Active Immunity Produced by So-Called Balanced or Neutral Mixtures of Diphtheria Toxin and Antitoxin.
Abstract: The foregoing and earlier data taken together demonstrate that an active immunity lasting several years can be produced in guinea-pigs, by the injection of toxin-antitoxin mixtures which have no recognizable harmful effect either immediate or remote. They also show, what might have been anticipated, that under the same conditions mixtures which produce local lesions and which, therefore, contain an excess of toxin produce a much higher degree of immunity than the neutral mixtures, and that an excess of antitoxin reduces the possibility of producing an active immunity, and may extinguish it altogether. There is, therefore, a certain definite relation between the components of the mixture and the degree of immunity producible. Furthermore, toxin-antitoxin mixtures do not change materially within five days at room temperature. They are apparently more efficacious at the end of forty-eight hours than immediately after preparation. The experiments finally prove that a relatively high degree of active immunity can be induced by a harmless procedure, whereas the use of toxin alone leading to very severe local lesions is incapable of producing more than an insignificant protection. The method, therefore, invites further tests in regard to its ultimate applicability to the human being. Unless the subcutis of the guinea-pig reacts to toxin-antitoxin mixtures in a manner peculiar to itself, a practical, easily controlled method for active immunization can be worked out which should afford a larger protection than the serum alone and avoid the complications associated with horse serum. That proportion of toxin and antitoxin which would produce the highest desirable immunity consistent with the least discomfort would have to be carefully worked out for the human subject. From the nature of the immunity induced it is obvious, however, that such a method of immunization cannot take the place of a large dose of antitoxin in exposed individuals who must be protected at once. It would be applicable only as a general protective measure without reference to any immediate danger, since it would take several weeks, perhaps longer, to perfect the attainable immunity. Passing to the theoretical aspects of the facts observed, we find no publications bearing directly upon the subject before us. Madsen has, however, approached it very closely in his experiments on the immunization of animals with mixtures not fully balanced, or, in other words, in which the "toxones" were still free. He found that the injection of such mixtures in rabbits, goats and horses produces an active immunity. He makes the significant remark that perhaps in the immunizing capacity we may possess the keenest reagent for a poison which is not able to exert any toxic action in the body. This is fully borne out by the experiments described, for in these we pass beyond the visible spectrum, so to speak, of the toxin-antitoxin effects, and we are able to recognize toxic action only by the lasting immunizing effects. Another publication which touches upon some phases of the same problem is that of Morgenroth on the union between toxin and antitoxin. Morgenroth brought out the fact that a given toxin-antitoxin mixture is more toxic when injected directly into the circulation than when injected under the skin. Thus, an L(+) dose of 0.78 c.c. toxin + one unit antitoxin applied subcutaneously was of the same toxicity as 0.68 c.c. toxin + one unit antitoxin injected into the circulation. When the mixture had stood twenty-four hours this (L(+)) dose was still 0.78 c.c. subcutaneously, but it had risen to 0.74 c.c. when introduced by the intracardiac route. The author makes two deductions from these results. He assumes that the velocity of reaction between toxin and antitoxin is slow, and that the union is not completed until the mixture has stood twenty-four hours. Hence, the L(+) dose of toxin injected into the blood is higher after twenty-four hours than immediately after mixing the toxin and antitoxin. He furthermore explains the fact that the subcutaneous L(+) dose remains the same whether the mixture is injected at once or after twenty-four hours, by assuming that in the subcutis of the guinea-pig there is a catalytic acceleration of the union of toxin and antitoxin. In view of the writer's results it seems that not only immediately, but four to five days after the preparation of the mixture of toxin and antitoxin, there are still toxic substances available for the production of immunity in the body of the guinea-pig, when the dose of toxin in the mixture is far below the L(0) or neutral level. These toxins may be free, either because uncombined in vitro, or else because the mixture is partially dissociated in vivo, or there may be a third possibility. It is obvious that Morgenroth's investigations, however extensive and thorough, have not exhausted the subject, for both these inferences are incompatible with his. Perhaps his recent important studies on the recovery of toxin from its combination with antitoxin with weak acids may throw more light on this subject. The only conclusion which we may safely draw at this time is that the toxin-antitoxin mixture produces two sets of effects, essentially identical, however. One is visible, as injury (oedema, loss of hair, superficial and deep necrosis of skin, paralysis and death), and corresponds to the toxin spectrum of Ehrlich. The other is invisible and manifests itself only in degrees of active immunity. At what ratio of toxin to antitoxin in the mixture active immunity is no longer produced will vary somewhat with the guinea-pig used, but it is evident that traces of immunity are still transmitted to the young when the amount of toxin approaches half the L(0) dose.
Publication Date: 1909-03-01 PubMed ID: 19867246PubMed Central: PMC2124709DOI: 10.1084/jem.11.2.241Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
- Journal Article
Summary
This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.
The research article presents an investigation into the active immunity produced by the injection of diphtheria toxin-antitoxin mixtures in guinea-pigs. It concludes that mixtures producing local lesions with an excess of toxin result in stronger immunity than neutral mixes, and a high level of active immunity can be achieved with no harmful effects.
Experiment Design and Results
- The research focuses on the use of toxin-antitoxin mixtures to induce active immunity in guinea-pigs. These mixtures were found not to change significantly within five days at room temperature.
- The researchers found that these mixtures are more efficacious at the end of forty-eight hours than immediately after preparation.
- The data also indicated that mixtures which produce local lesions contain an excess of toxin, resulting in a much higher degree of immunity than neutral mixtures.
- On the contrary, the use of an excess of antitoxin reduces the possibility of producing active immunity and can even extinguish it altogether.
Theoretical Implications
- The researchers note that their findings have significant theoretical implications. The result supports the hypothesis that in the immunizing capacity, we may detect a poison that does not manifest toxic action in the body.
- This is made evident by the experiments that reveal toxic action through persistent immunizing effects.
Comparisons and Conclusions
- The research referred to a work by Morgenroth on the union between toxin and antitoxin. Morgenroth found out that a certain toxin-antitoxin mixture is more toxic when injected directly into the bloodstream than when administered under the skin.
- The article concludes that a high level of active immunity can be induced without any harmful impacts by using toxin-antitoxin mixtures.
- However, the study acknowledges that the proportion of toxin and antitoxin that would produce maximum immunity with the least discomfort would be different for humans and should be carefully analyzed.
- They also note that this method of vaccination would not replace the administration of large antitoxin doses for individuals directly exposed to the disease, as it takes several weeks or even longer to attain the full level of immunity.
Cite This Article
APA
Smith T.
(1909).
Active Immunity Produced by So-Called Balanced or Neutral Mixtures of Diphtheria Toxin and Antitoxin.
J Exp Med, 11(2), 241-256.
https://doi.org/10.1084/jem.11.2.241 Publication
Researcher Affiliations
- Antitoxin and Vaccine Laboratory of the Massachusetts State Board of Health.
Citations
This article has been cited 19 times.- Inoue T, Kurosaki T. Memory B cells.. Nat Rev Immunol 2023 Jul 3;.
- Schaefer-Babajew D, Wang Z, Muecksch F, Cho A, Raspe R, Johnson B, Canis M, DaSilva J, Ramos V, Turroja M, Millard KG, Schmidt F, Dizon J, Shimelovich I, Yao KH, Oliveira TY, Gazumyan A, Gaebler C, Bieniasz PD, Hatziioannou T, Caskey M, Nussenzweig MC. Antibody feedback regulation of memory B cell development in SARS-CoV-2 mRNA vaccination.. medRxiv 2022 Aug 10;.
- Dahiya DS, Wani F, Guidi JC, Kichloo A. Gastrointestinal Adverse Effects of Immunotherapeutic Agents: A Systematic Review.. Gastroenterology Res 2020 Dec;13(6):227-232.
- Anania JC, Westin A, Heyman B. IgG Suppresses Antibody Responses to Sheep Red Blood Cells in Double Knock-Out Mice Lacking Complement Factor C3 and Activating Fcγ-Receptors.. Front Immunol 2020;11:1404.
- Martin B, Märkl B. Immunologic Biomarkers and Biomarkers for Immunotherapies in Gastrointestinal Cancer.. Visc Med 2019 Mar;35(1):3-10.
- Xu H, Zhang L, Heyman B. IgG-mediated immune suppression in mice is epitope specific except during high epitope density conditions.. Sci Rep 2018 Oct 16;8(1):15292.
- Hazama S, Tamada K, Yamaguchi Y, Kawakami Y, Nagano H. Current status of immunotherapy against gastrointestinal cancers and its biomarkers: Perspective for precision immunotherapy.. Ann Gastroenterol Surg 2018 Jul;2(4):289-303.
- Kaufmann SH. Remembering Emil von Behring: from Tetanus Treatment to Antibody Cooperation with Phagocytes.. mBio 2017 Feb 28;8(1).
- Cross AS. Anti-endotoxin vaccines: back to the future.. Virulence 2014 Jan 1;5(1):219-25.
- Cousens LP, Najafian N, Mingozzi F, Elyaman W, Mazer B, Moise L, Messitt TJ, Su Y, Sayegh M, High K, Khoury SJ, Scott DW, De Groot AS. In vitro and in vivo studies of IgG-derived Treg epitopes (Tregitopes): a promising new tool for tolerance induction and treatment of autoimmunity.. J Clin Immunol 2013 Jan;33 Suppl 1(Suppl 1):S43-9.
- Elyaman W, Khoury SJ, Scott DW, De Groot AS. Potential application of tregitopes as immunomodulating agents in multiple sclerosis.. Neurol Res Int 2011;2011:256460.
- Kidd JG. THE DETECTION OF A "MASKED" VIRUS (THE SHOPE PAPILLOMA VIRUS) BY MEANS OF IMMUNIZATION : RESULTS OF IMMUNIZATION WITH MIXTURES CONTAINING VIRUS AND ANTIBODY.. J Exp Med 1941 Sep 30;74(4):321-44.
- Cox HR, Olitsky PK. ACTIVE IMMUNIZATION OF GUINEA PIGS WITH THE VIRUS OF EQUINE ENCEPHALOMYELITIS : IV. EFFECT OF IMMUNE SERUM ON ANTIGENICITY OF ACTIVE AND INACTIVE VIRUS.. J Exp Med 1936 Jul 31;64(2):223-32.
- UHR JW, BAUMANN JB. Antibody formation. I. The suppression of antibody formation by passively administered antibody.. J Exp Med 1961 May 1;113(5):935-57.
- Karlsson MC, Wernersson S, Diaz de Ståhl T, Gustavsson S, Heyman B. Efficient IgG-mediated suppression of primary antibody responses in Fcgamma receptor-deficient mice.. Proc Natl Acad Sci U S A 1999 Mar 2;96(5):2244-9.
- Caulfield MJ, Stanko D. T-cell dependent response to immune complexes abrogates B-cell unresponsiveness to pneumococcal cell wall polysaccharide.. Immunology 1995 Nov;86(3):331-5.
- Dixon FJ, Jacot-Guillarmod H, McConahey PJ. The effect of passively administered antibody on antibody synthesis.. J Exp Med 1967 Jun 1;125(6):1119-35.
- Sterzl J, Johanovská D, Milerová J. Passive administration of antibodies during the primary immunization. The influence on the secondary response.. Folia Microbiol (Praha) 1969;14(4):351-8.
- Keith L, Halloway M, Stepto RC. The multiple use of RhoGAM.. J Natl Med Assoc 1973 Jan;65(1):40-4.
Use Nutrition Calculator
Check if your horse's diet meets their nutrition requirements with our easy-to-use tool Check your horse's diet with our easy-to-use tool
Talk to a Nutritionist
Discuss your horse's feeding plan with our experts over a free phone consultation Discuss your horse's diet over a phone consultation
Submit Diet Evaluation
Get a customized feeding plan for your horse formulated by our equine nutritionists Get a custom feeding plan formulated by our nutritionists