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Neutralization of bothropic and crotalic venom toxic activities by IgG(T) and IgGa subclasses isolated from immune horse serum

Authors :
UCL - MD/CHIR - Département de chirurgie
UCL - (SLuc) Service de biologie hématologique
UCL - (SLuc) Centre de thérapie tissulaire et cellulaire
Fernandes, I.
Takehara, H. A.
Santos, A. C.
Cormont, Françoise
Latinne, Dominique
Bazin, Hervé
Mota, I.
UCL - MD/CHIR - Département de chirurgie
UCL - (SLuc) Service de biologie hématologique
UCL - (SLuc) Centre de thérapie tissulaire et cellulaire
Fernandes, I.
Takehara, H. A.
Santos, A. C.
Cormont, Françoise
Latinne, Dominique
Bazin, Hervé
Mota, I.
Source :
Toxicon, Vol. 35, no.6, p. 931-936 (1997)
Publication Year :
1997

Abstract

IgG(T) and IgGa isotypes were isolated from horse hyperimmune anti-bothropic and anti-crotalic sera using a combination of two affinity chromatographic processes. IgG(T) and IgGa isotypes were isolated from these sera by chromatography on protein A-Sepharose followed by separation of the two isotypes by chromatography on a column of anti-IgG(T)-Sepharose. LO-HoGT-1, a rat anti-horse IgG(T) monoclonal antibody, was used. A comparative study of the efficiency of these isotypes in neutralizing the main toxic activities of the homologous venoms was carried out. It was found that IgG(T) was about three-fold and seven-fold more protective than IgGa for neutralization of the lethal activity of B. jararaca and C. d. terrificus venoms, respectively. IgG(T) was also more effective than IgGa for the neutralization of the haemorrhagic activity induced by B. jararaca venom, while both isotypes neutralized equally well the blood incoagulability induced by this venom. The results suggest that IgG(T) is the most protective isotype present in both anti-bothropic and anti-crotalic sera, followed by IgGa. Owing to their very low concentration in the serum, other IgG isotypes are not likely to be important in neutralizing the venoms' toxic activities.

Details

Database :
OAIster
Journal :
Toxicon, Vol. 35, no.6, p. 931-936 (1997)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1288280900
Document Type :
Electronic Resource