TY - JOUR
T1 - Application of SARS-CoV-2 Serology to Address Public Health Priorities
AU - Sherman, Amy C.
AU - Smith, Teresa
AU - Zhu, Yerun
AU - Taibl, Kaitlin
AU - Howard-Anderson, Jessica
AU - Landay, Taylor
AU - Pisanic, Nora
AU - Kleinhenz, Jennifer
AU - Simon, Trevor W.
AU - Espinoza, Daniel
AU - Edupuganti, Neena
AU - Hammond, Skyler
AU - Rouphael, Nadine
AU - Shen, Huifeng
AU - Fairley, Jessica K.
AU - Edupuganti, Srilatha
AU - Cardona-Ospina, Jaime A.
AU - Rodriguez-Morales, Alfonso J.
AU - Premkumar, Lakshmanane
AU - Wrammert, Jens
AU - Tarleton, Rick
AU - Fridkin, Scott
AU - Heaney, Christopher D.
AU - Scherer, Erin M.
AU - Collins, Matthew H.
N1 - Publisher Copyright:
Copyright © 2021 Sherman, Smith, Zhu, Taibl, Howard-Anderson, Landay, Pisanic, Kleinhenz, Simon, Espinoza, Edupuganti, Hammond, Rouphael, Shen, Fairley, Edupuganti, Cardona-Ospina, Rodriguez-Morales, Premkumar, Wrammert, Tarleton, Fridkin, Heaney, Scherer and Collins.
PY - 2021/11/23
Y1 - 2021/11/23
N2 - Background: Antibodies against SARS-CoV-2 can be detected by various testing platforms, but a detailed understanding of assay performance is critical. Methods: 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. Results: 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 (p = <0.0001, R2 = 0.26). Conclusions: We applied a validated SARS-CoV-2-specific IgG ELISA in multiple contexts and performed orthogonal testing on samples. This study demonstrates the utility of a simple serologic assay for detecting prior SARS-CoV-2 infection, particularly as a tool for efficiently testing large numbers of samples as in population surveillance. Our work also highlights that precise understanding of SARS-CoV-2 infection and immunity at the individual level, particularly with wide availability of vaccination, may be improved by orthogonal testing and/or more complex assays such as multiplex bead assays.
AB - Background: Antibodies against SARS-CoV-2 can be detected by various testing platforms, but a detailed understanding of assay performance is critical. Methods: 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. Results: 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 (p = <0.0001, R2 = 0.26). Conclusions: We applied a validated SARS-CoV-2-specific IgG ELISA in multiple contexts and performed orthogonal testing on samples. This study demonstrates the utility of a simple serologic assay for detecting prior SARS-CoV-2 infection, particularly as a tool for efficiently testing large numbers of samples as in population surveillance. Our work also highlights that precise understanding of SARS-CoV-2 infection and immunity at the individual level, particularly with wide availability of vaccination, may be improved by orthogonal testing and/or more complex assays such as multiplex bead assays.
KW - antibody response
KW - ELISA
KW - public health
KW - SARS-CoV-2
KW - serology
UR - http://www.scopus.com/inward/record.url?scp=85120917115&partnerID=8YFLogxK
U2 - 10.3389/fpubh.2021.744535
DO - 10.3389/fpubh.2021.744535
M3 - Artículo
C2 - 34888282
AN - SCOPUS:85120917115
SN - 2296-2565
VL - 9
JO - Frontiers in Public Health
JF - Frontiers in Public Health
M1 - 744535
ER -