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SARS-CoV-2-specific T cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of SARS-CoV-2

As of January 2022, at least 60 million individuals are estimated to develop post-acute sequelae of SARS-CoV-2 (PASC) after infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). While elevated levels of SARS-CoV-2-specific T cells have been observed in non-specific PASC, littl...

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Autores principales: Littlefield, Katherine M., Watson, Renée O., Schneider, Jennifer M., Neff, Charles P., Yamada, Eiko, Zhang, Min, Campbell, Thomas B., Falta, Michael T., Jolley, Sarah E., Fontenot, Andrew P., Palmer, Brent E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176759/
https://www.ncbi.nlm.nih.gov/pubmed/35617421
http://dx.doi.org/10.1371/journal.ppat.1010359
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author Littlefield, Katherine M.
Watson, Renée O.
Schneider, Jennifer M.
Neff, Charles P.
Yamada, Eiko
Zhang, Min
Campbell, Thomas B.
Falta, Michael T.
Jolley, Sarah E.
Fontenot, Andrew P.
Palmer, Brent E.
author_facet Littlefield, Katherine M.
Watson, Renée O.
Schneider, Jennifer M.
Neff, Charles P.
Yamada, Eiko
Zhang, Min
Campbell, Thomas B.
Falta, Michael T.
Jolley, Sarah E.
Fontenot, Andrew P.
Palmer, Brent E.
author_sort Littlefield, Katherine M.
collection PubMed
description As of January 2022, at least 60 million individuals are estimated to develop post-acute sequelae of SARS-CoV-2 (PASC) after infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). While elevated levels of SARS-CoV-2-specific T cells have been observed in non-specific PASC, little is known about their impact on pulmonary function which is compromised in the majority of these individuals. This study compares frequencies of SARS-CoV-2-specific T cells and inflammatory markers with lung function in participants with pulmonary PASC and resolved COVID-19 (RC). Compared to RC, participants with respiratory PASC had between 6- and 105-fold higher frequencies of IFN-γ- and TNF-α-producing SARS-CoV-2-specific CD4(+) and CD8(+) T cells in peripheral blood, and elevated levels of plasma CRP and IL-6. Importantly, in PASC participants the frequency of TNF-α-producing SARS-CoV-2-specific CD4(+) and CD8(+) T cells, which exhibited the highest levels of Ki67 indicating they were activity dividing, correlated positively with plasma IL-6 and negatively with measures of lung function, including forced expiratory volume in one second (FEV(1)), while increased frequencies of IFN-γ-producing SARS-CoV-2-specific T cells associated with prolonged dyspnea. Statistical analyses stratified by age, number of comorbidities and hospitalization status demonstrated that none of these factors affect differences in the frequency of SARS-CoV-2 T cells and plasma IL-6 levels measured between PASC and RC cohorts. Taken together, these findings demonstrate elevated frequencies of SARS-CoV-2-specific T cells in individuals with pulmonary PASC are associated with increased systemic inflammation and decreased lung function, suggesting that SARS-CoV-2-specific T cells contribute to lingering pulmonary symptoms. These findings also provide mechanistic insight on the pathophysiology of PASC that can inform development of potential treatments to reduce symptom burden.
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spelling pubmed-91767592022-06-09 SARS-CoV-2-specific T cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of SARS-CoV-2 Littlefield, Katherine M. Watson, Renée O. Schneider, Jennifer M. Neff, Charles P. Yamada, Eiko Zhang, Min Campbell, Thomas B. Falta, Michael T. Jolley, Sarah E. Fontenot, Andrew P. Palmer, Brent E. PLoS Pathog Research Article As of January 2022, at least 60 million individuals are estimated to develop post-acute sequelae of SARS-CoV-2 (PASC) after infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). While elevated levels of SARS-CoV-2-specific T cells have been observed in non-specific PASC, little is known about their impact on pulmonary function which is compromised in the majority of these individuals. This study compares frequencies of SARS-CoV-2-specific T cells and inflammatory markers with lung function in participants with pulmonary PASC and resolved COVID-19 (RC). Compared to RC, participants with respiratory PASC had between 6- and 105-fold higher frequencies of IFN-γ- and TNF-α-producing SARS-CoV-2-specific CD4(+) and CD8(+) T cells in peripheral blood, and elevated levels of plasma CRP and IL-6. Importantly, in PASC participants the frequency of TNF-α-producing SARS-CoV-2-specific CD4(+) and CD8(+) T cells, which exhibited the highest levels of Ki67 indicating they were activity dividing, correlated positively with plasma IL-6 and negatively with measures of lung function, including forced expiratory volume in one second (FEV(1)), while increased frequencies of IFN-γ-producing SARS-CoV-2-specific T cells associated with prolonged dyspnea. Statistical analyses stratified by age, number of comorbidities and hospitalization status demonstrated that none of these factors affect differences in the frequency of SARS-CoV-2 T cells and plasma IL-6 levels measured between PASC and RC cohorts. Taken together, these findings demonstrate elevated frequencies of SARS-CoV-2-specific T cells in individuals with pulmonary PASC are associated with increased systemic inflammation and decreased lung function, suggesting that SARS-CoV-2-specific T cells contribute to lingering pulmonary symptoms. These findings also provide mechanistic insight on the pathophysiology of PASC that can inform development of potential treatments to reduce symptom burden. Public Library of Science 2022-05-26 /pmc/articles/PMC9176759/ /pubmed/35617421 http://dx.doi.org/10.1371/journal.ppat.1010359 Text en © 2022 Littlefield et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Littlefield, Katherine M.
Watson, Renée O.
Schneider, Jennifer M.
Neff, Charles P.
Yamada, Eiko
Zhang, Min
Campbell, Thomas B.
Falta, Michael T.
Jolley, Sarah E.
Fontenot, Andrew P.
Palmer, Brent E.
SARS-CoV-2-specific T cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of SARS-CoV-2
title SARS-CoV-2-specific T cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of SARS-CoV-2
title_full SARS-CoV-2-specific T cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of SARS-CoV-2
title_fullStr SARS-CoV-2-specific T cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of SARS-CoV-2
title_full_unstemmed SARS-CoV-2-specific T cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of SARS-CoV-2
title_short SARS-CoV-2-specific T cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of SARS-CoV-2
title_sort sars-cov-2-specific t cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of sars-cov-2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176759/
https://www.ncbi.nlm.nih.gov/pubmed/35617421
http://dx.doi.org/10.1371/journal.ppat.1010359
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