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[Preprint]. 2020 Nov 18:2020.11.17.20233452. [Version 1] doi: 10.1101/2020.11.17.20233452

Patterns and persistence of SARS-CoV-2 IgG antibodies in a US metropolitan site

Alexis R Demonbreun, Thomas W McDade, Lorenzo Pesce, Lauren A Vaught, Nina L Reiser, Elena Bogdanovic, Matt E Velez, Ryan R Hsieh, Claire-Naoma Klaisner, Lacy M Simons, Rana Saber, Daniel T Ryan, Michael G Ison, Judd F Hultquist, John T Wilkins, Richard T D’Aquila, Brian Mustanski, Elizabeth M McNally
PMCID: PMC7685344  PMID: 33236031

Abstract

Background

Estimates of seroprevalence to SARS-CoV-2 vary widely. We ascertained IgG levels across a single US metropolitan site, Chicago, over the 2020 summer, a period when restrictions on activities had been lifted.

Methods

We utilized a self-sampled dried blood spot assay to quantitatively monitor antibodies to the receptor binding domain (RBD) of the spike glycoprotein of SARS-CoV-2 in 1545 participants, with return of blood spot cards either by mail or in-person drop-off.

Results

Seroprevalence was 19.8%, with no significant difference between method of contact, or between essential and non-essential workers. Only a small number (1.2%) of participants reported having had a diagnosis of COVID-19 based on virus detection, consistent with a 16-fold greater exposure to SARS-CoV-2 measured by serology than detected by viral testing. Only a modest correlation was observed between having antibodies to SARS-CoV-2 nucleocapsid compared to RBD, with many only having detectable anti-RBD antibodies. From a subset of those who participated in repeat testing, three-quarters of seropositive individuals retained detectable antibodies for at least 120 days. One seropositive individual experienced a strong boost in IgG levels following a symptomatic illness, suggestive of potential re-exposure.

Conclusions

These data underscore the importance of a self-collected, quantitative assay with adequate sensitivity to detect antibodies at the lower levels among non-hospitalized persons with community-acquired exposure to COVID-19.

Full Text Availability

The license terms selected by the author(s) for this preprint version do not permit archiving in PMC. The full text is available from the preprint server.


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