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Merck

Human Antibodies Protect against Aerosolized Eastern Equine Encephalitis Virus Infection.

Cell (2020-12-11)
Lauren E Williamson, Theron Gilliland, Pramod K Yadav, Elad Binshtein, Robin Bombardi, Nurgun Kose, Rachel S Nargi, Rachel E Sutton, Clarissa L Durie, Erica Armstrong, Robert H Carnahan, Lauren M Walker, Arthur S Kim, Julie M Fox, Michael S Diamond, Melanie D Ohi, William B Klimstra, James E Crowe, Lauren E Williamson, Theron Gilliland, Pramod K Yadav, Elad Binshtein, Robin Bombardi, Nurgun Kose, Rachel S Nargi, Rachel E Sutton, Clarissa L Durie, Erica Armstrong, Robert H Carnahan, Lauren M Walker, Arthur S Kim, Julie M Fox, Michael S Diamond, Melanie D Ohi, William B Klimstra, James E Crowe
RESUMEN

Eastern equine encephalitis virus (EEEV) is one of the most virulent viruses endemic to North America. No licensed vaccines or antiviral therapeutics are available to combat this infection, which has recently shown an increase in human cases. Here, we characterize human monoclonal antibodies (mAbs) isolated from a survivor of natural EEEV infection with potent (<20 pM) inhibitory activity of EEEV. Cryo-electron microscopy reconstructions of two highly neutralizing mAbs, EEEV-33 and EEEV-143, were solved in complex with chimeric Sindbis/EEEV virions to 7.2 Å and 8.3 Å, respectively. The mAbs recognize two distinct antigenic sites that are critical for inhibiting viral entry into cells. EEEV-33 and EEEV-143 protect against disease following stringent lethal aerosol challenge of mice with highly pathogenic EEEV. These studies provide insight into the molecular basis for the neutralizing human antibody response against EEEV and can facilitate development of vaccines and candidate antibody therapeutics.

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Saponin, for molecular biology, used as non-ionic surfactant
Sigma-Aldrich
Ouabain octahydrate, ≥95% (HPLC), powder
Sigma-Aldrich
Cyclosporin A, BioReagent, from Tolypocladium inflatum, for molecular biology, ≥95%
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Chk2 Inhibitor II hydrate, ≥98% (HPLC)
g-Strophanthin, phyproof® Reference Substance