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10.1101/2021.11.26.470157

http://scihub22266oqcxt.onion/10.1101/2021.11.26.470157
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suck abstract from ncbi


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pmid34873599      bioRxiv 2021 ; ä (ä): ä
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  • A large-scale systematic survey of SARS-CoV-2 antibodies reveals recurring molecular features #MMPMID34873599
  • Wang Y; Yuan M; Peng J; Wilson IA; Wu NC
  • bioRxiv 2021[Nov]; ä (ä): ä PMID34873599show ga
  • In the past two years, the global research in combating COVID-19 pandemic has led to isolation and characterization of numerous human antibodies to the SARS-CoV-2 spike. This enormous collection of antibodies provides an unprecedented opportunity to study the antibody response to a single antigen. From mining information derived from 88 research publications and 13 patents, we have assembled a dataset of a^(1/4)8,000 human antibodies to the SARS-CoV-2 spike from >200 donors. Analysis of antibody targeting of different domains of the spike protein reveals a number of common (public) responses to SARS-CoV-2, exemplified via recurring IGHV/IGK(L)V pairs, CDR H3 sequences, IGHD usage, and somatic hypermutation. We further present a proof-of-concept for prediction of antigen specificity using deep learning to differentiate sequences of antibodies to SARS-CoV-2 spike and to influenza hemagglutinin. Overall, this study not only provides an informative resource for antibody and vaccine research, but fundamentally advances our molecular understanding of public antibody responses to a viral pathogen.
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