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American Focus > Blog > Tech and Science > Blood of Man Who’s Had 200 Snakebites Helps Make a Potent Antivenom
Tech and Science

Blood of Man Who’s Had 200 Snakebites Helps Make a Potent Antivenom

Last updated: May 7, 2025 9:12 am
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Blood of Man Who’s Had 200 Snakebites Helps Make a Potent Antivenom
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A groundbreaking new antivenom has been developed using antibodies from a man who has survived over 200 snakebites. This innovative treatment combines existing medication with antibodies extracted from the blood of Tim Friede, a snake enthusiast who has built up a remarkable immunity to snake venom through repeated exposure.

The antivenom, which has been proven effective in protecting mice against the venom of 19 different species of deadly snakes, including the king cobra, represents a significant advancement in snakebite treatment. The research, outlined in a recent paper published in the prestigious journal Cell, has sparked both hope and ethical concerns within the scientific community.

While the potential of this new antivenom to address the dire need for more effective snakebite treatments is undeniable, the use of material derived from an individual who engaged in risky self-experimentation raises ethical questions. The authors of the study emphasize that they were not involved in Friede’s dangerous activities and caution against attempting to replicate his methods. Jacob Glanville, co-author of the study and CEO of Centivax, a biomedical firm in South San Francisco, stresses the dangers of handling snake venom and advises against following Friede’s example.

Traditional antivenoms are typically produced by injecting animals with snake venom to stimulate antibody production. However, this outdated method is limited in its effectiveness against a wide range of snake species. The new antivenom developed by Glanville and his team aims to provide broad-spectrum protection against the diverse array of venomous snakes found worldwide.

By focusing on the Elapidae family of snakes, which includes nearly half of all venomous snake species, the researchers identified key components in the venom that could be targeted for neutralization. By isolating antibodies from Friede’s blood and combining them with varespladib, an enzyme inhibitor that counteracts snake venom, the team created a potent cocktail that successfully protected mice against lethal doses of venom from various elapid snakes.

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While the ethical implications of using antibodies derived from a self-experimenting individual are a point of contention, experts acknowledge the potential of this new approach. Kartik Sunagar, a biologist specializing in antivenom development, commends the study for its scientific rigor but underscores the need for further research to determine the scalability and affordability of this treatment.

Moving forward, Glanville and his team are exploring ways to make the antivenom more accessible and cost-effective. Plans are underway to test the experimental cocktail on dogs in Australia bitten by snakes, with the goal of validating its efficacy before considering human trials.

In conclusion, the development of a novel antivenom utilizing antibodies from a man with a history of snakebites represents a significant milestone in snakebite treatment. While ethical concerns persist, the potential benefits of this innovative approach are promising. Further research and testing are needed to assess the real-world applicability of this groundbreaking antivenom.

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