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Scalable, Micro-Neutralization Assay for Assessment of SARS-CoV-2 (COVID-19) Virus-Neutralizing Antibodies in Human Clinical Samples

As the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic expanded, it was clear that effective testing for the presence of neutralizing antibodies in the blood of convalescent patients would be critical for development of plasma-based therapeutic approaches. To address the need f...

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Autores principales: Bennett, Richard S., Postnikova, Elena N., Liang, Janie, Gross, Robin, Mazur, Steven, Dixit, Saurabh, Kocher, Gregory, Yu, Shuiqing, Georgia-Clark, Shalamar, Gerhardt, Dawn, Cai, Yingyun, Marron, Lindsay, Lukin, Vladimir V., Holbrook, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8151879/
https://www.ncbi.nlm.nih.gov/pubmed/34065987
http://dx.doi.org/10.3390/v13050893
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author Bennett, Richard S.
Postnikova, Elena N.
Liang, Janie
Gross, Robin
Mazur, Steven
Dixit, Saurabh
Kocher, Gregory
Yu, Shuiqing
Georgia-Clark, Shalamar
Gerhardt, Dawn
Cai, Yingyun
Marron, Lindsay
Lukin, Vladimir V.
Holbrook, Michael R.
author_facet Bennett, Richard S.
Postnikova, Elena N.
Liang, Janie
Gross, Robin
Mazur, Steven
Dixit, Saurabh
Kocher, Gregory
Yu, Shuiqing
Georgia-Clark, Shalamar
Gerhardt, Dawn
Cai, Yingyun
Marron, Lindsay
Lukin, Vladimir V.
Holbrook, Michael R.
author_sort Bennett, Richard S.
collection PubMed
description As the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic expanded, it was clear that effective testing for the presence of neutralizing antibodies in the blood of convalescent patients would be critical for development of plasma-based therapeutic approaches. To address the need for a high-quality neutralization assay against SARS-CoV-2, a previously established fluorescence reduction neutralization assay (FRNA) against Middle East respiratory syndrome coronavirus (MERS-CoV) was modified and optimized. The SARS-CoV-2 FRNA provides a quantitative assessment of a large number of infected cells through use of a high-content imaging system. Because of this approach, and the fact that it does not involve subjective interpretation, this assay is more efficient and more accurate than other neutralization assays. In addition, the ability to set robust acceptance criteria for individual plates and specific test wells provided further rigor to this assay. Such agile adaptability avails use with multiple virus variants. By February 2021, the SARS-CoV-2 FRNA had been used to screen over 5000 samples, including acute and convalescent plasma or serum samples and therapeutic antibody treatments, for SARS-CoV-2 neutralizing titers.
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spelling pubmed-81518792021-05-27 Scalable, Micro-Neutralization Assay for Assessment of SARS-CoV-2 (COVID-19) Virus-Neutralizing Antibodies in Human Clinical Samples Bennett, Richard S. Postnikova, Elena N. Liang, Janie Gross, Robin Mazur, Steven Dixit, Saurabh Kocher, Gregory Yu, Shuiqing Georgia-Clark, Shalamar Gerhardt, Dawn Cai, Yingyun Marron, Lindsay Lukin, Vladimir V. Holbrook, Michael R. Viruses Article As the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic expanded, it was clear that effective testing for the presence of neutralizing antibodies in the blood of convalescent patients would be critical for development of plasma-based therapeutic approaches. To address the need for a high-quality neutralization assay against SARS-CoV-2, a previously established fluorescence reduction neutralization assay (FRNA) against Middle East respiratory syndrome coronavirus (MERS-CoV) was modified and optimized. The SARS-CoV-2 FRNA provides a quantitative assessment of a large number of infected cells through use of a high-content imaging system. Because of this approach, and the fact that it does not involve subjective interpretation, this assay is more efficient and more accurate than other neutralization assays. In addition, the ability to set robust acceptance criteria for individual plates and specific test wells provided further rigor to this assay. Such agile adaptability avails use with multiple virus variants. By February 2021, the SARS-CoV-2 FRNA had been used to screen over 5000 samples, including acute and convalescent plasma or serum samples and therapeutic antibody treatments, for SARS-CoV-2 neutralizing titers. MDPI 2021-05-12 /pmc/articles/PMC8151879/ /pubmed/34065987 http://dx.doi.org/10.3390/v13050893 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
Bennett, Richard S.
Postnikova, Elena N.
Liang, Janie
Gross, Robin
Mazur, Steven
Dixit, Saurabh
Kocher, Gregory
Yu, Shuiqing
Georgia-Clark, Shalamar
Gerhardt, Dawn
Cai, Yingyun
Marron, Lindsay
Lukin, Vladimir V.
Holbrook, Michael R.
Scalable, Micro-Neutralization Assay for Assessment of SARS-CoV-2 (COVID-19) Virus-Neutralizing Antibodies in Human Clinical Samples
title Scalable, Micro-Neutralization Assay for Assessment of SARS-CoV-2 (COVID-19) Virus-Neutralizing Antibodies in Human Clinical Samples
title_full Scalable, Micro-Neutralization Assay for Assessment of SARS-CoV-2 (COVID-19) Virus-Neutralizing Antibodies in Human Clinical Samples
title_fullStr Scalable, Micro-Neutralization Assay for Assessment of SARS-CoV-2 (COVID-19) Virus-Neutralizing Antibodies in Human Clinical Samples
title_full_unstemmed Scalable, Micro-Neutralization Assay for Assessment of SARS-CoV-2 (COVID-19) Virus-Neutralizing Antibodies in Human Clinical Samples
title_short Scalable, Micro-Neutralization Assay for Assessment of SARS-CoV-2 (COVID-19) Virus-Neutralizing Antibodies in Human Clinical Samples
title_sort scalable, micro-neutralization assay for assessment of sars-cov-2 (covid-19) virus-neutralizing antibodies in human clinical samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8151879/
https://www.ncbi.nlm.nih.gov/pubmed/34065987
http://dx.doi.org/10.3390/v13050893
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