» Articles » PMID: 33755598

Patterns and Persistence of SARS-CoV-2 IgG Antibodies in Chicago to Monitor COVID-19 Exposure

Abstract

BACKGROUNDEstimates of seroprevalence to SARS-CoV-2 vary widely and may influence vaccination response. We ascertained IgG levels across a single US metropolitan site, Chicago, from June 2020 through December 2020.METHODSParticipants (n = 7935) were recruited through electronic advertising and received materials for a self-sampled dried-blood spot assay through the mail or a minimal contact in-person method. IgG against the receptor-binding domain of SARS-CoV-2 was measured using an established highly sensitive and highly specific assay.RESULTSOverall seroprevalence was 17.9%, with no significant difference between method of contact. Only 2.5% of participants reported having had a diagnosis of COVID-19 based on virus detection, consistent with a 7-fold greater exposure to SARS-CoV-2 measured by serology than that detected by viral testing. The range of IgG level observed in seropositive participants from this community survey overlapped with the range of IgG levels associated with COVID-19 cases having a documented positive PCR test. From a subset of those who participated in repeat testing, half of seropositive individuals retained detectable antibodies for 3 to 4 months.CONCLUSIONQuantitative IgG measurements with a highly specific and sensitive assay indicated more widespread exposure to SARS-CoV-2 than observed by viral testing. The range of IgG concentrations produced from these asymptomatic exposures was similar to IgG levels occurring after documented nonhospitalized COVID-19, which were considerably lower than those produced from hospitalized COVID-19 cases. The differing ranges of IgG response, coupled with the rate of decay of antibodies, may influence response to subsequent viral exposure and vaccine.FundingNational Science Foundation grant 2035114, NIH grant 3UL1TR001422-06S4, NIH National Center for Advancing Translational Sciences grants UL1 TR001422 and UL1 TR002389, Dixon Family Foundation, Northwestern University Cancer Center (NIH grant P30 CA060553), and Walder Foundation's Chicago Coronavirus Assessment Network.

Citing Articles

Longitudinal determination of seroprevalence and immune response to SARS-CoV-2 in a population of food and retail workers through decentralized testing and transformation of ELISA datasets.

Djaileb A, Parker M, Lavallee E, Stuible M, Durocher Y, Theriault M PLoS One. 2024; 19(12):e0314499.

PMID: 39680559 PMC: 11649073. DOI: 10.1371/journal.pone.0314499.


A Dried Blood Spot protocol for high-throughput quantitative analysis of SARS-CoV-2 RBD serology based on the Roche Elecsys system.

Castelletti N, Paunovic I, Rubio-Acero R, Beyerl J, Plank M, Reinkemeyer C Microbiol Spectr. 2024; 12(4):e0288523.

PMID: 38426747 PMC: 10986497. DOI: 10.1128/spectrum.02885-23.


Individual Immune Response to SARS-CoV-2 Infection-The Role of Seasonal Coronaviruses and Human Leukocyte Antigen.

Rottmayer K, Loeffler-Wirth H, Gruenewald T, Doxiadis I, Lehmann C Biology (Basel). 2023; 12(10).

PMID: 37887003 PMC: 10603889. DOI: 10.3390/biology12101293.


Estimating the cumulative incidence of SARS-CoV-2 infection in Costa Rica: modelling seroprevalence data in a population-based cohort.

Fantin R, Agarwala N, Aparicio A, Pfeiffer R, Waterboer T, Abdelnour A Lancet Reg Health Am. 2023; 27:100616.

PMID: 37868648 PMC: 10589740. DOI: 10.1016/j.lana.2023.100616.


Omicron infection elicits a broad neutralizing response in hospitalized patients with COVID-19.

McNally E J Clin Invest. 2022; 132(23).

PMID: 36453549 PMC: 9711865. DOI: 10.1172/JCI165034.


References
1.
McDade T, McNally E, Zelikovich A, DAquila R, Mustanski B, Miller A . High seroprevalence for SARS-CoV-2 among household members of essential workers detected using a dried blood spot assay. PLoS One. 2020; 15(8):e0237833. PMC: 7428174. DOI: 10.1371/journal.pone.0237833. View

2.
Oved K, Olmer L, Shemer-Avni Y, Wolf T, Supino-Rosin L, Prajgrod G . Multi-center nationwide comparison of seven serology assays reveals a SARS-CoV-2 non-responding seronegative subpopulation. EClinicalMedicine. 2020; 29:100651. PMC: 7676374. DOI: 10.1016/j.eclinm.2020.100651. View

3.
Gudbjartsson D, Norddahl G, Melsted P, Gunnarsdottir K, Holm H, Eythorsson E . Humoral Immune Response to SARS-CoV-2 in Iceland. N Engl J Med. 2020; 383(18):1724-1734. PMC: 7494247. DOI: 10.1056/NEJMoa2026116. View

4.
Amanat F, Stadlbauer D, Strohmeier S, Nguyen T, Chromikova V, McMahon M . A serological assay to detect SARS-CoV-2 seroconversion in humans. Nat Med. 2020; 26(7):1033-1036. PMC: 8183627. DOI: 10.1038/s41591-020-0913-5. View

5.
Stringhini S, Wisniak A, Piumatti G, Azman A, Lauer S, Baysson H . Seroprevalence of anti-SARS-CoV-2 IgG antibodies in Geneva, Switzerland (SEROCoV-POP): a population-based study. Lancet. 2020; 396(10247):313-319. PMC: 7289564. DOI: 10.1016/S0140-6736(20)31304-0. View