a fundus which at first 464 INFECTION AND IMMUNITY. "Biastomv- lie WHS inclined to consider as an oidiuni, but later cetic" Der- n i i i , -,• i i j • matitis. calletl a blastomyces. femce that tnne many simi- lar cases, especially in Chicago and the adjacent territory, have been discovered and reported by Wells. Hektoen, Hessler, Hyde and Montgomery, Ricketts and others. In many instances the spe- cific fungi have been cultivated. Systemic Further investigations by Eixford and Gilchrist, Busse, Ophiils and Moffit, Hyde and Montgomery and others have brought to light the existence of systemic infections by fungi which resemble closely those found in blastomycetic dermatitis, and, in fact, cases in which the infection primar- ily was limited to the skin have gone on to general- ized infection. The Saccharomycosis hominis of Busse and Curtis, blastomycetic dermatitis, gen- eralized blastomycosis, and about a dozen cases in California, which at one time were considered to be of protozoon etiology (Eixford and Gilchrist), are closely related or identical processes which have as their cause a group of fungi, the individual strains of which may show considerable differences. Nature of In thoso cases usually described as blastomycetic dermatitis or systematic blastomycosis, the fungus proliferates in the tissues by budding, and is found chiefly in the intraepithelial and subcutaneous abscesses, and in the granula- tion tissue and nodules of internal organs. Its appearance in culture media and its bio- logic properties are subject to considerable variations, at one time growing as a mold, at an- other time more like the typical oidium, and again resembling some form of yeast. Eicketts considers that the genus oidium is sufficiently broad to in- clude all the types which have been described, and Fungi. OIDIOMYCOmH. 465 that blaslomycGs is too narrow. The organisms which have been cultivated from tlie cases in Cali- fornia grow as molds, and they differ from those described by Gilchrist, Hektoen, Eicketts and oth- ers in that they form endospores and apparently do not bud in the tissues of the host (Ophiils, Wol- bach). Ophiils calls this parasite Oiclium cocci- dioides, agreeing with Eicketts as to the generic character of the group. The skin infection usually appears as a coarse Histology. warty and ulcerative lesion, in which the large papillas and cutaneous areola are beset with mi- nute abscesses; the process extends gradually and eventually may involve large areas. Histologically, the tissue shows an enormous epithelial hyper- plasia with intraepithelial abscesses, and a richly cellular, granulomatous condition of the subepithe- lial tissue, in which giant cells and small abscesses are found. When the disease is systemic, various internal organs, especially the lungs, spleen and kidneys, are the seats of abscesses and nodules which contain the parasites in immense numbers. The lungs show lobular or more extensive consoli- dation. The skin infection occasionally follows slight infection traumatism, while in other instances no predispos- ing condition is known by the patient. The occur- rence of cutaneous lesions in crops has been noted, and suggests that in some instances they may orig- inate as embolic foci . from a pulmonary lesion which later heals or becomes latent. In the sys- temic infection the primary lesion appears to be in the lungs in most cases, from which the blood and other organs, including the skin, may be in- vaded. Pulmonary oidiomycosis simulates pul- Atria. Systemic Infection. 466 IXFECTl I \l Ml MTV. monary tuberculosis. In extensive involvnnont of the lungs the organisms may bo domonstrated in the sputum. At pi'osent nothing is known concern- ing immunity to these infections. TJtriisli. Ophiils very properly suggests that thrusli should be considered as one form of oidiomycosis. Thrush is of particular interest because of the early date at which its parasitic nature was recognized. Langenbeck and Berg, in 1839 and 1841, are cited as the discoverers of the fungus, and they repro- duced the disease by inoculations with fragments of the membrane. The parasite was studied a little later by Gruby, Eobin and others, and the latter gave it the name of Oidium albicans. Grawitz ob- tained it in pure culture in 1877 and demonstrated its pathogenicity for dogs and rabbits. Cultures of the organism show differences in size, morphology, chemical activities and methods of proliferation, although the variations are hardly so wide as those found among .the fungi cultivated from cases of "blastomycosis." Although thrush usually is considered a rather harmless affection, Virchow long ago showed that its filaments may penetrate the submucous tissues and even the lumens of blood vessels. In rare in- stances systemic infection, with abscesses in the brain, kidney and spleen or with nodules in the lungs, has been noted; in these cases the condi- tions resemble those found in systemic "l^lastomy- cosis." The healthy person has little or no susceptibility to thrush, although a few eases of infection have been noted in individuals wlio were otherwise nor- OIDIOMYCOHIH. 467 mal. Customarily it attacks only those wlio are in a low state of vitality, as poorly nourished chil- dren or those in advanced age, or those whose re- sistance is much lowered by some other disease (ty- phoid, diabetes, etc.). Phagocytosis of yeast and oidium-like cells takes Phagocytosis place when they are placed in the abdominal cav- *"'' '"""""'*v. ity of experiment animals (guinea-pigs). A num- ber of leucocytes may fuse to form a plasmodial mass around one or more of the parasitic cells. Eoger and Noisette caused an increase in the re- sistance of rabbits to thrush infection by the intra- venous injection of small doses of the parasite. Ac- cording to Koisette, an immune serum agglutinates only the strain used in the immunization. _ Infections of other animals (horses, cattle) by oidium-like organisms, the trichophyton and other fungi which cause superficial diseases in the skin of man, and other fungi (aspergillus, mucor), which occasionally are pathogenic for man, will not be discussed. GEOUP V. PllOTOZOOX INFECTIONS. I. MALAEIA. Etiology. The etiolog}' of malaria, which for long was supposed to be associated with impure and swampy atmospheres (malaria is from mal' aria, Italian meaning bad air), remained unknown until 1880, when Laveran discovered ameboid, half-moon shaped and flagellated forms of a parasite in the blood of the patients. In following years Golgi, Grassi, Marcliiafava and Celli and many others took prominent parts in working out the different forms of parasites, their sexual characters and their relation to the different types of malaria. Ross and The Conception that mosquitoes may be influen- tial m transmittmg malaria is a very old one and its origin is unknown. In 1894 Manson suggested that the malarial organism may utilize the mos- quito as an intermediate host where, after under- going further development, it again becomes in- fectious for man. He was inclined to think that the flagella are reproductive forms, which are essential for an extra corpus life of the parasite. The proof of this came from MacCallum in 1897, who showed that the flagellated forms are really spermatozoites, the function of which is to im- pregnate female cells of the parasite. This was observed first in relation to halteridium, one of the organisms of avian malaria, and later in rela- tion to the parasites of human malaria. In the same year Eoss found the pigmented, half-moon shaped parasites of ffistivo-autumnal MALARIA. 469 fever in the stomach of the anopheles mosquito. Through the work of Eoss and others it is now established that the malarial parasite undergoes further development;, a sexual cycle, in anopheles, and that man is inoculated only by the bites of such infected insects. From the standpoint of the zoologist, man is an intermediate host for the parasite, since the latter undergoes its higher de- velopment only after it reaches the mosquito. The malarial parasites of man belong to the class of Sporozoa; order, Coccidiomorpha ; family, Hemosporidia ; genus, Plasmodium. The follow- ing are the names given to the three species : 1. Plasmodium prgecox (parasite of gestivo-autumnal fever) ; 2. Plaismodium vivax (of tertian fever) ; 3. Plasmodium malarias (of quartan fever) . When the blood of one suffering from tertian fever is examined at the end of the febrile parox- ysm, or at the beginning of the afebrile stage, the parasites are found within the erythrocytes as pale, rather clear bodies, about one-fifth the diameter of the corpuscle, and in fresh specimens showing an active ameboid movement. They are very difficult to recognize in unstained specimens. They increase in size gradually, and after eighteen hours, when they begin to acquire pigment, they are recognized more easily. After twenty-four hours the pig- ment has increased markedly and the erythrocytes are swollen and pale. In stained preparations the periphery of the parasite stains more deeply than the center and gives it a pronounced ring form. At the end of thirty-six hours they have increased noticeably in size and their ameboid motion is less. Shortly before the next attack — i. e., forty- six to forty-eight hours after the preceding one — Species of Plasmodium. Tertian Fever. 470 ISFECTION AXJ) IMMIMTY. Sexual Cells. Segmentation I lie pigiucut asscmblcs iiilo oiic 01" two gvoups in ^ceUs. tlie center of the parasite and clear hyaline points begin to appear. These are the young endocellular parasites which are formed by division of the nu- cleus of the mother cell. They gradually increase in size and number, and as the red corpuscles disin- tegrate they are discharged, from fifteen to twenty- five in number, as young parasites. This completes the cycle, an asexual cycle, which has lasted forty- eight hours, and the young forms then begin a new cycle after penetrating other red corpuscles. The mother cell is called the sporocyte and its ofl'spring are merozoites, and the process of divi- sion schizogony. In addition to the asexual cell just described, two sexual cells, a male and a female, grow to adult size in the erythrocytes, acquire pigment and eventually become free. They differ from the asexual cell in that the pigment continues to be uniformly distributed, and neither gives rise to young parasites by division. The male cell (micro- gametocyte, 8-9 microns) has a clear protoplasm and is smaller than the female (macrogamete, 10-14 microns) ; the female has a granular proto- plasm. There are many more male than female cells. They undergo no further development in the body of man, and in order that the sexual pro- cess be completed the two cells must first gain en- trance into the stomach of the female anopheles mosquito. Impregnation. A further step in the sexual process may be seen in drop preparations of the blood, although this step does not occur in the human body. Ten to twenty minutes after such a preparation has been made the male cells, after a period of agitation, MALARIA. 'ill discharge from four to eight long, thin flagella (microgametes or spermatozoa), which thrash about violently and eventually come in contact vi'ith a female cell, which they enter and become un- recognizable. This same process is instituted and completed Life in the (sporogony) in the stomach of the mosquito, the penetration of the female cell by the spermatozoon resulting in the impregnation of the former. Pol- lowing impregTiation, the female cell gradually assumes a Avorm-like or sickle shape (ookinet), penetrates the wall of the stomach and becomes encapsulated (oocyst). Forty-eight hours after the mosquito has sucked malarial blood all the female cells have reached this stage and no more free parasites are found in the stomach. About five days after the blood was taken the Formation of , -, . •',.. 1J.-.- n Sporozoites. oocyst has increased m size about six times and has formed within itself a number of small spheres, which are called daughter cysts or sporo- blasts. The latter soon acquire a finely striated ap- pearance, which is due to the formation of hun- dreds of "germinal rods" or sickle-like bodies (sporozoites). The latter are nothing less than young malarial parasites, which are thrown into the body cavity by the rupture of the oocyst, and are carried to the salivary glands of the mosquito by the lym]3hatic circulation. If the mosquito has been kept at a temperature of 24° to 30° C. these sickle forms first appear in the salivary gland after eight to ten days. Such are the cells which are inoculated into man by the bite of the mosquito. The changes which they undergo before they ap- pear as clear oval bodies in the erythrocytes are unknown. 472 IXFECTIOy AXD IMMLXITY Parasite of Quartan Fever. Parasite of Aestivo-Au- tumnal Tever. "Half-moon" Cells. The asexual cycle of the quartan parasite is identical Avith that of the tertian, with the excep- tion that seventy-two hours are required for its completion. It contains more pigment, and wlien division takes place eight, or at most fourteen, young parasites are formed, in contrast to the lifteen to twenty-five of the tertian parasites. The er3^throcytes do not become large and pale (Ruge). The sexual cells practically are indistinguishable from those of the tertian parasite, although they are, on the whole, slightly smaller. The sexual cycle also is completed only in the body of the female anopheles mosquito, and is identical with that of the tertian parasite. The parasite of aestivo-autumnal fever is one- half to two-thirds the size of the tertian parasite, a difference which is constant in the various stages of development of the asexual cell. It divides eventually into eight to twenty-five young para- sites, the cycle occupying from twenty-four to forty-eight hours. Here, as in quartan fever, the erythrocytes do not become swollen and pale, but even appear darker in color, because of some shrinking (Euge). The sexual cells in asstivo-autumnal fever are characteristic. Whereas they at first do not differ in shape from the asexual cells, as they grow older they gradually assume the shape of a half moon in one edge of the erythrocyte, reaching a length equal to one and one-half diameters of the red cell. At this time a fine line drawn across the concavity of the parasite represents the margin of the ery- throcyte. This form is only temporary, however; they subsequently assume first a vspindle and then a spherical form. As in the other parasites, the MALARIA. 473 male cell is rather clear and the female granular. When mounted in a hanging drop the male cell liberates flagella, which penetrate the female cell. This does not occur in the human body. In this respect, and also in the completion of the sexual cycle in the body of the mosquito, they resemble the other two parasites. The parasites of tertian and quartan fevers un- dergo division while they are in the circulating blood, and when peripheral blood is examined at the end of the afebrile stage the young cells may be found extracellular. This is not the case, how- ever, in the gestivo-autumnal fever. In this in- stance, for unknown reasons, the adult cells with- draw to the internal organs, especially the spleen, bone-marrow and brain, where division takes place in the minute vessels. Hence if the peripheral blood is examined preceding and during the febrile stage few or no dividing cells or young parasites are seen. Following inoculation by an infected mosquito, ten to twelve days are required for the onset of a paroxysm. In rare instances the incubation period may be as short as five to six days. This probably depends to some extent on the number of organisms inoculated. Malarial infection of the mosquito is- not transmitted to the offspring the latter,* hence the bites of young mosquitos do not convey the disease unless they also have sucked malarial blood. The conditions are different in relation to Texas fever, in which the infection is trans- mitted by the female tick to her young. The ffistivo-autumnal parasite apparently is virulence more virulent than the tertian or quartan. Not Incubation Period. * This is questioned by Schaudinn. 474 IXFECTIOy A\n IMMUNITY. Relation of S>niptonis to the Bioloqv of the Parasites. all cases of tertian or quartan fever are equally severe, and these variations may depend on diU'cr- ences both in virulence and in the resistance of in- dividuals. "When all the parasites divide within a period of two to four hours, the paroxysm is more intense but shorter than when division extends over six to eight hours (Ruge in relation to ter- tian fever). Some of the severer symptoms are due to the localization of the jiarasitcs (brain and intestines), rather than to special toxicity. The melanemia of malarial fevers is due to the fact that the parasites absorb the hemoglobin from the erythrocytes, transform it into melanin by their metabolic activities and liberate the melanin at the time of cell division. The anemia results from destruction of the erythrocytes. The cause of the fever and its periodic recur- rence is more difficult to explain. As stated above, the fever begins in both tertian and quartan fevers at the time division forms of the parasites are en- countered in the perif)heral blood. Although all the parasites do not divide simultaneously, the process is complete within a period of four to eight hours and the parox}'sm begins early in this Fever and period. It is quitc natural, then, to infer that by the division of the parasite and the escape of the young cells from the erythrocytes, toxic substances are thrown into the circulation, and that the febrile reaction is due to the action of these toxins. Methylene blue has the power of preventing seg- mentation of the parasites (Ehrlich), and it has been shown that the paroxysm of fever may be averted by administering methylene blue at the proper time. This corroborates the view that the segmentation of the parasites causes fever in some Schizogony. MALARIA. 475 way. The paroxysm would seem to represent the time required for the exhaustion of the toxins set free at the time of the cell division.* On the basis of the conditions just cited, the brief duration, sharp limitation and regular re- currence of the paroxysms in tertian and quartan fevers become intelligible. In a similar manner the longer paroxysms and shorter intermissions which characterize the typical ffistivo-autumnal in- fection (i. e., in first attacks) are related to the habits of division of the corresponding parasite. All the cells do not divide within a relatively short period, as in tertian and quartan fevers, but the process of division rather stretches out over from twenty-four to forty-eight hours. This accounts for the longer duration of the paroxysm. When the last cells of one generation are dividing, per- haps after the fever has gone down, the first cells of the succeeding generation are well on toward maturity and their division within a short time inaugurates a new paroxysm; the brief intermis- sion would seem to be explained by this condition. As the disease lasts longer, or as relapses develop, the periods of division of the parasite are less sharply limited and a course with an irregularly continuous (?) fever may be established. Quotidian malarial fever is caused either by a double infection with tertian parasites or a triple infection with quartan parasites. In either instance a generation of parasites matures and divides ever}' twenty-four hours. The cause of Duration of Paroxysms. Quotidian Fever. * Ivosenan, Parker, Francis and Beyer produced a typical paroxysm in a healthy person by injecting filtered serum taken from a tertian patient during the chill. This was intoxication, not infection. 476 IXFECTIOX AXD IMMIXITY. the double or triple infection is not known definite- ly. In some instances it is possible that successive inoculations by different mosquitoes has occurred. On the other hand a fever which is primarily ter- tian or quartan may gradually change into the quotidian variet}', and in this condition it is pos- sible that the organisms may gradually separate themselves into two or three distinct generations, which reach maturity on successive days. Mixed In other instances mixed infection witli two Infections. , . , „ . . , t mi • • n kinds of parasites is encountered. This is usually ffistivo-autumnal fever combined either with ter- tian or with quartan. Either the asstivo-aiitumnal may be primary on the one hand or the tertian or quartan on the other. The clinical course is com- plicated correspondingly. It is doubtful if tertian infection is ever mixed with quartan. Eugc speaks of experiments by Dr. Mattel which indicate that a mixed infection does not continue indefinitely as such. A patient suffering from quartan fever was inoculated with sestivo-autumnal blood; in time all the quartan parasites disappeared, leav- ing only the gestivo-autumnal. In malarial cachexia there is not only an in- sufficiency of the blood-forming organs, but other parenchymatous organs have suffered as a result of prolonged intoxication. The blood-forming or- gans can not keep pace with the destruction of the erythrocytes. . Trigeminal and supraorbital neuralgias and periodic headaches occur sometimes as accompani- ments of malarial infection, even when there is little or no fever, and no parasites may be dis- coverable in the blood. That they are malarial in origin is concluded from the fact that they subside under quinin treatment. MALARIA. 477 In some forms, and particularly m a3stivo- Cerebral , 1 J. 11 , / X and Intesti- autumnal lever, cerebral symptoms (e. g., coma) nai Symptoms. are marked by accumulations of the parasites in the small vessels of the brain; tbc vessels may be completely occluded. The conditions arc similar in the small vessels of the intestines in malarial diarrheas. The so-called "black-water fever," or hemo- "Black-water ' Fever." globinuric fever, is not a special form of malaria, but a complication which, it is thought, is pre- cipitated by insufficient or improper administra- tion of quinin (Koch and others). It is most fre- quent in the tropics, hence in sestivo-autumnal fever, but may occur in the tertian and quartan types. Various observers have found that in all the way from 56 per cent, to 97 per cent, of the cases quinin precipitated attacks. Stephens and Christopher were not able to exclude quinin as a factor in any of the cases- they encountered. The essential process is a massive destruction of the erythrocytes which is entirely out of proportion to the number of cells occupied by parasites: few or no parasites may be present. The amount of hemoglobin thus liberated is so great that it is ex- creted largely by the kidneys; anuria may result from occlusion of the tubules by pigment. How the quinin, or the quinin plus parasites, produce this extensive hemolysis is entirely obscure; the effect is that of an intense intoxication, in which the erythrocytes suffer primarily and chiefl3^ The essential epidemiologic features of malaria Epidemiology. are the following : It prevails especially in tropical and subtropical zones and less in temperate zones. It is most abundant in low, swampy regions, and in other places which afford quiet streams, ponds 478 IXFECriOX AM) nnil MTY. or other standing Avater. Malaria is not directly contagious. In order to hocoine infected it is necessary, customarily, for one to enter or be in close proximity to a "malarial district." That the virus is not carried far from an infected dis- trict is shown by the exemption of the crews of vessels which lie within two or three miles of such a district. Infection has long been supposed to take place chiefly by night. The disease may be introduced into new regions (of suitable climate) by the importation of malarial subjects. These and many other phenomena of malaria which were once very obscure have been cleared up by the mosquito theory. Anopheles. There arc many species of anopheles and they are distributed throughout the world in warm and moderate climates. Anopheles inacuUpennis is the most numerous species, and for it, as well as for Anopheles punctipennis, Howard has found several natural breeding places in this country. It is probable that many, but not all, species of anopheles may transmit malaria. The female only is a blood-sucker, the male living on vegetable material exclusively. After the female has ob- tained blood from man or another mammal it flies to a suitable pond or other collection of w^ater, where it deposits its eggs. Development "The adult mosquito lays its eggs on the surface of the water. The eggs float on the water for some days (tw^o to four), after wliieh tlicy hatch and permit the escape of the larva. "The larva is a free-swimming, worm-like ani- mal, which eats greedily and grows rapidly, cast- ing its skin several times in the process, till it reaches its full development. At this stage it sud- MALARIA. 479 denly changes its form; casting its skin, the worm- like larva assumes a comma shape and so becomes the pupa or nymj)ha. "During the pupal period the insect ceases to eat; profound anatomical changes take place with- in the pupal skin, whereby the masticatory mouth - parts of the larva are converted into the suctorial apparatus of the adult insect or imago. After a certain number of days the pupa case ruptures and the adult insect is liberated, furnished with wings and legs adapted for a life in the air." (James and Liston.) In one instance Howard found the life cycle of Anopheles macuUpennis to be: "Egg stage, three days; larval stage, sixteen days; pupal stage, five days, making a total period in the early stages of twenty-four days." The rapidity with which this process takes place depends largely on the tem- perature; it is more rapid in the hot weather of July and August than in the cold days of May. Anopheles usually does not lay its eggs in tin cans or barrels of water, but preferably in more open or cleaner water. Excavations which have become filled with water are favorable places, as are also collections of water from springs'. The anopheles leads an adult life for many months and may even hibernate under suitable conditions either in the adult or larval form. It is generally stated that the insects do not fly more than half a mile from their breeding and feeding- grounds. Their dispersal certainly extends beyond these limits, however. James and Liston enumer- ate the following methods of dispersal : 1. By direct flight over considerable distances. 2. By the eggs and larvae being carried in streams and Migration of Anopheles. 480 IXFECTIOX AXD IMMUNITY. Prophylaxis. General Measures. canals. 3. By a multiplication of successive short flights by adults. 4. In conveyances. Anopheles avoicls high winds and rains, seeks shelter on excessively hot days and feeds and bites chiefly or only after sunset and before sunrise. The latter habit confirms the old belief that ma- larial infection occurs chiefly at night. For further details as to the morphology and habits of the insect in its different stages, and for differentiation of the different genera and spe- cies, one should consult a textbook of entomology, or, for example, the book on "Mosquitos," by How- ard (McClure, Phillips & Co., New York). Individual prophylaxis may be accomplished and maintained by taking small daily doses of quinin, or larger doses (1 gram) every few days. One who has had malaria may likewise prevent recurrence by suitable quinin treatment. Quinin has the power of preventing division of the parasites, and, therefore, the power of preventing the paroxysms. "R. Koch's procedure consists in this, that one takes a gram of quinin every tenth and eleventh day, and if fever still develops, every ninth and tenth day." (Euge.) Other points in individual prophylaxis are, first, the application of ethereal oils (clove oil, oil of pennyroj^al) to the exposed skin, and, second, the use of mosquito netting. The important practices for general prophylaxis are the following: 1. The draining of swampy places and of jdooIs of water W'here anopheles may deposit its eggs. This in many instances manifest- ly can not be accomplished. 2. Covering pools of water with petroleum. This is to a degree success- ful. Every square meter requires i/o liter of pe- MALARIA. 481 troleiim (Kerschbatimer), and the oil must be added fresh every seven or eight days. The layer of oil excludes the air from the larval mosquitoes and they drown. If fresh oil is not added occa- sionally new eggs may hatch. 3. Koch's method of extermination of malaria. This consists of the searching out of all cases of malaria and the de- struction of the parasites by appropriate quinin treatment. Koch practiced this method in an in- fected locality of New Guinea and in a relatively short time freed it of malaria. If all the plasmodia in a community are destroyed the disease can not again become endemic unless it is introduced from without or unless infected mosquitoes are imported. Manifestly this method must be practiced on an ex- tensive scale in order to render it permanently successful. It seems to have been demonstrated, however, that the number of cases in any given locality may be materially decreased by pursu- ing it. So far as is known, susceptibility to malaria is immunity. universal. The belief is very general that one attack of malaria not only does not protect against reinfection, but even predisposes to it. Two facts, however, show that acquired immunity (relative or absolute) is possible. First, in certain regions of Africa where malaria is endemic the adult na- tives rarely suffer from the disease, and then only from light attacks, whereas European visitors con- tract the disease in severe form. The cause of this immunity was explained by Koch. "Koch found that the native adults of malarial countries were free from malaria, but that the children suffered almost universally from malarial diseaises. If they recovered from the original infection they 482 INFECTION AM) IMMUNITY. became immunized in time through continued new attacks or relapses, the number of malarial chil- dren gradually decreased with their age, and in the vicinity of the tenth year the only evidence, in general, of a previous infection was an enlarged spleen, and even this disappeared during puberty, so that the adult natives finally appeared as healthy and malaria-immune persons." (Ruge.) The objection raised by many that such immunity is not observed in Italy and other civilized coun- tries where malaria is endemic, is met by the fact that the disease in these countries is not permitted to run an uninterrupted course. Treatment with quinin is instituted and the immunizing process is thereby broken off. Koch also established that immunity against one type of parasite is not effi- cient against other types. Second, in civilized countries it has often been noted that subsequent attacks are of a milder char- acter than the primary; the disease may in time "wear itself out," even without quinin treatment. Ruge gives as an accompaniment of this immuniz- ing process the occurrence of the sexual cells in large numbers, even up to 50 per cent, of the total number of parasites (tertian fever). In such cases large numbers of the parasites die before they reach maturity, their death being indicated by shrinking and clouding of the cells and altera- tions in or disappearance of the chromatin. It is somewhat characteristic of quartan fever, and still more so of sestivo-autumnal, that the sexual cells are much more numerous in recurrences than in primary attacks. One may be able to differentiate a relapse from the primary attack by the number of sexual cells encountered (Ruge). TUYPANOSOMIASIS. 483 Proteosome. N'o thing in the way of serum therapy has been accomplished, and it is doubtful if any serum could equal quinin in efficacy. MALARIA OF BIRDS. Wliat is considered as true malaria also occurs in birds. One of these diseases is caused by a proteosome {Pro- teosoma Labhe, Cystosporon danielewslcy, Hemameha re- licta). Sparrows, hawks, buzzards, crows and pigeons are aflfected. Like the malarial parasites in man, the parasite enters the erythrocytes and has both a sexual and an asexual cycle of development, the latter taking place in the infected animal, the former in the stomach -of the common mosquito (Culex pipiens) . Hence in its development proteosoma is perfectly analogous to Plasmodium. The disease is transmissible from bird to bird by the inoculation of infected blood. Halteridium is still another hemosporidium which in- 'Halteridium. -fects birds. It was in the study of this organism that MacCallum first saw the phenomenon of impregnation. All the cells seen in the blood appear to be divisible into male and female, and although MacCallum had seen im- pregnation in microscopic preparations the life cycle for a long time was obscru-e. Recently Schaudinn has found that the sexiial cycle is completed in Culex pipiens. He considers the organism to be a trypanosome. "I have been able to prove that the halteridium is the sexual stage of a trypanosome which multiplies in the common mosquito — Culex pipiens — and after a complicated mi- gration through the body of the mosquito is again in- troduced by its bite into the blood of the owl, where, a,fter a period of sexual multiplication, it is transformed into the Avell-known male and female halteridium." II. TETPANOSOMIASIS. Gruby created the genus Trypanosoma in 1843^ when he gave the name of Trypanosoma sanguinis to a flagellate protozoon which he found in the ialood of frogs. Since that time similar organisms have been found in the bloods of many animals and the genus Trypanosoma has grown to considerable Genus Trypanosoma. 484 IXFECTIOX AM) IM.yUMTY. dimensions. It is not improbalile. liowcver, that a niunber which now bear indepcmU'iit names will be shown to be identical. This suggests itself par- ticularly in relation to trypanosomiasis in horses, in which the infections are loiown under four sep- arate names in different countries, and the para- sites are given separate specific names. The study of these infections is so young and has been prose- cuted in such widely separated countries that the existing chaos is quite natural and can be adjusted only as time and circumstances permit of close comparative study. Until such a time the prevail- ing views as to independence of species and of in- fections must be recognized. Morphorogy. Trypanosomas vary a great deal in size and mor- phology. Eoughly, they are from one to five mi- crons thick and fifteen to forty-five microns long, including the flagellum. All species possess active eel-like movements, some traveling rapidly, others slowly. A long, actively-motile flagellum projects from the anterior end, and where it joins the cell body is continuous with an "undulating mem- brane," which extends along a border of the or- ganism to a point near the centrosome or micronu- cleus in the posterior portion of the cell. The centrosome is sometimes spoken of as analagous to the "eye spot" of some other protozoa. The un- dulating membrane is more or less wavy or folded and its breadth varies. The centrosome presum- ably has a close relationship to the undulating membrane, and, through the latter, with the flagel- lum. The nucleus is in the anterior portion of the parasite. In relation to some species a con- tractile vacuole is spoken of. An endoplasm and an ectoplasm may be differentiated. TRYPANOSOMIASIS. 485 Division of trypanosomes is nearly always longi- Division tudinal, rarely transverse. According to Piimmer and Bradford, conjugation may occur, "followed by an ameboid stage and division by segmenta- tion." The ameboid stage at times occurred inde- pendently of conjugation. (Musgrave and Clegg.)* In the process of longitudinal fission the order of division of the different parts of the cell is as fol- lows : 1, Centrosome ; 3, flagellum ; 3, nucleus and protoplasm (Laveran and Mesnil). After division has occurred the two cells may remain attached at their posterior ends for some time. By a re- peated division of young cells, the posterior ends remaining attached, rosettes are said to be formed. Others consider rosette formation as a phenomenon of agglutination. Possibly both phenomena occur. Trypanosomas are differentiated on the basis of size, pathogenicity, motility and certain points in morphology, as the position and size of the micro- nucleus or centrosome, the presence of a contractile vacuole, the size and tinctorial qualities of the nucleus, the degree of granulation of the proto- plasm and the location of the granules, appearance of the undulating membrane, length of flagellum and shape of the posterior non-flagellated end. Differentiation. TRYPANOSOMIASIS I^^ MAJ^^. Kepreu in 1898 flrst found trypanosomes in the blood of man in Algiers in eight cases. His ob- servations were passed over temporarily. The para- site bears his name (T. neprevi). Again in 1901 Forde discovered similar parasites in Western Trypanoso- ma tic Fever. * Knowledge is very deficient concerning the questions of conjugation and sexual cycles. An exception is to be made in relation to halteridium, a parasite of bird malaria, which is a trypanosomc, according to Scliaudinn. (See page 483.) 486 I\FEVT10\ AM> IMMrXlTY. Africa (Gambia), and since that time a number of cases of "Gambian fever" or trypanosomatic fever in man have been imported. In this in- stance the parasite was called T. gamhicnsc b}^ But- ton and 2\ liomlnis by Manson. The disease is said to follow the bite of a tsetse-fly (Glossina palpalis). at least in some instances. The tissues around the bite become inflamed and in from a few days to two weeks recurring attacks of fever set in, and a patchy and ringed crythenurtous erup- tion appears on the skin. Forde gives as the chief clinical findings in his case: 1, the irregular intermittent temperature; 2, the edematous con- dition of the face and lower extremities ; 3, the rapid and variable pulse and respiration, unac- companied by any evident cause ; 4, loss of weight, with marked debilitj^, wasting and lassitude; 5. the persistence of these symptoms and their re- sistance to treatment. The parasites are most numerous in the blood at the time of the febrilfe attacks. Eecovery has not been reported. Sleeping Sleeping sickness has been endemic in certain districts of Africa for a long time, and, although confined to a very limited district at one time, it ap- pears now to have extended to distant parts. Speak- ing of trypanosomatic fever and sleeping sicloiess collectively, Ruata says that while originally con- fined to a small rlistrict in Western Africa between the latitudes 15' ISTorth and 15' South, it is now found one thousand miles up the Congo (Bangola, Stanley Falls) and in East-central Africa on the shores of the A^ictoria Nyanza Lake. "ISTow it ex- tends from the mouth of the Katonga Eiver through Uganda (1901, Cook), Kome Island. Busaga, Buvuma, Kavirondo, Kisumu, Lumbwa, TRYPANOSOMIASIS. 487. Homa, Kasagiuiga, Lnsinga Island, the eastern shores of the lake, joining the south of the bound- ary river Gori in the Udcmi district of the Sultina of Obo" (Kuata). Its extension supposedly has been facilitated by rapid transit. "The disease is most prevalent amongst the inhabitants of low-lying shambas (ba- nana and potato plantations) in places along the shores of the Victoria ISTyanza, or in wooded dis- tricts not far from the water" (Christy). Those living on high ground are much less infected than those living in the low moist places near water. A great deal of stress is laid on its close association with inland bodies of water. It apparently has no relation to sex, age, sea- sons, food or drinking water, and is related to oc- cupation only in so far as the occupation carries one into the low places mentioned. At one time (1891) Manson advanced the idea that sleeping sickness is caused by the minute Filaria perstans. It has since developed that this parasite occurs in 70 per cent, of the natives in certain districts, and that sleeping sickness may occur in areas in which Filaria perstans does not exist; Manson has abandoned this view. A num- ber of investigators also found cocci in the cerebro- spinal fluid, but this occurred very rarely during life and at a late stage of the disease; such organ- isms are probably secondary or agonal invasions in spite of their rather frequent occurrence. Fur- ther investigations by Castellani disclosed the pres- ence of a trypanosome {T. castellani) in the cere- bro-spinal fluid of a large percentage of the cases, and a little later Bruce found this organism in all the cases he had examined. This observation has Occurrence. Trypanosomes in-Sleeping Sickness. 488 INFECTION AND IMMUNITY. been confirmed so many times that the trypan- osome is noAv generally considered as the cause of the disease. Tsetse Sleei)iug sickness is not contagious in the or- '"'>'• dinary sense, and Bruce furnishes rather strong evidence that it is transmitted by the bite of a tsetse-fly (Glossina palpaUs). The distribu- tion of the disease corresponds to the habitat of this fly, and Bruce transferred the infection to monkeys by means of flies which had bitten those suffering from sleeping sickness. Sambon does not consider the experiments above criticism. Symptoms. ^^ pronounccd lethargy or somnolence is the most striking clinical feature of the disease. "The appearance of the somnolent condition is preceded, often for a long time, by prodromal signs, which are so characteristic that the patient's neighbors cannot possibly be deceived as to the fate that awaits him. The victim complains of wealcness, langour, dejection, disinclination for work, head- aches, particularly localized over the occiput, a sensation of weight in the head and giddiness. His eyelids tend continually to close and he has a tendency to go to rest at unusual hours of the day ; for this purpose he seeks out lonely quiet spots, where he spends a long time in dozing" (Scheube). For some time he is able to resist the somnolence, and when aroused gives intelligent answers. He eventually acquires an unsteady gait and walks about like a drunken man. The temperature of the body appears to be lowered, although irregular attacks of fever occur. The somnolence gradually becomes more intense, the patient grows very weak, the pulse small and thready, respiration difficult, the edema seen in trvausoniatic fever is rather TRYPANOSOMIASIS. 489 constant, incontinence of the urine and feces may develop; the patient commonly dies after passing into a state of deep stupor. Convulsions and pa- ralyses are noted; the mind usually is clear when the patient is conscious, although maniacal at- tacks and delusions are occasionally noted. The cervical and superficial lymphatics are frequently but not constantly enlarged. A papulo-vesicular eruption is quite characteristic and persistent and the skin becomes very dry. The incubation period varies from six to eighteen months, and the som- nolent state from three to twelve months. Eecov- ery rarely occurs. The essential anatomic change is meningo-en- cephalitis, the soft membranes being thickened, containing a milky fluid and the vessels of the pia and brain being surrounded by an extensive infil- tration of mononuclear leucocytes. Meningo- Encephalitis. The discoverv of trypanosomes in sleeping sick- identity of jry- •t -J i- J. o panosomatic Fever and Sleeping ness suggested that tryanosomatic fever may really represent the long prodromal stage of sleep- ing sickness. This view has been greatly strength- ened by a case reported by Manson in which a typical case of tryanosomatic fever was seen to pass into typical and fatal sleeping sickness. The wife of a missionary in upper Congo was bitten by a tsetse-fly, and following an inflammatory re- action at the seat of the bite, she developed and ran a long course of tryanosomatic fever. After a year and a half to two years of remittent attacks of fever, the organisms being found in the blood repeatedly, she grew weaker, became somnolent and died in a comatose condition. The anatomic changes at autopsy were typical of sleeping sick- ness. Some who are not quite willing to accept the Sickness. The Parasite. 490 IXFECTION AM) IMMU^'ITY. unity of the two diseases suggest that the sleeping sickness may have been superimposed on trypann- matic fever. Assuming that the two conditions represent dif- ferent stages of the same disease, we would have to recognize trypanosomatic fever as the first stage and the letharg}^ of sleeping sickness as the second. If this proves to be correct the name of T. neprevi should be retained for the organism and the other names dropped (T. gamhicnse, T. hominis, T. castellani) . It is believed that T. castellani is a distinct species of trypanosome. It is hardly possible to as- sociate it "s\dth nagana, since sleeping sickness and nagana do not coincide in their distribution, and, moreover, the morphology and pathogenicity of T. castellani differ from that of T. hrucei. The former is not infectious for the "donkey, ox, guinea-pig, dog, pup, goat and sheep" (Kuata). T. castellani is from 18 to 25 microns long and 2 to 2.5 broad. Its morphology in general is like that of other trypanosomes, although there are sufficient differences to establish its independence. Its motility is rather slow, and in contrast to other trypanosomes it moves in the direction of its non- flagellated end. The failure to find any distinc- tive difference between this organism and T. neprevi (T. gamhiense) is an additional point in favor of the unity of trypanosomiasis fever and sleeping sickness. TRYPAXOSOMIASIS IN" ANIMALS. On account of the prevailing general interest in the subject, the more important trypanosomatic infections in animals and the corresponding parasites will be sketched briefly. TRYPANOSOMIA HIH. 491 Musgrave and Clegg speak of certain general symp- toms which are common to surra, nagana, nuil do cederan and dourine, as follows: "After an incubation period, which varies in the same class of animals and in those of different species as well as with the conditions of infec- tion, and during which the animal remains perfectly well, the first symptom to be noticed is a rise of tem- perature, and for some days a remittent or intermittent fever may be the only evidence of illness. Later on the animal becomes somewhat stupid; watery catarrhal dis- charges from the nose and eyes appear; the hair becomes somewhat roughened and falls out in places. Finally the catarrhal discharges become more profuse and the secretion more tenacious and even purulent; edema of the genitals and dependent parts appears; a staggering gait, particularly of the hind parts, comes on and is fol- lowed by death." The incubation period varies from a few to several days. Pronounced anemia develops, the method of de- struction of the erythrocytes being unknown. Lymphatic enlargement is the rule, and during the incubation period the parasites probably undergo great proliferation in the lymph glands. It is somewhat characteristic that mas- sive invasion of the blood stream occurs periodically. With a paryoxism of fever their numbers increase in the blood, and during the intermission they decrease and may be so few as not to be found microscopically. Even when few or no parasites are found in the circulation, however, the blood usually is infectious for other ani- mals. During the intermissions it is possible that they are largely within the lymph glands or other internal organs. The cause of these variations is not known, and it can not be said now that they are related to cycles of development like those of the malarial parasites. Voges suggests that they may represent the establishment of successive periods of temporary immunity (mal de cederas ) . These are only general features, and varia- tions occur in infections in different animals and by dif- ferent parasites. Trypanosoma lewisi, recognized in the blood of the rat by Lewis in 1879, and given its present name by Kent in 1882, infects wild rats throughout the world, and in some localities a very high percentage of the animals are General Symp- tomatology. Infectiousness of Blood. Trypanosomia- sis of Rats. 492 INFECTIOX AM) IMMUNITY. infected. Tlie parasite is readily found in the peripheral blood (as from tl\e tail), where a large number may be present in a single held of the microscope ; sometimes, however, prolonged search is necessary for their discov- ery. Its dimensions vary: 1.4 to 3 microns in diameter, 10 to 2.'5 microns in length, according to dill'crcnt ol)s('rv- ers. It is of lancct-forni. possesses a hnley granular cndo- plasm and a clear ectoplasm, and from the latter spring the ilagcllum and the undulating membrane. "The for- mer (llagcllum) is about as long as the body itself; it originates at the posterior end of the animal in a grannie-like structure, called the llagellar root, extends forward as a marginal thickening of the undulating membrane and becomes free only at the anterior end of the animal from which it extends into the surrounding medium as a flagellum" (Doflein). At its posterior ex- tremity the parasite ends in a sharp point. In its an- terior portion it contains a strongly staining nucleus; a contractile vacuole is not described. Its motility is, per- haps, more active than that of any other trypanosome, and in a fresh mount of rat's blood it may move across the field so rapidly as to be followed with difficulty. Division takes place by longitudinal fission (rarely transverse), and by repeated division rosettes are formed. Cultivation. No\^ and McXeal succeeded in cultivating this organ- ism artificially on a medium consisting of rabbit's blood, 2 parts, agar, 1 part. The growth occurs in the con- densation fluid, and the organisms were carried through many generations. In cultures they vary greatly in size ( from 1 to GO microns in length ) . "The existence of the small forms accounts for the fact that we have repeat- edly been able to infect rats with Berkefeld filtrates of such cultures." It is remarkable that so many of the rats which harbor the parasites appear to be perfectly healthy. However, the animals not infrequently die from the infection, and in some instances fairly severe epidemics have been noted. The infection is found also in the hamster, a European rodent, and in white rats. \'\liite mice are susceptible to inoculation (Doflein). Trypanosoma britcei, found by Bruce in 1894 in the blood of animals suffering from nagana or the tsetse-fly disease, in Zululand, is somewhat different morphologi- TRYPANOHOMIAHIH. 493 cally from T. lewisi, being more worm-like in form, hav- Nagana. ing a blunt posterior extremity, less motility and greater pathogenicity. "The undulating membrane is broader and more plicate, the protoplasm colors more easily and more deeply" than in T. lewisi. Its length is said to vary, depending on the animal which harbors it, being largest in the rat and shorter and thicker in the dog. Its dimensions as given by Laveran and Mesnil are 1 to \Y2. by 26 to 27 microns. Its structure is similar to that of T. lewisi, containing a nucleus near the middle of the body and a deeply staining centrosome in the posterior portion in or near which the flagellum has its origin. A contractile vacuole lies anterior to the centrosome. Natural infection (nagana) with this organism occurs in horses, cattle, mules, and also in some wild animals, as camels, buffaloes and hyenas. It is, however, a tropi- cal disease, occurring chiefly in various parts of South Africa. Nearly all animals are susceptible to artifi- cial infection by the injection of diseased blood. The distribution of nagana corresponds with the dis- tsetse tribution of the tsetse-fly, and Bruce discovered that this Fly. fly, after feeding on the blood of an infected animal, transfers the disease to others by biting. Horses, asses, cattle and hogs were infected artiflcially in this way, but man appears not to be susceptible. It is assumed, but perhaps not definitely proved, that no other fly or insect transmits the disease. Immediately after it has fed on infected blood it is capable of transferring the disease; hence, further development of the parasite in the tsetse- fly is not essential for its continued infectiousness, and, indeed, it is not certain that any further development occurs. Nagana presents a remittent or intermittent type of fever, catarrhal secretion from the nose and eyes, sub- cutaneous edema, particularly of the abdominal region, prepuce and posterior extremities, roughening and shed- ding of the hair, marked emaciation, weakness and ane- mia develop, and the animal dies in a state of exhaus- tion. The spleen is greatly swollen, the red corpuscles are diminished in number, and the urine may be blood stained. The parasites are found in enormous numbers in the blood. The disease is almost invariably fatal. It may last 494 /.V/'A'('77(>.V .1\7> / 1/1/ r\ /'/■)". for weeks or months in horses, and even much longer in cattle. It occurs not infrequently in epidemic form, wiping out the horses and cattle of infected regions. In wild animals it is suggested that the disease may be more chronic, and the shifting of siicli animals may serve to introduce the infection to new regions, but only to such regions as harbor the tsetse-fly. Cultivation. Now and McNeal cultivate T. brucei on a medium similar to that used for T. leioisi. The former is more exacting in its conditions for growth, preferring a me- dium containing blood and agar in a ratio of two to one or three to one. Cultures were kept alive for at least one hundred days through eight generations, although virulence was soon lost. Surra. Trypanosoma evansi is the name given by Steele to a parasite discovered by Evans (1880), in India, in the blood of horses suffering from surra. It has the same general morphologic features as T. brucei, with dimen- sions of 1 to 3.5 or 4 microns by 20 to 35 microns, in- cluding the flagellum ( Musgrave and Clegg ) . It con- tains a nucleus and possibly a contractile vacuole. The whole posterior extremity is contractile, according to Musgrave and Clegg, and this may also be true of other trypanosomes. Its motility is moderate and eel-like. It differs from the trypanosome of rats (T. leicisi) in its larger diameter and in its greater pathogenicity; T. evansi is pathogenic for "nearly all animals." It is longer than T. brucei. Surra affects horses chiefly, and has caused immense losses in India and in the Philippine Islands. In India it is certainly transmitted by certain flies, and the same probably is true in the Philippines. Musgrave and Clegg demonstrated also that fleas may be of great importance as carriers. By this means they were able to transfer the disease from dog to dog, rat to rat, and rat to dog. They frequently found the parasites in native rats and believe that this animal may serve as a host in which the disease is maintained. Cattle are susceptible to infec- tion, but the disease is less malignant in them and runs a long course; hence, they may be an important factor in maintaining an epidemic. The disease is also trans- mitted from horse to horse. In India, camels, elephants TliVrANOSOlMIAHIH. 495 and buffaloes also suffor from the disease. Surra resem- bles nagana in its clinical and anatomic aspects. Doflein gave the name of Trypanosoma equiperdum to Q^^fi^^ an organism described by Rouget in horses and asses suffering from dourine. Laveran and Mesnil call it T. rougetii. According to Rouget, the parasite resembles T. brucei closely. Doflein ( 1901 ) states that a nucleus and vacuole have not been seen. Dourine occurs in Algiers, southern France, Navarre and in the Pyrenees districts of France and Spain. The infection is trans- mitted by coitus and is limited largely to animals which are used for breeding. Ulcerations, particularly of the genitals, are characteristic. That it is not transmitted by insects may be due to the absence of suitable insects from these localities. The identity of dourine vpith surra or nagana is not yet determined. It is said to be more chronic than surra. Doflein recognizes the organ- ism as an independent parasite. Infection may be trans- ferred to dogs, white mice and other animals. Trypanosoma equinum (Voges) or T. elmassianii is Mai de the parasite found in mal de cederas, a disease of horses Cederas. in South America, resembling surra, nagana and dourine. Two different species have been found in the blood of infections of South African cattle: T. theileri (Bruce, 1902) and T. Other Animals transvaaliense (Laveran and Mesnil, 1902). The char- acteristic feature of the latter is the location of the centrosome near the nucleus near the center of the para- site. The following trypanosomes are found in fish: T. cohitis, T. carassii, T. remaJcii, T. solecB, T. borrelUi; the folloAving in birds: T. avium, T. eberthii. T. balbianii occvirs in oysters, T. rotatorium in frogs. Between various animals and the different try- immunity panosomes a number of exainples of natural im- munit}^ are known. The extent to which man is susceptible to sleeping sickness is not known, but since the disease may occur in Europeans as well as in native Africans, it is probable that suscepti- bility is general. Laveran and Mesnil state that sheep, deer and cattle which have recovered from nagana have an active immunity to the disease, 4!)G IM'KCTfOX AM) niMlMTY. • and it is thought that tlio imiminity of some ani- mals (e, g., cow) may be increased by injecting infected blood. Koch, and also Schilling, have at- tempted to render trypanosomas suitable for vacci- nation by passing them through asses, and a cer- tain degree of success was reported. The serums of actively immunized animals do not exert a pro- nounced protective or curative action, although they may in some instances j^rolong the incubation j)6riod. Human serum has a certain protective and curative power for rats and mice which have been inoculated with the parasite of nagana. In some instances immune and normal serums kill trypanosomes, as shown by rapid loss of mobility. 'Trypanroth." A most interesting bit of experimental therapy is that of Ehrlich and Sachs in curing and pro- tecting mice against mal de ccderas by injecting and feeding "trypanroth," a sj-nthetic dye. The dye was less efficient in experimental nagana and in trypanosomatic infections of rats, guinea-pigs and dogs. Among hundreds of other dye-stuffs no other was effective. The immunity and cure established in this way is very temporary and is to be referred to a reaction caused in the body rather than to a direct effect on the parasites.. The latter are not killed by the dye in test-tube experi- ments. "One may conceive of the action of try- panroth in this way, that as a result of a fresh injection of the dye a reaction takes place in the animal's body, which leads to the death of the trypanosomes; the reaction products possess only a temporary character and cease to be formed as soon as the dye is disposed of." Laveran reports a favorable influence on try- panosomiasis in mice and rats by a combined treat- ment with sodium arsenite and "trypanroth." PYROPLAmiOHlH. 497 Spontaneous agglutination and agglutination by normal and immune serums have been described. At the present time agglutination is of no value from the standpoint of diagnosis, III. ''spotted fever" of the rocky MOUNTAIN" STATES. In the valley of the Bitter Eoot Eiver of Mon- tana, and in certain sections of Idaho, Wyoming and Washington an acute febrile disease, known in those localities as sjootted fever, is encountered in the spring months. The disease is defined by Maxey as "an acute, endemic, non-contagious, Irat probably infectious, febrile disease, characterized clinically by a continuous moderately high fever, severe arthritic and muscular pains, and a pro- fuse petechial or purpural eruption in the skin, appearing first on the ankles, wrists and forehead, but rapidly spreading to all parts of the body." (Cited by Stiles.) In 1902-03, Wilson and Chowning studied many cases of the disease in Montana, and described as the cause a protozoon organism which they con- sider as a pyroplasma {Pyroplasma liominis). The organism is a hematozoon, occurring within the erythrocytes. Young cells resemble the "hyaline bodies" of malaria, are of ovoid shape, 1 micron thick and 1 to 2 microns long, and usually occur in pairs, but sometimes in numbers of 4 to 16, within an erythrocyte. The smaller ends of pairs often are directed toward each other, and they may be connected by a fine filament. They occur both in the red corpuscles and in the plasma. As they grow larger, two to three by three to five microns, only one parasite usually is found within an ery- throcyte, and in this stage they show active ame- Limited Occurrence. Pyroplasma Homfnis. 498 INFECTIOX AXD IMMUNITY. Transmission by Ticks. Intermediate Host. bold movement with tlic formation of pseudopodia. Eventually they assume a spherical form in fresh preparations, 'i'hey ^vere al)le to transfer the in- fection to rabbits by tlie inoculation of infected blood. After identifying the oi'ganisni as a pyroplasma and having in mind the part that ticks play in the transmission of Texas fever, and perhaps pyroplas- niosis in other animals (horse, sheep, dog), Wilson and Cho\vning directed their attention to the ques- tion of tick bites in those who become infected. It developed that of the 23 cases examined in 1903 all had been bitten by ticlcs, and fourteen had been bitten in from two to eight days before the onset of the disease. They concluded that the disease is transmitted in this manner. They also searched for some other host than man, in which the parasites might flourish contin- uously and constitute a source of infection for the ticks. This tliey believe was found in a certain gopher {Spcnnophilus columhianus) . On the west side of the river — that side in which the disease attacks man — they found the erythrocytes of about 20 per cent, of the gophers infected with a parasite similar to that found in man. On the other hand, the blood of sixty-two gophers from the uninfected side of the river showed no parasites. "Early in the spring the spermophile is said to harbor great numbers of ticks." Similar parasites Avere found in no other species of animals. Stiles, in later investigations, could not confirm the results of Wilson and Chowning, being unable either to find the parasites which they described in man, or to accept the tick-gopher hypothesis. Fur- ther investigation of this disease is needed. PYR0PLASM08I&. 49!) The Parasite. TEXAS FEVER. Texas fever of cattle may be considered briefly as a well-established example of pyroplasmosis. Th. Smith and Kilbourne (1893) discovered a pear- shaped protozoon (Pyroplasma bovis) , which occurs in pairs in the erythrocytes of infected cattle. The para- site measures from 2 to 4 microns long by 1.5 to 2 microns broad, the smaller ends of the pairs lying in apposition. The organisms have a rapid but rather coarse ameboid movement. About 1 per cent of the corpuscles are invaded ordinarily, but in fatal cases the proportion may rise from 5 to 10 per cent. The method of prolifera- tion of the parasite has not been followed out definitely. According to Smith and Kilbourne, numerous minute motile forms (coccus-like bodies) penetrate the corpus- cles and eventually reach the pear-shaped form. The breaking up of the adult pear-shaped parasites into such small forms has not been observed. A characteristic symptom of Texas fever is the pro- nounced hemoglobinuria which has given to the disease the additional name of hemoglobinuric fever. The disease is transmitted by means of a tick (Boophi- lus hovis) . The six-legged larvae fill themselves with blood, and in about eight days have been changed into eight-legged nymphse. In eight days more they have changed into fully-formed sexual animals, and, after filling themselves with blood and after having been im- pregnated, they drop off the cattle and lay their eggs. The eggs in from 3 to 4 weeks have again gro\vn into larvse, which are then ready to attach themselves to cattle ( cited from Kossel ) . Inasmuch as infected ticks transmit the parasites to their offspring, the bites of the larvse are able to give rise to the disease in cattle. A mature tick may deposit from 2,000 to 4,000 eggs. It has not been possible to transmit the disease to other species. The disease is endemic in the southwestern states, Transmission and the cattle in that region are supposed to acquire an immunity similar to that described by Koch in relation to malaria. Presumably the cattle first acquire the dis- ease when they are young, and those which withstand it show resistance to the infection in later life. Cattle 500 INFECTION AND IMMrXITY. from uninfected districts are more susceptible than those coming from localities in which the disease is endemic, and the latter even when apparently healthy may intro- duce the disease into new herds. This is done through transportation of the ticks. Partialh' successful attempts at active immunization have been made, and in Australia this is practiced on a fairly extensive scale. Five to ten cubic centimers of blood, taken from an infected animal, during the course of the disease or after recovery has been established, are injected into non-immune cattle. The disease is thereby reproduced in the latter with typical parasites in the blood. If the blood is taken from animals which have recovered, a milder infection results than when the blood of an actively infected animal is used (Pound, cited by Kossel). The resulting immunity is not an absolute one, however, and the percentage of mortality is fairly high. According to Dodson, the serum of animals which have completely recovered has no protective power for other animals. For prophylaxis it is important to free the cattle from ticks (as by an oil bath) and to avoid infected fields. If cattle are kept from an infected pasture for two years, the ticks die out very largely (Morgan). IV. AMEBIC DYSENTERY. Amebae. Aiiieba? ai'c uiiiccUular animal organisms -whiL-li contain one or more nuclei, a "contractile" vacuole. a granular endoplasm and a tougher more hyaline ectoplasm, having the power of locomotion by means of pseudopodia or by a gradual flowing for- ward of the cytoplasm. They nourish themselves by digesting bacteria and other lower organisms or solid particles of decaying matter, which they in- gest after the manner of phagocytes. They pro- liferate by division of an adult cell into two daugh- ter cells, and certain of them reach a cystic stage in which hundreds of endospores are formed {A.meha proteus). Some of them utilize higher animals as hosts only occasionally, while others AMEBIC DYSENTERY. 501 are known only as parasites. They frequently are encountered in the intestines of mice, frogs and other animals. Amebge are widely distriljuted in nature, exist- Distribution. ing to the depth of 3 meters in tropical soils, in the water of springs and wells and practically all surface waters (hot countries), and in stagnant or sluggish waters in higher altitudes. They exist on hay, fruits and vegetables of all kinds, especially those grown on or near the earth; e. g., beets and lettuce. Encystation takes place under certain unfavor- Resistance. able conditions, and in this condition the parasites "withstand a temperature of — 15° C. for twenty- five days (Musgrave and Clegg), and desiccation for ten to fifteen months. A temperature of 50° C. kills the vegetative and encysted forms. Sunlight for three hours and the a;-ray kill them readily in the vegetative form, but not so readily when they are encysted. Most chemical bactericides destroy them, although they show a particular resistance to alkalies, even 20 per cent. ISTaOH (Frosch), and strong acids. They resist the action of 0.3 per cent. HCl, i. e., the acidity of the stomach con- tents. Quinin (1/3500 of the hydrochlorate) is strongly germicidal for Ameha coU. Under artificial conditions amebse proliferate Cultivation. in the presence of other micro-organisms, and suitable mixtures they may be kept alive in- definitely on slightly alkaline bouillon agar. The only condition in which ameba are found unassociated with bacteria is in the liver ab- scesses which occur as a complication of amebic dysentery. It is true that the bacteria may have been present original^, but in their absence it is 502 IXFECriON AND IMMUNITY. supposed tliat onzvines noniially present in the liver stimulate the growth ami proliferation of the parasites. Amebae show a peculiar selective property for certain bacteria, although tiieir affinities may be gradually moililled. Aincba coU apparently pre- fers those organisms which Hourish in the human intestines (B. coll, B. typhosus, Sp. cholerce, Staph, pyog. aureus). Almost any strain will, however, grow with a variety of bacteria. Growth occurs only on the surface of the agar plates. When a pure strain of ameba is grown with a single species of bacterium the culture is spoken of as a "pure mixed culture." Amebic dysentery is primarily a disease of the tropics, where the natural conditions are favorable for the growth of the amebae and their conveyance to man. First found by Lambl (18G0), then by Cunning- ham and Lewis (1870), the organisms were de- scribed more accurately and given the name of Ameba coli by Losch (1875). Losch recognized them as the cause of a chronic form of dysentery, but it was Kartulis, in particular, who found the amebte constantly in the discharges and ulcers of the disease, and also in the liver abscesses which accompany the infection. Since ameba? demand the presence of living bacteria for their growth. Pathogenicity, their independent pathogenic nature has been ques- tioned by many who assume that the bacteria are the primary agents in causing the intestinal lesions and that the amebae are only incidental or second- ary factors. Many others, and particularly Mus- ■ grave and Clegg, consider that amebae have essen- tial pathogenic properties and are the primary agents in producing ameljic dysentery. By the feeding of encvsted cultures grown with other or- Ameba Coli. AMEBIC DYSENTERY. 503 ganisms, Musgravc and Clegg reproduced the dis- ease, typically in many monkeys. In one instance the amebse were fed in conjunction with cholera vibrios; typical dysentery developed and during the course of the disease the vibrios disappeared from the stools. The vibrio alone proved to be non-pathogenic Avhen fed to monkeys, and on this account they held the amebte to be the sole cause of the dysentery. The principal lesions occur in the large intes- tine, in which are found round or oval ulcers with infiltrated or undermined edges. The ulcers may increase in size, or coalesce with others, and cause the sloughing of large areas of the mucosa or even of the muscular coats. The organisms are found in the intestinal contents, on the surface of the ulcers, in the infiltrated base and edges, and in the underlying tissues. They have been found as- sociated with both chronic and acute appendi- citis. Amebic liver abscesses are not infrequent in those regions in which the disease is endemic. The organisms probably extend to the liver from the intestines through the lymphatic or portal vessels. Not infrequently the association of the amebae with bacteria is missed in the abscesses, and in these instances a "cold^' abscess containing much necrotic material and detritus is produced. If contaminated with bacteria the abscesses have a more purulent character. Suitalale prophylaxis against amebic infection is suggested by the known distribution of these or- ganisms. Of principal importance is the use of fil- tered or boiled waters and the avoidance of un- cooked vegetables in regions in which the disease is endemic, as in the Philippine Islands. Lesions Prophylaxis 504 IXFECTIOX AXD niMVMTY. inim«nity. Froiii thc fact tliat foreigners going into tropical countries are more susceptible to infection than the natives, it is concluded that the latter have some natural (or acquired) inuuuuity to the disease. Children are said to be less susceptible than adults and in them the disease yields to treatment more easily. There is no serum therapy for the infec- tions. The salts of quinin in strengths of 1-1500 to 1-750 are aiuebieidal Avlion injected into the colon. V. SAHCOSrORIDIA. Morphology. Sarcosporidia are unicellular parasites which are found within the muscle cells of some animals, but very rarely in man. They are more or less tubular or oval in shape and are frequently referred to as Miescher's tubules. Their size varies greatly and certain species may reach a length of two centi- meters. When well developed they possess two capsules — a dense outer capsule, which is perfor- ated with minute canals (?) directed toward the center of the parasite, and an inner thin hyalin membrane. Both represent differentiated ecto- plasm (Doflein). The endoplasm, even in young cells, gives rise to numerous small nucleated spheres (pansporoblasts), which increase in size and each of which eventually becomes multinu- cleated and forms numerous kidney or sickle- shaped, nucleated sporoblasts. Each sporoblast finally gives rise or is changed into a well-charac- terized spore with a membrane and a nucleus. This process takes place first in the central part of the parasite, but eventually extends to the ends as well. The central part of the old parasites con- tains only the empty network of endoplasm, the /SM liCOHPORlblA. 505 spores having disappeared, and a section at this point strongly resembles that of a tubule. The parasites are nourished through osmosis. None of the forms have definite motility. When the parasite outgrows the muscle cell which con- tains it, it is freed and becomes an intercellular parasite. Rather vague references are made to tumor-like formation as a consequence. Sarcosporidia have been found only in verte- occurrence. brates, particularly in mammals; most often in sheep and hogs, but also in the horse, ox, mouse, rat. The muscles adjacent to the alimentary tract are involved principally (esophagus, intestines, diaphragm and abdominal muscles) and on this account it is supposed that infection takes place through the intestines. The exact method of in- oculation is not known. Sarcocystis lindemanni (Sarcocystis liominis or Gregarina lindemanni) is the only sarcosporidium definitely identified in man. The parasites were as large as 1.6 millimeters long and 170 microns broad. They possessed a thin capsule, thickened at the ends. The spores were banana-shaped and eight to nine microns long. The organisms were found in the muscles of the larynx. VI. BALANTIDIUM COLI. B. Co'li is an infusorian (ciliate), with a more or less oval body, mouth opening and a short pharynx, is covered rather uniformly with short cilia, and presents longitudinal striations. It con- tains a bean-shaped chief nucleus and a secondary nucleus and two vacuoles on the right side. It meas- ures 70-100 microns in length and 50-70 in breadth. Proliferation is through simple division. 506 INFECTION AXD IMMUNITY. ■ Conjuuation ha? beeu noted. Involution cysts are splierioal and surrounded b}' a dense membrane. Pathogenic The parasite is found in the intestines of the hog Significance, ^^g ^^.^^l as in num, and the former may be its nor- mal host. It occurs also in sewage waters and has been found in drinking water. Infections have been noted in those having nothing to do Avith hogs. The organisms may reach the intestines of man in an encapsulated state ( ?) . It is found in diar- rheal conditions in man rarel}^, and the question is still open as to wdiether the parasite is able to cause enteritis independently or whether it merely aggravates and prolongs an enteritis due to other causes. The cecum and colon show the principal changes at autopsy, and are of an inflammatory and ulcera- tive nature. A smaller species, B. minutuin, has also been oliserved in the intestines of man. VII. CERCOMONAS INTESTINALIS. Morphology. This Organism is small and colorless, the form spherical or oval. The single flagellum is for the most part very large and is situated at the anterior end (in the direction in which the parasite moves) ; the posterior end is long drawn out and is subject to changes in form. Sharp pseudopodia are sometimes formed. The nucleus lies in the anterior half of the body, and either here or on the sides are one or more vacuoles. A mouth opening is not differentiated, but at the base of the flagel- lum food is taken in at a particular point through a vacuole. Proliferation takes place through con- jugation, binary division and the formation of ■swarm spores (?) within encysted forms. They abound in fresli water and in infusions of 2:rasses. TRICHOMONAS. 507 The}' are not of great parasitic importance, al- significance, though cercomonas has been found in the intes- tines, especially in inflammatory conditions (chol- era, typhoid), in pulmonary gangrene, putrid plu- .ritis, and several forms have been observed in other animals. It is not yet certain that cercomonas may be an independent cause of enteritis. VIII. TRICHOMOISrAS. Eather small, of a general pear-shape, rounded Morphology. or pointed anterior end, and possessing three or four long flagella. When only three flagella are present an undulating membrane surrounds the body like a spiral beginning at the base of the flagella and may prolong itself into a flagellum. The posterior extremity is moderately pointed, a nucleus lies in the anterior end, and toward the posterior are several non-contractile vacuoles. Methods of proliferation unknown (Doflein). Two species are found in man. Trichomonas species. vaginalis: possesses three flagella and an undu- lating membrane, and is of large size (15-35 mi- crons in length). It is found in the vaginal mu- cus, when of acid reaction, in a large percentage of women (Dolflein), particularly in vaginal catarrhs. It disappears in an alkaline reaction. Trichomonas hominis s. intestinalis: also pos- sesses three flagella and an undulating membrane, but is smaller than T. vaginalis. It is found as a parasite in the human intestines, particularly in diarrheas (typhoid, cholera, mucous colitis, etc.,) .and inhabits especially the upper and middle por- tions of the intestines. It is evacuated in consid- eral numbers following administration of cathar- tics. It appears not to be of much pathogenic sig- 508 INFECTIOX A.\l> IMMUMTY. nilifanoo, but tiiuls in the liquid stools and in an alkaline reaction conditions ^vhich favor its prolif- eration. It may be transmitted as a contagion (Ejv^tein). Other Otlier species of trichomonas occur in the intes- riagellates. . n i-nc , ^ tines ot diiierent animals. Other less important flagellates are: Lamhlia intesiinalis, found in the intestines of many ani- mals and in man in Germany, Italy, Russia and Sweden; Bodo urinarius [Cystomonas urhiarius. Plagiomonas urinaria), found in the urine in cys- titis (Kiinstler). IX. COCCIDIOSIS. Coccidia are essentially cell parasites, preferring the epithelial cells of the intestines and liver, al- though they may be carried to other organs. They have an alternating asexual and sexual cycle of development. The 3'oung sickle-shaped and nu- cleated sporozoite penetrates an epithelial cell, grows in size, and the nucleus subdivides many times to form new young cells, which eventually escape again as sickle-shaped sporozoites. This asexual process is called schizogony. Several stages of schizogony may follow successively, but event- ually the organisms lose their proliferative power unless they are fortified by a sexual cycle. In the sexual cycle (sporogony) some of the sporozoites become differentiated into larger granular cells (female) and others into smaller cells (male). Of these two cells the male eventually divides into many flagellated microgametes, each of which is al)le to penetrate and fertilize a female cell (macro- gamete). The female cell then forms a capsule, becomes an oocyst, divides into sporoblasts, each of which eventually forms sickle-shaped spores, Life Cycles. L'OaCIIJIOHIH. oOO which when liberated are again called sporozoites. Several species are recognized, depending on the number of spores formed by the oocyst. In some instances the spore formation takes place in the outer world, and when the oocysts are ingested the sporozoites are liberated. Goccidvum cuniculi s. oviforme is a frequent parasite in the intestines and liver of the rabbit, occurs occasionally in the same organs in man from association with rabbits (?), and causes a hemor- rhagic dysentery in the cattle of some countries (Switzerland). Horses, goats and swine may also be infected. Spore formation takes place outside the host. The oocyst' is discharged in the feces and produces four spores, each of which forms two sporozoites. A new host is infected by the ingestion of spores. Diarrhea and emaciation result from infection of the intestines, and in the liver cheesy nodules (coccidia nodules) are formed, containing para- sites, degenerated cells and proliferated epithe- lium. A papillomatous proliferation of the epi- thelium of the bile passages and intestines may be produced. Coccidium higeminuriij a coccidium in which the oocyst divides into two spore-containing cysts, has been found in man several times. Species. Results of Infection. GROUP VI. DISEASES OF DOUBTFUL OR UXKXOWX ETIOLOGY. Negri. I. II ^■|>l;()l•lln|•,lA. Following the investigations of Pasteur, in which it was found that the virus of hydrophobia exists in the central nervous system in pure cul- ture, the conditions seemed favorable for the dis- covery of the specific agent. As in the case of many other diseases, various bacilli, cocci, yeasts and so-called 2>i'otozoa have been dcseriljcd as the cause, but satisfactory proof of their etiologic role has not been provided. Bodies of Among the recently described parasites ( ?) cer- tain protozoon-like bodies (Negri bodies) found by jSTegri in the ganglionic cells are of a suggestive nature. Their average diameter is about five mi- crons, l)ut it varies between one and twenty-seven microns. They possess a "round, oval, elliptical, or coarse triangular form" (Marx), are differen- tiaterl into a central granular and a peripheral structure and may be surrounded by a doubly- contoured membrane. Negri considers these bod- ies specific for hydrophobia and reliable as a basis for anatomic diagnosis. They are found particu- larly in the pyramidal cells in the cornu Ammonis, the cells of Purkinje in the cerebellum, and the large cells of the cerebral convolutions. Many oth- ers have confirmed the findings of Negri. Against the hypothesis that these bodies are the cause of hydrophobia, the following points are cited : The distribution of the Negri bodies does not corre- spond with the greatest concentration of the virus HYDROPHOBIA. 511 in the nervous tissue, the latter being most abun- dant in the medulla and pons where the Negri bodies are encountered rarely. They are not found invariably in animals dying of hydrophobia. They present certain analogies with "protoplasmic in- clusions" seen in other conditions, as in carcinoma, variola, etc. Eemlinger found that the virus passes through appropriate Berkefeld filters, and for this reason Schlider holds that the bodies of Negri, being too large for filtration, can not be considered as the specific organism. The view of Schlider may be criticized, since the smallest Negri bodies are so minute that their filtration would seem to be possible. Nevertheless, it must remain doubtful Avhether bodies one micron in di- ameter, the proliferation of which has not been proved, may be considered as parasites. The hy- pothesis of Negri is hardly on a satisfactory basis at present. Eemlinger considers the bodies as "involution forms" of the tissue cells which have been invaded by the true parasite. The filterability of the viriis argues for its mi- Fiiterabinty croscopic size. By means of filtration one may isolate it even from brains which are badly decom- posed, and the method renders it possible to ob- tain pure cultures for purposes of immunization. Inoculation Avith filtered virus is sometimes fol- lowed by a prolonged incubation period which may depend on the retention of many of the organisms by the filter. A similar effect was produced by Hogyes by inoculating with diluted virus. By prolonged centrifugation of an emulsion of infected nervous tissue the overlying fluid loses its infectiousness. The possibility that the organism secretes a sol- of Virus. 512 INFECTION AND IMMUNITY. Toxin, ublc toxin is inii)ortant from the stanilpoint of im- munization. A number of observers, particularly Babes, and Heller and Bertarelli, noted that fil- trates of infected nervous tissue sometimes cause emaciation, paralyses and eventual death witiiout producing a disease which is transmissible to other animals. The organism is without doubt toxic, but these results give us no idea of the nature of the toxin. Resistance The virus of hydrophobia as contained in the central nervous system of infected animals exhib- its strong resistance to chemical germicides. Five per cent, carbolic acid destroys it in fifty minutes, 1 per cent, in three hours, and 1-1000 corrosive sublimate in three hours (Marx). It resists the action of putrefactive bacteria, and has been found virulent in animals which had been buried for two to four weeks, even when the brain was putrid. Di- rect sunlight destroys it, however, in a very short time. According to Tizzoni and Bongiovanni, the rays of radium have a destructive action on the virus. It is less resistant to heat, being destroyed in one-half hour at a temperature of 52-58° C. (Hog5'es), but is not affected by the temperature of liquid air for three months. Chlorin destroys it very rapidly. It is gradually weakened by desiccation, as first shown by Pasteur, the virus probably undergoing gradual death rather than mere attenuation. It is said to be attenuated by the action of the gastric juice and by the bile. When the nervous tissue is emulsified in glycerin, virulence is retained for months (Eoux). On the other hand, glycerin appears to destroy the viru- lence of filtrates (Di Vestea). Pasteur gave the name of street virus {virus HYDROPHOBIA. 513 de rue) to that obtained from the nervous tissue of street _ - , Virus and dogs m which the disease develops spontaneously. Fixed virus. When the street virus is injected subdurally into the rabbit the latter develops hydrophobia only after an incubation period of from two to three weeks. If, however, this virus is passed from one rabbit to another, its virulence gradually increases until the incubation period decreases to six days. At this point it is called fixed virus {virus fixe), and its virulence can not be further increased. Passage through the cat, fox and wolf also in- creases virulence. On the other hand, by passing it repeatedly through the monkey (Pasteur), the chicken (Kraus) or the dog it becomes attenuated for the rabbit and virulence may be lost entirely. Although virus fixe represents its highest degree Low virulence £ ■ T £ m -i. XI f £ of Fixed Viru» ot Virulence lor rabbits, there is good reason lor for Man. believing that repeated passage through the rab- bit decreases the virulence of the virus for man. In other words, street virus is more infectious for man than fixed virus. This may to some extent ac- count for the success of the Pasteur treatment. Ferran, indeed, uses unaltered virus fixe for the protective inoculation of man. B}^ means of inoculation experiments the virus Distribution of m.ay be demonstrated invariably in the brain, Body.'" spinal cord, and usually in the salivary glands and saliva of animals which have died of the disease. These tissues are specifically affected, and the virus probably proliferates in thein. By one or another observer its presence in the following organs and excretions has been demonstrated : Suprarenal gland, lachrymal gland, vitreous humor, urine, tes- ticular secretion, lymph, milk, in the peripheral nerves and cerbrospinal fluid. Marx states that 514 INFECTIOy AXD ntMUMTY. it has not been J'ouml in the liver, spleen, blood and aqueous Ininioi-. C'ounnont and Xicolas found it, however, in the aqueous liumor of rabbits after death. The possibility of postmortem invasion of this fluid has been suggested. It has been found occasionally in human saliva during life, and at the site of the wound following death (Pace). Means of Hydroplioljia is transiiiilted almost exclusively by the bites of infected animals, the virus being conveyed in the saliva. Accidental inoculation may occur in handling infected tissues. The virus does not penetrate the intact skin, and it is customary to consider a bite as harmless unless the continuity of the skin is broken. Experimentally, infection has been caused by placing the virus on the mu- cous membranes of the conjunctiva, nose and mouth, in the absence of discernible lesions. Pace mentions a man who contracted the disease after his rabid dog had inserted the tip of its tongue in his (the patient's) nose. But one authentic ex- ample of transmission from man to man is found in medical literature. This occurred through kiss- ing or biting, during coitus. In rare instances it seems to have been transmitted from the mother to the fetus in rabbits. The dog is the most common carrier of hydro- phobia. In some countries (Russia, Hungary) rabid wolves cause many infections. The disease has been conveyed by the bite of tlie cat, mouse and horse. and possibly by the skunk in some of our western states. The dog is. however, the natural host of the parasite, and either by his bite or by experi- mental inoculation practically all animals, at least mammalians, may be infected. The incubation period in animals varies from HYDROPHOBIA. 515 two weeks to several montlis. In man it varies between twenty and sixty days usually, but may be as short. as seven or ten days, or as long as twenty months (rare). In children it is shorter than in adults. The location of the bite is also of impor- tance in determining the length of incubation. It is shortest following wounds of the head and neck, somewhat longer when the injury is in the hand or arm, and still longer when in other parts of the body. The degree of laceration is also a factor, de- pending possibly on the introduction of largei; quantities of virus, and on larger surfaces for its absorption. The bite of the wolf is said to be most virulent, and next in virulence is the bite of the cat and dog. Not all who are bitten by rabid animals develop hydrophobia. Correct figures on this point are dif- ficult to obtain, since in many instances the ani- mals are only suspected of being rabid. According to Hogyes, 15 to 16 per cent, of those who are bit- ten contract hydrophobia. The percentage is much higher following bites by the wolf. The disease is invariably fatal to man. The symptoms of hydrophobia in man differ in no essential respects from those seen in animals. The immediate determination of hydrophobia in dogs which have bitten man is of the greatest importance. In many instances the behavior of the animal is sufficiently characteristic to justify clin- ical diagnosis of the disease. The disposition of the animal changes suddenly, it ceases to play, eats various indigestible substances, as glass, iron and wood, utters pathognomonic (?) long-drawn-out howls, may become ferocious, or, on the • other hand, quiet and sullen. At autopsy the meninges Incubation Period. Diagnosis in Dogs. olti l\J'j:rTI().\ AM) IMMIMTY. and iKTvous tissue are congested il' tlie disease is advanced, and the indigestible mentioned sub- stances may be found in the stomach, although the latter finding has little or no diagnostic importance. So-called ^ number of histologic changes have been de- Spcciic Lesions, scribcd as characteristic. Among these are the bodies of Negri, described above. Remlinger at- taches a great deal of importance to them as a means of diagnosis. Babes describes perivascular nodules of lymphoid cells (Wutknotchen) in the medulla and cord. The lesion of Van Geliuchten consists of a proliferation of the endothelial cells (neuronophages) surrounding the ganglionic cells, the latter at the same time undergoing atrophic and degenerative changes. This change is most marked in the cervical ganglia. One group of ob- servers finds these lesions constant in animals ■which have died of hydrophobia, but they may be absent if the animal is killed during the course of the disease; hence their absence does not exclude the diagnosis of hydrophobia. Others have found similar changes in other diseases. Metchnikoff, it will be remembered, observed the destruction of ganglionic cells, by neuronophages in aged dogs (page 179). We are hardly able at present to consider these changes as pathognomonic. Particularly in early stages of the disease they may be absent. The bite of a rabid dog is infectious in from two to four days in advance of the development of symptoms, and autopsy performed at this time may show neither gross nor microscopic changes which are characteristic. In communities in which hydro- phobia is known to be endemic, all cases of dog bite accompanied by penetration of the skin should re- ceive the Pasteur treatment. HY nun I' no HI A. 517 A great deal of experimental work wliich can not Eyiensipn be given in detail snows conclusively that the virus Nerves. is conveyed to the central nervous system by means of the peripheral nerves. The conditions then arc similar to those in tetanus with this exception : In hydrophobia the living virus reaches the central nervous system^ whereas in tetanus the bacilli re- main at the site of the wound. This condition ex- plains the shorter incubation period in hydropho- bia, as in tetanus, when the infection atrium is near the central nervous system (e. g., face). When the infection is introduced into any particular part of the body surface, the virus is first demon- strable in the corresponding segment of the cen- tral nervous system. Although transmission by the nerves is the rule, infection may be accom- plished in rabbits by intravascular injection. On the whole, however, infection is closely associated with the wounding of nerves. It has indeed been shown that if wounding of nerves is. entirely avoided, as in intraperitoneal injections into rab- hits (Marx) the full virulent nervou^s tissue may be used for immunization. A single injection of a large quantity brought about immunity in twelve days. The muzzling of dogs is a general prophylactic Prophylaxis. measure, which should be enforced in communities in which hydrophobia is known to occur. No mat- ter how thoroughly the cauterization and antisep- tic treatment of wounds is carried out it can in no case be depended on to destroy the virus. Even within five minutes the virus may be carried to a point which is beyond the reach of the cautery. In spite of this fact, however, cauterization should not be neglected, even when the Pasteur treatment 518 IXFECTIOX AM> IMMiMTY. Preparation of \irus for Pas- teur Treat- ment. Teclinic of Treatment. can be instituted at once. Tiie greater tlie quantity of virus introduced by the bite the shorter will be the incubation period, and there is good reason to believe that cauterization (actual cautery) prop- erly carried out destroys a sufficient amount of virus to prolong the incubation period. A long incubation period is greatly in favor of the success of the Pasteur treatment. Pasteur's first protective inoculations were car- ried out with virus which had been attenuated by passage through the monkey. The virus fixe ob- tained from the rabbit, as described above, was soon substituted for that of the monkey. In order that an antirabic institute may continuously have on hand a sufficient amount of vaccine,, it is neces- sary to inoculate two or three rabbits daily. For this purpose an emulsion of the medulla of a rab- bit which has died of hydrophobia is inoculated be- neath the dura mater. A short time before the animals would die of the disease, they are killed by bleeding, and the spinal cords removed with all ]')0ssiblc precautions for asepsis. Each cord is cut into two parts and each part suspended in a prop- erly constructed jar which contains solid potas- sium hydrate. After the jar is sealed desiccation is allowed to proceed for fourteen days, at the end of which time the infectiousness of the tissue has so decreased that it is suitable for the first injec- tion. The vaccine should be free from bacteria. As is well Icno-wn, the Pasteur prophylactic treatment consists of the subcutaneous injection on successive days, of suitable quantities of vims fixe, prepared as described above, beginning with the cord which has been desiccated for fourteen davs and graduallv usine: fresher cord? until viru- HYDROPHOBIA. 519 lent virus lias been inoculated. The vaccine is jjre- pared for use by emulsifying one centimeter of a cord in 5 c.c. of salt solution or some "artificial serum," and in a single treatment from 1 to 3 c.c. of this emulsion is injected, usually into the sub- cutaneous tissue of the anterior abdominal wall. In this region there is less likelihood of injuring large nerves, and local complications, which, how- ever, occur rarely, are of less consequence. The rapidity with which one should pass from the fourteen-day cord to fresh virus depends on the urgency of the case. When there is good reason to suspect a short incubation period, or when some days have followed the bite an "intensive" treat- ment should be used ; in other cases the progression may be slower. The following conditions augur a short incubation period : Bites of children, who are more susceptible than adults, and in whom the injuries usually are on the face; bites on the face and neck in all cases; lacerated wounds in which there is a larger surface for absorption of the virus. The influence which proper cauteriza- tion exerts on the incubation period was mentioned above. The table on page 520, taken from Marx, illus- trates a "light" and an "intensive" treatment. This scheme is variously modified in different institutes, especially in the direction of a more rapid progression to virulent material. Other methods of attentuation are also used, as of^er ,1 o Ti • TT 1 ■ 1 • p p ^ Means of the lollowmg: Heating emulsions of fresh virus Attenuation. at 58° C. for different lengths of time, or at dif- ferent temperatures (80° to 30° C.) for ten min- utes (Babes-Puscari) ; digestion of virus with nat- ural or artificial gastric juice (Tizzoni and Cen- 520 INFECTION AND IMMUNITY. tanui) ; the use of fresh but very dilute virus (Hi)gyes). Ferran, in Barcelona, inoculates man with the fresh unaltered virus fixe, and in nearly 3,000 cases but two cases of hydrophobia devel- oped. This indicates clearly the low infectious- ness of virus fixe for man. Light. Intensive. Day of Age of Amount of Day of Age of Amount of Treat- Dried Cord Emulsion Treat- Dried Cord Emulsion ment. iu Days. Injected. ment. iu Days. Injected. 1 ~v 14 3 7^ 3 13 3 1 J 13 3 *> j 12 3 112 3 11 3 111 3 3 10 9 3 3 2 I? 3 3 4 • 8 7 3 3 3 3 5 . 6 6 2 2 3 \l 2 6 5 9 i 5 2 7 ") 2 5 5 2 8 4 2 6 4 2 9 3 1 7 3 1 10 5 2 8 4 2 11 5 2 9 3 1 12 4 2 10 5 2 13 4 9 11 5 2 14 3 2 12 4 9 15 3 9 13 4 2 16 5 2 14 3 9 17 4 2 15 3 2 18 3 2 16 5 2 17 4 2 18 3 9 19 5 2 20 4 2 21 3 2 It seems unnecessary at this date to quote sta- tistics to show the value of the Pasteur treatment. Observations indicate that immunity is not fully established until about fourteen days after the completion of the treatment, and in a certain num- ber of cases the disease develops before this time has passed. The number of deaths after this pe- riod is exceedingly small and has grown less with HYDRO/'flO/ifA. 521 improved technic. In 188G the number of deaths which occurred after fifteen days had passed amounted to 0.94 per cent.; in 1902 to 0.18 per cent. The immunity established by the Pasteur treat- immunity and ment is^ in all probability, antimicrobic in nature, enies. The serum of both man and animals, after immun- ization, is able to destroy the infectiousness of rabic nervous tissue, i. e., the serum is rabicidal (Babes and Lepp, 1889). The technic of Kraus and his co-laborers is well adapted to show the rabi- cidal properties of the immune serum. Eabid ner- vous tissue is made into an emulsion with salt solution in a dilution of 1-100, and then filtered through paper to remove coarse particles of tissue. To quantities of 0.5 to 1.0 c.c. of this emulsion varying amounts of fresh immune serum are added, and after eighteen hours' contact the mixtures are injected into rabbits to determine the degree of infectiousness. Small quantities of rabicidal sub- stance may be detected in this way. Natural resistance to hydrophobia does not go hand in hand with the antirabic power of an ani- mal's serum. Old pigeons, for example, develop the disease following intracerebral injection of the vims, although their serum is not rabicidal. Babes and Lepp also showed that the immune serum has protective powers which are analogous in their efficiency with those of bactericidal serums. Babes advocates and practices the mixed method of immunization in severe cases, immune serum be- ing injected in addition to the virus. The serum has little or no curative value. IM'KCTIO.S AXD IMMUNITY. II. SYPHILIS. H>potheticai It is iiiipossililo ill iliis place to describe or even mention tlie niany cocci, bacteria and protozoa (?) wliic-h liave been brougbt into etiologic relationship witli syphilis. Until very recent times the bacil- lus of Lustgarten (Bacillus syphilis (?) ), occu- pied a fairly prominent position as the possible cause. This organism resembles the tubercle bacil- lus in its morphology and staining properties, and is not to be differentiated from one of the smegma l)acilli. Its recognition in S5'philitic lesions has always been difficult, and by far the greatest num- ber of investigators have been unable to demon- strate it. It has never received general recognition as the cause of the disease, and its presence in le- sions of the genitals has no significance because of the occurrence of smegma bacilli in this locality. The bacillus of De Lisle and Julien, and that of Joseph and Piorkowski rest on no better basis. Two important discoveries of recent date lend to the hope that some light may be thrown on juany dark problems in relation to syphilis. Transmission The first has to do with the transmission of the to Monkeys. disease to lower animals. Such attempts have been very numerous, both by the inoculation of syphilitic tissues and of organisms cultivated from the tissues. We have not the space to describe in- dividual experiments, and can only say that trans- mission to various animals (monkey, guinea-pig, rabbit, hog, etc.) has been claimed in a number of instances. Leaving the monkey out of consideration, it is reasonably certain that none of these reported successes represented the production of syphilis ; this is shown decisively by experiments published HYrJ/JLIS. 523 Metchnikoff and Roux. by Neisser in 1902. This may not be true, how- ever, in regard to the inoculation of monkeys, in which successful experiments were reported by Ivlebs (1879), Martineau and Hamonic (1882) and Sperk (1886-8).* It is quite likely that Sperk, in particular, accomplished transmission several times. However, the successes were not uniform, and the possibility of such transmission has become an assured fact only in the most recent times. It occurred to Metchnikoff and Eoux as it had Experiments of occurred to others that the monkey, particularly the higher species (chimpanzees), should on ac- count of their biologic proximity to man, be the most suitable animal for the j)roduction of experi- mental syphilis. Attention has already been called to this proximity as indicated by the reaction of serum precipitins. Their first inoculation was performed on a fe- male chimpanzee, virus from a primary lesion and from"'Moni(ey from mucous patches being introduced by means of scarification into the prepuce of the clitoris and into the skin of the eyebrow. The wounds healed, and twenty-six days after inoculation a vesicle which soon was surrounded by induration appeared on the prepuce. This lesion was pronounced a typi- cal hard chancre by eminent dermatologists and S3'philologists. With the appearance of the chan- cre the inguinal lymph glands became enlarged and one month later a papular eruption appeared on the thighs, abdomen and back. The papules persisted for more than a month, and were still discernible when the animal died several weeks later of pneumococcus infection. Before this ani- Transmission * Flexner : "The Etiology of SyphUls." Med. News, Dec. 9, 1905. 524 IM'LX'TION AND IMMUNITY. iiial died a second ehinipanzee was inoculated from the primary and secondary lesions of the first ani- mal, resulting in the development of primary le- sions and of adenitis. Still another successful in- oculation resulted in secondary lesions with the formation of mucous plaques. They have since performed many similar experiments with positive results^ when the higher types of monkeys were used. Confirmation has come from a number of independent experimenters (e. g., Lassar, A. Neis- ser. Kraus, Flexner), and A. Neisser in particular has taken up the work on an extensive scale. Experiments Some of Neisscr's work is of the utmost impor- tance. The experiments of Metchnikoff and Eoux had already indicated that the higher monkeys (chimpanzee, etc.) acquired generalized syphilis more readily than the lower species. Neisser's work corroborates this, and he recognizes a scale of susceptibility which corresponds roughly with the proximity of the different species to man, as indi- cated by general morphology and the reaction of serum precipitins. The chimpanzee, orang-utan and gorilla are the most susceptible, and the syph- ilis produced in them approaches closely that seen in man, including the secondary symptoms. It is suspected that the cynocephalus varieties are less, and the macacus varieties least susceptible. Among the macaci the smaller t3^pes (rhesus) are more resistant than the larger. The lower susceptibility of these animals is recognized by the failure of secondary symptoms to develop, hence in them the syphilis may be purely local (Xeisscr). The study of experimental syphilis is so young that generali- zations at this time are out of the question. A second discovery of no less importance was HYPIflLIH. 525 Possible Cause. that of a spirochetal'' {Spirocketa pallida) in tho Spirocheta primaiy and secondary lesions' of syphilis by Hoff- mann and Schaudinn in 1905. ''The organism measures from 4 to 10 microns in lengthy the aver- age being about that of the erythrocyte of man. Its width varies from immeasurable thinness to one-half micron. It possesses from three to twelve, sometimes more, curves, which are sharp and reg- ular and resemble the curves of a corkscrew. The poles are sharpened. The organism is mobile, and the motions consist of rotations on the long axis, forward and backward movements, and the bend- ing of the entire body. Flagella have not been seen'' (Flexner). It may be stained by the azur of Giemsa or the Komanowsky stain or some one of its modifications. Confirmation has come from a large number of observers in rapid succession, little difficulty being found in demon^strating the spirals in preparations from chancres and mucous plaques, secondary lesions in the skiii and in fluid aspirated from the lymph glands which are regional to the chancre. Schaudinn found it once in fluid aspirated from the spleen, but its demon- stration in the blood has been accomplished in only a few instances after prolonged centrifugation of the blood. Levaditi and Petresco discovered it in the fluid of an artificially produced blister. Two additional facts make the case of Spirocheta pal- lida a strong one, i. e., its occurrence in the lesions of the congenitally syphilitic .and in the experi- mental lesions of the monke5\ even when the inoc- Distribution of Spirocheta. * The discovery of spirochetae in yaws, by Castellani and by Wellman, is a very suggestive one, in view of tlie tend- ency in many quarters to considers yaws as a manifestation of syphilis. 5-2ti IXFECTIOX AM) IMMIXITY. Illation iti made from a previousl}' infected monkey (Kraus). Iviiowledge concerning its relation to tertiary lesions is not yet of a satisfactory nature. Suggestive as these results are, we must appre- ciate that much remains to be learned before the causal relationship of Spirocheta pallida to syphilis can be an unquestioned one. Infection. Infection usually is venereal. It is not defi- nitely known whether a defect of the surface of the prepuce, glans, vagina, etc., is essential for infec- tion. The epithelium in these localities is so deli- cate that defects of microscopic dimensions may be easily produced, and infection may take place through such defects as through grosser lesions. It IS well known that the lip, tongue, conjunctiva and finger may be the seats of primary lesions, and it is probable that no part of tlie body surface is immune when the virus is introduced suitably. The secretions of all surface lesions in syphilis are infectious, except those of gummata. Concern- ing the infectiousness of different normal secre- tions and the situation of the virus in internal or- gan?, we may look forward to more positive infor- mation than we have had hitherto. Defibrinated blood and serum from cases of secondary syphilis did not produce lesions when injected subcuta- neously and intraperitoneally into monkeys (Neis- ser). Neisser had previously performed experi- ments on man which showed the serum not to be infectious. We can not conclude from these results, however, that the blood in syphilis is not infected. Inoculations into monkeys from the internal or- gans (liver, spleen, bone marrow) of syphilitic monkeys, gave negative results. The virus is non- filterable, i. e., it is so large or its form is such that it does not pass through a Berkefeld filter. Occurrence of Virus. HYI'IULIH. 527 Clinical e.\2)erience indicates that the virulence virulence. of the syphilitic virus is not uniform. It is pos- sible that certain strains are more likely to bring about "post-syphilitic" diseases than others. That the resistance of the virus outside the body is low seems evident from the fact that transmission is practically unknown except as it occurs by direct contact. Neisser destroyed it by heating to 60° C. for thirty minutes, but at this temperature for ten to twenty minutes its virulence for monkeys was retained. Prophylaxis demands no principles not generally known. Susceptibility to syphilis varies a great deal, not in the sense that some are immune, but in that a more virulent type of disease develops in some than in others. This is a condition, however, which is difficult to differentiate from variations in the virulence of the infecting agent. Syphilis is said to be particularly virulent when introduced into a race of people for the first time. The subject of immunity to syphilis is one of immunity. such proportions, the phenomena are so varied, and knowledge so inaccurate, that a thorough analysis can not be undertaken in this place. It is the customary belief that one attack confers permanent immunity to a second. To what ex- tent the acquired resistance to reinfection signifies a state of immunity is not satisfactorily settled. It seems well established that within a relatively short period following the appearance of a chancre a second primary lesion can not be acquired. It would be impossible to refer this resistance to ac- tual immunity in view of the fact that the indi- vidual is at the moment the subject of systemic infection. A second infection would be but a su- 528 INFECTION AND IMATUNITY. perimposed infection and may not be recogniz- able Avithout tbe formation of a new chancre. The resistance which is continued into the tertiary stage, at a time when the individual usually has lost infectiousness for others, is equally obscure. If the present hope that Spirocheta pallida will be shown to be the cause of the disease is realized, and if experimental work wdth the monkey yields the results which it seems to promise, those and many other questions of fundamental importance may be elucidated. Among such questions are: the immunity of a mother who gives birth to a child infected by the father at the time of concep- tion (Colle's law) ; the occasional occurrence of re- infection; the persistence of infectiousness and transmission of the disease into the third genera- tion, of Avliich there are a number of reported ex- amples. Serum Scruiii-the'rapv, or vaccination against syphilis, are possibilities of a future time. A truly anti- syphilitic serum has not yet been demonstrated. Neisser found the serum of syphilitics, from what- soever stage of the disease, without influence on the course of the infection. Also treatment Avith the normal serums of various insusceptible ani- mals has had no unqualified success. Metchnikoff and Roux observed a phenomenon which suggested to them the possibility of attenuating the virus so that it may be suitable for vaccination. A raa- cacus monkey reacted to inoculation by the produc- tion of a local lesion, the virus of which when transferred to the more susceptible chimpanzee likewise caused a local lesion, but no signs of gen- eralization appeared. The chimpanzee later showed himself resistant to the virus from man, and for Therapy YELLOW FEVEIi. 529 this reason it was assumed that immunization had been accomplished. Neisser reasonably criticises this conclusion on the ground that the chimpanzee, having been inoculated, with syphilis from the monkey, resisted inoculation from man, not be- ■ cause he was immunized, but because he was syphi- lized, i. e., he was already infected with syphilis. III. YELLOW EEVER. Yellow fever is peculiarly an American disease, occurrence. and it has reached other continents (e. g., Spain) only in accidental ways and for brief periods. It is possibly endemic in certain portions of West Africa (Sierra Leone), to which it, was probably carried from the Antilles (Scheube). Scheube regards the Antilles as the birthplace of yellow fever." Knowledge of it extends only to the middle of the seventeenth century, at which time it surely existed in the West Indies. The dis- ease has on several occasions been carried to Spain by vessels returning from Cuban ports. Until very recent times it was endemic in Cuba, especially Havana, and in Vera Cruz and other Spanish-American ports it has prevailed extensively. From such points extension frequent- ly takes place into adjacent tropical or subtropical regions, or even into temperate localities during the summer months. In the latter part of the eighteenth century Philadelphia suffered very se- verely. Baltimore was attacked similarly and Bos- ton to a less degree. Other northern ports, e. g., New York, have experienced attacks of limited duration, the disease, presumably, being intro- duced by means of infected ships. In addition to our southern coasts and that of Mexico, the Atlantic coast of South America has 530 IXFECTIOX AM) IMMLMTY. Bacillus Icteroides. The Mosquito Theory. lu'on infce-tcHl as far south as Buenos Ayres. and likewise the western coast of Mexico and Peiii. In the eighteenth century the coast of Spain and Portugal suflFerod severely, but since that time only minor epidemics have occurred in these coun- tries. Epidemics frequently have appeared on ships after they had left infected ports. The Southern States were invaded repeatedly in the last decade of the eighteenth century, in 1803, 1805, 1853, 18G7, 1873, 1878, 1905, and in lesser degrees at other times, in all ninety-six times. The severest epidemics w^ere those of 1853 and 1878. The many microbes which have been cited as the cause of yellow fever need not be described. The BaciUus icteroides of Sanarelli, which had at- tained more prominence than any other, was shown by Sternberg, by Reed and Carroll and by the more recent work on the mosquito theory, to bear no causal relationship to the disease. According to Eeed and Carroll it is identical witli the hog-chol- era bacillus. The monumental work of Reed, Carroll, Agra- monte and Lazear (1900), the last of whom lost his life from yellow fever, has made it possible to replace accurate knowledge of the epidemiology and prophylaxis of yellow fever and, to a certain extent, of its etiology, for many incorrect ideas which had prevailed up to that time. The conception that yellow fever is transferred from one person to another by moscpiitoes was first advanced positively by Carlos Finlay, a Cuban physician, in 1881, although several Ameri- can physicians had long before noted the preva- lence of mosquitoes during yellow fever outbreaks (Rush, 1793; Weightman,^ 1839; Wood, 1853; YELLOW FMVMR. 531 Barton, 1853). He reported tlie trariHnnssJon of the disease, experiinentally, by the bites of inos- quitoes which liad fed on yellow fever patients, and stated that light attacks which followed the bites resulted in the establishment of immunity. The subsequent observations of Eeed and his co- workers indicate, however, that Finlay's technic was such that he could not possibly have produced experimental fever, and that the development of the disease in his subjects was purely a coincidence. The reason for this will appear below. Having satisfied themselves that Bacillus icte- The work of roides is but an accidental organism in yellow Etc., with stego- n 1 J.^ L -1. • J! -\ 1 ^ T myia Fasciata. fever, and that it is found under normal condi- tions as well, Eeed and his associates began work on the- mosquito hypothesis of Finlay. The first positive result was obtained in the case of Dr. Car- roll. Carroll "was bitten at 2 p. m., Aug. 27, 1900, by Btegomyia fasciata. This particular mosquito had • bitten a severe case of yellow fever on the second day of the disease, twelve days before; a mild case of yellow fever on the first day of the attack, six days preceding; a severe case of yellow- fever on the second day of the attack, four days before; a mild case of yellow fever on the second day of attack, two days before inoculation." After an incubation period of three days, Carroll devel- oped typical and severe yellow fever, from which he recovered. A similar result in one other case was reported at this time, and later Camp Lazear, with mosquito-proof houses, was established for the continuation of the study. The experiments of Eeed and his co-workers, and confirmatory work by Guiteras and the French commission, can not be described in this place. We ma}^ feel sure, how- 532 IXFECTION AXD IMMUNITY. Important Facts evGi", that witli all tliG conditioiis of experiineuta- Been Learned, tioil lindcr absolutC COntlol thc followillg poillts ' have been determined with scientific certainty: 1. Yellow fever may be transferred from a patient to a non-immune by the bite of a mosquito — Stego- inijia fasciala — which has previously fed on the yellow fever patient. 3. In order that the mos- quito become infected it is necessary for him to feed on yellow fever blood within the first few days (three days) of the fever. 3. The mosquito can not transfer yellow fever directly and imme- diately from the patient to a non-immune, but it is necessary for a period of not less than twelve days to elapse before he becomes infectious. When this time has been reached the insect continues in- fectious for at least fifty-seven days and probably throughout his life. 4. Yellow fever can not be transferred by "fomites.'^ 5. The subcutaneous in- jection of yellow fever blood into a non-immune produces yellow fever, hence the infecting agent exists in the circulation. 6. The serum of a yel- low fever patient, after being diluted and filtered through a Bcrkefeld filter (Eeed and Carroll) or Chamberland B porcelain filter (Eosenau, Parker, Francis and Beyer) is infectious, hence the in- fecting agent at some stage of its development is very minute, possibly ultramicroscopic. 7. "An attack of yellow fever produced by the bite of a mosquito confers immunity against the subsequent injection of the blood of an individual suffering from the nOn-experimental form of this disease" (Eeed, Carroll and Agramonte). 8. The period of incubation usually is three days, but may vary within the limits of two to six days. 9. "A house may be said to be infected with yellow fever only and Stegomyia. YJ^JLLOW FEVER. ' 533 Avhen there are present within its walls contami- nated mosquitoes capable of conveying the parasite of the disease." 10. "The spread of yellow fever can be most effectually controlled by measures directed to the destruction of mosquitoes and the protection of the sick against the bites of these insects." 11. No mosquito other than Stugomyia fasciata has been found capable of transmitting the disease, and analogies suggest the probability that no other insect is concerned. These discoveries explain many facts in rela- Epidemiology tion to yellow fever which had been obscure hither- to. For example, yellow fever is a tropical and subtropical disease only because Stegomyia fas- ciata breeds in tropical and subtropical climates. The disease is found in low, moist localities rather than in the high and dry, because the mosquito in- habits the former and not the latter. Yellow fever dies out with the first severe frost or on the advent of cool weather because these conditions either kill the mosquito or cause him to hibernate. The advent of an initial case of yellow fever in a suitable region is followed by the appearance of the disease in epidemic form only after a period of two or three weeks, because the mosquito first becomes infectious in about two weeks after it has fed on yellow fever blood; this may correspond with a certain stage of development of the as yet unrecog- nized parasite. The observation often made that yellow fever, like malaria, is not contagious in the ordinary sense, in spite of its rapid extension, is readily understood, as is the irregular method in Avihch the disease spreads. It is now clear why the disinfection of fomites has never been able to check the advance of an epidemic, and why the ■>:!4 i\j'j:cti().\ \\I) nnii mty. ordinary quarantine measures wliieh (.lid not take tlie mosquito into consideration were not eU'oetive in keeiiinu' tlie disease out of a ra\()i-able port; and lu' ii J'avorahle port is meant one which can harhor Stegonii/ia fasciata. These discoveries also c.\- })lain liow yellow fever could be" stamped out oi" Havana^ Texas and Xcw Orleans by i)rophylactic, hygienic and quarantine measures, which had as their objects tlie destruction of the mosquito and its breeding places and prevention of the infection of the mosquitoes l)y suitably screening the pa- tients. Distribution of ]t is thus sccn that the epidemic occurrence of yellow fever is strictly- associated witli the distribu- tion of Stegomyia fasciata. Howard, in Bulletin Xo. 46 of the Public Health Eeports. gives this distribution as known on Sept. l:i-> gold (Rio Urando-Ludlow). Houth Carolina: Charles- ton, Columbia, Fort Freniont, Sullivan's Island. Ari- mona: Nogales. Maryland: Baltimore (Carter) — breed- ing in fresh water'on fruit wharf. North Carolina: Beau- fort, Winston, Raleigh, Greensboro, Charlotte, Salisbury. Indiana: Jefl'ersoftville. Missouri: St. Louis. Eeed and Carroll found the larvffi of stegomyia Breeding Places "(1) in rain-water barrels; (2) in tin cans that had been used for removing excreta and which still contained a small amount of fecal matter; (3) in sagging gutters containing rain water; (•f) in cesspools; (5) in tin cans placed about table legs to prevent the inroads of red ants; (6) in the collection of water at the base of the leaves of the agave americana; (7) in one end of a horse trough that was in daily use." These in- stances are cited to show the general character of the places in which the eggs and larvae of stegomyia may be found. The eggs are deposited during the night, in about seven days after the ingestion of blood, and "in pairs, in groups of three or more or singly," to the number of forty-seven on the average (Eeed and Carroll). The eggs are very resistant to drying and extreme cold ( — 17° C). With a favorable temperature they hatch in from three to seven days ; the larval stage lasts for seven days, the pupal two days, the total cycle being completed in about twelve days. As in the case of anopheles, only the female stegomyia sucks blood. The insect prefers the hours from 3 p. m. to 9 a. m. for feeding, but is most active from 4 p. m. to midnight. "In captivity the hungry impreg- nated female will bite at any hour of the day or night." In a state of freedom it will not bite a second time for from five to seven days. It ap- pears not to bite when the temperature is lower 536 IM'ECnOX AM) IMMLMTy.. Time of tliau 6"i° F., auotliei factor in the subsidence ' '"*'■ of yellow fever with the advent of cool weather. For further details concerning the morphology, biology and habits of stegomyia consult Howard on "The lilosquito" ; Eeed and Carroll, "The Pre- vention of Yellow Fever," Medical Record, Oct. 26. 1901; Parker. Beyer and Pothier, "Eeport of Working Party No. 1," Yellow Fever Institute Bulletin Xo. 13, 1903, Washington. Importation YcUow fcvcr cascs and stegomyia work together "**' in the extension of the disease just as malarial . cases and anopheles do in the extension of ma- laria; for the principles involved the chapter on malaria may be consulted. Of particular interest is the importation of the disease by means of ships, since the invasion of the United States usually comes about in this way. It is frequently stated that ships lying one-half mile from shore are safe from yellow fever; Grubbs, however, believes that stegomyia may reach vessels lying within fifteen miles of the shore if the wind is favorable. The insect readily boards a vessel lying in an infected port and may remain there at least during a sev- enteen days' voyage. It may also breed in suitable barrels or tanks of water on the ship. Under these conditions it is readily imderstood how a ship, leaving a harbor with a healthy crew, may be at- tacked by yellow fever a few days after leaving port; and how any quarantine measure at a new port which does not involve the destruction of the mosquitoes on the boat and the protection of the patients from the bites of mosquitoes is inadequate. Resistance As statcd, the nature of the virus is unknown. Its filterability was mentioned. A temperature of 55° C. for ten uiiinitos renders innocuous YELLO W FE VER. 537 the defibrinated blood of tlic infected; according to the French Commission (Marchoux, Salimbeni and Simond) the virus is destroyed in five minutes at this temperature. Tlie latter also found that defibrinated blood when sealed under vaselin re- tained its virulence for five, but not for eight days. The toxic substance appears to have a strong af- finity for the parenchymatous organs, particularly the liver and kidney. The essential jorinciples of prophylaxis have Prophylaxis. been alluded to : 1, the destruction of breeding places for the mosquito as described in the section on malaria; 2, the isolation of patients, screened, to exclude mosquitoes; 3, the destruction of mos- quitoes found in infected houses or ships; 4, the individual factor of avoiding the bites of mos- quitoes, which involves the screening of houses, and individual care. One may go about more safely in the middle of the day than before 9 a. m. and after 3 p. m. For the disinfection of Jiouses, i. e., for the destruction of mosquitoes, two pounds of tobacco or two pounds of pyrethrum powder per 1,000 cubic feet of space may be burned after the rooms are sealed. When smaller quan- tities are used the insects. may be only stupified, and should be collected and burned (Eosenau, Par- ker, Beyer and Pothier) . Sulphur dioxid is highly efficient, but formaldehyd is valueless as an in- secticide (Rosenau). The negro is less susceptible to yellow fever than Susceptibility. the white man and in him the mortality is lower. Among the natives the mortality is from 7 to 10 per cent., among the whites from 20 to 80 per cent. (Scheube). The statement that Caucasians may become "acclimated" so that they are less suscep- Immunitv and Serum Prop ry,is i.\j'K("no.\ amj lumlmty. tiblc needs additional investigation. Tt seems im- ])ossil)le that aoeliinatization eouM iiiran anytliing else than aetive iininunizatimi. CliiUlren and the aged are attacked less i'reqiuiilly than those be- tween the ages of ten and thirty. An attack of yellow fever, whether experimental erties. or natural, confers immunity of long or lasting du- ration. According to the French Commission, a certain degree of immunity could he conferred In" the injection of infected serum wliich liad hwn heated to 55° C. for five minutes, or ol' delll)i-i- nated blood Avhich had been kept under vaselin oil at room temperature for eight days. They also claimed that the serum of convalescents has pro- phylactic and curative properties to a certain de- gree. • IV. TYPHUS FEVER. In addition to a streptobacillus obtained by Hlawa and the diplococci described by a number of investigators, a supposed, protozoon, resembling pyroplasma, was found in six cases by Gotschlich. The etiologic role of none of these organisms can be accepted at the present time. ocxurrence Tvphus is uow a tare disease. It is endemic on and Conta- • J^ t r^^ i t • giousness. a Small scalc m London, Glasgow and Ijiverpool, and cases occur in the larger cities of Ireland. In epidemic form it attacks localities in which the hygienic conditions are bad. The contagion seems to fasten itself in such localities and does not ex- tend with rapidity to neighboring communities in which good hygiene and cleanliness prevail ; it is particularly a disease of the poor, the filthy and the underfed. Healthy, clean and well-nour- ished persons who enter an infected district and come in contact witli tlie patients arc subject to TYPHUS. FKVEIt. 539 attack. 'I'yplius has always been considered a very contagious disease. It has been noted repeatedly, however, that when patients are removed to a hos- pital and kept under clean and hygienic conditions with plenty of fresh air that infection of attend- ants and physicians is relatively infrequent. From observation of 600 hospital cases Eobinson and Potts draw particular attention to -this point and lay great stress on the importance of liberal ven- tilation in decreasing contagiousness. The method of transmission is not known. It has been sug- gested repeatedly that the disease may be spread by the bites of insects, perhaps fleas and bed-bugs. Gotschlich emphasizes the latter as possible car- riers, discrediting the significance of the flea. He notes that in Alexandria fleas are everywhere, whereas typhus is confined largely to the poorer and unclean localities. Transmission by means of clothing and other fomites is said to occur. Usual- ly the development of typhus in a hitherto unin- fected community is traceable to the importation of the disease; in some instances, however, the origin could not be learned. Proph3daxis demands the isolation and disinfec- tion usually practiced in combating contagious diseases, particular attention being paid to hj^giene, cleanliness, the admission of fresh air to the sick room, and the destruction of vermin ( !). The serum of convalescents is said to be cura- tive in a moderate degree (Legrain). V. DENGUE FEVEE. Dengue occurs in numerous countries which af- occurrence. ford a warm climate. It is endemic in Egypt, Arabia, Senegambia, Honduras, the Bermudas, 540 I.XFJ-JCTWX AM) IMMUNITY and the Sandwich Jshuuls. Important centers for the origin of epidemics are the lesser Antilles of the Western Hemisphere, the Red Sea Coast, and Senegambia (de Brun, cited by Scheiibe). It occurs in our southern states and In Mexico. It may be introduced into new regions by means of infected ships. Organisms. The specific agent is unknown. The "plasmeba" described by Eberle (190-i) and his hypothesis that Cidex fatigans may transmit the disease await con- firmation. The same may be said of an influenza- like organism seen by Carpenter and Sutton (1905) in stained preparations from the throat. "Dengue fever is an acute infectious disease, distinguished by the appearance of an initial and terminal polj^morphous eruption and accompanied by severe articular and muscular pains." Corre- sponding with the two eruptions, there are charac- teristically two periods of temperature separated by a short period of apyrexia. The intense muscu- lar pains and asthenia resemble those of influenza, the respiratory affections of the latter being absent, however. The incubation period varies from a few hours to four or five days, usually one or two, and the entire duration from six to seven days. Transmission. Dcngue fever extends epidemically with all the rapidity which characterizes influenza. "In some respects the spread of the disease suggests some peculiarity in the method of propagation differing from that of the well-known diseases, influenza, scarlet fever, measles, etc. It appeared to spread particularly to contiguous houses, whole streets Ijcing attacked seriatim.^^* Dengue prevails espe- * "Iteport on the Dengue Epidemic in Brisbane in 100.5." rommittee of Queensland Brancli of the British Medical Association. .Tournal of Tropical Medicine, Dec. 1.5. 1005. DENGUE FEVER. 541 cially during the hot months. "A great fall of temperature and the appearance of absolutely cold weather always puts an end to the epidemics" (Hirsch;, cited by Scheube). The disease extends so rapidly, and the incuba- tion period is so short, that general measures of prophylaxis would seem to be of no avail. Susceptibility is general, even in infancy and old age. The disease has a very low mortality; it is more severe in very early and very late life. Eelapses are not infrequent, and one attack does not confer immunity. Second attacks may occur during the same year. Leucopenia is present from the first (Carpenter and Sutton). VI. ACUTE ARTICULAR RHEUMATISM. (See pp. 359, 360.) VII. SMALLPOX AND VACCINIA. Vaccinia and smallpox may be considered to- Relation of gether, having in mind the likelihood or, indeed, smai'ipox!" the certainty, that they have a common etiology. This view seems the only possible one, in spite of our uncertainty as to the exact nature of the cause. To hold a different view would be to aclcnowledge that immunization with one kind of microbe may confer immunity of the strongest and most spe- cific character against another, a condition for which we could find no parallel. More satisfactory knowledge, however, comes inocuiati«n of from actual conversion of smallpox virus into vac- Infanltox!***' cine virus by passing the former through cows. Abbot quotes W. J. Simpson as follows : "In ISTo- vember, 1885, with smallpox lymph from an un- vaccinated patient, ] inoculated a cow with fifth- day lymph and a ewe with eight-day lymph from 54_' IM'KCTIOX AMI I MM (MTV. the same patient. Both i)i'esentetl vesicles on tlio seventli dav, the lymph of which I sent to London to be used by Dr. Cory, the direi-tor of thi- Animal Yacciiic Institute of London. This call' lym[)h, which Dr. Cory passed through a second calf before using it on children, was the starting point of a now vaccine at the institute. Between Xov. 21, 1885. and May 6, 1886, 1,247 children had l)een vaccinated with this lymph and gave 98.4 per cent, insertions of success." Concerning the changes which smallpox virus undergoes in the cow, as a result of which it loses permanently the power of causing smallpox in man, we have no knowledge, aside from the hy- ])othesis of Councilman and others mentioned below. Etiology. We may pass over the various bacilli and cocci whicli have been described as causing vaccinia and smallpox with the remark that none of them are of primary significance, but that they have been either accidental contaminations or the causes of secondary infections during the course of the dis- ease. Theories. There are two chief theories as to tin' cause of smallpox (and vaccinia) to-day. One, that the virus is an ultra-microscopic and uncultivatable organ- ism ; and a second, that it is represented by certain protozoon-like bodies seen in the specific lesions (vesicles, pustules) of both vaccinia and smallpox. Concerning the first theory we know nothing be- yond the observation of Parke that the virus of both vaccinia and variola did not pass through Berke- feld and Chamberland filters under the conditions of his experiments. Of the second theory a brief review may be given. Protozoon-like bodies have been seen by many SMALLPOX AND VACCIMA. 543 observers and were lirst brought into causal rela- Cytoryties tion with smallpox by Van der Loeff and by L. Proto/oom?; Pfieffer (1887). Griiarnieri (1892), however, gave the subject its present impetus by a careful study of these forms as seen in vaccinia and gave to the hypothetical organism the name of Cytoryctes vac- cinice, s. variola'. The bodies were found within the deep' epithelial cells in the pustules of vaccinia and smallpox and in the lesions produced on the cornea of the rabbit by inoculation with the viruses of vaccinia and smallpox. They lie within clear spaces in the protoplasm of the cells, vary in size from that of a micrococcus to that of an epithelial nucleus and multiply, it was supposed, by binary division. When mounted in hanging-drops of the vesicular fluid they showed ameboid movements. Confirmatory work came from others, and partic- ularly Wasielewski, who concluded that the "vac- cine bodies" are perfectly characteristic, that they are never found in normal or other pathological conditions of the skin, that they can not originate from leucocytes or epithelial cells, and hence can not be accidental "cell inclusions." Filtered virus produced no lesions in the cornea of the rabbit. Eecently Councilman, Magrath and Brincker- Work of hoff have studied this supposed organism in great and others. detail and find, in addition to the forms in the cy- toplasm (cytoplasmic parasites), 'still others within the nucleus of the epithelial cells of the vesicles and pustules. They express the belief that the or- ganism first gains entrance in the cytoplasm of the cells, and after a period of "multiplicative prolif- eration," the products of the latter process pene- trate the nuclei of the epithelial cells and there undergo another type of proliferation. Calkins, 544 IMECTIOX AM) IMMLMTY. I ife History of Cytoryctes. the zoologist, after studying the material, shares their views and has constructed a life cycle of the parasite from the various forms Avliieh lie found in fixed and stained preparations. The smallest recognizable forms in the cytoplasm measure about 0.7 of a micron and lie in a vacuole in the cj'toplasm near the nucleus. Calkins interprets these as "gemmules" and as products of the prolifera- tion of the parasite at the primary point of' infection (lungs (?) ). Somewhat larger forms (3 microns) con- taining a vacuole with a central point staining with methylene blue, represent "gemmules" which have grown and have become somewhat differentiated. The periphery Cytoplasmic of the organism becomes diU'ercntiated also by the for- Stages. niation of minute dots which may eventually be stained by a special method. During this stage the organism "often is spherical, but may be fusiform, pyriform or ameboid, while pseudopodia are frequentlj'- caught in various degrees of extension." No definite nucleus is discernible, but material corresponding to nuclear sub- stance is distributed somewhat generally through the parasitic cell. Certain granules are distributed through- out the body of the organism, and these granules eventu- ally give rise to the "gemmules" or young parasites which become free by the disintegration of the mother cell. Howard and Perkins find, in addition to the cyto- plasmic stage of Councilman and his co-workers, a sec- ond cytoplasmic stage, the products of which penetrate the nucleus to institute the intranuclear stages. Cal- kins speaks of the fate of the gemmules as follows: "The germs formed by the multiplicative reproduction of the cytoplasmic "ameboid form of the parasite may develop into new cytoplasmic organisms or ultimately may become germ cells within the nucleus of the epithe- lial cell. In the latter case they develop into struc- tures which I regard as gametocytes. The resulting zygote (formed by conjugation of the gametes) is the ameboid pansporoblast mother organism." Nuclear The conclusion that conjugation takes place is based Stages. ^^ certain analogies with other micro-organisms, rather than on observation of the phenomenon. This intra- SMALLPOX AND VACCINIA. 545 nuclear mother organism, the product of conjugation, finally grows to a size of 10 to 12 microns and forms within it from eight to twenty "primary sporoblasts." The young sporoblasts are eventually liberated from the mother cell and are at first solid and homogeneous, like the gcmmules, but later when they have reached a size of li/o to 2 microns small vacuoles appear in the peripheral ring of substance and in each vacuole a young spore is formed. The formation of these spores terminates the "primary nuclear phase" of the organism. These spores, still Avithin the nucleus of the epithelial cell, become, in their turn, sporoblasts, and the formation of a large number of secondary spores within them constitutes the secondary nuclear phase of the parasite. In the mean- time the nucleus of the epithelial cell has degenerated, and the secondary sporoblast with its contained spores escapes first into the cytoplasm and eventually into the pericellular space. In accordance with this conception the intranuclear process is well calculated to give rise to a massive number of young parasites within the body. Councilman, Magrath and Brinckerhoflf state that after the tenth day of the disease the parasites become more and more difficult of recognition by microscopic methods. However, Brinckerhoff found that even the desiccated crusts of pustules and vesicles produce typical lesions on the cornea of the rabbit. These forms have never been recognized positively in the blood of patients, and Magrath and Brinckerhoff were not able to produce le- sions in the rabbit's cornea by inoculation of variolous blood. The general distribution of the lesions in the skin and the occurrence of fetal smallpox gives us abun- dant reason for believing that the blood stream is in- vaded by the jDarasites. It was stated above that bodies of the general nature Cytoryctes in of those described are found in vaccinia as well as in ^^ccinia. smallpox, and this occurrence is some added reason for believing that Cytoryctes variolw, s. vaccinkv. is the cause of these processes. It is a most interesting and important observation by the American authors cited that the intranuclear stage of the parasite does not occur in vaccinia (Tyzzer), and we are led to believe that this is an important differential point between 54G IXFECTIOX AXD niMVyiTY. Infection Atrium. Dissemination. vaccinia and smallpox. Assuming that the bodies in question cause the disease, the thought is pei-tinent that the dilTerence in virulence between vaccinia and variola inocuhita may depend on the failure of (he intranuclear cycle to appear in vaccinia. The work of Giiariiieri, and particularly that of Councilman, Magrath and Brinckerhoff, is most suggestive, and ardent supporters of their views have appeared with corroborative work (e. g., How- ard). At the same time man}^ skilled observers discredit entirely the parasitic nature of the bodies described, interpreting them rather as products of degeneration of the epithelial cells and nuclei or as inclusions of other tissue cells (e. g., leuco- cytes, Borrel) or fragments of other nuclei. Ewing expresses similar views. The state of the question is sueli that I'nrther study is urgently called for. We have no positive knowledge as to infection atrium in smallpox, although the existence of a "contagious zone'' of atmosphere about the patients is good ground for the belief that invasion takes place through the respiratory passages. The disease which follows introduction of the virus into the skin is spoken of as variola inoculata, and is much less severe than smallpox. We are also ignorant to a large degree of the means of excretion or dissem- mination of the virus. Osier states that the virus "exists in the secretions and excretions and in the exhalations from the lungs and skin." The dried epithelial cells which are continuously thrown off are no doubt a most important means of dissemina- tion. Infection may be transmitted by means of clothing or other materials which have been in con- tact with patients, and the disease may be carried to others from the sickroom by a healthy person. (SMALLPOX AND VACCINIA. 547 Epidemiologic experience teaches that the virus is one of great resistance and tenacity. The incubation period in variola falls within the Cyclic Nature extremes of eight to twenty days, most commonly from nine to fifteen days. The stage of invasion, or the primary fever, terminates the incubation period, and during this time the initial rash ap- pears, accompanied by moderate hyperleucocytosis. On the third to the fourth days the remission sets in, the number of leucocytes in the blood decreases to normal or below normal, and cutaneous lesions make their appearance, and in the course of forty- eight hours show a vesicular nature. When the umbilicated vesicles are changed into pustules the temperature again rises (secondary fever) and hy- perleucocytosis again develops. This much only of the clinical picture is mentioned to emphasize the cyclic nature of the phenomena ; one may well suspect that the organism causing such a disease undergoes particular phases of development which in some way are related to the well-known clinical cycle. Epidemics are sometimes of so mild a charac- variations in ^ Virulence. ter that the patients are not bed-ridden and may be found in the pursuit of their occupations in spite of well-marked eruptions. Such occurrences can be referred only to a virus of low pathogeni- city. Even mild epidemics, however, may be ac- companied by severe and fatal cases. Cases of am- bulatory smallpox are most important factors in spreading the disease. We have nothing more than presumptive knowl- "l^yfrusf"" edge concerning the distribution of the virus in the Body. the body aside from its occurrence in the skin and mucous membranes. We may feel certain, how- 548 INFECTION AND nnilMTY. Secondary infections. Prophylaxis. Discovery of Vaccination. ever, that the infection is systemic. The lesions of the skin are of such a nature that the}^ are generally regarded as of embolic character, which presupposes blood infection ; and transmission of the disease througli the placenta is decisive proof of a general distribution of the virus at some stage of the process. The failure to cause vaccinia in the cornea of the rabbit by inoculating the blood of i^atients (cited above) may indicate that the virus is present in the blood in small quantity or that circulating organisms are eventually de- stroyed. The intoxication of smallpox is mani- festly general. In few diseases does secondary infection play so important a role as in smallpox. Wlien the cu- taneous lesions have become pustular they usually contain pyogenic cocci, although they may be ab- sent. It is somewhat strange that streptococci are more often encountered than staph3dococci, in view of the normal presence of the latter in the epidermis. Fatal cases are almost without excep- tion accompanied by general streptococcus infec- tions, and Councilman believes these organisms are more important as a cause of death than the specific virus. Successful propliylaxis involves universal vac- cination, in addition to special measures which are demanded in the presence of the disease: isola- tion of the sick until desquamation is complete, antiseptic baths, and disinfection and fumigation as currently practiced. Interesting matters of history are the facts that protective inoculation against smallpox Avas prac- ticed in fairly ancient times by rather primitive races, and that Lady ]\Iary Wortley Montague HMALLl'OX AND VACCINIA. 549 introduced this method into Europe in 1718. This was not the vaccination in vogue to-day, however, but rather the inoculation of virulent virus from the pustules of the diseased into the healthy. As mentioned in one of the earlier chap- ters, this procedure commonly produced a mild type of disease (variola inoculata) which ren- dered the individual immune to virulent small- pox. Everyone knows that the vaccination of to-day, i. e., the substitution of the virus of cowpox for that of smallpox, was the discovery of Jenner (1798), and we need offer no comments concern- ing its efficacy nor repeat the well-earned epithets which have been applied to the rare species of dis- believers. Nothing is more certain than that smallpox has ceased to be a world pest only be- cause of the continued Jennerization of the race. The essential points established by Jenner are the following: 1. That the vaccine disease ■casually communicated to man has the power of rendering him insusceptible to smallpox. 2. That the specific co^^vpox alone, and not other eruptions affecting the cow which might be confounded with it, has this protective power. 3. That the cow- pox may be communicated at will from the cow to man, by the hand of the surgeon, whenever the requisite opportunity exists. 4. That the cowpox,. once engrafted on the human subject, may be con- tinued from individual to individual by successive transmissions, conferring on each the same im- munity against smallpox as was produced in the one first infected directlv from the cow (cited from S. W. Abbott). For at least half a centurv following Jenner's Jenner. 550 INFECTION A\n 1)1)11 WITY. Humanized L>mph. Cowpox. Preparation of Vaccine. discovery humanized lymph was used for vacci- nation, new patients being inoculated by means of points prepared from vesicles of previous cases, or with the fresh lymph from such cases. The not infrequent transmission of syphilis by this means was the source of many calamities. Following the precedent of Warlemont in 1868, the lymph of cowpox is now the universal source of vaccine. Cowpox probably occurs to a greater or less degree in all countries, especially in the spring and summer, attacks the udder and teats almost ex- clusively, and is accompanied by very mild con- stitutional symptoms. The incubation period is from three to eight days. There is first local heat, swelling and tenderness, followed by the for- mation of papules, which in three or four days after their appearance are transformed into vesi- cles. The disease reaches its maximum develop- ment at the tenth or eleventh day, the umbilicated vesicles going through the usual course to crust formation. Calves and heifers from the age of two months to two years are best suited for vaccination in the production of lymph for commercial purposes. The region of the flank or the Avhole ventral sur- face of the body may be inoculated, and in the lat- ter instance as many as a hundred or more inser- tions may be made. The skin is first shaved, cleansed with antiseptics, and the lymph from an- other calf is introduced by means of a syringe or by scarification. In some institutions long, very superficial parallel incisions are made and the virus rubbed in with a spatula. Within five days to a week the vesicles are in such condition that thp Ivmph may be collected, the contents either SMALLPOX AND VACCINIA. 551 being squeezed out with suitably formed forceps or scooped out with a sharp spoon. Depending on the area vaccinated, the lymph collected from a single calf may be sufficient for from 2,000 to 15,000 vaccinations in man. In view of tlio im- munity which is conferred calves can l)e used but once for the production of vaccine virus. All other methods of preserving lymph have been largely abandoned for the process of giycerinization, the glycerin being very inti- mately mixed with the virus by mechanical means and allowed to remain in this state in a cool place for from six to eight weeks before the product is put on the market. Dried vaccine on ivory jooints is still used to some extent, the points being coated directly from the vesicles. Dried vaccine retains its power for from two to four months or longer when kept in a cool, dark, dry place. Glycerinated lymph has many advan- tages, the most important of which relates to the bactericidal action of the glycerin by which the lymph is freed from the pathogenic bacteria (e. g., staphylococci) which in former times caused ser- ious complications in vaccination. The glycerin is supposed to destroy such organisms to a large degree without, however, injuring the vaccine virus itself. It is also stated that glycerinated lymph is much more durable than the dried ; that its potency may be retained for eight months or longer under suitable conditions. Eosenau has recently called attention to the fact that the bac- tericidal power of glycerin has been overestimated, and that while it kills pyogenic cocci within two weeks when at the body temperature, such organ- isms may live for months in glycerin when in the Giycerinization. Effect en Con- taminating Bacteria. o^rl IXrJX'TfOX A\n /l/l/r\77'V. ice chest ; aud^ of course, ouv glycerinated virus is kept in the ice chest. Tetanus spores live for months in glycerin and glycerin lias practically no neutralizing action on tetanus toxin. Glycerin docs liave tlio power, however, of attenuating the tetanus spores, and its slow bactericidal action is well established. As stated above, the vaccine should be gl3'cerinized for some weeks before it is put on the market. Glycerin has the added ad- vantage for the manufacturer of enal)ling him to dilute his lymph moderately (50 to GO per cent.) without impairing the virus. Of much more importance for the safety of virus than glycerinizatidn arc pi'npci- hygiene and cleanliness during the whole process of prepara- tion. The powers recently conferred on the Sur- geon-General by an act of Congress have resulted in a great improvement in the purity of the vac- cine now on the market.* While it can not be expected that vaccine will be entirely free from bacteria, it is possible to re- duce their number to a low minimum and to elim- inate pathogenic forms, particularly pathogenic cocci, tetanus and tubercle bacilli. Vaccination The tcclinic of vaccination is so well known that no description is needed. It need only be stated that in scarifying it is undesirable to cause hemorrhage and that the operation is a sur- gical ijrocedure, demanding surgical cleanliness and surgical care of the wound. As a rule vac- cination in man protects against smallpox for a period of six to ten years, after which revaccina- tion is necessary for continued protection. It * John F. Anderson "Federal Control of Vaccine Virus," Jour, of the Amer. Med. Assn., June 10, 1905. SMALLI'O.y AM) VACCIMA. 553 should not be concluded from the negative out- come of a single vaccination that the individual is immune to vaccination and hence immune to smallpox, but rather, repeated attempts should be made with virus known to be fresh. It is quite possible that certain individuals are immune to vaccinia, as often stated, but they are very rare, and the condition should not be recognized hastily. Among 38,000 vaccinations Dr. Cory encountered but one in which a "take" could not be gotten on second trial (Abbott). The ideal condition is that all children should when to Vaccinate. be vaccinated at an early age by requirement of law as in certain European countries, where it is demanded within the first few months or the first year or two of life. Some countries require re- vaccination before the children are admitted to school and recommend repetitions at suitable in- tervals. We have no national law on the subject and the state laws differ. In many states children must be vaccinated before they are admitted to the pub- lic schools, the responsibility sometimes falling on the school and sometimes on the city or tc^Ti authorities. A number of states have no laws on the subject, although vaccination is for the most ]3art assvired through the requirements of the State Boards of Health and the local authorities. When there is danger of an epidemic, and in known cases of exposure, vaccination should be practiced thoroughly. Inasmuch as the incuba- tion period of vaccinia is about three days less than that of smallpox, successful vaccination pro- tects within a limited period following exposure. Immediate vaccination is demanded in case of 554 INFECTIOy A\n IMMLMTY. Imniunity and Susceptibility. Leucocytes. Serum. exposure. Healthy infants may be vaccinated within the first six weeks or two months of life and at any earlier period in case of exposure. An attack of smallpox confers prolonged and, with few exceptions, lasting immunity. Second and even third attacks have been described. It is known that those who have had smallpox may be- come susceptible to vaccination after a period of time. Susceptibility varies a good deal with age. During the ages of from two to fourteen years the disease is less common than between fifteen and forty, and after this period it again decreases in frequency. Undoubted instances of natural immunity to smallpox occur, but they are very rare. Smallpox is accompanied by a leucocytosis wliich is peculiar because of the large number of mononuclears. There is a slight rise in the number of leucocytes during the first febrile on- set, a fall to almost normal during the remission, followed by a second rise, which may be as high as 16,000 to 20,000. Fatal cases show a terminal hypoleucocytosis (]\Iagrath, Brinckerhoff and Ban- croft). Large numbers of lymphocytes are also found in the pustules (Eoger). ISTothing of a sat- isfactory nature is known concerning the relation- ship of the leucocytes to recovery and immunity. There is no serum therapy for smallpox. The interesting observation has been made, however, that the serum of convalescents or of vaccinated man or animal will, when mixed with vaccine virus, prevent its action. Horsepox is identical with cowpox. Sheeppox (clavel6e) is an independent disease. The virus of cow- pox produces a local lesion in the sheep, but does not CHICKENPOX. 555 cause immunity to sheeppox. The virus of sheeppox, on the other hand, has no effect on horses and cattle (Nocard and Leclainche). The virus of sheeppox is filterable ( Borrel ) . VIII. CHICKENPOX (vAEICELLA), Although the skin manifestations of varicella often resemble those of smallpox to such an extent that differentiation is difficult, the two diseases are distinct. Nothing indicates this more clearly than the fact that one who has recovered from varicella is susceptible to vaccination, and it is loiown further that an attack of chickenpox does not protect against smallpox. The etiology is unknown, and no organism which has been described can be considered the probable cause. Varicella occurs epidemically and sporadically. The virus probably exists in the lesions of the skin and in the scales, and the latter may be the chief source of contagion. There is no definite knowledge concerning the resistance of the virus, nor its distribution; the conclusion is justified, however, that it exists in the circulation at least in an early stage of the disease. The infection atrium likewise is a matter of conjecture, but probably is to be found in the lungs or upper respiratory tract. The patients should be isolated and school chil- dren should not be allowed to return to school until desquamation is complete. Disinfection should be practiced. • Susceptibility and virulence wo\ild seem to vary, since the severity of the cutaneous lesions is not constant. In delicate and tuberculous children, the lesions may become gangrenous. Hemorrhagic 55(; i\i'i:(Ti()\ i\7> nnii \//v. varicella is observed oceasionally. Such compli- cations as nephritis and otitis media occur. Varicella is a disease of childhood, although it may occur in adults. Infants are attacked less frequently. Second or even third attacks occur, although they are rare. There is no serum therapy. IX. SCAELET FEVER. The role -which the streptococcus plays in scarlet fever was considered on page 361. The ^'TDodies" recently observed by Mallory may be referred to briefly. TheProto- In 1903 Mallory described certain protozoon- '**Maiiory. Hkc Ijodics found in the skin of four cases. They could be divided into two groups, one of which consisted of "round, oval, elongated, lobulated bodies" from 2 to 7 microns in diameter ; the indi- viduals of the second group "contain a central round body, around which are grouped, on optical section, from 10 to 18 narrow segments, which, in some cases, are united, but in others are sharply separated laterally from each other." They occur within and between the epithelial cells and in the superficial part of the corium. He gives the name of Cydaster scarlatinal is to these bodies, and, al- though expressing the belief that they are protozoa and have a causal relation to scarlet fever, does not claim to have proved such a relation. Duval corroborated the discovery of Mallory, and demonstrated the bodies in five out of eighteen cases in blisters which were produced artificially during the height of the eruption. Field found them not only in the skin of scarlet fever, but also ill tliat of measles and concludes that manv of HCARLET FEVER. 557 them at least represent artifacts or degeneration forms of tissue cells. More extensive observations seem to be necessary to establish the nature of these supposed parasites. Other micro-organisms which have been de- scribed as the cause of scarlet fever, including the Diplococcus scarlatince of Class, we may pass over with the remark that the claims concerning them have not been upheld. The contagiousness of scarlet fever is extreme, ^^j^j^an"-"* and the virus undoubtedly is thrown into the sur- mission. rounding air from the skin of the patient. It is highly probable that the virus also reaches the sur- rounding air from the respiratory passages by means of "drop infection," since transmission may occur before the skin shows involvement. Patients continue to be infectious for from 4 to 6 weeks or longer after the appearance of the eruption. The disease may be transmitted by an intermediate healthy person, or by contaminated clothing or furnishings. The origin of epidemics from milk which has in some way been contaminated seems to have been proved in a number of instances. Of great importance for the persistence of an epidemic is the resistance of the virus, which re- mains viable and virulent for months and possibly for years, when under suitable conditions. Prophylaxis demands isolation of the patients Prophylaxis. until desquamation is complete; the use of anti- septic baths or ointments, or vigorous scrubbing with soap as desquamation proceeds; antiseptic treatment of the mouth cavity; disinfection of all utensils, linen, etc., with which the patient has been in contact ; avoidance of stirring up the dust in the room, Avhich demands moist rather than dry 558 l.\J'JX"J10.\ AM) IMML.MTY. Susceptibility and Immunity. Leucocytes. Serum Therapy. cleansing; the disinfection of the sputum and other discharges of the patient; an abundance of f resli air and sunshine in tlie sick room ; tlie final disinfection of the room. Physicians and nurses, when in the presence of the patient, should wear long gowns, which can he discarded on leaving, and other Avell-known precautions should be ob- served to avoid spreading of the disease. Scarlet fever is particularly a disease of clii Id- hood, "a large proportion of cases occurring before the tenth year" (Osier). Adults are attacked not infrequently. Infants are less susceptible than older children. Many examples of family immun- ity, which probably is relative, are encountered, and likewise instances in which there is a family susceptibility. In a given family examples of in- dividual immunity and susceptibility are fre- quently met with. One attack usually confers im- munity against a second, but not invariably. Scarlatina is characterized by a leucocytosis, the degree of which bears some relation to the severity of the infection. In mild cases the aver- age is from 10,000 to 18,850 (Bowie), in moder- ately severe cases from 20,000 to 40,000, or even as high as 78,000 (Klotz) ; in malignant uncompli- cated cases there is a tendency to a low leucocyto- sis (Klotz). How much of this leucocytosis de- pends on co-existing streptococcus infection re- mains "uncertain. Treatment with antistreptococcus serum is the only serotherapeutic measure which has been ad- vocated in relation to scarlet fever. This is done either on the assumption that the disease is of streptococcus etiology, satisfactory proof of which has not yet been obtained, or with the hope that MI'JAHfjEH. 551) the serum will iuUuencc favorably secondary in- fections with the streptococcus. The serums of Aronson, Moser and of Menzer have been tried more than others. Moser is probably more enthu- siastic than others, and he claims a reduction in the mortality from an average of 13.08 per cent, to 8.9 per cent, in 400 cases. Others have observed a favorable influence- in some cases, but the re- sults are not uniform. The development of sec- ondary streptococcus infections can not be pre- vented by the use of the serums, although it is stated that their severity may be moderated. Of theoretical interest is the report by Weiss- becker and by v. Leyden that the serum of con- valescents causes a reduction of the temperature and a shortening of the course of the disease. The results published up to the present time indicate that we have not as yet an efficient serum for scarlet fever (see also p. 367). X. MEASLES. Bacilli which have been recognized in the con- Micro- , . J -, ^ p organisms. ]unctiva, sputum and nasal passages m cases oi measles have, for the most part, resembled either the diphtheria or the influenza bacillus. Pseudo- diphtheria bacilli are normal residents in the eye, and influenza-like bacilli are found in the sputum in various conditions; hence, there is insufficient reason to associate such organisms with the etiol- ogy of measles. The micrococci found by Lasage (1900) have not received recognition as the cause of the disease. Measles is highly contagious, even during the Distribution of . * the Virus prodromal stage. The contagion doubtless is ex- creted from the lungs as well as the skin, and. in oUO IXFECTIOX .l.\7> LMMl MTV. view of the early broueliial syinptoms, the virus probably gains entrance through the lungs. Suc- cessful inoculation into man with blood taken from the involved skin shows that the virus exists in the circulation of the skin. Hektoen doubts the decisiveness of a number of these experiments since they were carried out in the presence of epidemics and natural infection could not be ex- cluded; at the same time he does not question the results of Mayr (1852) . In two experiments on man Hektoen determined the presence of the virus in the blood. ''The results of these two experiments per- mit the conclusion that the virus of measles is present in the blood of patients with typical measles some time at least during the first 30 hours of the eruption; furthermore, that the virus retains its virulence for at least 2-i hours when such blood is inoculated into ascites-broth and kept at 37° C. This demonstration shows that it is not difficult to obtain the virus of measles unmixed with other microbes and in such form that it may be studied by various methods." The virus is much less resistant than that of scarlet fever. The varying grades of severity of different epidemics show that it is subject to alteration in its virulence. Effect on Although measles is considered somewhat harm- Resistance. |^,g ^^^ ^YiQ whole, dangerous complications, such as broncho-pneumonia and otitis media, are suffi- ciently frequent. The development of tuberculosis following measles, an event which is not uncom- mon, shoe's that measles may greatly decrease gen- eral resistance. Prophylaxis. The prophvlaxis of measles is not different from that of other exanthemata. The isolation should continue for four weeks after the appearance of the MEASLES. 501 Susceptibility and Recur- rence exanthem (Gotschlich). The sickroom sliould bo disinfected eventually. The view not uncommonly encountered that measles is a good thing for a child to have and be over with is in no way justifi- able. The development of serious complications ean in no case be foreseen, and fatalities may occur even in mild epidemics. Very young children^ the rachitic and tubercu- lous, and those in a poor state of nutrition should be guarded against exposure, for in them measles is often malignant. Infants are less susceptible than older children. Measles occurs in adults more frequently than scarlet fever. Eecurrences, on the whole, are frequent, as many as four attacks hav- ing been noted in an individual. Hence, the im- munity caused by infection is not uniformly of a permanent character. It is very probable that the inhabitants of a country in which measles is endemic gradually become immunized, with the result that the disease prevails in a mild form. On the contrary, regions in which measles has hitherto been unknown, or has been absent for many decades, are susceptible to visitations of great malignancy. Such epi- demics have occurred in the Faroe Islands and in Iceland, with a mortality exceeded by few epi- demic diseases. A moderate leucocytosis is excited in measles. Leucocytes, "which begins soon after infection, reaches its maximum six days before the appearance of the eruption, and lasts into the first part of the stage of invasion" (Tiliston). We are ignorant of the significance of this phagocytosis. There is no serum therapy for measles. Weiss- Racial Immunization. j()2 T\FEfT10\ 1\7> /)/l/r.Y/7') . becker states tliat tlic serum of convalescents in- fluences the course of the disease favorably. XI. GERMAX MEASLES (iJOTTIELy), Eotheln is considered as distinct from measles, in spite of clinical similarities. It is recognized because of certain peculiarities in the eruption and its uniformly mild course. Perhaps the strongest reason for believing the two diseases to be distinct lies in the fact that an attack of rotheln does not leave an immunity against measles. Eotheln is contagious. Efforts should be made to prevent extension, as in measles, the methods of transmission being the same in the two diseases. XII. WHOOPING COUGH. Various jjrotozoa (?) and bacteria (cocci and bacilli) have been assigned as the cause of whoop- ing cough. Many of the so-called protozoa found in the throat were undoubtedly tissue cells (leuco- cytes, ciliated epithelium). Among the cocci, the diplococcus of Eitter (1892) acquired some promi- nence. He is said to have found it constantly in 146 cases. Investigations by others failed to jus- tify his conclusions. The Influenza- Disregarding some other bacilli which certain like Bacillus of j-i i n j -i i i • -i i sprengierand mvcstigators liavc attempted to bring into rela- tion with pertussis, we may note the essential facts concerning an influenza-like bacillus which has l)een found with great constancy and by many competent investigators in the sputum of patients. First observed by Sprengler (1897) in pertussis sputum, this organism or bacilli similar to it have been found by Czaplewski and ITensel, Zusch, Cavasse, Vincenzi, Elmassian, Luzzatto, Arnheim, Jochmann and Kruse. Eeyher, Smit. "Wollstein, of Jochmann. W J J 00 /'I NO COUdll. 503 and Davis. The organism is said to be somewliat larger and thicker than the true influenza bacillus, but has the same bipolar staining afKnity and the same demand for hemoglobin for its growth in pure cultures. There is some difference of opinion as to whether the organisms described by these different observers are all identical and as to whether all have worked with pure cultures. The conclusion of Davis would seem to sum up the situation : "With the exception of Manicatide, probably all of the investigators, at least in more recent years, have been dealing, either in pure or impure cultures, with the influenza-like bacillus, first described by Sprengler and later by Joch- mann." Culturally they are not to be differen- Hemophilic tiated from the influenza bacillus. When in pure anTsym^^ culture they demand hemoglobin for their develop- ''"'*'*• ment, although the amount of hemoglobin may be so small as not to color the medium. When in mixed culture with the streptococcus, staphylo- coccus, pneumococcus and B. xerosis, they grow abundantly even in the absence of hemoglobin. Hence, in relation to symbiosis, also they resemble the influenza bacillus. For symbiotic development it is necessary that the secondary organisms be living; when killed or when the filtrates of bouil- lon cultures are used, the "pertussis bacilli" are not stimulated to growth. Inoculation of pure cultures on the mucous Pathogenicity. membrane of the upper respiratory passages in various animals, including the monkey, does not produce a pertussis-like infection. The organisms have, however, a low degree of virulence for ani- mals, particularly the guinea-pig. Davis found that three blood-agar cultures injected intraperi- 564 INFECTIOy AM> IMMI MTV. toueally killed guinea-pigs in 24: hours or less. The virulence of the organism is augmented when mixed with certain other bacteria. By injecting it, mixed witli a non-pathogenic staphylococcus, its virulence, after six passages, was so increased that one blood-agar culture killed guinea-pigs in 24 hours (Davis). In this respect, also, it resembles the influenza bacillus. Significance. Inoculatcd in the throat of an adult, who pre- sumedly had never had whooping cough, a distinct febrile reaction, lasting two or three days, devel- oped after an incubation period of two days (Davis). Headache and pharyngitis were accom- paniments of the reaction and the pharj^ngitis continued for at least four weeks. There was lit- tle cough, and it Avas concluded that the micro- organism had not produced whooping cough, although it had shown toxic and infec- tious properties. The bacillus proliferated enor- mously in the pharynx and nose and was still to be cultivated after four weeks; Such an organism may well be an important factor in whooping cough, even though it is not the essential cause. Davis is inclined to regard its relation to whoop- ing cough as similar to that of the streptococcus to scarlet fever — i. e., a very important compli- cating organism. Davis finds still further reason for doubting its specific relationship to whooping cough from the fact that it was found frequently in measles, acute influenza, epidemic meningitis, bronchitis, vari- cella and in normal throats. The organism is disseminated extensively by coughing, and the same is probably true of the es- sential virus. Close contact, as by kissing, or the W IIOOI'ING COUGH. 505 coininon use of eating utensils is a means of trans- Contaoious- mission. Tlie opinion has been advanced by Weill and Pclin that pertussis is contagious only during the catarrhal stage of the disease. "Of ninety- three non-immune children who were placed with fifteen children who were in the convulsive stage, none became sick" (cited by Gotschlich). This point is not sufficiently established, however, to warrant modifications of prophylactic measures. Whooping cough is often epidemic and is more common in cities where contact with the infected is more likely to occur than in the country. The incubation period is from seven to fourteen days. Isolation is more difficult than in the more acute contagious diseases, yet contact with other chil- dren should be avoided as much as possible, and the patients should be withdrawn from school until recovery is complete. Pertussis is almost exclusively a disease of chil- dren, although older people may be attacked. Sus- ceptibility is not general. One attack usually con- fers immunity. A varying degree of leucocytosia is excited by the infection (13,000 to 45,000), the significance of which is not knovni. It is chiefly mononuclear. Serum therapy for whooping cough has not ad- serom vanced to a point where we can speak with as- ^''°''^''^- surance concerning it. Manicatide (1903) im- munized horses and sheep with the organism which he cultivated from a large number of cases. He reports that cure may be accomplished in from two to twelve days when the serum is used within the fi.rst fifteen days of the disease. The bacillus of Manicatide differs from the influenza-like organ- ism of other observers, hence, his antiserum can 5(50 i\ri:cTi()\ w n nnirxirv. not be accepted imreservedly as a specific serum for whooping cough. Smit found that an anti- serum for the influenza-like organism exerted no influence on the disease. XIII. MUMPS (epidemic PAROTITIS). Mumps occurs epidemically in children, particu- larly in schools, in other institutions, and in sol- diers confined to barracks. It is most frequent in the spring and autumn and probably is endemic in large centers of population. It is contagious, the virus probably being disseminated from the upper respiratory passages with infected droplets of spu- tum and saliva. The disease has an incubation period of two to three weeks and runs its course in from seven to ten days. Involvement of the testis, ovary or female breast are complications to be feared in adult life ; "orchi- tis, albuminuria, with convulsions, acute uremia, endocarditis and peripheral neuritis are occasional complications" (Osier). Fatal meningitis devel- ops rarely. Very young infants and adults are at- tacked less frequently than children of school age. Patients should be isolated for three weeks from the time s}Tnptoms appear (Gotschlich). One attack usually establishes protection. A peculiar form of parotitis sometimes follows injury of the abdominal and pelvic viscera, the so- called "postoperative" parotitis. The parotid glands may also be invaded by a number of kno-wTi micro-organisms, e. g., the pneumococcus. cAPPENDIX, I. — The Hypothesis of Welch. What has come to be known as the hypothesis of Welch is of such practical and theoretical importance that ref- erence to it should not be passed over. It may be put in the form of the following question: If bacterial tox- ins and the constituents of bacterial cells so act on the tissue cells that the latter produce bodies (antibodies) Avhich are inimical to the bacteria, why may not the body fluids in turn so act on the bacteria that the latter produce bodies (antibodies) which are inimical to the tissue cells? "Looked at from the point of view of the bacterium, as well as from that of the animal host, ac- cording to the hypothesis advanced, the struggle be- tween the bacteria and the body cells in infections may be conceived as an immimizing contest in which each participant is stimulated by its opponent to the produc- tion of cytotoxins hostile to the other, and thereby en- deavors to make itself immune against its antagonist." (Welch.) A more reasonable hypothesis could hardly be ad- vanced, and no small number of facts known at the pres- ent time are in harmony with it. Walker had already performed Avork of a fundamental character, which showed that the typhoid bacillus, when grown in the presence of its antiserum, acquires greater virulence for animals. Furthermore, a greater dose of protective serum was required to save guinea-pigs from infection with the immunized culture than from the same strain which had not been immunized. The fact has been known for a long time that the typhoid bacillus resists agglu- tination when freshly cultivated from a patient ha^nng the disease, whereas it becomes easily agglutinable after a period of artificial cultivation. It may well be assumed that the bacillus, when playing the part of an infecting organism, gradually was immunized against the agglu- tinating properties of the patient's serum; and, on the 5GS Al'J'EXDfX. otlier hand, that it lost tiiis resistance after it had been removed from the stinuihiting influence of the infected body. This immunization with agglutinins may be car- ried on in the test glass, and bacteria which have been so treated acquire the power to absorb a greater quantity of agglutinin from the homologous serum (Bail). Another pertinent observation w\as that by Wechsberg, who found that a strain of the diphtheria bacillus when grown in a medium containing diphtheria ant itoxin could ue made to produce diphtheria toxin more abund- antly. We may assume that the antitoxin combined with the corresponding receptors situated in the bacilli (diphtheria toxin), and that the bacilli were, as a result, stimulated to produce a greater number of such recep- tors (toxin). Consistent as these observations are with the hypo- thesis under discussion, Welch meant a great deal more than the immunization of the bacteria against the de- fensive powers of the animal body. Not only may a bac- terium during infection become more resistant to the bactericidal action of the body by producing antibodies for those bactericidal agencies, or by its ability to ab- sorb and dispose of a greater quantity of bacteriolysin ; and not only may a bacterium be able to respond to the presence of natural antitoxins in the body by the pro- duction of more toxin; but, in addition, certain constitu- ents of our body fluids may, by combining with suitable bacterial receptors, stimulate the bacterium to the pro- duction of a Avhole shower of cytotoxins, which attack the leucocytes, erythrocytes, nerve cells, liver, kidney, etc. The nature of the animal substances which may combine with the bacterial receptors and thus cause the formation of the bacteriogenic cytotoxins is left an open question, and is not of essential importance for the theory : it is not at all necessary that they be toxic for the bacterium, and they may even be taken up as food substances. Likewise the possible nature of the cytotoxins produced bv the bacterium is of secondary importance. It so hap- pened that Welch assumed that they might be of the nature of amboceptors, which may become complemented by bacterial complement, by the circulating comple- ment of the body or by endocomplements of the tissue cells. One could with equal reasonableness assume that Ar/'ENDfX. .509 they may be complete toxins, receptors of the second order, with a haptophorous and a toxophorous structure. A well-known statement of Metchnikoff is to the effect that a particular bacterium when virulent is not so readily taken up by leucocytes as is an avirulent strain, 'ihis fact has been noted repeatedly in recent times in tne study of phagocytosis in the test tube. This may be because the organism, in its virulent parasitic state, secretes substances which repel the phagocytes, neu- tralize the opsonins, or because of the formation of actual leucocytic toxins. One of the most widely known phenomena in relation to the virulence of some organisms is that their patho- genicity may be increased by passing them through suit- able animals repeatedly. The best results are obtained when intermediate artificial cultivation is avoided and the inoculations are made directly from the dead into the living animal. It may, with all reason, be assumed that by continued residence in the host the bacterium has been trained to produce a greater quantity of toxic substances which are inimical to the host, and that the increased virulence of the parasite depends on this con- dition. Although up to the present time systematic attempts to place the hypothesis of Welch on a firm experimental basis appear not to have been made, the observations cited, as well as others which could be enumerated, pro- vide cumulative evidence of its correctness. II. — The Aggressins of Bail. Not entirely foreign to the subject discussed above is the so-called aggressin theory of Bail, the essential points of which may be given without entering into a detailed discussion. Bail attributes to pathogenic bacteria the property of "aggressiveness," through which they directly antagonize the protective agencies of the body. The micro-organ- isms of highest parasitic powers, the "true parasites," as those belonging to the hemorrhagic septicemia group, possess the greatest aggressiveness, since they are able to proliferate in the blood stream while the antibacterial activities of the body (phagocytosis, etc.) are held in abeyance. Other bacteria. Avhich in causing disease tend .-)70 AITESDIX. to remain localized, and, if by any means they reach the blood stream, are not able to proliferate greatly in this place, are "half parasites" and have a lower degree of aggressiveness; they are more siisce])tible to ))hagocyto- sis and to the action of bacteriolysins (typhoid, cholera, dysentery ) . [Saprophytes have no aggressive action. This is very general, but Bail and liis co-workers have attempted to put the conception on an experimental basis by demonstrating the existence of a substance on which i..e aggressiveness of bacteria depends; to this substance tney give the name of "aggressin.' Intraperitoneal inoculation of the tubercle bacillus into the guinea-pig leads to more or less general tuber- culosis and to the death of the animal in the course of a few weeks. If, during the course of the disease, a second injection of a large quantity of the bacillus is made into the peritoneal cavity, or if an injection of tuberculin is given, the animal dies very quickly. This is, of course, nothing more than the well-known hypersusceptibility of tuberculous animals to the products of the tubercle bacillus. In addition to this fact, however, a similar result was obtained in another manner. If a large quan- tity of bacilli is placed in the peritoneal cavity of a liealthy guinea-pig, and the exudate is removed after twenty-four hours and freed from leucocytes and bacilli, the aggressin of the bacillus is said to be present in the clear lluid. This is demonstrated by injecting some of the iluid, together with tubercle bacilli, into the peri- toneal cavity of another healthy guinea-pig. The rapid death of the animal is the result, whereas the bacilli alone cause death only after a long period, and the cell- free exudate alone is without toxicity. A similar condition has been found in experimental in- fections with a number of bacteria (typhoid, cholera, dysentery, plague, chicken cholera), the essential fact being the same: that, following intraperitoneal or intra- pleural inoculation, the resulting exudate, when freed from leucocytes and bacteria, has the power of intensify- ing an infection by the corresponding organism. There seems at present to be no definite knowledge concerning the nature of these aggressins. although Bail thinks they may resemble true toxins in some respects. Likewise the precise character of their action is un- APPENDIX. 571 known, altlioiigli Bail and liis ('(j-woikcr.s are strongly inclined to the view that they inhibit phagocytosis by some direct action of the leucocytes. It is further interesting that immunization with ag- gressins is said to give rise to the formation of anti- aggressins, and that by the use of antiaggressive serum the action of the aggressins is neutralized, and the bac- teria consequently become the prey of the leucocytes. The action of the antiaggressive serum is said not to depend on the presence of bacteriolysins. One can hardly attempt a serious criticism of the aggressin theory at this time, and the above statements are made only to signify its general character. III. — COBBA-LECITHID. Too late to be incorporated in its proper place in the text, it is learned that the chemical identity and mole- cular weight of cobra-lecithid have been determined by Dr. Kyes in the laboratory of Ehrlich, and that work descriptive of the characteristics of the substance is in process of publication. "BIBLIOGRAPHY:' Ilopf: Immunlt-it unci Immuulsiorun^, Tubiugeii, l.i)02. lihrlich (and his lHlI>il^^• : Collecicd Studies on Immunity. Autlioiized Translation by diaries Bolduan, M. D. (Ju prep- araiion). .lolin WiU-.v iJt Sons, New Yoii<. Metclinii;oir : Immunity in Infectiye Diseases, Masson et C'ie.. Taris, 1!)01. Translated by Binuie. MacMlllan & Co. $r>.L'5 net. !»ieudonne: Inununitiit, Scliutzimpfung nnd Serumtlierapy. 4tli Edition. .Toll. Ambr. Bartb, Leipzig, 1905. (Gives the fundamental literature.) Roger : Les Maladies Infectieuses. Masson et Cie.. Paris, 1002. (Detailed treatise on the infectious properties of different micro-organisms.) Kolle and Wassermann : Handbuch der I'athogenen Mi- kro-organisiiaen, Giistav Fischer, Jena, 1902-1904. Kour volumes. Ritchie : Current Theories of Immunity. Journal of Hy- giene, 1902, pp. 21.-), 2.52, .344. Charrin : I.os Defenses Naturelles de I'Organisras. Masson et Cie.. Taris. 189S. Bosanquet : Serums, Vaccines and Toxins. Keener & Co., Chicago. 1904. :i44 pages. Oppenheimer, Carl : Toxine und Antitoxine, Fischer, Jena, 1904. (Gives the important literature.) Wassermann : Immune Sera. Hemolysins. Cytotoxlns and Precipitins. Translated by Charles Bolduan. 1904. Sachs : Die Ilomolvsine. From Lubarscli-Ostertag's Kr- gebniss^. Bergmann. Wiesbaden, 1902. (Literature to date of publication is given. Reprint may be purchased.) Sachs : Die Cvtotoxine dcs Blutserums. Binchemisches Centralblatt, i, l^O.*?, .'573 fif. (Literature to date of publi- cation.) Bensaude : Le Ph^nom^ne de I'Agglutination des Mi- crobes. Paris, Carr4 et C. Naud, 1897. (Gives the early literature on agglutination.) V. Dungern : Die Antikfirper. Fischer, Jena. 1903. Wcigert. E. : Les Tuberculiues. Storck et Clc., Lyon, France. 1902. Wright : A Short Treatise on Antityphoid Inoculation. Archibald Constable. Westminster. 1904. (An exposition of the methods and principles of Wright.) Scbenbe : Diseases of Warm Countries. Second Edition, 1903. Translated by Cantlie. Manson : Lectures on Tropical Diseases. Chicago. Keener & Co.. 190.-. Nocard and Leclainche : Les ^Maladies Microbienne dea Animanx. Two volumes, third Edition. Masson et Cie., Paris. lOO.^i. Welch : The Huxley Lecture on Recent Studies of Im- munity with Special Iteference to Their Bearing on Path- ology.' Medical News, 1902, vol. Ixxxi, 721. * Si->e nolo in tlio Profnce concerning Bibliography. INDEX, PAGE. Abrin 0, 104, 204 Achalme, bacillus of, in rheumatic fever 359 Acne, staphylococcus in 370 Acquired Immunity (see Immunity, acquired). Active immunity (see Immunity, active). Actinomyces iovis et hoininis (ray fungus) 10, 458 Classification of, 459, 460 ; cultivation and morphology of, 459 ; lungs, in, 337 ; occurrence of, in nature, 460 ; phagocystosis of, 461 ; resistance of, 459 ; species of, and virulence of, 460. Actinomycosis 10, 450-462 Animals, susceptibility of, to, 460 ; connective tissue, formation of, in, 5, 45S, 461 ; immunity and sus- ceptibility to, 461, 462 ; infection atria, 460 ; iodld of potassium In treatment of, 462 ; lesions, charac- ter of, 45S, 460 ; phagocytosis In, 461 ; prophylaxis of, 461 ; transmission of, 460. Acute articular rheumatism (see Rheumatic fever) .... 541 Adrenal gland, cytotoxln for . 173 Agglutination 92, 118 Of erythrocytes, 103 ; of erythrocytes with silicic acid, 129 ; etiology, determined by. 7 ; group agglutina- tion, 110, 113 ; immunity, relation to, 96, 97 , macroscopic and microscopic, 102 ; prognostic im- portance of, 95 ; sodium chlorld, influence on, 110 ; stages in the reaction, 110 ; substances concerned, 105 ; serum dilutions, 113 ; specificity. 111 ; technlc, 98; theories of mechanism of, 116; see also under Agglutinins and under dlfCerent diseases and micro- organisms. Agglutinins 92-118 Absorption of by bacteria, 2u3 ; agglutinophorous group, 108 ; autoagglutlnlns, 104 ; chief agglutinins. Ill : congenital, 93, 96 ; definition, 105 ; distribution of, in the body, 95 ; Ehrllch's theory of the produc- tion of, 114 ; ferments, action of, on, 96, 107 ; for- mation of, following vaccination, 233 ; haptophorous group of, 108 ; Hauptagglutinin, 111 ; immune, 62, 93 ; Isoagglutinins, 104 ; mixed infections. Influence of, on, 113 ; Mitagglutinin, 109 ; normal, 55, 92 ; origin of, 96 ; precipitation of, by chemicals, 107 ; produc- tion of. 93 : receptors of 2d order, 108 ; resistance to acids and alkalies, 109 ; resistance to heat, 97, 108, 109 ; somatic and flagellar, 107 ; specificity of. 92 ; structure of, 108 ; union with cells, character of, 203, 204 ; unit of measure of, 103 ; variations of, in animals, 114 ; variations in the quantity of, 95 ; ^ymotoxic group of, 108 ; see Agglutination, Agglutinogens, Agglutinoids, and also under the dif- ferent micro-organisms. 574 INDEX. }'AG1'.. AKiiluiliiosenlc power of bacteria 04 AgKlutino-iens. or asfilutiuable substances 10r> Diffiisibility of, 1M7 ; distribution of, lUG ; flagellar and somatic. loT ; nuiltipllcity of, 107 ; resistance of, to heat, 107 : structure of, 108 ; see Agglutinins and Asrshitination. Agglutinoids 109 Aggressins 509 Alexins 411, 130 Delinition of. 40; identity of, with complement, 134, 13r( : nature and selective action of, 131 ; see Com- plement. Alkaloids. Failure to cause formation of antibodies, 198; state of. within the cells, 198, 205. Amboceptold • • 209 Amboceptors 134, 141 Absorption of, by cells, 144. 140. 203 ; bacteriolytic, 143 ; complementophllous haptophore of, 147 ; cyto- philous haptophore of, 14G ; formation of, 150 ; for- mation following vaccination, 233 ; hemolytic, 141 ; influence in phagocytosis. 190 ; Isolation of, 14G ; manner of action of, with complement, 145. 148, 207, 208 ; occurrence of. In animal secretions. 158 ; origin from leucocytes, 183, 190; origin in cholera, 190; receptors of the 3d order, 207 ; sensitization by, 142. 145 ; solutions of, 144 ; specificity of, 152, 153 ; structure of, 147 ; svnonvms for, 148. 217 ; union with cells, nature of," 147. 148, 203. 204; see Hem- olysins (serum), Bacterlolyslns, Cytotoxins and Venoms. Ameba coli. Discovery of. 502 : pathogenicity of. 502 ; symbiosis of. 502 ; see Amebic dysentery. Ameba proteus 500 Ameba. Cultivation and distribution of, 501 ; phagocytic action of. 170; resistance of, 501; symbiosis, 501, 502. Amebic dysentery 500 Anatomic changes in, 503 ; immunity to, 504 ; liver abscess in, 503 ; occurrence of. 502 ; prophylaxis, 503 ; see Amebns, and Ameba coll. Amlbodiastase 176 Amyloid degeneration, production of by staphylococcus. . 375 "Anatomic tubercle" (see Tuberculosis j. Animals, susceptibility of, to Actinomycosis. 460; anthrax, 330, 331; B. influenza, 304; ji. melUensis, 335; cholera, 309; hydrophobia. 513, 514 ; leprosy, 447 ; Micrococcus catarrhaUn, 384 ; Micrococcus meninc/itidis. 390 ; oidiomycosis. 4ii7 ; pneuraococcus. 339 ; pseudotuberculosis, 444 ; relapsing fever, 404 ; staphylococcus. 375. 376 ; streptococcus. 352 ; syphilis. 522 ; trypanosomiasis, 490, 495: tuberculin, 414; tuberoilosis, 427. 441. Animal experiments, in testing value of serums 201 Anopheles mosnnitoes. A. inaciiUpennis, 478; A. punctipennis, 478; habits of. 478 ; life cycle of. 478. 479 ; malaria, rule in. 468 ; migration of, 479 ; occurrence, 478. INDEX. 575 PAGE. Antliracase-ImmiinpvnteUlin ',',?,2 Anthrax 32T-;i:i3 Animals, Immunity and susceptibility of, 330, 331 ; bacillemia, 330 ; discovery of its microbic nature, 27, 28, 29 ; immunity, 332 ; immunization, mixed, 333 ; influence of streptococcus on, 362 ; malignant pustule, 329 ; occurrence, 327 ; opsonins, 331, 333 ; phagocytosis in, 190, 331 ; prophylaxis, 330 ; serum- therapy, 332 ; toxic results, 330 ; transmission, 329 ; vaccination, 28, 29, 332 ; wool-sorters' disease, 329 ; see also B. anthracis. Antiabrin 90 Antiaggressins 571 Antiamboceptors 150 Danger in formation of, 157 ; as receptors of the lirst order, 207. Antibacterial serums (see Bacteriolysins) 22G-231 Antibodies. Mechanism of production, 199 ; origin of, 210, 314 ; scheme of, 216 ; specificity of, 208 ; union with antigens, 200 ; see Antitoxins, Amboceptors, Ag- glutinins, Precipitins, Hemolysins, Bacteriolysins and C'ytotoxins. Anticomplements 154, 207 Anticrotin 90 A.ncicytotosins 165 Antiferments G3, 90 Antigens. Scheme of, 216 ; union with tissue cells, character of, 200. Antiglobulin 124 Anti-immune serum 156 Antilaccase 90 Antile\icocidin 90, 372 Antileucotoxic serum 169 Antinephrotoxin 170 Antineurotoxin 171 P^or venom, 266. Antipepsin • 90 Antiprecipitins 123 Antirennet 90 Antiricin 90, 201. 202 Antirobin 90 Antispermotoxin 166 AntJstaphylolysin 380 Antisteapsin 90 Antistreptocolysin 353 Antitoxins 65, 91. 221, 235 Early administration of, 223, 224 ; curative action of, 222, 223 ; discovery of, 33 ; examination of by U. S. Hygienic Laboratory, 76 ; for animal toxins, 90 ; for B. botuHnus, 359 ; for B. diphtheriw, 241. 243 ; for B. pyocyaneus, 260, 261 ; for B. ietani, 223, 252 ; for bacterial toxins, 89, 90 ; for plant toxins (abrin, crotin, ricin, robin, phallin), 90, 264: for pollen toxin, 263 ; for zootoxins, 268 ; formation of. 85 : haptophorous group of, 79 ; infections charac- terized by the formation of, 235, 268 ; leucocytic :)7(i i\ni:x. I'AGK. origin, question ol', 191 ; niauul"acture ol', O'J ; mode of action of, I'Ol, 221, 220; nature of, lUl ; toxins, neutralization of, by, 78, 201, 2U3 ; normal, 45 ; pres- ervation of, 71, 73 ; propliylactic action of, 226 ; receptors, free, S9 ; receptors of tlie lirst order, 207 : relation of, to toxins. In tlie body, 222 : rela- tion of, to toxins, in vitro, 221 ; standardization of, 72, 25.") ; unit of, 72 ; see Part II, Group 1, and also tlic dill'erent micro-organisms. Antitrypsin 90 Antiurease ''" Antivenin 70, 90, 207, 208 Aniilyrosinase 90 Arachnolysin (spider poison) 10, 268 Arrhenius and Madsen, views of 210 Anltritis 344, 348, 354, 378, 386, 391 Asperj;illus 6. 407 Atropliy, phagocytosis in 178, 179 Attenuation. Importance' of in vaccination, 57 ; methods of, 219. Autougi,'lutinins 104 .A.ulocytotoxins 103, 174 Autolytic products, vaccination witli 220, 312 .^.uiouephrotoxins 169 Autoprecipitins 121 Autospermotoxin 160 Bucillus ii'drogenes capsulatun 14, 185, 359 liaLillus alcaligencs 270 IJfiilliis aiithracis 10, 327-329 Antagonism of, bv other bacteria, 329 ; antiserums for, 32^; attenuation of, 58, 219 ; cultivation of, 328 ; discovery of, 27, 327 ; gastric juice, effect of, on, 39, 329 ; iicmunity, active, 332 ; immunity, acquired, 186, 331 ; immunity, natural, 330 ; immunity, passive, 332 ; infection atria, 39 ; opsonins, 331 : phagocytosis of, 331 ; serums, effect of, on, 48, 49, 331 ; spores of, 29, 327, 328 ; toxic properties of, 330 ; vii-ulence of, 329 ; see Anthrax. Bacillus botulinus 250, 257 Animals, susceptibility of, 257, 258 ; antitoxin for, 259 ; morphology, etc., 257 ; occurrence in meat, 257 ; saprophytic nature of, 258 ; spores of, 257 ; toxin, action of, 258 : toxin, detection of in meat, 257 ; toxin, preparation and resistance of, 258 ; see Botulism. Bacillus chanori mollis (bacillus of Ducrcy ; bacillus of soft chancre) , 10. 399 Cultivation, morphology, phagocytosis of, susceptibil- ity of animals to, 400. Bacillus of chicken cholera 58 Bacillus coli cominunis 298-304 Agglutination of, 92, 94. Ill, 304 ; autagoni.sm for pu- trefactive bacteria, 299, 300 ; antiserums, properties of, 303 ; beneficial functions of, 299 ; in cystitis, 303 : in enteritis, 40, 301, 303; group agglutination. 111; group of, 298 ; in meningitis, 389 ; morphology and staining of, 298; occurrence in intestines, 298, 299; occurrence in nature. 29S ; in pneunionin. 330: ro- INDEX. 577 PAGE. sistance of, 208, 290 ; serums, effect of, on, 200 ; sym- biosis with Amelta coli, 502 ; toxin of, 303 ; typicai strains of, 290; virulence of, 300, 301, 302. Bacillus diplitheriw 10, 235, 236 Agglutination of, 243 ; antitoxin for, 89, 241, 242 ; morphology, staining, cultivation, resistance, viabil- ity of, 236 ; occurrence of, in the body, 237, 238 ; phagocytosis of, 240 ; pneumonia, in, 33G ; toxic ac- tion of, 15 : toxins of, 66, 67, 237, 238, 242 ; toxin, attenuation of, 40, 210 ; tuberculosis, in, 425 ; see Diphtheria. Bacillus of Ducrey. See Bacillus chancri mollis. Bacillus dysenteriw 10, 288-290 -Agglutination of, 92, 94, 288, 289, 294 ; antiserums for, properties of, 293 ; cultivation and morphology of, 288, 280 ; dissemination of, 292 ; endotoxin of, 291 ; etiologic role of, 280 ; "Flexner" type of, 289 ; pseudodysentery bacilli, 288 ; toxicity of, 291 ; toxin, autolytic, of, 201 ; types of, 288 ; see Dysentery, acute epidemic. Bacillus edemor, maligna) 1, 14 Bacillus enteritidis 294-298 Agglutinins and agglutination of, 94, 298 ; Bacillus paratypliosus , resemblance to, 285 ; discovery of, 295 ; fermenting powers of, 295 ; group agglutina- tion, 111 ; group of, 295 ; meat poisoning by, 294-208 ; morphology and staining of, 295 ; occur- rence of, in meat of horses and cattle, 295, 296, 297 ; poisoning by oysters and fish, in, 297 ; resist- ance of, 297 ; toxin, 295-206 ; toxin, occurrence in , meat, 297 ; toxin, resistance of, 297. Bacillus of Friedlander ; see Bacillus pneumonice. Bacilli from butter, grass and milk 444 Bacillus icteroides, in yellow fever 11, 530, 531 Bacillus influenzos 10, 394 Agglutination of, 399 ; animals, virulence for, 395 ;' antiserum, properties of, 390 ; in conjunctivitis. 396 ; cultivation of, 394 ; discovery of, 394 ; excre- tion of, 395 ; hemophilic properties of, 394 ; im- munization with, 399 ; in meningitis, 389-306 ; morphology and staining of, 394 ; occurrence of. in the' body. 396 ; otitis media, in, 396 ; peritonitis, in, 396 ; resistance of, 395 ; symbiosis of, 394 ; toxin of, 395 ; tuberculosis, in, 425 ; see ' Influenza. Bacillus lactis aerogenes. Antagonistic action on putrefactive bacteria, 300 ; oc- currence in intestines, 401. Bacillus lepras 10, 446 Animals, insusceptibility of, to, 447 ; antiserums for, 452 ; discovery of, 446 ; endotoxin, question of, 450 ; excretion and occurrence in nature of. 447 ; incul- tivability of, 447 ; morphology of, 447 ; occurrence in the body, 449 ; phagocytosis of, 449, 451 ; see Leprosy. Bacillus of Lustgarten 443, 552 Bacillus mallei 10, 453 Agglutination of, 458 ; cultivation, morphology and resistance of, 453 ; mallein, varieties, and prepara- 57S IXDEX. PAGE. lion ol", 4."(4 ; im'iiiii.uilis. in, :1^'.' ; i)ha,:j;oc.vtosis of, 4riG, Bacitliis melitensis 334, 335 AgTfil'itination of. o34 ; animals, siisceiilibility of, to, 3;>o ; morphology of, 334 : opsonins, iulhieuce of In phagocytosis of, . 334 ; serums, effect of, on, 334; see Malta fever. Ba< illiis inucosus vupsulutiis 401 Bacillus of ozena 402 BaciUus vai-'ityphosus 284 Agglutination of, 11, 2S4, 287 ; antiserums for. jm-oi)- erties of, 287 ; blood cultures, 288 ; endotoxin, 287 ; excretion of, 28G ; meat poisoning by, 285 ; occur- rence in the body. 280 ; "paracolon" bacilli, rela- tion to, 285 ; resistance of, 280 ; toxicity, 287 ; tvpes of. 285 ; see Paratyphoid fever. Bacillus pestis 10, 316-319 Agglutination of, 94, 320 ; cultivation of, 310, 317 ; endotoxin, resistance of, 319 ; excretion of. 321 ; involution forms. 317 ; meningitis, in, 389 : mor- phology, 310; phagocytosis of, 325; pleomorphism, 316 ; pneumonia, in, 330 ; resistance and viability, 317, 318 ; staining of, 310 ; toxicity of cell bodies, 310 ; toxiu of Lustig and Galeotti, 318 ; toxin, soluble, question of, 318 ; virulence, 318, 319 ; see I'lague. Bacillus pneumonia- (bacillus of Friedlander) . 337, 401, 402 Agglutination of, 94, 402 ; antagonism for B. anthra- cii?, 329 ; antiserum. 402 ; influenza, 397 ; lesions caused bv, 402 ; meningitis, in, 389 ; pneumonia, in, 336, 344.' 402 ; tuberculosis, in, 425. BaciUus proditJiosus. Antagonism for B. anthracis, 329; Coley"s mixture, in, 362 ; symbiotic action of. 185. BaciUus psittacosis, agglutination of 94, 111 Bacillus pseudotuberculosis, varieties of 445 Bacillus pyocyaneus 259-261 Agglutination of, 92, 94 ; agglutinins for, 261 ; agonal invasion by, 259 ; antagonism for B. anthracis, 329 ; antitoxin, 261 ; bactericidal serum for, 261 ; fer- ments of, 260 ; endocarditis, in. 259 ; endotoxin of, 260 ; enteritis, in, 40 ; infections, symptoms of. 260 ; meningitis, in, 259 ; pigments of. 200 ; pyo- cyanase. 260 ; pyoc.vanolysin. 260 ; p.vocyanin, 360 ; secondary infections by, 259 ; septicemia, in. 259 ; toxic action of, 16 ; toxin, soluble, 06, 260, 261 ; tu- berculois. in, 425. Bacillns of rhinoscleroma 402 Bacillus of symptomatic anthrax 185 Bacillus tetam 244-256 Agglutination. 256: anaerobic property of, 247; ani- mals, susceptibility of, to toxin, 51 ; avirulent strains, 249 ; discover.v of, 244 ; morpholog.v, stain- ing, cultivation, 244. 245 ; occurrence in intestines. 246; occurrence in nature. 245; parasitic power of, 247: pnthogenlc properties of. 249; resistance of spores of. 246 : toxins of. 15. 20. 00, 07, 249 ; toxin, absorption of. by leucocytes. 191: toxin, fixation of. INDEX. 579 PAGF by tissues, 52, ij.'i, 204. 205, 222, 251 ; toxin, attenuation of, 21!) ; toxin, action of gastric .juice on, ."'.0 ; toxin, neutralization of, by antitoxin, 224 ; action of pancreatic juice on, 40 ; virulence, 185 ; see Tetanus. Bacillus tuberculosis 10, 407 Agglutination, 438, 440 ; agglutination, relation of to immunity, 97 ; animals, susceptibility of to, 427 ; antiserums, properties of, 4.38 ; attenuation of, 410 ; avian, 442 ; bacteria resembling, 443 ; bovine, differentiation of bovine, from human, 417 ; con- stituents, 411 ; cultivation, 409 ; discovery of, 407 ; effect on tissues, 42, 44, 422-425 ; ex- cretion of, 414, 415, 419 ; fever producing s!il)stance of, 411 ; of iish, 443 ; gastric juice, re- sistance to, 39. 410 ; immunization with, 411, 430- 432 ; inflammation of lungs, in, 337 ; lesions pro- duced by, 411 ; morphology of, 408 ; occurrence in nature, 414 ; pathogenic properties of, 411 ; pha- gocytosis of, 421, 422 ; proteins in, 411 ; resistance of, 409 ; staining properties of, 408, 411 ; strepto- coccus, influence of. on cultui'es, 356 ; "toxalbumin" of, 411; toxic substances, effects of, 411; toxin of Marmorek, 404 ; toxins, 439, 440 ; virulence of, 410, 427 ; see Tuberculosis. Bacillus tuphosus 10, 269 Agglutination of, 92, 94, 116, 283, 284 ; antitoxin, question of, 271 ; autolysis of, 271 ; blood cultures of, 273, 284 ; discovery of, 269 ; dissemination of, 270 ; endotoxin, 271 ; excretion of, 273, 274 ; ex- tracts of, 282 ; gastric juice, action of, on, 39 ; im- munization with, 280, 281, 283 ; leucocytes, relation of, to, 277 ; meningitis, in, 380 ; morphology of, 269 ; occurrence in body, 9, 270, 274 ; occurrence in na- ture, 270"; phagocytosis of, 274 ; pueumonia, in, 336 ; resistance of, 270 ; symbiosis with Ameha coli, 502 ; toxin of Chantemesse, 282 ; vaccines, 279, 232 ; see Typhoid fever. Bacillus xerosis 244 Bacterium coli commune; see Bacillus coli communis. Bactericidal serum, substance, etc. ; see Bacteriolysins. Bacteriolysins 130 Absorption of. by bacteria. 136; composition of, 134; curative value of, 227, 231 ; endotoxins, action on, 136, 228 ; group reaction with, 135 ; immunity, relation of, to, 135 ; inactivation and reactivation of. 133, 134 ; nature and selective action of, 131 ; ori- gin of, from body cells, 45. 138 ; properties, general. 130 ; prophylactic value of, 227 ; specificity of, 135 ; standardization of, 138 ; technic of testing. 139 ; therapeutic use of, 226 ; see Amboceptors and Com- plements. Bacteriolysis and bacteriolysin 130 Bacteriolysis. Group reaction. 153; mechanism of. 145: Pfeilfer's phenomenon. 131 ; similarity to hemolysis, 134 ; see Bacteriolysins. Bacteriolytic enzymes, relation to immunity 61, 62 5S0 y.\7>/;.v. FAOB. Bacteriotropic substances 227, 346. 309, 381 Balaiitidiinn roli, morphology, occurrence and patho- genicity 505, 506 Balaiitidiiitii, miniitttm 506 Keuzol ring; use of, as an analogy in ICIirli.-h's theory 106. Bile. Bactericidal and antitoxic propenies ot, 4ii ; iinnnine agglutinins in, i)'^. Biologic test Tor species; see I'lecipiiin^. "Blacl< Death" ; see Plague. "Blaekwater fever" in malaria 477 Blastoniycetic dermatitis ; see Oidiomycosis. Blastomycosis ; see Oidiomycosis. Blue pus 259 Bodo Hfinariiifs 508 Botulism 10, 250-259 Absorption of toxin, 258 ; antitoxin, 90, 259 ; immun- ity, 25!) ; infected meats, 250, 257 ; phagocytosis, 258 ; prophylaxis, 259 ; susceptibility, 258 ; symp- toms, 250 : tissues affected by lo.vin, 258 ; see BaciUii-i hotKliniis. Bovine pest 11 Bronchitis. In epidemic cerebrospinal meningitis, 391 ; meningo- coccus in, 391 ; Micrococcus catarrhulis in, 384, 391 ; staphylococcus in, 377 ; streptococcus in, 354. Capsulated bacilli 401, 402 ('arbuncle, staphylococcus in 370, 377 Carcinoma, hereditary susceptibility to 18 Cell receptors ; see Receptors. Cercomonas iiilcstiiialis, morphology and pathogenicity of 506, 507 Chancroid ; see soft chancre. Chemicals in relation to antibody formation.; 198 Chemotaxis -13, 44, 177, 185 Chicken cholera, attenuation of microbe of 219 Chicken pox (varicella I 555, 556 Chicken typhus or chicken-pest 11 Cholera 10, 304-315 Accidental, in man, 313; agglutination reaction, 315; animals, susceptibility of, to, 309 ; anti-bodies, origin of, 190. 314 ; antitoxic serum, 315 ; bacteri- cidal power of body fluids, 313 ; "cholera-carriers," 304, 313 ; diagnosis, bacteriologic. 315 ; epidemiol- ogy, 307. 308, 311, 312; experimental, in man, 313; gastric .inice. protective action of, 313; geographic distribution of. 307. 308 ; immunity and susceptibil- ity to. 50, 00, 190, 313, 314 ; infection atrium, 307 ; lesions, intestinal, 310 ; effect of leucotoxic scrum on Infections, 168 ; mechanism of intoxi- cation. 310 : mixed immunization in. 234, 314 ; phag- ocytosis, 188. 189, 313, 314 ; phagolysls. 188 ; proph- ylaxis, 218, 307, 311 : serum properties in, 20, 97 ; serum therapy, 230. 314. 315 ; sources of infection and transmission. 307-309 ; vaccines and vaccina- tion. 58, 312, 313 ; see Vibrio cholera;. Cholesterin, neutralizing action on tetanolysin 91 Chromophages 179 ITS/DEX. 581 PAGE. Cladothrix, infections witli 463 Clavelf'e (slieep-pox) 11, 554 Co-agglutinins HI Cobra-lecitliid ICO, 200, .=571 Col^ra venom ; see Venoms. Coccidia, life cycle', morphology, spore formation and patbogenicity, 508, 500. Coccidiosis 508, 509 Coccidium Mgeminum 500 Coccidium cuniculi s. oviforme 509 Corodacteria septica (Billroth) 349 Coleys mi.^tnre 362 Colle's law ; see Syphilis. Colloids 127, 128 Complement. Absorption of, 145. 229 ; decrease of during disease, 280 : diversion of, 157, 229, 230 ; isolation of, 140 ; lecithin as a. 160 : multiplicity of, 153. 210 ; origin of, 138, ISO ; neutralization of, by salts, 91, 161 ; receptors of second order, 207 ; resistance to heat, 184 : solutions of. 144 : sources of, for bactericidal serums. 228, 229 ; specificity of, 152 ; structure of. 149 ; unicity, theory of. 210 ; see Cytase. Complemintophilous haptophore ; see Haptophore. Compleraentoid . 149, 209 Complementnid-'Verstopfung 150 Conjunctivitis. B. influensce, in, 396, 397 ; diphtheritic, 237 ; menin- gococcus in, 391 ; pneumococcus in, 348, 349 ; staphylococcus in, 377. Connective tissue, role of, in innammation 5, 42, 46 Contact infection 3 Contagion and contagiousness 2 Contagious disease, definition 2 Copula of Mtiller. synonyms for 148 Cow pox 550, 554 Crotin 104. 264 Cr.vstalloids. properties of 127 Culex fatigans 540 Culex pipiens, in transmission of malaria of birds. . . . 483 Curative injections 220 Cyclasier scarlatinalis 556 See Scarlet fever. Cystomonas urinariiis 508 Cytase 178, 181, 182 See Complement. Cytorifctex variolm s. vctccinw 543 Conjugation, 544, 545 ; cytoplasmic stages, 544 ; life history of, 54-546 ; nuclear stages, 544 ; smallpox, in, 543 : vaccinia, in, 545. Cytotoxins (Cytolyslns) 55, 62, 162-175 Activity, determination of, 164 ; amboceptors in, 165 ; antileuco toxin, 169; antinephrotoxm, 170; anti- spermotoxin, 166 ; autocytotoxins, 163. 174 ; auto- nephrotoxins, 169 ; autospermotoxin, 166 ; ciliated epithelium, cytotoxin for, 167 ; complements In, 165 ; for malignant tumors, 164 ; hepatotoxins. 171 ; infections, effect of leucotoxins on, 168 ; leucotoxin, oS-2 INDEX. PAGE. 167 ; nephrotoxin, 169 ; neurotoxins, 171 ; origin, 180; of venoms, 2(55, 12GG ; pancrootoxln, 173; specificity, lack ot". IGl' : sporiuotoxln, H'>,"> ; structure of, 105; syncytiotoxiii, 171; technlc of i)roductlon, 104 ; thyrotoxin. 17;^ ; utility, theoretical, Hj2, 108. Cytolysins ; see Cytotoxins. Dacryocystitis, pucumococcus in 348 Daplinla, phagocytosis of 183 Dengue fever 539, 541 iharacteristics of, 546 ; contagiousness of, 540, 541 ; Culex fathjaiix in transmission of, 540 ; etiology, 540 ; occurrence. 530 ; "plasmelja" in. 540 ; recur- rences and relapses, 541 ; suscepiibillty to, 541 ; transmission, 540. Desmon 148 Deuterotoxin 83. 209 Diphtheria 10. 13. 20, 235-244 Agglutination reaction, 243 : bacilli, localization of, 2;)8 : conjunctivitis, diphtheritic, 237 ; forms of, 237 ; immunity and susceptibility, 50, 01, 230, 240 ; infection atria, 237 ; latent. 237 ; leucocytes in, 240 ; mixed infections in, 14, 238, 186, 358 ; paralysis, influence of antitoxin on. 242 ; predisposing causes, 240 ; pneumonia in, 344 ; prophylaxis, 240, 241 ; pseudodiphtherla bacilli in. 243 ; recurrences, 50, 240 ; septic, 230 ; serum therapy, 225, 241 ; sources of infection, 236, 237 ; tissues Injured by toxin, 23S : transmission, 237 ; vulva, of, 237 ; see Bacillus di/jlithcriw. Diplococcus iiitraccllularis mciiiiif/ilidis ; see Micrococcus meiiinpitidis. Diplococcus pneumonia; 336-349 Agglutination of, 347 ; alveolar abscess, in, 348 ; ani- mals, susceptibility of, 339 ; antiserums, properties of, 340 ; conjunctivitis, 348. 349 ; dacryocystitis, 348 ; discovery of, 337 ; endotoxins, 339 ; enteritis, 348, 349 ; group agglutination, 348 ; Immunization with, 345, 346, 347 ; influenza, in, 397 ; meningitis, 348, 349, 389 ; morphology, staining, and cultiva- tion, 337, 338 ; neurotoxic strains of, 339 ; occur- rence in blood. 343 ; occurrence, normal, 339 ; op- sonins in phagocytosis of, 346 ; otitis media, in, 348. 349 : peritonitis, in. .348, 349 ; phagocytosis of, 346 ; pneumonia, in. 337-348 ; pneumotoxin, 339, 346 ; pulmonary hemorrhage, in, 344 ; resembljince to streptococcus, 338 ; resistance, 338 ; rhinitis, in, 348; septicemia. 348; serpent ulcer, 348, 340; tuberculosis. In, 425 ; virulence, 338 ; virulence, in- crease of, 342 ; see Pneumonia. Diplococcus (streptococcus) in rheumatic fever 359 Donrine ; see Trypanosomiasis in animals. Droplet infection 237 In diphtheria, 237 ; in influenza, 397 ; in tuberculosis, 415. Drug habituation 22 Dust infection 237 In diphtheria. 237 ; in influenza, 3!t7 ; in tuberculosis, 415 ; in typhoid fever, 272. INDEX. 583 PAGE. Dvsenterv, acute opidemic 8, 10, 288-204 "Agglutination reaction, 204 ; antiserums, properties of, 203 ; bacilli, clisseminatlon of, by stools, 292 ; bacilli, distribution of. in the body, 290 ; chronic, 288, 292 ; immunity and susceptibility, 60, 202, 293: incubniion period, 288; institutions, occurrence in. 202: iiilcslinal lesions in, 200; occurrence of, 288 ; predisposing causes of, 202 ; prophylaxis, 292 ; serum therapy, 293 ; summer diarrheas of infants, 289 ; transmission, 292 ; vaccination, 293 ; see Ba- cillus (lysentericE. Eclampsia, relation of syncytiotoxin to 171 Eczema, relation of staphylococcus to 376, 377 Eel serum, antitoxin for 90 Ehrlich's partial saturation method 80, 209 Ehrlich's "side-chain" theory. See "Side-chain" the- ory of Ehrlich. Emboli, bacterial 4 Endocarditis. Colon bacillus in, 302 ; gonorrheal, 386 ; pneumococcus in. 344, 348 ; staphylococcus in, 359, 377 ; strepto- coccus in. 354. 358, 359. Encephalitis, in epidemic cerebrospinal meningitis.... .391 Endocomplement 159, 266 Endotheliotoxin, of venom 265 Endotoxins 330 Anthrax bacillus, 330 ; Bacillus pyocyaneus. 260, 261 ; bacteria containing, 226, 231 ; cholera vibrio, 300 ; diseases associated with, 269 ; dysentery bacillus, 291 ; failure of bactericidal serums to neutralize, 227 ; glanders bacillus. 453 ; of gonococcus, 385 ; leprosy bacillus, 450 ; liberation of, by bacteriolytic serums, 136, 228; meningococcus, 390; paratyphoid bacillus, 287 ; plague bacillus, 318 ; pneumococcus, 330 ; staphylococcus, 262, 373 ; streptococcus, 262. 353 ; tubercle bacillus, 411 ; typhoid bacillus, 271. Enteritis. Amcha coli in ; see Amebic dysentery ; Balantidiiim coli in, 505 ; Cercomanas intestinalis in, 506 ; colon bacillus in, 303 ; pneumococcus in, 348, 349 ; staph- ylococcus in, 377 ; streptococcus in, 354, 355, 357 ; Trichomonas intestinalis in, 507. Enzymes, bacteriolytic, relation to immunity 61, 62 Enzymes, intracellular 176 Epilepsv. cytotoxin in 174 Epithelioma contagiosum of fowls 11 Epitoxoids 81 Erysipelas 355 Effect on tumors, 362 ; experimental production of, by streptococcus, 355 ; in course of tuberculosis, 356 ; recurrence of, 56 ; staphylococcus in, 355 ; strepto- cocci in, 350, 354. Etiology, infectious 7 Etiology, unknown 10, 510 Exhaustion, toxin of 174 Farcin da bwuf 463 584 IXDEX. PAGE. Farcy, sec Glanders 10 Fermentation, early studies on 27 Fibrin, mechanical value of in inllammation 45 Fixator, aynonyms for 148 See Amboceptors. Filaria perstans 487 Filaiia sanguinis hominis 4 Fish, B. cntcfitidis in poisonous 297 Fish poisons, antitoxins for 90 Fleas, in the transmission of plague ^520, 321 Flies, as carriers of tvphoid fever 272 Fomites 3, 532, 539 Food-substances. Fixation of, by amboceptors. 208 ; manner of union with cells, 197 ; non-formation of antibodies for, 109. Foot and mouth disease 11, 12 Fowls, epithelioma contasiosum of 11 "Gambian Fever" ; see Trypanosomatic Fever. Gastric juice. Protective role of, 39. 313. 329. Gelatinase 371 German measles (Rotheln) 562 Glanders (Farcy) 10. 30. 452-458 Agglutination reaction. 458 ; animals, susceptibility of. 452 ; bacilli, distribution of, in the body. 454 ; connective tissue development in, 456 ; diagnosis, bacteriologic. 457; healing processes in. 456; im- munity, 456 ; infection atria, 454. 455 ; mallein in diagnosis of, 457 ; organs involved, 456 ; pha- gocytosis, 456 ; serum therapy, 457 ; tissue reactions, 455 ; see RaciUus mallei. GJossina palpalis in transmission of sleeping sickness.. 488 Gonococcus ; see Micrococcus yonorrhea;. Gonorrhea 10, 56, 384-388 Acute and chronic, 387. 388 ; complications of, 380, 387 ; immunity, 56, 387, 388 ; ophthalmia in, 386 ; phagocytosis, 385, 389 ; reinfection, 387, 388 ; su- perinfection, 388 ; susceptibility of different tissues to, 386 ; urethral changes. 387 ; see Micrococcus gonorrhea;. Gonotoxin 386 Grass bacilli 444 Oregarina lindemanni ; see Sarcosporidia. Group agglutination 110. 113, 284, 287. 298, 348, 369 Gruber-Widal reaction ; see Agglutination. Hairs, phagocytosis of pigment by chromophages .... 179 Halteridium. r Impregnation of parasite, 468 ; in malaria of birds, 483. Haptophores T9, 197, 199, 207 Ilaptophorous groups ; see Haptophores. llaupiagglutinins HI Hav fever 262, 263 Antitoxin (pollantin). 90, 263; pollen as cause of, 262 ; toxin of, 262. Hanging-drop preparation 98 INDEX. 585 PAGE. Hemagglutinins. Of plants, 103 ; of serums, 104 ; of venom, 2G5. Hemoglobinuric fever, in malaria 477 Hemolysins. Animal, 264, 268 ; bacterial, 202 ; cobra lecithld, 160, -O'j, 571 ; colloids as, 160 ; e'xperimental value of, 141 ; from organ extracts, 180 ; immune, in serums, 62. 141 ; intraleucocytic, ISO ; normal, in serums, .'54 ; pyocyanolysin, 260 ; serum hemolysins, structure of, 141 ; staphylococcus, see Staphylolysin ; streptococ- cus, see Streptocolysin ; tetanolysin, 249 ; venom, of, 265. Hemolysis, see Hemolysins. Hemolytic experiments. Technic of, 141 ; value of, in study of immunity, 142 Hemorrhagic septicemia group of bacteria .316 Hemorrhagin 159, 265 Hemotoxins 67 Hepatotoxins 171 Heterologous serum 94 Homologous serum 94 "Horror autotoxicus" 174 Horsepox 554 Hydrophobia 10, 510-521 Animals, in, 51.3, 514 ; antiserum, properties of, 421 ; diagnosis, in dogs. 515, 516 ; extension through nerves, 517 ; fixed virus of, 51.3 ; immunity, charac- ter of, 521 ; immunization, mixed, 521 ; incubation period, 514, 515, 517, 518 ; micro-organisms found in, 510 : Negri bodies. 510. 511 ; Pasteur treatment, 518, 52] : prophylaxis of, 517, 521 ; specific ( ?) le- sions, 516 : street virus of, 512 ; transmission of, 514: toxin, question of, 511; vaccination, 29. 30, 519 : vaccine, preparation of. 518, 519 ; virulence for man. 513, 517, 520 ; virulence, increase and de- crease of. by passage, 513 : virus, attenuation of, 58. 23 9. 511, 518-520; virus de rue, 513; virus, dis- tribution and excretion of, 518 : virus, filterability of. 12. 511; virus 1ixe, 513, 518: virus, resistance of, 512. Ichthyosismus 256 Ichthyotoxin 268 Immunitv. Absolute. 21 : acquired, 18, 56-64 : active. 21. 56. 59 ; antibacterial. 19. 47, 48, 49, 211 ; antitoxic, 19, 49, 50, 210 ; definition of, 17 ; in families, IS ; leuco- cytes, relation to ; see Phagocytosis ; natural, 18, 35-55 : early theories of. 24 ; passive. 21, 60 ; rela- tive, 21 ; theories of, 30-34 ; types of, 22 ; see An- titoxins, Bacteriolysins, Phagocytosis and the indi- vidual diseases. Immunization. Active, as curative measure, 220 ; active, for prophyl- axis, 232 ; classification of methods, 218 ; choice of animals for, 229 ; mixed, 220, 234 ; passive, as cura- 586 INDEX. PAGE. tlve measure, 220 ; passive, In prophylaxis, 220 ; with tissue cells, 1G4 ; with toxins, 33. Impetisro contagiosa. Staphylococcus in. 3o4 ; streptococcus in. .".■"iT. Incubation period -'10 Infection. "Air borne." 3 ; atrium of. 3. 35, 30 ; contact, b.v, 3 ; mixed, 11, 14. 15. 113; see individual diseases; "water borne," 3 ; infectious agents, classification of. 6. Infectiousness and contagiousness 2 Infestation 2 Inflammation. Antagonism of, to infections, 4G ; chemotaxis, 43 ; connective tissue, inflammatory rSle of, 41, 40 ; fibrin, influence of. 45 ; injurious effects of, 41, 42 ; leucocytes in. 43-45 ; nature of, 41 ; organization in, 45 ; pha^rocytosis in, 43-45 ; plasma, influence of, 45 ; relation of, to virulence of bacteria, 42, 43 ; role of, in immunity and resistance, 41 ; variations in intensity, 42-44. Influenza 10, .393-399 Conjunctivitis in, 37, 397 ; chronic, 397 ; contagiousness of, 303 ; epidemics of. 308 ; immunity, 308 ; infec- tion atrium. 307 ; intestinal, 30G ; intoxication, 39G ; meningitis in, 300. 307 ; mixed and secondary infections in, 397 ; otitis media in, 39G, 307 ; peri- tonitis in, 306, 307 ; phagocytosis in, 396 ; pneu- monia during. 344, 30G ; prophylaxis, 308 ; recur- rence of, 56. 308 ; susceptibility. 308 ; transmission of. 307 ; tuberculosis during. 307 ; see liacilliis in- flcnzw. Injuries, mechanical and toxic, by bacteria 4 "Intestinal group" of bacteria 270 Intoxications, infectious 15 Isoagglutinins 104 Isoprecipitins 121 Lactoserum 120, 125 Lamblia hitefituiaUs 508 "Leistungskern" 8G, 195 Lecithin as endocomplement 159 "Leprolin" 450 Leprosy 10. 445-452 Animals, insusceptibility of. to. 447 ; contagiousness of. 44G ; distribution of bacilli in the body. 440; extension and occurrence of. 445 ; fish, relation of to, 448 ; infection atria. 448 ; intercurrent infections, 450 ; phagocytosis in, 440. 451 ; potassium iodid in treatment of, 450 ; prophylaxis, 451 ; protective factors in, 451 ; serum therapy of. 452 ; spontaneous disappearance of, 450 ; susceptibility to, 451 ; trans- mission of. 448 ; tubercular, 450 ; see Bacillus le/irw. Leptothrix, infections by 463 Leptothri.v hnrcali-t 4G3 Leptothrix var/iiialis 4G3 INDEX. 587 PAGE. Leucocidin 67, 202, 373, 380, 382 Antitoxin for, 372 ; influence on phagocytosis, 372. Leucocytes. Absorption of toxins by, 191 ; complement in, 154 ; for- mation of precipitins by, 121 ; immunity, relation to, 176-194 ; in inflammations, 43 ; phagocytic prop- erties of, 43, 44, 45 ; see also individual diseases ; see Phagocytosis. Leucocytic exudates, bactericidal action of .■;78, 379 "Loop," standard 101 Leucotoxic serum 107, 168 Leucotoxin ; see Leucotoxic Serum. "Lumpy jaw" ; see Actinomycosis. Lupus, influence of streptococcus on 362 Lymphangitis, streptococcus in 354-356 Lymphatotoxin ; see Leucotoxic Serum. Macrocytase 178 Macroparasites 6 Macrophages 44, 168, 178, 184 Madura foot ; see Mycetoma. Mai de cederas ; see Trypanosomiasis in animals. Malaria ." 468-483 /Estivo-autumual, 469 ; sestivo-autumnal, parasite of ; see Plasmodium prcecox ; anemia in, 474; "black- water fever" in, 477 : cachexia in, 476 ; cerebral symptoms, 477 ; epidemiology of, 477 ; etiology of, 468 ; fever, relation of to developmental cycles of parasites, 474 ; hemoglobinuric fever in, 477 ; immunity, acquired, 481, 482 ; incubation period, 473 ; intestinal symptoms. 477 ; melauemia in, 474 ; methylene blue in, 474 ; mixed infections, 476 ; mosquitoes, transmission by, 468 ; neuralgia In, 476 ; parasites, localization of, 477 ; prophylaxis of, 480, 481; quartan, 469; quartan, parasite of; see Plasmodium malatiw; quinin in prophylaxis and treatment of, 470, 477, 481 ; quotidian, 475 ; para- sites, localization of, 473, 474, 477 ; relation of clinical symptoms to developmental cycles of para- sites. 473 : susceptibility to, 481 ; tertian, 469 ; tertian, parasite of; see Plasmodium vivax ; toxins, 474. 475 ; transmission ; see Anopheles ; see Plas- modiurti of malaria. Malaria of birds, halteridium in ; proteosoma in 483 Malignant pustule ; see "Anthrax." Mallein 220, 454, 457 Malta Fever 333-335 Accidental infections. 335 ; agglutination reaction in, 334 ; difference from typhoid fever, 334 ; distribu- tion of bacillus in body, 334, 335 ; immunity, 335 ; occurrence, 333 ; serum, properties of, 334 ; serum therapj', 335 ; transmission, 335 ; see Bacillus meli- tensis. Measles 559-562 Complications and sequelas. 560 ; contagiousness of, 559 ; immunity and susceptibility. 561 ; leprosy, influence on, 450 ; leiicocytes in. 501 ; Micrococcus •"•^^'^ iXDi:x. PAGE. vtttanhalis in, 384; microorganisms In, 559; propliyluxis, 5G0 ; racial Iminunl/.ation, oOl ; resist- ance of virus, 500 ; recurrences, 501 ; serum therapy, 561 ; virus, distribution of, 559, 560. Meat poisoning. Iiaiilhis botiiliniiK in. 1250: liacillus cntcritidis in. :.:'.>4-'JltS ; Bacillus paratuphosus in, 285 ; relation of ptuiiiaiues to, i;95. Mechanical and toxic injuries 4 Mediterranean fever, see Malta fever. Meningitis. n. iineitmoiiivc in. 402; colon bacillus in. .iOL' : in in- fluenza. 396 : micro-organisms causing, 3S8, 189 ; pneumococcus In, 344, 348, 349 : secondary, 356, 357 ; streptococcus in, 354, 356, 357 358 ; tubercu- lous, 420. Meningitis, epidemic cerebrospinal 388-393 Agglutination test. 393; cerebrospiiuil cliaracter of, ■i'M : complications, 391 ; contagiousness of. 392 ; immunity, acquired, 392 : lumbar puncture for diag- nosis, .''.91 : metastatic Infections, 391 : mixed and secondary infections in, 391 : prophylaxis of, 392 ; secondary to rhinitis, 390 ; serum, properties of, 393 : susceptibility to. 392 : transmission of, 392 ; see Micrococcus meuingitidis. Meningococcus ; see Micrococcus mcninyifidix. Metchnikoff's theory ; see Phagocytosis. Methylene blue, effect of, on malarial parasites 474 Microbic speciQcity 27 Micrococcus cutarrhalis 'AS'.i. 384 Animals, susceptibility of, to, 384; bronchitis, in. :;.S4, 391 ; measles, in, 384 ; occurrence in i-espirarory passages, 383 ; occurrence under normal conditions, 384 ; pneumonia, in, 337, 344. 384. 392 ; resemblance to meningococcus, 392 ; scarlet fever, in, 3s4 ; whooping-cough, In, 383. Micrococcus gonorrhccc (gonococcus^ 383 Antiserum for, 388 ; cultivation of. 384, 385 ; discovery of, 384 ; endotoxin of, 385 ; gonotoxin, 386 ; Im- munization with, 388 ; infections with. 384, 388 ; morphology, 384 : phagocytosis of, 385, 387 ; re- sistance of, 385 ; toxin, soluble, 388 ; see Gonorrhea. Micrococcus hcmatodes 374 Micrococcus mclitensis, see liacillus melitensis. Micrococcus nieuiit(iitidis (Diplococcus intruccUularis mtiilngitidis, or the meningococcus) 10, 388-393 Agglutination of. 393 ; animals, susceptibility of, 390 ; antiserum, properties of, 392, 393 ; bronchitis, in. 391 ; conjunctivitis, in, 391 ; cultivation. 390 ; dis- covery, 389 ; endotoxin, 390 ; excretion of, 392 ; im- munization with, 39.'{ ; morphology, 390 ; pneumonia, in, 391 ; resemblance to gonococcus, 389 ; resem- blance to Micrococcus cutarrhalis, 392; resistance, 390 ; rhinitis, in, 391 ; virulence, 390 ; see Mei^in- gltls, epidemic cerebrospinal. Microbic specificity 27 Mlcrocj'tase 17S-189 IVDEX. 589 PAGE. Micro-organisms. Early belief in, 25 ; recognition of, 20 ; ultrami- croscopic, 6. Microparasites 6 Microphages 44, 178, 184, 100 Microsporon scpticum (Klebs) 349 Milk bacilli 444 Mitagylutinin Ill "Monadinin" of Klebs 359 Mucor 467 Mumps (epidemic parotitis ) ■. 56<5 Mycetoma 462 Nagana ; see Trypanosomiasis in animals 493 Natural immunity ; see Immunity. "Negative phase" following vaccinations 233 Negri bodies ; see Hydrophobia. Nephrotoxin 169, 170 Neurouophages 179 Neurotoxin of serums 171 Neurotoxin of venom 07, 265 Oldia 6. 10 Oidiomycosis 463-467 In animals, 467 : cutaneous, 463 ; infection atria, 465 • organisms of. 464 ; resemblance to tubercu- losis, 465 ; systemic, 464 ; thrush, 466. Oidium 464 Agglutination, immunization and phagocytosis, 467. Oidium alhicans 466 Oidium coccidioules 465 Old age. Metchinkoff's theory of 168 Ophthalmia. Cytotoxins in, 173 ; gonorrheal, 386. Opsonic index 382 Opsonins 61, 193, 227, 369 Action of salts on, 194 ; in acquired immunity, 6 ; see Phagocytosis in different diseases. Opsonoid 194 Otitis media. B. infliienzw in. 396. 397 : pneumococcus in, 348 : staphylococcus in. 377 : streptococcus in, 358 : tuber- culous. 420. Oxytuberculin 413 Ozena 402 Pancreatic juice, action on toxins 40 Pancreotoxin 173 "Paracolon" bacilli 285 Parasites, pathogenic 1, 6 Parasitism 1 Parotitis, epidemic ; see Mumps. Passive immunity ; see Immunity. Paratyphoid fever 284-288 Agglutination reaction in, 287, 288 ; blood cultures in, 288 : characteristics of the disease. 286 ; endotoxin of bacilli. 287 ; epidemiology of, 285 : as meat pois- oning, 285 : occurrence of bacilli in the body, 286 : properties of serum, 287 : prophylaxis. 287 : trans- mission, 285, 286 : see Bacillus paratijpliosus. Passage 58 r.'.Mi ixni-:x. TAGE. rasteur troiitmeut : see Ilyilruphobia. I'athogenesis 4, 5 roripneiimonia of cattle 11, 12 Periostitis albuminosa 377 Periostitis, staphylococcus in 377 Peritonitis. Colon liacillus in. SO."} : b.v influenza bacillus. 300. 307 : pneuniocoocus in. 34S. 340 : staphylococcus in. 377: streptococcus in, 354. 357; tuberculous, 420. Pertussis ; see Whooping-cough. Pfeiffer's phenomenon 06, 131, 132 In identifying the vibrio of cholera, 305 ; role of leu- cocytes in, ISS. Phagocytic (Metchnikoff's) theory of immunity .... 17('>. 104 Comparison of. with the side-chain theory of Ehr- lich. 212, 215: see Phagocytosis. Phagocytosis 31, 44, 176-194, 215 In active immunity. 50, 00, 102. 103 : chemotaxis in, 177. 185: fixators, influence of, 100: in inflamma- tions. 43 : intestinal, 41. 177 : intravascular, 188 ; leucocidin, influence of, 372 ; in nutrition. 172 : op- sonins., role of. 103 : in passive inimunitj-, 60, 102, 103 : relation of to virulence of bacteria, 184, 187 ; in resorption, 178 : serum, influence of. 187. 193 ; in vitro. 40. 103 : see under the individual micro- organisms and diseases ; see Opsonins. Phagolysis 181, 182, 188. 190 Phallin 264 Phrynolysin 268 Phytoprecipitins 120 Plaoiomonas urinaria 508 Plague lU, 315-327 Agglutination reaction. 320. 327 : animals, suscepti- bility of. 310 : conthgiousness, 322 : diagnosis, bac- teriologic. 323 : dissemination of bacillus by urine, feces, sputum. 322 ; epidemiology. 320. 323 : foci of, 320 : immunity, 56, 60, 324, 325 : infection atria, 322 : mixed immunization in, 234. 324 : mixed in- fection in. 323 : occurrence, 315 : houses. 321 : prophylaxis. 323 : in rats, 320 : serum therapy. 325, 32(". : transmission by fleas. 320, 321 : transmission from rat to man. 320, 321 : vaccination, 58, 218, 323 : vaccines. 323, 324 : see Bacillus pestis. Plasmin of Buchner 68, 219 Plasmodia of malaria 4, 10, 468 Anopheles mosquito as host of, 9, 469 ; asexual cycle. 469 : development in anopheles. 470 : development in man. 469 : discovery of. 468 : flagella of. 468 : macrogamete. 470 : merozoites. 470 : methylene blue, effect of. 474 : microgaraete, 471 ; microgametocyte, 470 i oocyst, 471 : ookinet, 471 : schizogony, 470 ; sexual cycle. 470 : species of. 400 : spermatozoites. 408: sporocyte. 470: sporogony. 471: spnrozoites. 471 ; see Malaria. Plasmodium vialariw ■ 469 Relation to clinical symptoms, 473: sexual and asex- ual cycles of, 472 : virulence, 474. PlasniofUt'm prcecox 469 INDEX. 591 PAGE. Relation to clinical syniptoms, 47:i ; sexual and asexual cycles of, 472 ; virulence, 473. Plasmodium vivax 4G9 Asexual cycle of, 4G0, 470 ; relation of to clinical symptoms, 473 ; sexual cycle of, 470, 471 ; virulence 474 Pneumococcus ; see Diplococmis pneiimonUe. Pneumonia 330-348 Agglutination reaction, 347 ; B. pneumoniai in, 402 bacteria causing, 336, 337 ; causes, predisposing, 343 ; complications, 343, 344, 348 ; contagiousness, 342 : immunity and susceptibility, .56, 34.5 ; infection atrium and method of infection, 340 : influenza bacil- lus in, 396 ; leucocytes, 345 ; metastatic infections, 348 ; phagocytosis, 345 ; meningococcus in, 301 ; Micrococcus catarrhalis in, 384, 392 ; mixed infec- tions in, 344 ; polyvalent serum for. 347 ; prophy- laxis, 344 ; recurrences, 345 ; Roemer's serum, 347 ; serum properties, 345 ; serum therapy, 346. 347 ; staphylococcus in, 377 ; streptococcus in, 354, 355, 356 : vaccination, 345 ; see Diplococcus pneumonicB and other bacteria enumerated on page 336. Pneumotoxln 339 Pollantin 263 Pollens. As cause of hay fever, 262 ; antitoxin for, 263. Polyceptors 155 Polyvalent serums. For pneumococcus, 347 ; for staphylococcus, 383 ; for streptococcus, 232, 306. "Positive phase" following vaccination 233 Postmortem invasion 302 Precipitate 120, 124, 125 Precipitation reaction 106, 119 Agglutination, relation to, 117 ; as clinical reaction, 119 : with colloids and electrolytes, 128, 129 ; forensic use of, 63, 125 : precipitation, group reac- tion. 125, 126 : meats, differentiation of, 127 ; physi- cal chemistry in the study of, 129 ; specific inhibi- tion. 122 ; technic, 126 ; use of in studying reactions of immunity, 206. Precipitins 119-129 Antiprecipitins, 123 : autoprecipitins 121 : bacterial, 63, 119, 233, 314 ; formation of, 121 : isoprecipitins, 121 : lactoserum, 120 : phytoprecipitlns, 120 : re- sistance to ferments, heat, etc., 122 : serum precipi- tins, immune, 63 : serum precipitins, normal, 55 ; structure of, 122 ; zooprecipitins, 120. Precipitogens 120 Precipitoids 12§ Pregnancy, serum diagnosis 172 Preparator 148 Proagglutinoids 109 Prophylactic injections, classification of methods 218 Protective inoculation ; see Vaccination. Proteins 220 Proteosoma in malaria of birds 483 Prototoxin 83, 20v> Protoxoids 82, 209 o!>2 IXDKX. PAGE. Protozoa, infoctlons with 408, 509 rseudodiphihiTia baoilli 243, 244, 425 I'seiuioinlliH'iiza bacilli 394 rseudotuberculosis of animals 444 Ptomalns in meat 205 Pyocyanase 61, 260 Pyocyanin 260 Pyocyanolysin 2G0 Ptiroplasma hovis : see Texas fever. Pi/rophif^iitn ho7tiiiiis: sec Spotted fever Pyroplasmosis : see Spotted fever and Texas fever. Rabies ; see Hydrophobia. Hadium, effect on venom 207 Rats .in epidemics* of plague 320, 321 Rattlesnake venom. Antiserum for, 207 ; immunization with. 210. Ray fungus ; see* Actinomyces 320, 321 Receptors. Bacterial. 152: function of. 52. f<~. RS : immunify. re- lation to. 100; loss of. as cause of immunity, 240; multiplicity of. SO. 208; new formation of, 100, 205, 207; nutrition, relation to. 105: of first order, 89, 200. 207; of second order, 114 203. 207. 209; of the third order, 150. 203, 207 : synonym for side chain. 107 ; tetanophile receptors of nervous tissue, 252 : types of. 207 ; see different antibodies. Kelapsinir fever 10, 40.3-406 Agerlutination test, 406 ; immunity and susceptibility, 404, 400; organism of; see Rpirocheta nhcr- mrieri : phagocytosis in. 405 ; propliylaxis, 404 ; serum properties. 405. 400 ; serum tlierapy, 400 ; transmission of by bedbugs, 404. Resistance, natural ; see Immunity, natural. Resorption. Of foreign cells, 179 ; of native cells, 178. Rheumatic fever 359, 360 "Agonal invasions in, 359 : antistreptococcus serum in, 308 ; bacillus of Achalme in. 359 : diplococcus Cstrentococcus) in. 300 ; experimental. 359. 360 ; micro-organisms found in lesions, 350 ; staphylococ- cus in, 359 ; streptococcus in, 354, 359. 360 ; /.innctosis transTiicens, 359. Rhinitis. Meningococcus in. 301 ; pneumococcus in, 348 ; pri- mary to meningitis. 390; staphylococcus in, 377; Ixhiiiitis fiJ}ri)>osa, 237. Rhinoscleroma 402 Ricin 0, 264 Antiricin, 63 ; Ehrlich's use of in studying nature of antitoxic action, 201, 202; hemagglutinin in, 104. Robin 264 R()theln. see German measles. SnccJiaromi/cosis homiiih 464 Salamjvnder poison, antitoxin for 90 Saprophytes 1 In tetanus 248 Sarcnrjistis liominifi: see Sarcosporidia. INDEX. r/J3 PAGE. Sarcosporidia. Morphology, occurrence and proliferation, r»04, ijO.") ; SarcocysMs liommis, 505. Scarlatina ; see Scarlet fever. Scarlet fever (scarlatina) 55G-559 Agglutination of streptococci by serum, 369, 370 ; con- tagiousness, 557 ; Cyclastcr scarlatinalis in, 55G ; Diplococcus scarlatinoe, 11 ; leucocytes in, 558 ; Micrococcus catarrhalis, 384 ; micro-organisms in, 557 ; prophylaxis, 557 ; protozoa in, 10, 556 ; resistance of virus, 557 ; serum therapy, 558, 559 ; streptococcus in. 14, 15, 186, 354, 355, 358, 361, 556; Streptococcus scarlatina;, 361; immunity and susceptibility, 56, 558; serum therapy (antistrep- tococcus), 366, 368, 558; transmission, 557. Scorpion, toxin and antitoxin 90, 268 Sensitization 145 Serpent ulcer. Pneumococcus in, 348, 349 ; treatment with antipneu- mococcus serum (lloemer), 349. Serums, purity of 76, 221 Serum therapy, principles of 218-234 Antitoxins, 221, 226 ; bactericidal serums, 226, 232 ; classification of methods, 218 ; curative injections, 220, 223, 227 ; prophylactic injections. 218, 226, 227 ; see also under the different diseases. Sheep-pox ; see Clavelde. Side-chain theory of Ehrlich 195-217 Amboceptor formation, 150 ; agglutinin formation, 114 ; antitoxin formation, 86, 89 ; applied to cell nutrition, 195 ; as applied to immunity, 199 ; chem- ical processes, 78, 200, 205, 208 ; complements, 153, 210 ; essential tenets of, 200 ; haptophores, 197 ; "Leistunf/skern/' 195 ; Metclinikoff's phagocytic the- ory, comparison with, 212. 217 ; precipitin forma- tion, 121 ; receptor proliferation, 205 ; receptors, types of, 207 ; side chains, 195. Sleeping sickness 486-490 Anatomic lesions of, 489 ; bacteria in, 487 ; occur- rence. 486. 487 ; symptoms of, 488, 489 ; transmis- sion of, 488 ; Trypanosomatic fever, relation to, 489, 490 ; ti'ypanosomes in, 487 ; see Trypanosomiasis. Smallpox 541-555 Bacteria in. 542, 548 ; conversion, into vaccinia, 541, 542 ; cyclic nature of symptoms, 547 ; Cytoryctes variolw s. vacciniw, 548 ; dissemination of virus, 546 ; etiology. 542 ; fetal, 548 ; immunity and sus- ceptibility, 56, 554 ; incubation period, 547 ; infec- tion atrium, 546 ; inoculation into calves, 541 ; Jennerization, 549 ; leucocytes in, 554 ; mixed (sec- ondary) infections, 15, 548 ; nonfiltrability of virus, 542 ; prophylaxis, 548 ; protozoon-llke bodies in, 11, 542 ; relation to vaccinia. 57, 541 ; revaccina- tion, 552, 553 ; serum properties, 554 ; transmis- sion, 546 : vaccination, 548 ; vaccine, contamina- tions of, 551, 552 ; vaccine, durability of, 551 ; .viru- lence, variations in, 547 ; virus, distribution in the body, 547. ; 594 IXDEX. PAGE. Smallpox and vaccinia 541, 5")") Smegma bacilli 443 Snako bitos 264, 2G8 Soft chancre or chancroid 8!)9-401 In animals, 400: bacillus of. 400; Immunity, 401 ; in- dependence, .300 ; infectiousness of, 309 ; phago- cytosis, 400, 401. Specific infections 9 Spcrmnphiliis columhiaiuts as host of Pyroplasma hominis . 498 Spermotoxin '.' . 165, 160 Spider poison, antitoxin foi- 90 Spirochrta nhcnn cirri 10, 403 Agghuinins for, 400 : animals, susceptiblllly of. 404 ; antiserums, properties of. 405 ; distribution in the body, 403 ; morphology, 403 ; occurrence in bedbugs, 404 : phagocytosis of, 405 ; see Kelapsing fever. SpirocJieta rinUida (see syphilis) 525, 526 "Spotted fever" '. 497, 498 Piiroplaaiiia hominis in 497 StaphiilocnccK.i pyoqcnea. or staphylococcus 370-383 Agglutination, 02. 3S2 : amyloid degeneration. 375 ; animals, susceptibility of. 375, 376 ; antiserums, properties. 3S0 : bactericidal action of leucocytic exudates. 378. 370 : bacterlolysln. 379. 380 ; dis- covery. 350 : endotoxin, 373 ; ferments of, 371 ; hemolytic action, 5. 371. 372: Immunity, 186. 379, 380 ; leucocidin. 372. 373. 380. 382 ; leucocytes in infections. 378. 379 : leucotactic substance. 375 : mixed infections. 378 : morphology, 370 ; necrotiz- ing substance, 375 : pathogenic powers. 37. 336. 344, 354, 359. 376, 378. 389 ; opsonins in phagocv- tosls of, 382 ; phagocytosis, 378. 370, 380, 382 : pigment formation. 374 : polyvalent serum. 383 : resistance. 374. 375 ; staphylolysin, 271. 372, 373, 375. 380 : symbiosis with Amelia coli, 502 : symbio- sis with 7?. influenza;, 394 : toxicity of culture filtrates, 372, 373 : toxin, soluble, 375 ; vaccination against, 381 ; varieties. 373. 374 ; virulence, 37G. Staphylolysin ; see Staphylococcus. S Organisms of, 40(3 ; susceptibility to, 407 ; systemic infections, 466. Thyrotoxin 1"3 "Tick fever" ; see "Spotted fever." Timothy bacillus 444 Toxins. Animal. 0. 204-2G8 ; attenuation of, 70 ; l>ac- terial, 0. 2:i5 ; see individual bacteria ; cliem- otaxls, influence on, ISo, 354, 372 ; crotln, 204 ; degenerative changes in, 80, 209 ; dis- covery of. 33 ; effects of, 4, 5 ; endotoxins, 6. 20, OS ; see individual bacteria ; gastric juice, de- structive action, 30 ; haptophores of, 70, 209 ; see side-chain theory ; immunization with, 00. 70, 220 ; incubation period of, C5, 251 ; intracellular ; see Endotoxins ; leucocidin. 372 : leucocytes in absorp- tion of. 45, 101 ; modifications by age, 85 ; neu- tralization by antitoxins, 48. 78, 200 ; pancreatic juice, destructive action, 40; phallin, 204; of pollens. 202 ; precipitation of, 06 ; preparation. t>0 ; properties of, 05, 208 ; as receptors of, second order, 207 ; ricin. 204 ; robin. 204 ; secondary or adven- titious, 07 ; selective action of, 5 ; toxin spectrum, 81, 200 ; standardization of, 72 ; staphylolysin, 371 ; structure. 78 ; toxophores, 80, 200 ; see side-chain theory ; union with tissue cells. 66, 87, 200, 204. 224, 222, 252 ; vegetable, 6, 262-264 ; see individ- ual micro-organisms. Toxoids 80-83, 209 Toxon 82, 209, 242 Toxophorous group, toxophore 80, 207 Trichomonas iiitestinalis, morphologv and pathogenicity of 507, 508 Tricfwmonas vaginalis 507 Trichoijhvton 467 Tritotoxin 83, 209 Trypanosoma 483 Agglutination of, 485 ; cultivation of, 492, 404 ; ■ morphology of, 484 ; multiplication of, 485 ; rosotte formation by, 485 ; sleeping sickness. 487 ; species of. 484, 485. 490 ; trypanosomatic fever, 480. Trypanosomatic fever 485, 486 Sleeping slclcness. relation to. 480, 400 ; symptoms of, 480 : trypanosomes in, 486. Trypanosomiasis 483-497 Agglutination reactions, 497: immunity and suscep- tibility, 405; in man. 485-400; parasites, occurrence of in the blood, 491 ; serum therapy of. 406 ; 'trypanroth" in treatment of. 490 ; vaccination in," 496 ; see Sleeping sickness and Trypanosomatic fever. Trypanosomiasis in animals 490-495 bourine, 495 ; horses, cattle and mules, 493-405 ; mat de rederas, 405 ; nagana, 403 ; in rats, 491 ; surra, 404 ; symptomatology, 491. INDEX. 597 PAGE. "Trypanroth" In treatment of trypanosomiasis 490 Tsetse flies, in transmission of trypanosomiasis ; see Trypanosomiasis. Tuberculin of Kocli and others 219, 220, 412, 413, 414 Dangers, errors and limitations in use, 434, 435 ; diagnostic use of, 432-436, 442 ; disturbances caused by, 433; Immunization with, 411, 431, 432; prepara- tion of, 412 ; principles of action, 437 ; _speclficlty of. 434, 435 ; standardization of, 412, 414 ; therapy, 436, 437. Tuberculocidin 413 Tuberculosis 10, 407-443 Agglutination as an index of immunity to, 437 ; agglutination reaction, 438, 440 ; amy- loid degeneration in, 424 ; "anatomic tubercle," 419 ; m animals, 427, 441 ; avian, 442 ; bovine, 441 ; bovine, relation of, to human, 415-417 ; congenital, 417 ; disinfection in, 426 : dissemination by means of phagocytes, 421 ; "droplet infection," 418 ; "dust infection," 418 ; healing, spontaneous, 420 ; heredity in, 429 ; immunity and susceptibility, 18, 19. 61, 427, 430-432, 437 ; Immunization, mixed, 439 ; Infection atria, 418, 420 ; infectiveness of, 407 ; latent. 418 ; lupus vulgaris, 419 ; metastases in, 420 ; miliary, 421 ; mixed infections in, 424 ; organs attacked, 419-421 ; phagocytosis, 421, 422 ; pneumonia during, 344 ; predisposing factors to, 42S, 429 ; primary and secondary, 421 ; prophy- laxis. 425, 427 ; pulmonary. 418 : serum therapy, 425, 438 : streptococcus in, 355, 350 ; tissue changes in, 5. 422-425 ; tuberculin in diagnosis. 432-430 ; ulcerative, 419 ; vaccination against, 439. Tumors, influence of streptococcus on 302 Turtle poison, antitoxin for 90 Typhoid fever 10, 209-284 Agglutination reaction, 7, 95. 283, 284 ; antibodies, origin of, 190 ; bacillemia. 272, 273 ; bacilli, distri- bution in the body, 273, 274 ; blood cultures for di- agnosis. 273. 284 ; "dust" infection, 272 ; epidemi- ology of, 271 ; flies as carriers, 272 ; immunity and susceptibility, 56, 60, 61. 275 ; infection atrium, 272 ; leucocytes, 274. 277 ; leucotoxin in experi- mental infections, 168 ; mixed immunization, 234, 282 ; mixed infections in, 275 ; serum properties, 20 prophylaxis. 278 ; serum prophylaxis, 279 ; serum therapy, 230, 282 : therapy, active immunization, 283 ; therapy of Jez. 283 ; vaccines and vaccina- tion, 58, 218, 279, 282 ; see B. typhosus. Typhus fever 10, 538-541 Conditions for development, 538 ; contagiousness, 539 ; fomites, 539 ; micro-organisms in, 538 ; occurrence, 538 ; prophylaxis, 539 ; pyroplasma ( ?) in, 538 ; serum therapy, 539 ; transmission, 539. Ultramicroscopic micro-organisms 12 Uncinaria duodenalis 4 Undulant fever ; see Malta fever. Univalent serums 366 Urease ' . ' 90 598 IXDKX. PAGE. Vaccination I'S, 57. 21S-220, 232-234 Antibodies proiiiicetl by, 23;? ; duration of resistance caused by, 2.'{2 ; incubation period, relation to, 234; see Smallpox and Hydrophobia; opsonins, in-. crease of, 234 ; •■positive'' and "negative phases," 233 : substances used for, 21S-22U ; see the indi- vidual diseases. Vaccines 218-220, 232-234 See the Individual diseases. Vaccinia ; see Smallpox and Vaccinia. Varicella; see Chlckenpox. Variola inoculata o4G, 591 Variola ; see Smallpox. Venoms 24, G6, 78, S5, 15S-1G0, 2G4-2G8 Amboceptors and complements, 150, 266 ; antiveiiins, 63. 267, 268 ; character of, from different snaljes, 2(!5 ; cobra-Iecithid, 160, 266 ; cytotoxins of, 265 ; endocomplements for, 159, 266; endotheliotoxin of, 265 ; ferments of, 266 ; hemagglutinins of, 158, 265 ; hemolysin of. 158, 265 : hemorrhapin, 159. 265 ; incubation period, 66, 267; lecithin as comple- ment, 159, 266 ; neurotoxin of, 158, 265 ; radium, effect of, 267 ; structure of cytotoxins of, 266 ; tox- ins of, 158 ; toxoids of, 265. Vibrio cholera:. Acquired immunity to, 186; action of gastric juice on, 39 ; active' immunity, formation of specific precipi- tin in, 314 ; agglutination of, by normal serum, 02 ; agglutination of, 315; agglutinins, 314; attenua- tion of, 57 ; autolytic products, vaccination with, :U3 ; discovery, 304 ; endotoxin of, 309 ; identifica- tion of, by agglutination reaction and by Pfeiffer experiment. 305 ; in Pfeiffer's phenomenon, 131 ; in stools of convalescents, 307 ; location in infected body, 310 ; morphology, staining properties and cultivation of, 304, 305 ; non-neutralization of endo- toxin of, by its specific bactericidal serum, 137 ; oc- currence of water, 307 ; resistance and viability of, 306 ; see Cholera ; symbiosis with Ameha coll, 502 ; soluble toxin ( ?) 310 ; specificity of. 9 ; toxicity of culture filtrates, 309 ; toxicity of killed cultures, 309. Vihrio metchnikovi 33 Virulence. Increase of, in the presence of other micro-organisms, 14 ; influence of, on inflammatory reaction, 42 ; rela- tion of, to phagocytosis, 184 ; see different micro- organisms. Wasp poison, antitoxin for 90 Whooping cough (pertussis) 562-566 Contagiousness, 564, 565 ; cultural characteristics and lithogenicity of the influenza-like bacillus, 562 563 ; immunity and susceptibility, 505 : influeuza- like bacillus in, 562 ; influenza-like bacillus, rela- tion to whooping cough, 564 ; Micrococcus catar- rhnlis in, 383 ; micro-organisms in, 562 ; prophyl- axis, 565 ; pseudo-influenza bacilli in, 395 ; serum therapy, 505 ; virus, dissemination of, 564. MDEX. 599 „,i' i 1 >! ■ -. . PAGE. Water-borne eiademics ; cholera, dysentery, typhoid. 071 OflO '>i\Si Welch, hypothesis of ' " ' r/^ Widal reaction '.'.'.'.'.'.'.'.'. 02' 111 See Agglutination. "' Wool-sorters' disease; see An(hra.\-. Wright's method of vaccination. Staphylococcus infections, 381 ; typhoid fever, 279, Yellow fever Kj goo-SSS Acclimatization, question of, 537 ; altitude and mois- ture, relation to, 583 ; Bacillva icteroidcs in. 530 531 ; cold, relation to, 533 ; epidemiology, 533 ; fo- mites, 532, 533 : immunity acquired, 332, 538 • importation by ships, 530 ; incubation period, 532 • mosquito theory of, 530; see also Steriomyia fasci- ata; non-contagiousness of, 533; occurrence, 529- prophylaxis and quarantine of. 533, 534. 536 537 ' virus, filterability of, 532 ; virus, resistance of,' 536 ; serum therapy, 538 ; susceptibility to, 537. Zone, contagious _ 2 3 Zo(5precipitins ' 120 Zootoxins ' 268 Zwischenl-ih-per, synonyms for 14.8 Zymotoxic groups 108 000 i\in:\. CORRECTIONS. I'a^c S, 14th line fioiii hoitdin: iiistoad of "Strong," rend "Miisjirave and ClogK." I'ago 12, 4th line from top: instead of "Unstained ability," read "Unstainability." I'age 27 : between the 12th and i;Uh lines from top a line is omitted. It should read : "Other students, especially I'asteur and Koch, soon took up the study of anthrax." etc. ; the i;Uh line is repeated. l*ai,'e 57, 14th line from bottom : instead of "s-arloloid," read "variolata Inoculala. ' Page Gl, 4tli line from top : instead of "poisons," read "opsonins." Page So, 18th line from bottom : instead of "Part II, Chapter III," read "pages 158-100." Page 85, 4th line from bottom : instead of "equaled," read "equalled." Page 107, i;>th line from bottom: instead of "flagellffi" read "flagoUa." I'age 158, footnote : instead of "Chapter III," read "page 204." Page 181, 3rd line from bottom : instead of "phenomena" read "phenomenon." Page 200. 4th line from top : instead of "crawfish," read "spider-crab." Page 217 : instead of "opsinogenous." read "opsonigenous." Page 231, 9th line^ from bottom : instead of "simulating." read "stimulating." Page 204 : The description of the poison fangs of snalies applies to the chief poisonous snakes of North America, which are "pit vipers" ; another class of poisonous snakes, among wliich are included the cobra, and the coral snake of North America, possess immovable poison fangs. Page 413, 3rd line from bottom : instead of "toxins of tuberculins," read "toxins or tuberculins." Page 485. 5th line from bottom : instead of "Nepreu," read "Nepveu." I'age 485, 2d line from bottom, and page 490, 8th line from bottom : Instead of "T. ncprevi" read "T. nepveui." Page 511. 14th line from bottom: instead of "microscopic," read "ultramicroscopic." ^j^^ //o'^ />i>^^^^ :v-, ^ ^-^y.^;:^^^^ z4^.