| Literature DB >> 33720905 |
Abdelilah Majdoubi1,2, Christina Michalski1,2, Sarah E O'Connell3, Sarah Dada1,2, Sandeep Narpala3, Jean Gelinas4,5, Disha Mehta4,6, Claire Cheung1,2, Dirk Fh Winkler7, Manjula Basappa3, Aaron C Liu1,2,8, Matthias Görges1,6, Vilte E Barakauskas9, Mike Irvine1, Jennifer Mehalko10, Dominic Esposito10, Inna Sekirov9,11, Agatha N Jassem9,11, David M Goldfarb1,2,12, Steven Pelech7,13, Daniel C Douek3, Adrian B McDermott3, Pascal M Lavoie1,2.
Abstract
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.Entities:
Keywords: Adaptive immunity; COVID-19; Immunology
Year: 2021 PMID: 33720905 DOI: 10.1172/jci.insight.146316
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708