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Prospective mapping of viral mutations that escape antibodies used to treat COVID-19
Tyler N. Starr; Allison J. Greaney; Amin Addetia; William H. Hannon; Adam S. Dingens; Jesse D Bloom.
Afiliación
  • Tyler N. Starr; Fred Hutch Cancer Research Center
  • Allison J. Greaney; Fred Hutch Cancer Research Center
  • Amin Addetia; Fred Hutch Cancer Research Center
  • William H. Hannon; Fred Hutch Cancer Research Center
  • Adam S. Dingens; Fred Hutch Cancer Research Center
  • Jesse D Bloom; Fred Hutchinson Cancer Research Center
Preprint en En | PREPRINT-BIORXIV | ID: ppbiorxiv-405472
ABSTRACT
Antibodies are becoming a frontline therapy for SARS-CoV-2, but the risk of viral evolutionary escape remains unclear. Here we map how all mutations to SARS-CoV-2s receptor-binding domain (RBD) affect binding by the antibodies in Regenerons REGN-COV2 cocktail and Eli Lillys LY-CoV016. These complete maps uncover a single amino-acid mutation that fully escapes the REGN-COV2 cocktail, which consists of two antibodies targeting distinct structural epitopes. The maps also identify viral mutations that are selected in a persistently infected patient treated with REGN-COV2, as well as in lab viral escape selections. Finally, the maps reveal that mutations escaping each individual antibody are already present in circulating SARS-CoV-2 strains. Overall, these complete escape maps enable immediate interpretation of the consequences of mutations observed during viral surveillance.
Licencia
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Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Observational_studies / Prognostic_studies Idioma: En Año: 2020 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Observational_studies / Prognostic_studies Idioma: En Año: 2020 Tipo del documento: Preprint