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Analysis of SARS-CoV-2 antibodies in COVID-19 convalescent blood using a coronavirus antigen microarray

The current practice for diagnosis of COVID-19, based on SARS-CoV-2 PCR testing of pharyngeal or respiratory specimens in a symptomatic patient at high epidemiologic risk, likely underestimates the true prevalence of infection. Serologic methods can more accurately estimate the disease burden by det...

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Autores principales: de Assis, Rafael R., Jain, Aarti, Nakajima, Rie, Jasinskas, Algis, Felgner, Jiin, Obiero, Joshua M., Norris, Philip J., Stone, Mars, Simmons, Graham, Bagri, Anil, Irsch, Johannes, Schreiber, Martin, Buser, Andreas, Holbro, Andreas, Battegay, Manuel, Hosimer, Philip, Noesen, Charles, Adenaiye, Oluwasanmi, Tai, Sheldon, Hong, Filbert, Milton, Donald K., Davies, D. Huw, Contestable, Paul, Corash, Laurence M., Busch, Michael P., Felgner, Philip L., Khan, Saahir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782488/
https://www.ncbi.nlm.nih.gov/pubmed/33397903
http://dx.doi.org/10.1038/s41467-020-20095-2
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author de Assis, Rafael R.
Jain, Aarti
Nakajima, Rie
Jasinskas, Algis
Felgner, Jiin
Obiero, Joshua M.
Norris, Philip J.
Stone, Mars
Simmons, Graham
Bagri, Anil
Irsch, Johannes
Schreiber, Martin
Buser, Andreas
Holbro, Andreas
Battegay, Manuel
Hosimer, Philip
Noesen, Charles
Adenaiye, Oluwasanmi
Tai, Sheldon
Hong, Filbert
Milton, Donald K.
Davies, D. Huw
Contestable, Paul
Corash, Laurence M.
Busch, Michael P.
Felgner, Philip L.
Khan, Saahir
author_facet de Assis, Rafael R.
Jain, Aarti
Nakajima, Rie
Jasinskas, Algis
Felgner, Jiin
Obiero, Joshua M.
Norris, Philip J.
Stone, Mars
Simmons, Graham
Bagri, Anil
Irsch, Johannes
Schreiber, Martin
Buser, Andreas
Holbro, Andreas
Battegay, Manuel
Hosimer, Philip
Noesen, Charles
Adenaiye, Oluwasanmi
Tai, Sheldon
Hong, Filbert
Milton, Donald K.
Davies, D. Huw
Contestable, Paul
Corash, Laurence M.
Busch, Michael P.
Felgner, Philip L.
Khan, Saahir
author_sort de Assis, Rafael R.
collection PubMed
description The current practice for diagnosis of COVID-19, based on SARS-CoV-2 PCR testing of pharyngeal or respiratory specimens in a symptomatic patient at high epidemiologic risk, likely underestimates the true prevalence of infection. Serologic methods can more accurately estimate the disease burden by detecting infections missed by the limited testing performed to date. Here, we describe the validation of a coronavirus antigen microarray containing immunologically significant antigens from SARS-CoV-2, in addition to SARS-CoV, MERS-CoV, common human coronavirus strains, and other common respiratory viruses. A comparison of antibody profiles detected on the array from control sera collected prior to the SARS-CoV-2 pandemic versus convalescent blood specimens from virologically confirmed COVID-19 cases demonstrates near complete discrimination of these two groups, with improved performance from use of antigen combinations that include both spike protein and nucleoprotein. This array can be used as a diagnostic tool, as an epidemiologic tool to more accurately estimate the disease burden of COVID-19, and as a research tool to correlate antibody responses with clinical outcomes.
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spelling pubmed-77824882021-01-11 Analysis of SARS-CoV-2 antibodies in COVID-19 convalescent blood using a coronavirus antigen microarray de Assis, Rafael R. Jain, Aarti Nakajima, Rie Jasinskas, Algis Felgner, Jiin Obiero, Joshua M. Norris, Philip J. Stone, Mars Simmons, Graham Bagri, Anil Irsch, Johannes Schreiber, Martin Buser, Andreas Holbro, Andreas Battegay, Manuel Hosimer, Philip Noesen, Charles Adenaiye, Oluwasanmi Tai, Sheldon Hong, Filbert Milton, Donald K. Davies, D. Huw Contestable, Paul Corash, Laurence M. Busch, Michael P. Felgner, Philip L. Khan, Saahir Nat Commun Article The current practice for diagnosis of COVID-19, based on SARS-CoV-2 PCR testing of pharyngeal or respiratory specimens in a symptomatic patient at high epidemiologic risk, likely underestimates the true prevalence of infection. Serologic methods can more accurately estimate the disease burden by detecting infections missed by the limited testing performed to date. Here, we describe the validation of a coronavirus antigen microarray containing immunologically significant antigens from SARS-CoV-2, in addition to SARS-CoV, MERS-CoV, common human coronavirus strains, and other common respiratory viruses. A comparison of antibody profiles detected on the array from control sera collected prior to the SARS-CoV-2 pandemic versus convalescent blood specimens from virologically confirmed COVID-19 cases demonstrates near complete discrimination of these two groups, with improved performance from use of antigen combinations that include both spike protein and nucleoprotein. This array can be used as a diagnostic tool, as an epidemiologic tool to more accurately estimate the disease burden of COVID-19, and as a research tool to correlate antibody responses with clinical outcomes. Nature Publishing Group UK 2021-01-04 /pmc/articles/PMC7782488/ /pubmed/33397903 http://dx.doi.org/10.1038/s41467-020-20095-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
de Assis, Rafael R.
Jain, Aarti
Nakajima, Rie
Jasinskas, Algis
Felgner, Jiin
Obiero, Joshua M.
Norris, Philip J.
Stone, Mars
Simmons, Graham
Bagri, Anil
Irsch, Johannes
Schreiber, Martin
Buser, Andreas
Holbro, Andreas
Battegay, Manuel
Hosimer, Philip
Noesen, Charles
Adenaiye, Oluwasanmi
Tai, Sheldon
Hong, Filbert
Milton, Donald K.
Davies, D. Huw
Contestable, Paul
Corash, Laurence M.
Busch, Michael P.
Felgner, Philip L.
Khan, Saahir
Analysis of SARS-CoV-2 antibodies in COVID-19 convalescent blood using a coronavirus antigen microarray
title Analysis of SARS-CoV-2 antibodies in COVID-19 convalescent blood using a coronavirus antigen microarray
title_full Analysis of SARS-CoV-2 antibodies in COVID-19 convalescent blood using a coronavirus antigen microarray
title_fullStr Analysis of SARS-CoV-2 antibodies in COVID-19 convalescent blood using a coronavirus antigen microarray
title_full_unstemmed Analysis of SARS-CoV-2 antibodies in COVID-19 convalescent blood using a coronavirus antigen microarray
title_short Analysis of SARS-CoV-2 antibodies in COVID-19 convalescent blood using a coronavirus antigen microarray
title_sort analysis of sars-cov-2 antibodies in covid-19 convalescent blood using a coronavirus antigen microarray
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782488/
https://www.ncbi.nlm.nih.gov/pubmed/33397903
http://dx.doi.org/10.1038/s41467-020-20095-2
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