TY - JOUR
T1 - Processing of pro-tumor necrosis factor-α by venom metalloproteinases: A hypothesis explaining local tissue damage following snake bite: A hypothesis explaining local tissue damage following snake bite
AU - Moura-da-Silva, Ana Maria
AU - Laing, Gavin David
AU - Paine, Mark
AU - Dennison, Jeremy Michael Thomas Jonathan
AU - Politi, Vincenzo
AU - Crampton, Julian Moray
AU - Theakston, Robert David Geoffrey
PY - 1996/1/1
Y1 - 1996/1/1
N2 - Venom-induced necrosis is a common local debilitating sequela of bites by many vipers, frequently resulting in severe permanent scarring and deformity. Antivenoms are not effective under these circumstances unless administered within a few minutes of the bite; this is unlikely to occur in the rural tropics where most victims take a long time to reach medical care. We have shown that two venom zinc metalloproteinases (jararhagin from Bothrops jararaca venom and a metalloproteinase from Echis pyramidum leakeyi, venom) successfully cleaved the recombinant glutathione-S-transferase - tumor necrosis factor-α fusion protein (GST-TNF-α) substrate to form biologically active TNF-α which was shown to be neutralized by ovine TNF-α Fab antibodies. This resulted in a reduction of venom-induced necrosis in mice when injected intravenously or intradermally both before and after intradermal injections of E.p, leakeyi venom. A peptidomimetic (POL 647) was also found to inhibit the Echis metalloproteinase, thus preventing the processing of the TNF precursor; this was shown using a TNF-α-sensitive cell culture assay and electrophoresis. These observations demonstrate the possible importance of TNF-α in the development of the resulting necrotic lesion and leads to the hypothesis that increased levels of venom metalloproteinases following snake bite release active TNF-α. This cytokine may contribute to the local necrosis and also induce the production of endogenous matrix metalloproteinases, which in turn generate a positive feedback mechanism resulting in continued cleavage of pro-TNF-α. The results indicate that inhibition or neutralization of endogenous TNF-α appears to result in a significant reduction in venom-induced necrosis. This could help to explain the clinical observations that treatment of local necrosis following snake bite by antivenom is only minimally successful.
AB - Venom-induced necrosis is a common local debilitating sequela of bites by many vipers, frequently resulting in severe permanent scarring and deformity. Antivenoms are not effective under these circumstances unless administered within a few minutes of the bite; this is unlikely to occur in the rural tropics where most victims take a long time to reach medical care. We have shown that two venom zinc metalloproteinases (jararhagin from Bothrops jararaca venom and a metalloproteinase from Echis pyramidum leakeyi, venom) successfully cleaved the recombinant glutathione-S-transferase - tumor necrosis factor-α fusion protein (GST-TNF-α) substrate to form biologically active TNF-α which was shown to be neutralized by ovine TNF-α Fab antibodies. This resulted in a reduction of venom-induced necrosis in mice when injected intravenously or intradermally both before and after intradermal injections of E.p, leakeyi venom. A peptidomimetic (POL 647) was also found to inhibit the Echis metalloproteinase, thus preventing the processing of the TNF precursor; this was shown using a TNF-α-sensitive cell culture assay and electrophoresis. These observations demonstrate the possible importance of TNF-α in the development of the resulting necrotic lesion and leads to the hypothesis that increased levels of venom metalloproteinases following snake bite release active TNF-α. This cytokine may contribute to the local necrosis and also induce the production of endogenous matrix metalloproteinases, which in turn generate a positive feedback mechanism resulting in continued cleavage of pro-TNF-α. The results indicate that inhibition or neutralization of endogenous TNF-α appears to result in a significant reduction in venom-induced necrosis. This could help to explain the clinical observations that treatment of local necrosis following snake bite by antivenom is only minimally successful.
KW - Metalloproteinases
KW - Necrosis, local
KW - Snake venom
KW - Tumor necrosis factor
U2 - 10.1002/eji.1830260905
DO - 10.1002/eji.1830260905
M3 - Article
SN - 0014-2980
VL - 26
SP - 2000
EP - 2005
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 9
ER -