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PMID: 8814237 Published · ppublish English Journal Article

Processing of pro-tumor necrosis factor-alpha by venom metalloproteinases: a hypothesis explaining local tissue damage following snake bite.

European journal of immunology ·Vol. 26 ·No. 9 ·1996-09-00 ·Pages 2000-5

Moura-da-Silva AM, Laing GD, Paine MJ, Dennison JM, Politi V, Crampton JM, Theakston RD

Abstract

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-alpha fusion protein (GST-TNF-alpha) substrate to form biologically active TNF-alpha which was shown to be neutralized by ovine TNF-alpha 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-alpha-sensitive cell culture assay and electrophoresis. These observations demonstrate the possible importance of TNF-alpha 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-alpha. 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-alpha. The results indicate that inhibition or neutralization of endogenous TNF-alpha 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.

MeSH Terms
Amino Acid Sequence Animals Immunoglobulin Fab Fragments/immunology Male Metalloendopeptidases/physiology Mice Molecular Sequence Data Necrosis Protein Precursors/metabolism Snake Bites/metabolism Snake Venoms/metabolism,toxicity Tumor Necrosis Factor-alpha/metabolism
Chemicals
Immunoglobulin Fab Fragments Protein Precursors Snake Venoms Tumor Necrosis Factor-alpha Metalloendopeptidases
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Moura-da-Silva A M
Laboratorio de Imunopatologia, Instituto Butantan, São Paulo, Brasil.
Laing G D
Paine M J
Dennison J M
Politi V
Crampton J M
Theakston R D
Article Info
Journal
European journal of immunology
Abbr.
Eur J Immunol
ISSN
0014-2980
Published
1996-09-00
Pages
2000-5
Language
English
Region
Germany
NLM ID
1273201
Subset
IM
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