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A flow cytometry-based proliferation assay for clinical evaluation of T-cell memory against SARS-CoV-2
In general, the method of choice for evaluating immunity against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is detection of antibodies against the virus in patient sera. However, this is not feasible in patients who do not produce antibodies, either due to a primary immunodeficienc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484816/ https://www.ncbi.nlm.nih.gov/pubmed/34597619 http://dx.doi.org/10.1016/j.jim.2021.113159 |
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author | Lind Enoksson, Sara Bergman, Peter Klingström, Jonas Boström, Fredrik Da Silva Rodrigues, Rui Winerdal, Malin Elisabeth Marits, Per |
author_facet | Lind Enoksson, Sara Bergman, Peter Klingström, Jonas Boström, Fredrik Da Silva Rodrigues, Rui Winerdal, Malin Elisabeth Marits, Per |
author_sort | Lind Enoksson, Sara |
collection | PubMed |
description | In general, the method of choice for evaluating immunity against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is detection of antibodies against the virus in patient sera. However, this is not feasible in patients who do not produce antibodies, either due to a primary immunodeficiency or secondary to treatment with immunosuppressive drugs. Assessment of the antiviral T cell response is an alternative to serological tests, but most T cell assays are labor-intensive and unsuitable for a clinical routine laboratory. We developed a flow cytometry-based assay for T cell proliferative responses against SARS-CoV-2, based on the detection of blast transformation of activated cells. The assay was validated on previously SARS-CoV-2 infected individuals and healthy seronegative blood donors, displaying 74% sensitivity and 96% specificity for previous infection with SARS-CoV-2. The usefulness of the assay was demonstrated in a patient with common variable immunodeficiency with a history of COVID-19. The described T-cell assay is a clinically relevant complement to serology in the evaluation of cellular immunity against SARS-CoV-2, which can be emulated by any routine lab with flow cytometric competence. |
format | Online Article Text |
id | pubmed-8484816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84848162021-10-01 A flow cytometry-based proliferation assay for clinical evaluation of T-cell memory against SARS-CoV-2 Lind Enoksson, Sara Bergman, Peter Klingström, Jonas Boström, Fredrik Da Silva Rodrigues, Rui Winerdal, Malin Elisabeth Marits, Per J Immunol Methods Short Communication In general, the method of choice for evaluating immunity against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is detection of antibodies against the virus in patient sera. However, this is not feasible in patients who do not produce antibodies, either due to a primary immunodeficiency or secondary to treatment with immunosuppressive drugs. Assessment of the antiviral T cell response is an alternative to serological tests, but most T cell assays are labor-intensive and unsuitable for a clinical routine laboratory. We developed a flow cytometry-based assay for T cell proliferative responses against SARS-CoV-2, based on the detection of blast transformation of activated cells. The assay was validated on previously SARS-CoV-2 infected individuals and healthy seronegative blood donors, displaying 74% sensitivity and 96% specificity for previous infection with SARS-CoV-2. The usefulness of the assay was demonstrated in a patient with common variable immunodeficiency with a history of COVID-19. The described T-cell assay is a clinically relevant complement to serology in the evaluation of cellular immunity against SARS-CoV-2, which can be emulated by any routine lab with flow cytometric competence. Elsevier B.V. 2021-12 2021-09-28 /pmc/articles/PMC8484816/ /pubmed/34597619 http://dx.doi.org/10.1016/j.jim.2021.113159 Text en © 2021 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Short Communication Lind Enoksson, Sara Bergman, Peter Klingström, Jonas Boström, Fredrik Da Silva Rodrigues, Rui Winerdal, Malin Elisabeth Marits, Per A flow cytometry-based proliferation assay for clinical evaluation of T-cell memory against SARS-CoV-2 |
title | A flow cytometry-based proliferation assay for clinical evaluation of T-cell memory against SARS-CoV-2 |
title_full | A flow cytometry-based proliferation assay for clinical evaluation of T-cell memory against SARS-CoV-2 |
title_fullStr | A flow cytometry-based proliferation assay for clinical evaluation of T-cell memory against SARS-CoV-2 |
title_full_unstemmed | A flow cytometry-based proliferation assay for clinical evaluation of T-cell memory against SARS-CoV-2 |
title_short | A flow cytometry-based proliferation assay for clinical evaluation of T-cell memory against SARS-CoV-2 |
title_sort | flow cytometry-based proliferation assay for clinical evaluation of t-cell memory against sars-cov-2 |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484816/ https://www.ncbi.nlm.nih.gov/pubmed/34597619 http://dx.doi.org/10.1016/j.jim.2021.113159 |
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