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Characteristics of Anti-SARS-CoV-2 Antibodies in Recovered COVID-19 Subjects

Coronavirus Disease 2019 (COVID-19) is a global pandemic caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). While detection of SARS-CoV-2 by polymerase chain reaction with reverse transcription (RT-PCR) is currently used to diagnose acute COVID-19 infection, serologica...

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Autores principales: Huynh, Angela, Arnold, Donald M., Smith, James W., Moore, Jane C., Zhang, Ali, Chagla, Zain, Harvey, Bart J., Stacey, Hannah D., Ang, Jann C., Clare, Rumi, Ivetic, Nikola, Chetty, Vasudhevan T., Bowdish, Dawn M. E., Miller, Matthew S., Kelton, John G., Nazy, Ishac
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073159/
https://www.ncbi.nlm.nih.gov/pubmed/33923828
http://dx.doi.org/10.3390/v13040697
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author Huynh, Angela
Arnold, Donald M.
Smith, James W.
Moore, Jane C.
Zhang, Ali
Chagla, Zain
Harvey, Bart J.
Stacey, Hannah D.
Ang, Jann C.
Clare, Rumi
Ivetic, Nikola
Chetty, Vasudhevan T.
Bowdish, Dawn M. E.
Miller, Matthew S.
Kelton, John G.
Nazy, Ishac
author_facet Huynh, Angela
Arnold, Donald M.
Smith, James W.
Moore, Jane C.
Zhang, Ali
Chagla, Zain
Harvey, Bart J.
Stacey, Hannah D.
Ang, Jann C.
Clare, Rumi
Ivetic, Nikola
Chetty, Vasudhevan T.
Bowdish, Dawn M. E.
Miller, Matthew S.
Kelton, John G.
Nazy, Ishac
author_sort Huynh, Angela
collection PubMed
description Coronavirus Disease 2019 (COVID-19) is a global pandemic caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). While detection of SARS-CoV-2 by polymerase chain reaction with reverse transcription (RT-PCR) is currently used to diagnose acute COVID-19 infection, serological assays are needed to study the humoral immune response to SARS-CoV-2. Anti-SARS-CoV-2 immunoglobulin (Ig)G/A/M antibodies against spike (S) protein and its receptor-binding domain (RBD) were characterized in recovered subjects who were RT-PCR-positive (n = 153) and RT-PCR-negative (n = 55) using an enzyme-linked immunosorbent assay (ELISA). These antibodies were also further assessed for their ability to neutralize live SARS-CoV-2 virus. Anti-SARS-CoV-2 antibodies were detected in 90.9% of resolved subjects up to 180 days post-symptom onset. Anti-S protein and anti-RBD IgG titers correlated (r = 0.5157 and r = 0.6010, respectively) with viral neutralization. Of the RT-PCR-positive subjects, 22 (14.3%) did not have anti-SARS-CoV-2 antibodies; and of those, 17 had RT-PCR cycle threshold (Ct) values > 27. These high Ct values raise the possibility that these indeterminate results are from individuals who were not infected or had mild infection that failed to elicit an antibody response. This study highlights the importance of serological surveys to determine population-level immunity based on infection numbers as determined by RT-PCR.
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spelling pubmed-80731592021-04-27 Characteristics of Anti-SARS-CoV-2 Antibodies in Recovered COVID-19 Subjects Huynh, Angela Arnold, Donald M. Smith, James W. Moore, Jane C. Zhang, Ali Chagla, Zain Harvey, Bart J. Stacey, Hannah D. Ang, Jann C. Clare, Rumi Ivetic, Nikola Chetty, Vasudhevan T. Bowdish, Dawn M. E. Miller, Matthew S. Kelton, John G. Nazy, Ishac Viruses Article Coronavirus Disease 2019 (COVID-19) is a global pandemic caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). While detection of SARS-CoV-2 by polymerase chain reaction with reverse transcription (RT-PCR) is currently used to diagnose acute COVID-19 infection, serological assays are needed to study the humoral immune response to SARS-CoV-2. Anti-SARS-CoV-2 immunoglobulin (Ig)G/A/M antibodies against spike (S) protein and its receptor-binding domain (RBD) were characterized in recovered subjects who were RT-PCR-positive (n = 153) and RT-PCR-negative (n = 55) using an enzyme-linked immunosorbent assay (ELISA). These antibodies were also further assessed for their ability to neutralize live SARS-CoV-2 virus. Anti-SARS-CoV-2 antibodies were detected in 90.9% of resolved subjects up to 180 days post-symptom onset. Anti-S protein and anti-RBD IgG titers correlated (r = 0.5157 and r = 0.6010, respectively) with viral neutralization. Of the RT-PCR-positive subjects, 22 (14.3%) did not have anti-SARS-CoV-2 antibodies; and of those, 17 had RT-PCR cycle threshold (Ct) values > 27. These high Ct values raise the possibility that these indeterminate results are from individuals who were not infected or had mild infection that failed to elicit an antibody response. This study highlights the importance of serological surveys to determine population-level immunity based on infection numbers as determined by RT-PCR. MDPI 2021-04-16 /pmc/articles/PMC8073159/ /pubmed/33923828 http://dx.doi.org/10.3390/v13040697 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Huynh, Angela
Arnold, Donald M.
Smith, James W.
Moore, Jane C.
Zhang, Ali
Chagla, Zain
Harvey, Bart J.
Stacey, Hannah D.
Ang, Jann C.
Clare, Rumi
Ivetic, Nikola
Chetty, Vasudhevan T.
Bowdish, Dawn M. E.
Miller, Matthew S.
Kelton, John G.
Nazy, Ishac
Characteristics of Anti-SARS-CoV-2 Antibodies in Recovered COVID-19 Subjects
title Characteristics of Anti-SARS-CoV-2 Antibodies in Recovered COVID-19 Subjects
title_full Characteristics of Anti-SARS-CoV-2 Antibodies in Recovered COVID-19 Subjects
title_fullStr Characteristics of Anti-SARS-CoV-2 Antibodies in Recovered COVID-19 Subjects
title_full_unstemmed Characteristics of Anti-SARS-CoV-2 Antibodies in Recovered COVID-19 Subjects
title_short Characteristics of Anti-SARS-CoV-2 Antibodies in Recovered COVID-19 Subjects
title_sort characteristics of anti-sars-cov-2 antibodies in recovered covid-19 subjects
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073159/
https://www.ncbi.nlm.nih.gov/pubmed/33923828
http://dx.doi.org/10.3390/v13040697
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