Comparing Traditional and Toxin-Oriented Approaches towards Antivenom Production against Bitis arietans Snake Venom

被引:0
作者
Guidolin, Felipe Raimondi [1 ]
de Godoi, Kemily Stephanie [1 ]
Megale, Angela Alice Amadeu [1 ]
da Silva, Cristiane Castilho Fernandes [2 ]
Kodama, Roberto Tadashi [2 ]
Cajado-Carvalho, Daniela [3 ]
Iwai, Leo Kei [3 ]
Spencer, Patrick Jack [4 ]
Portaro, Fernanda Calheta Vieira [2 ]
da Silva, Wilmar Dias [1 ]
机构
[1] Butantan Inst, Immunochem Lab, BR-05503900 Sao Paulo, Brazil
[2] Butantan Inst, Lab Struct & Funct Biomol, BR-05503900 Sao Paulo, Brazil
[3] Butantan Inst, Ctr Toxins Immune Response & Cell Signaling CeTICS, Lab Appl Toxinol LETA, BR-05503900 Sao Paulo, Brazil
[4] Univ Sao Paulo, Nucl & Energy Res Inst, BR-05508000 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
snake venom; antivenom; antibody; sub-Saharan Africa; Bitis; Bitis arietans; PUFF-ADDER; PROTEINS; ANTIBODY; METALLOPROTEINASES;
D O I
10.3390/toxins15090584
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Accidents with snakes are responsible for about 32,000 deaths annually in sub-Saharan Africa, caused mostly by snakes from the genus Bitis, in particular Bitis arietans. B. arietans venom is composed of a complex mixture of toxins, mainly metalloproteases, serine proteases, phospholipases, lectins, and disintegrins. In this work, we compared two approaches to anti-B. arietans antivenom production: immunization with crude snake venom ("traditional approach") and immunization with selected key toxins isolated from the snake venom ("toxin oriented" approach). Fractions from B. arietans venom were isolated by size exclusion chromatography. Crude venom and samples containing serine proteases or metalloproteases were selected for the immunization of BALB/c mice. Anti-B. arietans and anti-serine proteases plasmas showed a similar recognition profile and higher titers and affinity than the anti-metalloproteases plasma. Cross-recognition of other Bitis venoms was observed, but with low intensity. Although the plasma of all experimental groups inhibited the enzymatic activity of B. arietans venom in vitro, in vivo protection was not achieved. Our results have shown limitations in both approaches considered. Based on this, we proposed a model of polyclonal, species-specific, monovalent antivenoms that could be used as a base to produce customizable polyvalent sera for use in sub-Saharan Africa.
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页数:20
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