Author:
Glanville Jacob,Andrade Joel Christian,Bellin Mark,Kim Sangil,Pletnev Sergei,Tsao David,Verardi Raffaello,Bedi Rishi,Liao Sindy,Newland Raymond,Bayless Nicholas L.,Youssef Sawsan,Tully Ena,Zhang Baoshan,Bylund Tatsiana,Kim Sujeong,Liu Tracy,Kwong Peter D.
Abstract
AbstractSnake envenomation is a neglected tropical disease, causing >100,000 deaths and 300,000 permanent disabilities in humans annually. Could monoclonal antibody technology provide a solution? Here, we recover Centi-3FTX-D09, a potent broadly neutralizing antivenom antibody from the B-cell memory of a human subject with snake venom exposure. Centi-3FTX-D09 recognized a conserved neutralizing epitope on long 3-finger toxins (3FTXs), a dominant snake neurotoxin. Crystal structures of Centi-3FTX-D09 in complex with 3FTXs from mamba, taipan, krait, and cobra revealed epitope mimicry of the interface between these neurotoxins and their host target, the nicotinic acetylcholine receptor. Centi-3FTX-D09 providedin-vivoprotection against diverse recombinant long 3FTXs,in-vivorescue from whole venom challenge from cobras, black mamba, and king cobra, and, when combined with the phospholipase inhibitor varespladib,in-vivoprotection extending to a majority of tested elapid venoms. Thus, a single antibody can broadly neutralize long neurotoxins and contribute to broad protection from envenomation.
Publisher
Cold Spring Harbor Laboratory
Cited by
9 articles.
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