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An infectious SARS-CoV-2 B.1.1.529 Omicron virus escapes neutralization by therapeutic monoclonal antibodies
by
Errico, John M.
, Zost, Seth J.
, Kawaoka, Yoshihiro
, Crowe, James E.
, Corti, Davide
, Diamond, Michael S.
, Purcell, Lisa A.
, VanBlargan, Laura A.
, Halfmann, Peter J.
, Fremont, Daved H.
in
631/326/596/2558
/ 631/326/596/4130
/ Antibodies, Monoclonal - pharmacology
/ Antibodies, Monoclonal - therapeutic use
/ Antibodies, Monoclonal, Humanized
/ Antibodies, Neutralizing - therapeutic use
/ Antibodies, Viral - therapeutic use
/ Biomedical and Life Sciences
/ Biomedicine
/ Biotechnology
/ Cancer Research
/ Coronaviruses
/ COVID-19
/ COVID-19 Drug Treatment
/ Humans
/ Immunoglobulin G
/ Infectious Diseases
/ Metabolic Diseases
/ Molecular Medicine
/ Monoclonal antibodies
/ Mutation
/ Neurosciences
/ Neutralization
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ Spike Glycoprotein, Coronavirus - genetics
/ Spike protein
/ Viral diseases
/ Viruses
2022
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An infectious SARS-CoV-2 B.1.1.529 Omicron virus escapes neutralization by therapeutic monoclonal antibodies
by
Errico, John M.
, Zost, Seth J.
, Kawaoka, Yoshihiro
, Crowe, James E.
, Corti, Davide
, Diamond, Michael S.
, Purcell, Lisa A.
, VanBlargan, Laura A.
, Halfmann, Peter J.
, Fremont, Daved H.
in
631/326/596/2558
/ 631/326/596/4130
/ Antibodies, Monoclonal - pharmacology
/ Antibodies, Monoclonal - therapeutic use
/ Antibodies, Monoclonal, Humanized
/ Antibodies, Neutralizing - therapeutic use
/ Antibodies, Viral - therapeutic use
/ Biomedical and Life Sciences
/ Biomedicine
/ Biotechnology
/ Cancer Research
/ Coronaviruses
/ COVID-19
/ COVID-19 Drug Treatment
/ Humans
/ Immunoglobulin G
/ Infectious Diseases
/ Metabolic Diseases
/ Molecular Medicine
/ Monoclonal antibodies
/ Mutation
/ Neurosciences
/ Neutralization
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ Spike Glycoprotein, Coronavirus - genetics
/ Spike protein
/ Viral diseases
/ Viruses
2022
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An infectious SARS-CoV-2 B.1.1.529 Omicron virus escapes neutralization by therapeutic monoclonal antibodies
by
Errico, John M.
, Zost, Seth J.
, Kawaoka, Yoshihiro
, Crowe, James E.
, Corti, Davide
, Diamond, Michael S.
, Purcell, Lisa A.
, VanBlargan, Laura A.
, Halfmann, Peter J.
, Fremont, Daved H.
in
631/326/596/2558
/ 631/326/596/4130
/ Antibodies, Monoclonal - pharmacology
/ Antibodies, Monoclonal - therapeutic use
/ Antibodies, Monoclonal, Humanized
/ Antibodies, Neutralizing - therapeutic use
/ Antibodies, Viral - therapeutic use
/ Biomedical and Life Sciences
/ Biomedicine
/ Biotechnology
/ Cancer Research
/ Coronaviruses
/ COVID-19
/ COVID-19 Drug Treatment
/ Humans
/ Immunoglobulin G
/ Infectious Diseases
/ Metabolic Diseases
/ Molecular Medicine
/ Monoclonal antibodies
/ Mutation
/ Neurosciences
/ Neutralization
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ Spike Glycoprotein, Coronavirus - genetics
/ Spike protein
/ Viral diseases
/ Viruses
2022
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An infectious SARS-CoV-2 B.1.1.529 Omicron virus escapes neutralization by therapeutic monoclonal antibodies
Journal Article
An infectious SARS-CoV-2 B.1.1.529 Omicron virus escapes neutralization by therapeutic monoclonal antibodies
2022
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Overview
The emergence of the highly transmissible B.1.1.529 Omicron variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is concerning for antibody countermeasure efficacy because of the number of mutations in the spike protein. In this study, we tested a panel of anti-receptor-binding domain monoclonal antibodies (mAbs) corresponding to those in clinical use by Vir Biotechnology (S309, the parent mAb of VIR-7831 (sotrovimab)), AstraZeneca (COV2-2196 and COV2-2130, the parent mAbs of AZD8895 and AZD1061), Regeneron (REGN10933 and REGN10987), Eli Lilly (LY-CoV555 and LY-CoV016) and Celltrion (CT-P59) for their ability to neutralize an infectious B.1.1.529 Omicron isolate. Several mAbs (LY-CoV555, LY-CoV016, REGN10933, REGN10987 and CT-P59) completely lost neutralizing activity against B.1.1.529 virus in both Vero-TMPRSS2 and Vero-hACE2-TMPRSS2 cells, whereas others were reduced (COV2-2196 and COV2-2130 combination, ~12-fold decrease) or minimally affected (S309). Our results suggest that several, but not all, of the antibodies in clinical use might lose efficacy against the B.1.1.529 Omicron variant.
New in vitro data suggest that the new SARS-CoV-2 Omicron variant is likely to escape neutralization by most therapeutic antibodies currently available.
Publisher
Nature Publishing Group US,Nature Publishing Group
Subject
/ Antibodies, Monoclonal - pharmacology
/ Antibodies, Monoclonal - therapeutic use
/ Antibodies, Monoclonal, Humanized
/ Antibodies, Neutralizing - therapeutic use
/ Antibodies, Viral - therapeutic use
/ Biomedical and Life Sciences
/ COVID-19
/ Humans
/ Mutation
/ Severe acute respiratory syndrome coronavirus 2
/ Spike Glycoprotein, Coronavirus - genetics
/ Viruses
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