Login / Signup

Rapid isolation and profiling of a diverse panel of human monoclonal antibodies targeting the SARS-CoV-2 spike protein.

Seth J ZostPavlo GilchukRita E ChenJames Brett CaseJoseph X ReidyAndrew TrivetteRachel S NargiRachel E SuttonNaveenchandra SuryadevaraElaine C ChenElad M BinshteinSwathi ShrihariMario OstrowskiHelen Y ChuJonathan E DidierKeith W MacRenarisTaylor JonesSamuel DayLuke MyersFrances Eun-Hyung LeeDoan C NguyenIgnacio SanzDavid R MartinezPaul W RothlaufLouis-Marie BloyetSean P J WhelanRalph S BaricLarissa B ThackrayMichael S DiamondRobert H CarnahanJames E Crowe
Published in: Nature medicine (2020)
Antibodies are a principal determinant of immunity for most RNA viruses and have promise to reduce infection or disease during major epidemics. The novel coronavirus SARS-CoV-2 has caused a global pandemic with millions of infections and hundreds of thousands of deaths to date1,2. In response, we used a rapid antibody discovery platform to isolate hundreds of human monoclonal antibodies (mAbs) against the SARS-CoV-2 spike (S) protein. We stratify these mAbs into five major classes on the basis of their reactivity to subdomains of S protein as well as their cross-reactivity to SARS-CoV. Many of these mAbs inhibit infection of authentic SARS-CoV-2 virus, with most neutralizing mAbs recognizing the receptor-binding domain (RBD) of S. This work defines sites of vulnerability on SARS-CoV-2 S and demonstrates the speed and robustness of advanced antibody discovery platforms.
Keyphrases