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A multiplex chemiluminescent immunoassay for serological profiling of COVID-19-positive symptomatic and asymptomatic patients
The COVID-19 pandemic affects more than 81 million people worldwide with over 1.7 million deaths. As the population returns to work, it is critical to develop tests that reliably detect SARS-CoV-2-specific antibodies. Here we present results from a multiplex serology test for assessing the antibody...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854643/ https://www.ncbi.nlm.nih.gov/pubmed/33531472 http://dx.doi.org/10.1038/s41467-021-21040-7 |
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author | Grossberg, Allison N. Koza, Lilia A. Ledreux, Aurélie Prusmack, Chad Krishnamurthy, Hari Krishnan Jayaraman, Vasanth Granholm, Ann-Charlotte Linseman, Daniel A. |
author_facet | Grossberg, Allison N. Koza, Lilia A. Ledreux, Aurélie Prusmack, Chad Krishnamurthy, Hari Krishnan Jayaraman, Vasanth Granholm, Ann-Charlotte Linseman, Daniel A. |
author_sort | Grossberg, Allison N. |
collection | PubMed |
description | The COVID-19 pandemic affects more than 81 million people worldwide with over 1.7 million deaths. As the population returns to work, it is critical to develop tests that reliably detect SARS-CoV-2-specific antibodies. Here we present results from a multiplex serology test for assessing the antibody responses to COVID-19. In an initial large cohort, this test shows greater than 99% agreement with COVID-19 PCR test. In a second outpatient cohort consisting of adults and children in Colorado, the IgG responses are more robust in positive/symptomatic participants than in positive/asymptomatic participants, the IgM responses in symptomatic participants are transient and largely fall below the detection limit 30 days after symptom onset, and the levels of IgA against SARS-CoV-2 receptor binding domain are significantly increased in participants with moderate-to-severe symptoms compared to those with mild-to-moderate symptoms or asymptomatic individuals. Our results thus provide insight into serology profiling and the immune response to COVID-19. |
format | Online Article Text |
id | pubmed-7854643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78546432021-02-11 A multiplex chemiluminescent immunoassay for serological profiling of COVID-19-positive symptomatic and asymptomatic patients Grossberg, Allison N. Koza, Lilia A. Ledreux, Aurélie Prusmack, Chad Krishnamurthy, Hari Krishnan Jayaraman, Vasanth Granholm, Ann-Charlotte Linseman, Daniel A. Nat Commun Article The COVID-19 pandemic affects more than 81 million people worldwide with over 1.7 million deaths. As the population returns to work, it is critical to develop tests that reliably detect SARS-CoV-2-specific antibodies. Here we present results from a multiplex serology test for assessing the antibody responses to COVID-19. In an initial large cohort, this test shows greater than 99% agreement with COVID-19 PCR test. In a second outpatient cohort consisting of adults and children in Colorado, the IgG responses are more robust in positive/symptomatic participants than in positive/asymptomatic participants, the IgM responses in symptomatic participants are transient and largely fall below the detection limit 30 days after symptom onset, and the levels of IgA against SARS-CoV-2 receptor binding domain are significantly increased in participants with moderate-to-severe symptoms compared to those with mild-to-moderate symptoms or asymptomatic individuals. Our results thus provide insight into serology profiling and the immune response to COVID-19. Nature Publishing Group UK 2021-02-02 /pmc/articles/PMC7854643/ /pubmed/33531472 http://dx.doi.org/10.1038/s41467-021-21040-7 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 Grossberg, Allison N. Koza, Lilia A. Ledreux, Aurélie Prusmack, Chad Krishnamurthy, Hari Krishnan Jayaraman, Vasanth Granholm, Ann-Charlotte Linseman, Daniel A. A multiplex chemiluminescent immunoassay for serological profiling of COVID-19-positive symptomatic and asymptomatic patients |
title | A multiplex chemiluminescent immunoassay for serological profiling of COVID-19-positive symptomatic and asymptomatic patients |
title_full | A multiplex chemiluminescent immunoassay for serological profiling of COVID-19-positive symptomatic and asymptomatic patients |
title_fullStr | A multiplex chemiluminescent immunoassay for serological profiling of COVID-19-positive symptomatic and asymptomatic patients |
title_full_unstemmed | A multiplex chemiluminescent immunoassay for serological profiling of COVID-19-positive symptomatic and asymptomatic patients |
title_short | A multiplex chemiluminescent immunoassay for serological profiling of COVID-19-positive symptomatic and asymptomatic patients |
title_sort | multiplex chemiluminescent immunoassay for serological profiling of covid-19-positive symptomatic and asymptomatic patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854643/ https://www.ncbi.nlm.nih.gov/pubmed/33531472 http://dx.doi.org/10.1038/s41467-021-21040-7 |
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