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10.1126/science.abf9302

http://scihub22266oqcxt.onion/10.1126/science.abf9302
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33495308!7963219!33495308
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suck abstract from ncbi


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pmid33495308      Science 2021 ; 371 (6531): 850-854
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  • Prospective mapping of viral mutations that escape antibodies used to treat COVID-19 #MMPMID33495308
  • Starr TN; Greaney AJ; Addetia A; Hannon WW; Choudhary MC; Dingens AS; Li JZ; Bloom JD
  • Science 2021[Feb]; 371 (6531): 850-854 PMID33495308show ga
  • 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.
  • |*Mutation[MESH]
  • |Amino Acid Substitution[MESH]
  • |Angiotensin-Converting Enzyme 2/metabolism[MESH]
  • |Antibodies, Monoclonal, Humanized/*immunology/metabolism/therapeutic use[MESH]
  • |Antibodies, Viral/*immunology/metabolism/therapeutic use[MESH]
  • |COVID-19 Serotherapy[MESH]
  • |COVID-19/*therapy[MESH]
  • |Cells, Cultured[MESH]
  • |Drug Combinations[MESH]
  • |Humans[MESH]
  • |Immunization, Passive[MESH]
  • |Protein Binding[MESH]
  • |Protein Domains[MESH]
  • |Receptors, Coronavirus/metabolism[MESH]
  • |SARS-CoV-2/*genetics/*immunology[MESH]


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