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Patterns and persistence of SARS-CoV-2 IgG antibodies in Chicago to monitor COVID-19 exposure.
Demonbreun, Alexis R; McDade, Thomas W; Pesce, Lorenzo; Vaught, Lauren A; Reiser, Nina L; Bogdanovic, Elena; Velez, Matthew P; Hsieh, Ryan R; Simons, Lacy M; Saber, Rana; Ryan, Daniel T; Ison, Michael G; Hultquist, Judd F; Wilkins, John T; D'Aquila, Richard T; Mustanski, Brian; McNally, Elizabeth M.
Afiliação
  • Demonbreun AR; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine.
  • McDade TW; Department of Pharmacology, Northwestern University Feinberg School of Medicine.
  • Pesce L; Department of Anthropology and Institute for Policy Research, Northwestern University.
  • Vaught LA; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine.
  • Reiser NL; Department of Pharmacology, Northwestern University Feinberg School of Medicine.
  • Bogdanovic E; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine.
  • Velez MP; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine.
  • Hsieh RR; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine.
  • Simons LM; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine.
  • Saber R; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine.
  • Ryan DT; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine.
  • Ison MG; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine.
  • Hultquist JF; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine.
  • Wilkins JT; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine.
  • D'Aquila RT; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine.
  • Mustanski B; Division of Infectious Diseases, Department of Medicine, Northwestern University Feinberg School of Medicine.
  • McNally EM; Institute for Sexual and Gender Minority Health and Wellbeing and Department of Medical Social Sciences, Northwestern University.
medRxiv ; 2021 Mar 16.
Article em En | MEDLINE | ID: mdl-33236031
ABSTRACT

Background:

Estimates 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.

Methods:

Participants (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 to the receptor binding domain of SARS-CoV-2 was measured using an established highly sensitive and highly specific assay.

Results:

Overall 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 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 positive test. From a subset of those who participated in repeat testing, half of seropositive individuals retained detectable antibodies for 3-4 months.

Conclusions:

Quantitative IgG measurements with a highly specific and sensitive assay indicate more widespread exposure to SARS-CoV-2 than observed by viral testing. The range of IgG concentration produced from these asymptomatic exposures is similar to IgG levels occurring after documented non-hospitalized COVID-19, which is considerably lower than that 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2021 Tipo de documento: Article