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Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19
Although T cells are likely players in SARS-CoV-2 immunity, little is known about the phenotypic features of SARS-CoV-2-specific T cells associated with recovery from severe COVID-19. We analyzed T cells from longitudinal specimens of 34 COVID-19 patients with severities ranging from mild (outpatien...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852243/ https://www.ncbi.nlm.nih.gov/pubmed/33532792 http://dx.doi.org/10.1101/2021.01.22.21250054 |
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author | Neidleman, Jason Luo, Xiaoyu George, Ashley F. McGregor, Matthew Yang, Junkai Yun, Cassandra Murray, Victoria Gill, Gurjot Greene, Warner C. Vasquez, Joshua Lee, Sulggi Ghosn, Eliver Lynch, Kara Roan, Nadia R. |
author_facet | Neidleman, Jason Luo, Xiaoyu George, Ashley F. McGregor, Matthew Yang, Junkai Yun, Cassandra Murray, Victoria Gill, Gurjot Greene, Warner C. Vasquez, Joshua Lee, Sulggi Ghosn, Eliver Lynch, Kara Roan, Nadia R. |
author_sort | Neidleman, Jason |
collection | PubMed |
description | Although T cells are likely players in SARS-CoV-2 immunity, little is known about the phenotypic features of SARS-CoV-2-specific T cells associated with recovery from severe COVID-19. We analyzed T cells from longitudinal specimens of 34 COVID-19 patients with severities ranging from mild (outpatient) to critical culminating in death. Relative to patients that succumbed, individuals that recovered from severe COVID-19 harbored elevated and increasing numbers of SARS-CoV-2-specific T cells capable of homeostatic proliferation. In contrast, fatal COVID-19 displayed elevated numbers of SARS-CoV-2-specific regulatory T cells and a time-dependent escalation in activated bystander CXCR4+ T cells. Together with the demonstration of increased proportions of inflammatory CXCR4+ T cells in the lungs of severe COVID-19 patients, these results support a model whereby lung-homing T cells activated through bystander effects contribute to immunopathology, while a robust, non-suppressive SARS-CoV-2-specific T cell response limits pathogenesis and promotes recovery from severe COVID-19. |
format | Online Article Text |
id | pubmed-7852243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-78522432021-02-03 Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19 Neidleman, Jason Luo, Xiaoyu George, Ashley F. McGregor, Matthew Yang, Junkai Yun, Cassandra Murray, Victoria Gill, Gurjot Greene, Warner C. Vasquez, Joshua Lee, Sulggi Ghosn, Eliver Lynch, Kara Roan, Nadia R. medRxiv Article Although T cells are likely players in SARS-CoV-2 immunity, little is known about the phenotypic features of SARS-CoV-2-specific T cells associated with recovery from severe COVID-19. We analyzed T cells from longitudinal specimens of 34 COVID-19 patients with severities ranging from mild (outpatient) to critical culminating in death. Relative to patients that succumbed, individuals that recovered from severe COVID-19 harbored elevated and increasing numbers of SARS-CoV-2-specific T cells capable of homeostatic proliferation. In contrast, fatal COVID-19 displayed elevated numbers of SARS-CoV-2-specific regulatory T cells and a time-dependent escalation in activated bystander CXCR4+ T cells. Together with the demonstration of increased proportions of inflammatory CXCR4+ T cells in the lungs of severe COVID-19 patients, these results support a model whereby lung-homing T cells activated through bystander effects contribute to immunopathology, while a robust, non-suppressive SARS-CoV-2-specific T cell response limits pathogenesis and promotes recovery from severe COVID-19. Cold Spring Harbor Laboratory 2021-02-05 /pmc/articles/PMC7852243/ /pubmed/33532792 http://dx.doi.org/10.1101/2021.01.22.21250054 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Neidleman, Jason Luo, Xiaoyu George, Ashley F. McGregor, Matthew Yang, Junkai Yun, Cassandra Murray, Victoria Gill, Gurjot Greene, Warner C. Vasquez, Joshua Lee, Sulggi Ghosn, Eliver Lynch, Kara Roan, Nadia R. Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19 |
title | Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19 |
title_full | Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19 |
title_fullStr | Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19 |
title_full_unstemmed | Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19 |
title_short | Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19 |
title_sort | distinctive features of sars-cov-2-specific t cells predict recovery from severe covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852243/ https://www.ncbi.nlm.nih.gov/pubmed/33532792 http://dx.doi.org/10.1101/2021.01.22.21250054 |
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