Publication:
Immunochemical and biochemical comparisons of equine monovalent and polyvalent snake antivenoms

dc.contributor.authorRutai Raweerithen_US
dc.contributor.authorKavi Ratanabanangkoonen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.date.accessioned2018-06-21T08:34:38Z
dc.date.available2018-06-21T08:34:38Z
dc.date.issued2005-03-01en_US
dc.description.abstractAlthough the merit of polyvalent antivenoms is well-recognized, there is still doubt in some medical circles as to the relative efficacy and the propensity to cause adverse reactions of polyvalent (pAV) as compared to monovalent (mAV) antivenoms. Immunochemical and biochemical comparisons of equine polyvalent and monovalent antivenoms prepared under the same immunization protocols were therefore made. These antivenoms were prepared against Naja kaouthia (NK), Ophiophagus hannah (OH) and Bungarus fasciatus (BF) venoms. SDS-PAGE analysis of both types of antivenoms showed similar serum protein profiles. The total amount of immunoglobulin (IgGT+IgG) in pAVs was slightly but significantly higher than that of mAVs, while the total serum protein content in mAVs was slightly but significantly higher than that of pAVs. The amounts of total hyperimmune IgGT, determined by ELISA, were similar in mAVs and pAVs. pAVs contained specific antibodies against the principal NK postsynaptic toxin (NK 3) to the same extent as that observed with the anti-N. kaouthia mAV. The antibodies against OH and BF principal postsynaptic toxins (OH II and BF IX) in pAVs were significantly higher than those of the corresponding anti-O. hannah and anti-B. fasciatus mAVs. These results were in concordance with the comparable in vivo neutralization activities of mAVs and pAV previously reported. The apparent dissociation constant (Kd) of anti-OH II antibody in pAVs was comparable to that of the anti-O. hannah mAVs. The apparent Kds of anti-NK 3 and anti-BF IX antibodies in the corresponding mAVs were slightly lower than those in pAVs. The Kdvalues were all in nM range and were considered to be high affinity binding. It is concluded that pAVs could be prepared with potency and protein contents and thus the propensity to cause adverse reaction that were comparable to those of mAVs. © 2004 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationToxicon. Vol.45, No.3 (2005), 369-375en_US
dc.identifier.doi10.1016/j.toxicon.2004.10.019en_US
dc.identifier.issn00410101en_US
dc.identifier.other2-s2.0-15944421205en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/17172
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=15944421205&origin=inwarden_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleImmunochemical and biochemical comparisons of equine monovalent and polyvalent snake antivenomsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=15944421205&origin=inwarden_US

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