SARS-CoV-2 infections elicit higher levels of original antigenic sin antibodies compared with SARS-CoV-2 mRNA vaccinations

Cell Rep. 2022 Oct 18;41(3):111496. doi: 10.1016/j.celrep.2022.111496.

Abstract

It is important to determine if severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections and SARS-CoV-2 mRNA vaccinations elicit different types of antibodies. Here, we characterize the magnitude and specificity of SARS-CoV-2 spike-reactive antibodies from 10 acutely infected health care workers with no prior SARS-CoV-2 exposure history and 23 participants who received SARS-CoV-2 mRNA vaccines. We found that infection and primary mRNA vaccination elicit S1- and S2-reactive antibodies, while secondary vaccination boosts mostly S1 antibodies. Using absorption assays, we found that SARS-CoV-2 infections elicit a large proportion of original antigenic sin-like antibodies that bind efficiently to the spike of common seasonal human coronaviruses but poorly to the spike of SARS-CoV-2. In converse, vaccination modestly boosts antibodies reactive to the spike of common seasonal human coronaviruses, and these antibodies cross-react more efficiently to the spike of SARS-CoV-2. Our data indicate that SARS-CoV-2 infections and mRNA vaccinations elicit fundamentally different antibody responses.

Keywords: CP: Immunology; SARS-CoV-2; antibodies; coronavirus; mRNA vaccines; original antigenic sin.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antibodies, Viral
  • COVID-19* / prevention & control
  • Humans
  • RNA, Messenger / genetics
  • SARS-CoV-2
  • Spike Glycoprotein, Coronavirus / genetics
  • Vaccination

Substances

  • Spike Glycoprotein, Coronavirus
  • Antibodies, Viral
  • RNA, Messenger
  • spike protein, SARS-CoV-2