Production of monovalent anti-Bothrops asper antivenom: development of immune response in horses and neutralizing ability.
Abstract: A monovalent antivenom was produced by immunizing two horses with venom of the pit viper Bothrops asper (Ophidia: Viperidae). Although development of the immune response against four toxic and enzymatic activities of the venom was similar in both horses during the first two thirds of the immunization schedule, antibody response in one of the horses reached much higher levels in the last part of the immunization. Immunoelectrophoretic analysis indicates that there were precipitating antibodies in the sera of these horses during all the stages of immunization. However, immunoprecipitation did not correlate with the ability of sera to neutralize toxic activities of B. asper venom. Monovalent antivenom was more effective than the commercially available polyvalent antivenom in the neutralization of Bothrops asper venom. On the other hand, despite the fact that it neutralizes lethal and hemorrhagic activities of the venoms of Lachesia muta and Crotalus durissus durissus, it was less effective than polyvalent antivenom in these neutralizations. Moreover, it does not neutralize defibrinating activity induced by these two venoms, whereas it neutralizes this effect in the case of B. asper venom. It is proposed that monovalent antivenom may be highly effective in the case of envenomations induced by Bothrops asper venom; its use in treating accidents by L. muta and C. durissus would be indicated only if polyvalent antivenom is not available. Results also demonstrate that it is important to monitor antibody response individually in horses being immunized for antivenom production, due to the conspicuous variability in the response of different animals.
Publication Date: 1988-11-01 PubMed ID: 3078800
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- Journal Article
- Research Support
- Non-U.S. Gov't
- Review
Summary
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This study focuses on the production of a monovalent antivenom by immunizing horses with the venom of Bothrops asper, a species of pit viper. The researchers noted that the antivenom was particularly effective against B. Asper venom but less effective when used against other venoms. They conclude that the response to venom immunization can vary considerably between individual animals.
Development of Immune Response in Horses
- The research involved immunizing two horses with venom from Bothrops asper, a kind of pit viper snake. The goal was to stimulate an immune response in the horses and produce antivenom from their blood serum.
- While the horses’ immune response to the venom’s toxic and enzymatic activities was similar throughout most of the immunization schedule, one horse developed a significantly stronger antibody response during the last part of the schedule.
- Antibodies that precipitate, or cause an antigen to become solid, were present in the horses’ blood at all stages of the immunization. However, the presence of these antibodies did not correlate directly with the blood’s ability to neutralize the venom’s toxic activities.
Effectiveness of Monovalent Antivenom
- The monovalent antivenom (antivenom specific to one type of venom) produced from the horses’ blood was more effective than the commercially available polyvalent antivenom (antivenom effective against multiple types of venom) in neutralizing Bothrops asper venom. However, its effectiveness was lower when used against other types of venom from Lachesia muta and Crotalus durissus durissus.
- While the monovalent antivenom could neutralize the lethal and hemorrhagic activities of these venoms, it could not counteract their defibrinating activity (the ability to disrupt blood clotting). On the other hand, it could neutralize the defibrinating effect of B. asper venom.
Implications and Recommendations
- The results suggest that the monovalent antivenom could be particularly effective for treating bites from Bothrops asper snakes. It might also be useful in treating bites from L. muta and C. durissus if polyvalent antivenom is unavailable.
- The variability in immune response among horses highlights the need to monitor antibody response individually in order to effectively produce antivenom.
Cite This Article
APA
Gutiérrez JM, Chaves F, Rojas E, Elizondo J, Avila C, Cerdas L.
(1988).
Production of monovalent anti-Bothrops asper antivenom: development of immune response in horses and neutralizing ability.
Rev Biol Trop, 36(2B), 511-517.
Publication
Researcher Affiliations
- Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica, San José.
MeSH Terms
- Animals
- Antibody Formation
- Antivenins / biosynthesis
- Antivenins / isolation & purification
- Antivenins / supply & distribution
- Antivenins / therapeutic use
- Crotalid Venoms / immunology
- Horses / immunology
- Immunization
- Immunoelectrophoresis
Citations
This article has been cited 5 times.- Silva A, Hodgson WC, Tasoulis T, Isbister GK. Rodent Lethality Models Are Problematic for Evaluating Antivenoms for Human Envenoming. Front Pharmacol 2022;13:830384.
- Solano-Godoy JA, González-Gómez JC, Torres-Bonilla KA, Floriano RS, Miguel ATSF, Murillo-Arango W. Comparison of biological activities of Tityus pachyurus venom from two Colombian regions. J Venom Anim Toxins Incl Trop Dis 2021;27:e20210005.
- Kaul S, Sai Keerthana L, Kumar P, Birader K, Tammineni Y, Rawat D, Suman P. Cytotoxin antibody-based colourimetric sensor for field-level differential detection of elapid among big four snake venom. PLoS Negl Trop Dis 2021 Oct;15(10):e0009841.
- Oliveira CS, Caldeira CAS, Diniz-Sousa R, Romero DL, Marcussi S, Moura LA, Fuly AL, de Carvalho C, Cavalcante WLG, Gallacci M, Pai MD, Zuliani JP, Calderon LA, Soares AM. Pharmacological characterization of cnidarian extracts from the Caribbean Sea: evaluation of anti-snake venom and antitumor properties. J Venom Anim Toxins Incl Trop Dis 2018;24:22.
- Castillo JC, Vargas LJ, Segura C, Gutiérrez JM, Pérez JC. In vitro antiplasmodial activity of phospholipases A2 and a phospholipase homologue isolated from the venom of the snake Bothrops asper. Toxins (Basel) 2012 Dec 14;4(12):1500-16.
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