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Dynamic Assay for Profiling Anti-SARS-CoV-2 Antibodies and Their ACE2/Spike RBD Neutralization Capacity
Serological assays have been widely employed during the coronavirus disease 2019 (COVID-19) pandemic to measure antibody responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and to track seroconversion in populations. However, currently available assays do not allow determinatio...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8309970/ https://www.ncbi.nlm.nih.gov/pubmed/34372581 http://dx.doi.org/10.3390/v13071371 |
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author | Phelan, Thomas Dunne, Jean Conlon, Niall Cheallaigh, Clíona Ní Abbott, W. Mark Faba-Rodriguez, Raquel Amanat, Fatima Krammer, Florian Little, Mark A. Hughes, Gerry Bergin, Colm Kerr, Colm Sundaresan, Sudharshana Long, Aideen McCormack, William Brady, Gareth |
author_facet | Phelan, Thomas Dunne, Jean Conlon, Niall Cheallaigh, Clíona Ní Abbott, W. Mark Faba-Rodriguez, Raquel Amanat, Fatima Krammer, Florian Little, Mark A. Hughes, Gerry Bergin, Colm Kerr, Colm Sundaresan, Sudharshana Long, Aideen McCormack, William Brady, Gareth |
author_sort | Phelan, Thomas |
collection | PubMed |
description | Serological assays have been widely employed during the coronavirus disease 2019 (COVID-19) pandemic to measure antibody responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and to track seroconversion in populations. However, currently available assays do not allow determination of neutralization capacity within the assay protocol. Furthermore, commercial serology assays have a high buy-in cost that is inaccessible for many research groups. We have replicated the serological enzyme-linked immunosorbent assay for the detection of SARS-CoV-2 antibody isotypes, developed at the Icahn School of Medicine at Mount Sinai, New York. Additionally, we have modified the protocol to include a neutralization assay with only a minor modification to this protocol. We used this assay to screen local COVID-19 patient sera (n = 91) and pre-COVID-19 control sera (n = 103), and obtained approximate parity with approved commercial anti-nucleoprotein-based assays with these sera. Furthermore, data from our neutralization assay closely aligns with that generated using a spike-based pseudovirus infection model when a subset of patient sera was analyzed. |
format | Online Article Text |
id | pubmed-8309970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83099702021-07-25 Dynamic Assay for Profiling Anti-SARS-CoV-2 Antibodies and Their ACE2/Spike RBD Neutralization Capacity Phelan, Thomas Dunne, Jean Conlon, Niall Cheallaigh, Clíona Ní Abbott, W. Mark Faba-Rodriguez, Raquel Amanat, Fatima Krammer, Florian Little, Mark A. Hughes, Gerry Bergin, Colm Kerr, Colm Sundaresan, Sudharshana Long, Aideen McCormack, William Brady, Gareth Viruses Article Serological assays have been widely employed during the coronavirus disease 2019 (COVID-19) pandemic to measure antibody responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and to track seroconversion in populations. However, currently available assays do not allow determination of neutralization capacity within the assay protocol. Furthermore, commercial serology assays have a high buy-in cost that is inaccessible for many research groups. We have replicated the serological enzyme-linked immunosorbent assay for the detection of SARS-CoV-2 antibody isotypes, developed at the Icahn School of Medicine at Mount Sinai, New York. Additionally, we have modified the protocol to include a neutralization assay with only a minor modification to this protocol. We used this assay to screen local COVID-19 patient sera (n = 91) and pre-COVID-19 control sera (n = 103), and obtained approximate parity with approved commercial anti-nucleoprotein-based assays with these sera. Furthermore, data from our neutralization assay closely aligns with that generated using a spike-based pseudovirus infection model when a subset of patient sera was analyzed. MDPI 2021-07-15 /pmc/articles/PMC8309970/ /pubmed/34372581 http://dx.doi.org/10.3390/v13071371 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 Phelan, Thomas Dunne, Jean Conlon, Niall Cheallaigh, Clíona Ní Abbott, W. Mark Faba-Rodriguez, Raquel Amanat, Fatima Krammer, Florian Little, Mark A. Hughes, Gerry Bergin, Colm Kerr, Colm Sundaresan, Sudharshana Long, Aideen McCormack, William Brady, Gareth Dynamic Assay for Profiling Anti-SARS-CoV-2 Antibodies and Their ACE2/Spike RBD Neutralization Capacity |
title | Dynamic Assay for Profiling Anti-SARS-CoV-2 Antibodies and Their ACE2/Spike RBD Neutralization Capacity |
title_full | Dynamic Assay for Profiling Anti-SARS-CoV-2 Antibodies and Their ACE2/Spike RBD Neutralization Capacity |
title_fullStr | Dynamic Assay for Profiling Anti-SARS-CoV-2 Antibodies and Their ACE2/Spike RBD Neutralization Capacity |
title_full_unstemmed | Dynamic Assay for Profiling Anti-SARS-CoV-2 Antibodies and Their ACE2/Spike RBD Neutralization Capacity |
title_short | Dynamic Assay for Profiling Anti-SARS-CoV-2 Antibodies and Their ACE2/Spike RBD Neutralization Capacity |
title_sort | dynamic assay for profiling anti-sars-cov-2 antibodies and their ace2/spike rbd neutralization capacity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8309970/ https://www.ncbi.nlm.nih.gov/pubmed/34372581 http://dx.doi.org/10.3390/v13071371 |
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