In Vitro Immunological Cross-Reactivity of Thai Polyvalent and Monovalent Antivenoms with Asian Viper Venoms

The intravenous administration of polyclonal antibodies known as antivenom is the only effective treatment for snakebite envenomed victims, but because of inter-specific variation in the toxic components of snake venoms, these therapies have variable efficacies against different snake species and/or...

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Veröffentlicht in:Toxins 2020-12, Vol.12 (12), p.766
Hauptverfasser: Chaisakul, Janeyuth, Rusmili, Muhamad Rusdi Ahmad, Alsolaiss, Jaffer, Albulescu, Laura-Oana, Harrison, Robert A, Othman, Iekhsan, Casewell, Nicholas R
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Sprache:eng
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Zusammenfassung:The intravenous administration of polyclonal antibodies known as antivenom is the only effective treatment for snakebite envenomed victims, but because of inter-specific variation in the toxic components of snake venoms, these therapies have variable efficacies against different snake species and/or different populations of the same species. In this study, we sought to characterize the in vitro venom binding capability and in vitro cross-neutralizing activity of antivenom, specifically the Hemato Polyvalent antivenom (HPAV; The Queen Saovabha Memorial Institute (QSMI) of the Thai Red Cross Society, Thailand) and three monovalent antivenoms (QSMI) specific to , and venoms, against a variety of South Asian and Southeast Asian viper venoms ( , , , , , and ). Using ELISA and immunoblotting approaches, we find that the majority of protein components in the viper venoms were recognized and bound by the HPAV polyvalent antivenom, while the monospecific antivenom made against extensively recognized toxins present in the venom of related species, , and . In vitro coagulation assays using bovine plasma revealed similar findings, with HPAV antivenom significantly inhibiting the coagulopathic activities of all tested viper venoms and antivenom inhibiting the venoms from Malaysian arboreal pit vipers. We also show that the monovalent antivenom exhibits highly comparable levels of immunological binding and in vitro venom neutralization to venom from both Thailand and Malaysia, despite previous reports of considerable intraspecific venom variation. Our findings suggest that Thai antivenoms from QSMI may by useful therapeutics for managing snake envenomings caused by a number of Southeast Asian viper species and populations for which no specific antivenom currently exists and thus should be explored further to assess their clinical utility in treating snakebite victims.
ISSN:2072-6651
2072-6651
DOI:10.3390/toxins12120766