| Literature DB >> 33495308 |
Tyler N Starr1, Allison J Greaney1,2,3, Amin Addetia1,4, William W Hannon1,4, Manish C Choudhary5, Adam S Dingens1, Jonathan Z Li5, Jesse D Bloom6,2,7.
Abstract
Antibodies are a potential therapy for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), but the risk of the virus evolving to escape them remains unclear. Here we map how all mutations to the receptor binding domain (RBD) of SARS-CoV-2 affect binding by the antibodies in the REGN-COV2 cocktail and the antibody LY-CoV016. These complete maps uncover a single amino acid mutation that fully escapes the REGN-COV2 cocktail, which consists of two antibodies, REGN10933 and REGN10987, targeting distinct structural epitopes. The maps also identify viral mutations that are selected in a persistently infected patient treated with REGN-COV2 and during in vitro viral escape selections. Finally, the maps reveal that mutations escaping the individual antibodies are already present in circulating SARS-CoV-2 strains. These complete escape maps enable interpretation of the consequences of mutations observed during viral surveillance.Entities:
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Year: 2021 PMID: 33495308 PMCID: PMC7963219 DOI: 10.1126/science.abf9302
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728