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Oxford University Press - PMC COVID-19 Collection logoLink to Oxford University Press - PMC COVID-19 Collection
. 2021 Oct 12:jiab524. doi: 10.1093/infdis/jiab524

Anti-SARS-CoV-2 IgA Identifies Asymptomatic Infection in First Responders

Brian T Montague 1,, Matthew F Wipperman 2, Andrea T Hooper 2, Sara C Hamon 2, Rowena Crow 1, Femi Elemo 2, Lisa Hersh 2, Shaun Langdon 2, Jennifer D Hamilton 2, Meagan P O’Brien 2, Eric A F Simões 1,
PMCID: PMC8549282  PMID: 34636907

Abstract

Background

IgA is an important component of the early immune response to SARS-CoV-2. Prior serosurveys in high-risk groups employing IgG testing alone have provided discordant estimates. The potential added benefit of IgA in serosurveys has not been established.

Methods

Longitudinal serosurvey of first responders (police, emergency medical service providers, fire fighters, and other staff) employing three serologic tests: anti-spike IgA, anti-spike IgG, and anti-nucleocapsid IgG correlated with surveys assessing occupational and non-occupational risk, exposure to COVID-19 and illnesses consistent with COVID-19.

Results

Twelve percent of first responders in Colorado at baseline and 22% at follow-up were assessed as having SARS-CoV-2 infection. Five percent at baseline and 6% at follow-up were seropositive only for IgA. Among those IgA positive only at baseline, the majority 69% had a positive antibody at follow-up. 45% of those infected at baseline and 33% at follow-up were asymptomatic. At all time points, the estimated cumulative incidence in our study was higher than that in the general population.

Conclusions

First responders are at high risk of infection with SARS-CoV-2. IgA testing identified a significant portion of cases missed by IgG testing and its use as part of serologic surveys may improve retrospective identification of asymptomatic infection.

Keywords: SARS-CoV-2, COVID-19, serosurvey, IgA, first responders, epidemiology, cumulative incidence

Supplementary Material

jiab524_suppl_Supplementary_Tables

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

jiab524_suppl_Supplementary_Tables

Articles from The Journal of Infectious Diseases are provided here courtesy of Oxford University Press

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