4.7 Article

Longitudinal analysis of severe acute respiratory syndrome coronavirus 2 seroprevalence using multiple serology platforms

Journal

ISCIENCE
Volume 24, Issue 9, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.isci.2021.102937

Keywords

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Funding

  1. NIAID Collaborative Influenza Vaccine Innovation Centers (CIVIC) [75N93019C00051]
  2. NIAID Center of Excellence for Influenza Research and Surveillance (CEIRS) [HHSN272201400008C]
  3. JPB Foundation
  4. Open Philanthropy Project [2020-215611 (5384)]
  5. Serological SciencesNetwork (SeroNet)
  6. National Cancer Institute, National Institutes of Health [75N91019D00024, 75N91020F00003]

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This study analyzed the antibody responses of healthcare workers using different serological tests, finding a good correlation between RBD and spike-based assays. Antibody levels in HCWs declined over time, while the seroprevalence of NP-reactive antibodies significantly decreased.
Current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serological tests are based on the full-length spike (S), the receptor-binding domain (RBD), or the nucleoprotein (NP) as substrates. Here, we used samples from healthcare workers (HCWs) to perform a longitudinal analysis of the antibody responses using a research-grade RBD and spike-based enzyme-linked immunosorbent assay (ELISA), a commercial RBD and spike-based ELISA, and a commercial NP-based chemiluminescent microparticle immunoassay. Seroprevalence ranged around 28% early during the pandemic and a good correlation was observed between RBD and spike- based ELISAs. Modest correlations were observed between NP and both RBD and spike-based assays. The antibody levels in HCWs declined over time; however, the overall seroprevalence measured by RBD and spike-based assays remained unchanged, while the seroprevalence of NP-reactive antibodies significantly declined. Moreover, RBD and spike-based assays effectively detected seroconversion in vaccinees. Overall, our results consolidate the strength of different serological assays to assess the magnitude and duration of antibodies to SARS-CoV-2.

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