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Exploring beyond clinical routine SARS-CoV-2 serology using MultiCoV-Ab to evaluate endemic coronavirus cross-reactivity
The humoral immune response to SARS-CoV-2 is a benchmark for immunity and detailed analysis is required to understand the manifestation and progression of COVID-19, monitor seroconversion within the general population, and support vaccine development. The majority of currently available commercial s...
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/PMC7896075/ https://www.ncbi.nlm.nih.gov/pubmed/33608538 http://dx.doi.org/10.1038/s41467-021-20973-3 |
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author | Becker, Matthias Strengert, Monika Junker, Daniel Kaiser, Philipp D. Kerrinnes, Tobias Traenkle, Bjoern Dinter, Heiko Häring, Julia Ghozzi, Stéphane Zeck, Anne Weise, Frank Peter, Andreas Hörber, Sebastian Fink, Simon Ruoff, Felix Dulovic, Alex Bakchoul, Tamam Baillot, Armin Lohse, Stefan Cornberg, Markus Illig, Thomas Gottlieb, Jens Smola, Sigrun Karch, André Berger, Klaus Rammensee, Hans-Georg Schenke-Layland, Katja Nelde, Annika Märklin, Melanie Heitmann, Jonas S. Walz, Juliane S. Templin, Markus Joos, Thomas O. Rothbauer, Ulrich Krause, Gérard Schneiderhan-Marra, Nicole |
author_facet | Becker, Matthias Strengert, Monika Junker, Daniel Kaiser, Philipp D. Kerrinnes, Tobias Traenkle, Bjoern Dinter, Heiko Häring, Julia Ghozzi, Stéphane Zeck, Anne Weise, Frank Peter, Andreas Hörber, Sebastian Fink, Simon Ruoff, Felix Dulovic, Alex Bakchoul, Tamam Baillot, Armin Lohse, Stefan Cornberg, Markus Illig, Thomas Gottlieb, Jens Smola, Sigrun Karch, André Berger, Klaus Rammensee, Hans-Georg Schenke-Layland, Katja Nelde, Annika Märklin, Melanie Heitmann, Jonas S. Walz, Juliane S. Templin, Markus Joos, Thomas O. Rothbauer, Ulrich Krause, Gérard Schneiderhan-Marra, Nicole |
author_sort | Becker, Matthias |
collection | PubMed |
description | The humoral immune response to SARS-CoV-2 is a benchmark for immunity and detailed analysis is required to understand the manifestation and progression of COVID-19, monitor seroconversion within the general population, and support vaccine development. The majority of currently available commercial serological assays only quantify the SARS-CoV-2 antibody response against individual antigens, limiting our understanding of the immune response. To overcome this, we have developed a multiplex immunoassay (MultiCoV-Ab) including spike and nucleocapsid proteins of SARS-CoV-2 and the endemic human coronaviruses. Compared to three broadly used commercial in vitro diagnostic tests, our MultiCoV-Ab achieves a higher sensitivity and specificity when analyzing a well-characterized sample set of SARS-CoV-2 infected and uninfected individuals. We find a high response against endemic coronaviruses in our sample set, but no consistent cross-reactive IgG response patterns against SARS-CoV-2. Here we show a robust, high-content-enabled, antigen-saving multiplex assay suited to both monitoring vaccination studies and facilitating epidemiologic screenings for humoral immunity towards pandemic and endemic coronaviruses. |
format | Online Article Text |
id | pubmed-7896075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78960752021-03-03 Exploring beyond clinical routine SARS-CoV-2 serology using MultiCoV-Ab to evaluate endemic coronavirus cross-reactivity Becker, Matthias Strengert, Monika Junker, Daniel Kaiser, Philipp D. Kerrinnes, Tobias Traenkle, Bjoern Dinter, Heiko Häring, Julia Ghozzi, Stéphane Zeck, Anne Weise, Frank Peter, Andreas Hörber, Sebastian Fink, Simon Ruoff, Felix Dulovic, Alex Bakchoul, Tamam Baillot, Armin Lohse, Stefan Cornberg, Markus Illig, Thomas Gottlieb, Jens Smola, Sigrun Karch, André Berger, Klaus Rammensee, Hans-Georg Schenke-Layland, Katja Nelde, Annika Märklin, Melanie Heitmann, Jonas S. Walz, Juliane S. Templin, Markus Joos, Thomas O. Rothbauer, Ulrich Krause, Gérard Schneiderhan-Marra, Nicole Nat Commun Article The humoral immune response to SARS-CoV-2 is a benchmark for immunity and detailed analysis is required to understand the manifestation and progression of COVID-19, monitor seroconversion within the general population, and support vaccine development. The majority of currently available commercial serological assays only quantify the SARS-CoV-2 antibody response against individual antigens, limiting our understanding of the immune response. To overcome this, we have developed a multiplex immunoassay (MultiCoV-Ab) including spike and nucleocapsid proteins of SARS-CoV-2 and the endemic human coronaviruses. Compared to three broadly used commercial in vitro diagnostic tests, our MultiCoV-Ab achieves a higher sensitivity and specificity when analyzing a well-characterized sample set of SARS-CoV-2 infected and uninfected individuals. We find a high response against endemic coronaviruses in our sample set, but no consistent cross-reactive IgG response patterns against SARS-CoV-2. Here we show a robust, high-content-enabled, antigen-saving multiplex assay suited to both monitoring vaccination studies and facilitating epidemiologic screenings for humoral immunity towards pandemic and endemic coronaviruses. Nature Publishing Group UK 2021-02-19 /pmc/articles/PMC7896075/ /pubmed/33608538 http://dx.doi.org/10.1038/s41467-021-20973-3 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 Becker, Matthias Strengert, Monika Junker, Daniel Kaiser, Philipp D. Kerrinnes, Tobias Traenkle, Bjoern Dinter, Heiko Häring, Julia Ghozzi, Stéphane Zeck, Anne Weise, Frank Peter, Andreas Hörber, Sebastian Fink, Simon Ruoff, Felix Dulovic, Alex Bakchoul, Tamam Baillot, Armin Lohse, Stefan Cornberg, Markus Illig, Thomas Gottlieb, Jens Smola, Sigrun Karch, André Berger, Klaus Rammensee, Hans-Georg Schenke-Layland, Katja Nelde, Annika Märklin, Melanie Heitmann, Jonas S. Walz, Juliane S. Templin, Markus Joos, Thomas O. Rothbauer, Ulrich Krause, Gérard Schneiderhan-Marra, Nicole Exploring beyond clinical routine SARS-CoV-2 serology using MultiCoV-Ab to evaluate endemic coronavirus cross-reactivity |
title | Exploring beyond clinical routine SARS-CoV-2 serology using MultiCoV-Ab to evaluate endemic coronavirus cross-reactivity |
title_full | Exploring beyond clinical routine SARS-CoV-2 serology using MultiCoV-Ab to evaluate endemic coronavirus cross-reactivity |
title_fullStr | Exploring beyond clinical routine SARS-CoV-2 serology using MultiCoV-Ab to evaluate endemic coronavirus cross-reactivity |
title_full_unstemmed | Exploring beyond clinical routine SARS-CoV-2 serology using MultiCoV-Ab to evaluate endemic coronavirus cross-reactivity |
title_short | Exploring beyond clinical routine SARS-CoV-2 serology using MultiCoV-Ab to evaluate endemic coronavirus cross-reactivity |
title_sort | exploring beyond clinical routine sars-cov-2 serology using multicov-ab to evaluate endemic coronavirus cross-reactivity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896075/ https://www.ncbi.nlm.nih.gov/pubmed/33608538 http://dx.doi.org/10.1038/s41467-021-20973-3 |
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