Completed Cells, Biochemistry & Physiology

Antibody Discovery and Development Against Non-Immunogenic Snake Venom Toxins

In plain English

AI plain-English summary

Snake venom contains small toxins that the human immune system barely notices, so current antivenoms often fail to stop them. This matters because snakebites kill and disable tens of thousands of people each year, mostly in rural tropical regions. The toxins that cause the worst damage—bleeding, paralysis, tissue destruction—are often the smallest molecules in the venom. They slip past the immune response, so antibodies raised in horses or sheep (the standard way to make antivenom) rarely bind them effectively. The result: patients receive treatment that neutralises some venom components but leaves the most dangerous ones untouched. The researchers plan to outsmart this problem. They will design synthetic versions of these small toxins that the immune system *can* recognise, then use those to generate antibodies in the lab. They will also screen vast libraries of artificial antibodies to find ones that latch onto the real toxins with high precision. If this works, the antibodies could be added to existing antivenoms or developed into standalone treatments. The impact would be felt in rural clinics across Asia, Africa, and Latin America, where snakebite is a daily occupational hazard for farmers and herders. Better neutralisation of these hidden toxins could mean fewer amputations, less paralysis, and more people walking out of hospital alive.

View original technical description
This proposal aims to ultimately reduce global levels of morbidity and mortality from snakebite envenoming by discovering and developing antibodies that can neutralize the low molecular weight snake venom toxins – key contributors to the disease. These non-immunogenic toxins are poorly neutralized by currently available antivenoms produced by animal derived immunizations. This proposed project will discover neutralizing antibodies through immunization experiments using rationally designed immunogens and select for high-affinity antibodies via synthetic libraries using recombinant toxins.

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Researchers

Joseph Jardine (EPMC Awardee)Kartik Sunagar (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Utilising snake endogenous toxin inhibitors for the development of improved antivenom treatments
Recombinant snakebite antivenom for sub-Saharan Africa
Antibody development for geographically diverse hemotoxic snakebite envenoming
Structural characterization of key venom toxin neutralization vulnerabilities
Rational design of rapidly translatable, highly antigenic and novel recombinant immunogens to address deficiencies of current snakebite treatments

Original classification

Snakebite Grant – Next Generation Treatments

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.