| Literature DB >> 34011939 |
Ge Song1,2,3, Wan-Ting He1,2,3, Sean Callaghan1,2,3, Fabio Anzanello1,2,3, Deli Huang1, James Ricketts1, Jonathan L Torres4, Nathan Beutler1, Linghang Peng1, Sirena Vargas1,2,3, Jon Cassell1,2,3, Mara Parren1, Linlin Yang1, Caroline Ignacio5, Davey M Smith5, James E Voss1, David Nemazee1, Andrew B Ward2,3,4, Thomas Rogers1,5, Dennis R Burton6,7,8,9, Raiees Andrabi10,11,12.
Abstract
Pre-existing immunity to seasonal endemic coronaviruses could have profound consequences for antibody responses to SARS-CoV-2, induced from natural infection or vaccination. A first step to establish whether pre-existing responses can impact SARS-CoV-2 infection is to understand the nature and extent of cross-reactivity in humans to coronaviruses. Here we compare serum antibody and memory B cell responses to coronavirus spike proteins from pre-pandemic and SARS-CoV-2 convalescent donors using binding and functional assays. We show weak evidence of pre-existing SARS-CoV-2 cross-reactive serum antibodies in pre-pandemic donors. However, we find evidence of pre-existing cross-reactive memory B cells that are activated during SARS-CoV-2 infection. Monoclonal antibodies show varying degrees of cross-reactivity with betacoronaviruses, including SARS-CoV-1 and endemic coronaviruses. We identify one cross-reactive neutralizing antibody specific to the S2 subunit of the S protein. Our results suggest that pre-existing immunity to endemic coronaviruses should be considered in evaluating antibody responses to SARS-CoV-2.Entities:
Year: 2021 PMID: 34011939 DOI: 10.1038/s41467-021-23074-3
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919