Application of SARS-CoV-2 Serology to Address Public Health Priorities

Antibodies against SARS-CoV-2 can be detected by various testing platforms, but a detailed understanding of assay performance is critical. We developed and validated a simple enzyme-linked immunosorbent assay (ELISA) to detect IgG binding to the receptor-binding domain (RBD) of SARS-CoV-2, which was...

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Veröffentlicht in:Frontiers in public health 2021-11, Vol.9, p.744535-744535
Hauptverfasser: Sherman, Amy C, Smith, Teresa, Zhu, Yerun, Taibl, Kaitlin, Howard-Anderson, Jessica, Landay, Taylor, Pisanic, Nora, Kleinhenz, Jennifer, Simon, Trevor W, Espinoza, Daniel, Edupuganti, Neena, Hammond, Skyler, Rouphael, Nadine, Shen, Huifeng, Fairley, Jessica K, Edupuganti, Srilatha, Cardona-Ospina, Jaime A, Rodriguez-Morales, Alfonso J, Premkumar, Lakshmanane, Wrammert, Jens, Tarleton, Rick, Fridkin, Scott, Heaney, Christopher D, Scherer, Erin M, Collins, Matthew H
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Sprache:eng
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Zusammenfassung:Antibodies against SARS-CoV-2 can be detected by various testing platforms, but a detailed understanding of assay performance is critical. We developed and validated a simple enzyme-linked immunosorbent assay (ELISA) to detect IgG binding to the receptor-binding domain (RBD) of SARS-CoV-2, which was then applied for surveillance. ELISA results were compared to a set of complimentary serologic assays using a large panel of clinical research samples. The RBD ELISA exhibited robust performance in ROC curve analysis (AUC> 0.99; Se = 89%, Sp = 99.3%). Antibodies were detected in 23/353 (6.5%) healthcare workers, 6/9 RT-PCR-confirmed mild COVID-19 cases, and 0/30 non-COVID-19 cases from an ambulatory site. RBD ELISA showed a positive correlation with neutralizing activity ( =
ISSN:2296-2565
2296-2565
DOI:10.3389/fpubh.2021.744535