JCI Insight (Apr 2021)

A majority of uninfected adults show preexisting antibody reactivity against SARS-CoV-2

  • Abdelilah Majdoubi,
  • Christina Michalski,
  • Sarah E. O’Connell,
  • Sarah Dada,
  • Sandeep Narpala,
  • Jean Gelinas,
  • Disha Mehta,
  • Claire Cheung,
  • Dirk F.H. Winkler,
  • Manjula Basappa,
  • Aaron C. Liu,
  • Matthias Görges,
  • Vilte E. Barakauskas,
  • Mike Irvine,
  • Jennifer Mehalko,
  • Dominic Esposito,
  • Inna Sekirov,
  • Agatha N. Jassem,
  • David M. Goldfarb,
  • Steven Pelech,
  • Daniel C. Douek,
  • Adrian B. McDermott,
  • Pascal M. Lavoie

Journal volume & issue
Vol. 6, no. 8

Abstract

Read online

Preexisting cross-reactivity to SARS-CoV-2 occurs in the absence of prior viral exposure. However, this has been difficult to quantify at the population level due to a lack of reliably defined seroreactivity thresholds. Using an orthogonal antibody testing approach, we estimated that about 0.6% of nontriaged adults from the greater Vancouver, Canada, area between May 17 and June 19, 2020, showed clear evidence of a prior SARS-CoV-2 infection, after adjusting for false-positive and false-negative test results. Using a highly sensitive multiplex assay and positive/negative thresholds established in infants in whom maternal antibodies have waned, we determined that more than 90% of uninfected adults showed antibody reactivity against the spike protein, receptor-binding domain (RBD), N-terminal domain (NTD), or the nucleocapsid (N) protein from SARS-CoV-2. This seroreactivity was evenly distributed across age and sex, correlated with circulating coronaviruses’ reactivity, and was partially outcompeted by soluble circulating coronaviruses’ spike. Using a custom SARS-CoV-2 peptide mapping array, we found that this antibody reactivity broadly mapped to spike and to conserved nonstructural viral proteins. We conclude that most adults display preexisting antibody cross-reactivity against SARS-CoV-2, which further supports investigation of how this may impact the clinical severity of COVID-19 or SARS-CoV-2 vaccine responses.

Keywords