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Omicron (B.1.1.529): Infectivity, vaccine breakthrough, and antibody resistance

The latest severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant Omicron (B.1.1.529) has ushered panic responses around the world due to its contagious and vaccine escape mutations. The essential infectivity and antibody resistance of the SARS-CoV-2 variant are determined by its mutat...

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Autores principales: Chen, Jiahui, Wang, Rui, Gilby, Nancy Benovich, Wei, Guo-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cornell University 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647651/
https://www.ncbi.nlm.nih.gov/pubmed/34873578
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author Chen, Jiahui
Wang, Rui
Gilby, Nancy Benovich
Wei, Guo-Wei
author_facet Chen, Jiahui
Wang, Rui
Gilby, Nancy Benovich
Wei, Guo-Wei
author_sort Chen, Jiahui
collection PubMed
description The latest severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant Omicron (B.1.1.529) has ushered panic responses around the world due to its contagious and vaccine escape mutations. The essential infectivity and antibody resistance of the SARS-CoV-2 variant are determined by its mutations on the spike (S) protein receptor-binding domain (RBD). However, a complete experimental evaluation of Omicron might take weeks or even months. Here, we present a comprehensive quantitative analysis of Omicron’s infectivity, vaccine-breakthrough, and antibody resistance. An artificial intelligence (AI) model, which has been trained with tens of thousands of experimental data points and extensively validated by experimental data on SARS-CoV-2, reveals that Omicron may be over ten times more contagious than the original virus or about twice as infectious as the Delta variant. Based on 132 three-dimensional (3D) structures of antibody-RBD complexes, we unveil that Omicron may be twice more likely to escape current vaccines than the Delta variant. The Food and Drug Administration (FDA)-approved monoclonal antibodies (mAbs) from Eli Lilly may be seriously compromised. Omicron may also diminish the efficacy of mAbs from Celltrion and Rockefeller University. However, its impact to Regeneron mAb cocktail appears to be mild.
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spelling pubmed-86476512021-12-07 Omicron (B.1.1.529): Infectivity, vaccine breakthrough, and antibody resistance Chen, Jiahui Wang, Rui Gilby, Nancy Benovich Wei, Guo-Wei ArXiv Article The latest severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant Omicron (B.1.1.529) has ushered panic responses around the world due to its contagious and vaccine escape mutations. The essential infectivity and antibody resistance of the SARS-CoV-2 variant are determined by its mutations on the spike (S) protein receptor-binding domain (RBD). However, a complete experimental evaluation of Omicron might take weeks or even months. Here, we present a comprehensive quantitative analysis of Omicron’s infectivity, vaccine-breakthrough, and antibody resistance. An artificial intelligence (AI) model, which has been trained with tens of thousands of experimental data points and extensively validated by experimental data on SARS-CoV-2, reveals that Omicron may be over ten times more contagious than the original virus or about twice as infectious as the Delta variant. Based on 132 three-dimensional (3D) structures of antibody-RBD complexes, we unveil that Omicron may be twice more likely to escape current vaccines than the Delta variant. The Food and Drug Administration (FDA)-approved monoclonal antibodies (mAbs) from Eli Lilly may be seriously compromised. Omicron may also diminish the efficacy of mAbs from Celltrion and Rockefeller University. However, its impact to Regeneron mAb cocktail appears to be mild. Cornell University 2021-12-01 /pmc/articles/PMC8647651/ /pubmed/34873578 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Chen, Jiahui
Wang, Rui
Gilby, Nancy Benovich
Wei, Guo-Wei
Omicron (B.1.1.529): Infectivity, vaccine breakthrough, and antibody resistance
title Omicron (B.1.1.529): Infectivity, vaccine breakthrough, and antibody resistance
title_full Omicron (B.1.1.529): Infectivity, vaccine breakthrough, and antibody resistance
title_fullStr Omicron (B.1.1.529): Infectivity, vaccine breakthrough, and antibody resistance
title_full_unstemmed Omicron (B.1.1.529): Infectivity, vaccine breakthrough, and antibody resistance
title_short Omicron (B.1.1.529): Infectivity, vaccine breakthrough, and antibody resistance
title_sort omicron (b.1.1.529): infectivity, vaccine breakthrough, and antibody resistance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647651/
https://www.ncbi.nlm.nih.gov/pubmed/34873578
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