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Development of a new antigen-based microarray platform for screening and detection of human IgG antibodies against SARS-CoV-2
Strategies to contain the current SARS-CoV-2 pandemic rely, beside vaccinations, also on molecular and serological testing. For any kind of assay development, screening for the optimal antigen is essential. Here we describe the verification of a new protein microarray with different commercially ava...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109672/ https://www.ncbi.nlm.nih.gov/pubmed/35577791 http://dx.doi.org/10.1038/s41598-022-10823-7 |
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author | Burgold-Voigt, Sindy Müller, Elke Zopf, David Monecke, Stefan Braun, Sascha D. Frankenfeld, Katrin Kiehntopf, Michael Weis, Sebastian Schumacher, Thomas Pletz, Mathias W. Ehricht, Ralf |
author_facet | Burgold-Voigt, Sindy Müller, Elke Zopf, David Monecke, Stefan Braun, Sascha D. Frankenfeld, Katrin Kiehntopf, Michael Weis, Sebastian Schumacher, Thomas Pletz, Mathias W. Ehricht, Ralf |
author_sort | Burgold-Voigt, Sindy |
collection | PubMed |
description | Strategies to contain the current SARS-CoV-2 pandemic rely, beside vaccinations, also on molecular and serological testing. For any kind of assay development, screening for the optimal antigen is essential. Here we describe the verification of a new protein microarray with different commercially available preparations significant antigens of SARS-CoV-2 that can be used for the evaluation of the performance of these antigens in serological assays and for antibody screening in serum samples. Antigens of other pathogens that are addressed by widely used vaccinations were also included. To evaluate the accuracy of 21 different antigens or antigen preparations on the microarray, receiver operating characteristics (ROC) curve analysis using ELISA results as reference were performed. Except for a single concentration, a diagnostic sensitivity of 1 was determined for all antigen preparations. A diagnostic specificity, as well as an area under the curve (AUC) of 1 was obtained for 16 of 21 antigen preparations. For the remaining five, the diagnostic specificity ranged from 0.942 to 0.981 and AUC from 0.974 to 0.999. The optimized assay was subsequently also applied to determine the immune status of previously tested individuals and/or to detect the immunization status after COVID-19 vaccination. Microarray evaluation of the antibody profiles of COVID-19 convalescent and post vaccination sera showed that the IgG response differed between these groups, and that the choice of the test antigen is crucial for the assay performance. Furthermore, the results showed that the immune response is highly individualized, depended on several factors (e.g., age or sex), and was not directly related to the severity of disease. The new protein microarray provides an ideal method for the parallel screening of many different antigens of vaccine-preventable diseases in a single sample and for reliable and meaningful diagnostic tests, as well as for the development of safe and specific vaccines. |
format | Online Article Text |
id | pubmed-9109672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91096722022-05-16 Development of a new antigen-based microarray platform for screening and detection of human IgG antibodies against SARS-CoV-2 Burgold-Voigt, Sindy Müller, Elke Zopf, David Monecke, Stefan Braun, Sascha D. Frankenfeld, Katrin Kiehntopf, Michael Weis, Sebastian Schumacher, Thomas Pletz, Mathias W. Ehricht, Ralf Sci Rep Article Strategies to contain the current SARS-CoV-2 pandemic rely, beside vaccinations, also on molecular and serological testing. For any kind of assay development, screening for the optimal antigen is essential. Here we describe the verification of a new protein microarray with different commercially available preparations significant antigens of SARS-CoV-2 that can be used for the evaluation of the performance of these antigens in serological assays and for antibody screening in serum samples. Antigens of other pathogens that are addressed by widely used vaccinations were also included. To evaluate the accuracy of 21 different antigens or antigen preparations on the microarray, receiver operating characteristics (ROC) curve analysis using ELISA results as reference were performed. Except for a single concentration, a diagnostic sensitivity of 1 was determined for all antigen preparations. A diagnostic specificity, as well as an area under the curve (AUC) of 1 was obtained for 16 of 21 antigen preparations. For the remaining five, the diagnostic specificity ranged from 0.942 to 0.981 and AUC from 0.974 to 0.999. The optimized assay was subsequently also applied to determine the immune status of previously tested individuals and/or to detect the immunization status after COVID-19 vaccination. Microarray evaluation of the antibody profiles of COVID-19 convalescent and post vaccination sera showed that the IgG response differed between these groups, and that the choice of the test antigen is crucial for the assay performance. Furthermore, the results showed that the immune response is highly individualized, depended on several factors (e.g., age or sex), and was not directly related to the severity of disease. The new protein microarray provides an ideal method for the parallel screening of many different antigens of vaccine-preventable diseases in a single sample and for reliable and meaningful diagnostic tests, as well as for the development of safe and specific vaccines. Nature Publishing Group UK 2022-05-16 /pmc/articles/PMC9109672/ /pubmed/35577791 http://dx.doi.org/10.1038/s41598-022-10823-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Burgold-Voigt, Sindy Müller, Elke Zopf, David Monecke, Stefan Braun, Sascha D. Frankenfeld, Katrin Kiehntopf, Michael Weis, Sebastian Schumacher, Thomas Pletz, Mathias W. Ehricht, Ralf Development of a new antigen-based microarray platform for screening and detection of human IgG antibodies against SARS-CoV-2 |
title | Development of a new antigen-based microarray platform for screening and detection of human IgG antibodies against SARS-CoV-2 |
title_full | Development of a new antigen-based microarray platform for screening and detection of human IgG antibodies against SARS-CoV-2 |
title_fullStr | Development of a new antigen-based microarray platform for screening and detection of human IgG antibodies against SARS-CoV-2 |
title_full_unstemmed | Development of a new antigen-based microarray platform for screening and detection of human IgG antibodies against SARS-CoV-2 |
title_short | Development of a new antigen-based microarray platform for screening and detection of human IgG antibodies against SARS-CoV-2 |
title_sort | development of a new antigen-based microarray platform for screening and detection of human igg antibodies against sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109672/ https://www.ncbi.nlm.nih.gov/pubmed/35577791 http://dx.doi.org/10.1038/s41598-022-10823-7 |
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