Omicron (B.1.1.529): Infectivity, vaccine breakthrough, and antibody resistance
Jiahui Chen, Rui Wang, Nancy Benovich Gilby, Guo-Wei Wei

TL;DR
This study uses AI to comprehensively analyze Omicron's infectivity and antibody resistance, revealing it is significantly more contagious and capable of vaccine escape compared to previous variants, with implications for current antibody treatments.
Contribution
The paper provides the first extensive quantitative assessment of Omicron's infectivity and immune escape using AI and structural data, offering insights into vaccine and antibody effectiveness.
Findings
Omicron may be over ten times more contagious than the original virus.
Omicron could escape current vaccines twice as effectively as Delta.
FDA-approved monoclonal antibodies may be less effective against Omicron.
Abstract
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…
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Taxonomy
TopicsSARS-CoV-2 and COVID-19 Research · Bacillus and Francisella bacterial research · vaccines and immunoinformatics approaches
