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Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation
Numerous reports of vascular events after an initial recovery from COVID-19 form our impetus to investigate the impact of COVID-19 on vascular health of recovered patients. We found elevated levels of circulating endothelial cells (CECs), a biomarker of vascular injury, in COVID-19 convalescents com...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987341/ https://www.ncbi.nlm.nih.gov/pubmed/33752798 http://dx.doi.org/10.7554/eLife.64909 |
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author | Chioh, Florence WJ Fong, Siew-Wai Young, Barnaby E Wu, Kan-Xing Siau, Anthony Krishnan, Shuba Chan, Yi-Hao Carissimo, Guillaume Teo, Louis LY Gao, Fei Tan, Ru San Zhong, Liang Koh, Angela S Tan, Seow-Yen Tambyah, Paul A Renia, Laurent Ng, Lisa FP Lye, David C Cheung, Christine |
author_facet | Chioh, Florence WJ Fong, Siew-Wai Young, Barnaby E Wu, Kan-Xing Siau, Anthony Krishnan, Shuba Chan, Yi-Hao Carissimo, Guillaume Teo, Louis LY Gao, Fei Tan, Ru San Zhong, Liang Koh, Angela S Tan, Seow-Yen Tambyah, Paul A Renia, Laurent Ng, Lisa FP Lye, David C Cheung, Christine |
author_sort | Chioh, Florence WJ |
collection | PubMed |
description | Numerous reports of vascular events after an initial recovery from COVID-19 form our impetus to investigate the impact of COVID-19 on vascular health of recovered patients. We found elevated levels of circulating endothelial cells (CECs), a biomarker of vascular injury, in COVID-19 convalescents compared to healthy controls. In particular, those with pre-existing conditions (e.g., hypertension, diabetes) had more pronounced endothelial activation hallmarks than non-COVID-19 patients with matched cardiovascular risk. Several proinflammatory and activated T lymphocyte-associated cytokines sustained from acute infection to recovery phase, which correlated positively with CEC measures, implicating cytokine-driven endothelial dysfunction. Notably, we found higher frequency of effector T cells in our COVID-19 convalescents compared to healthy controls. The activation markers detected on CECs mapped to counter receptors found primarily on cytotoxic CD8(+) T cells, raising the possibility of cytotoxic effector cells targeting activated endothelial cells. Clinical trials in preventive therapy for post-COVID-19 vascular complications may be needed. |
format | Online Article Text |
id | pubmed-7987341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-79873412021-03-24 Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation Chioh, Florence WJ Fong, Siew-Wai Young, Barnaby E Wu, Kan-Xing Siau, Anthony Krishnan, Shuba Chan, Yi-Hao Carissimo, Guillaume Teo, Louis LY Gao, Fei Tan, Ru San Zhong, Liang Koh, Angela S Tan, Seow-Yen Tambyah, Paul A Renia, Laurent Ng, Lisa FP Lye, David C Cheung, Christine eLife Cell Biology Numerous reports of vascular events after an initial recovery from COVID-19 form our impetus to investigate the impact of COVID-19 on vascular health of recovered patients. We found elevated levels of circulating endothelial cells (CECs), a biomarker of vascular injury, in COVID-19 convalescents compared to healthy controls. In particular, those with pre-existing conditions (e.g., hypertension, diabetes) had more pronounced endothelial activation hallmarks than non-COVID-19 patients with matched cardiovascular risk. Several proinflammatory and activated T lymphocyte-associated cytokines sustained from acute infection to recovery phase, which correlated positively with CEC measures, implicating cytokine-driven endothelial dysfunction. Notably, we found higher frequency of effector T cells in our COVID-19 convalescents compared to healthy controls. The activation markers detected on CECs mapped to counter receptors found primarily on cytotoxic CD8(+) T cells, raising the possibility of cytotoxic effector cells targeting activated endothelial cells. Clinical trials in preventive therapy for post-COVID-19 vascular complications may be needed. eLife Sciences Publications, Ltd 2021-03-23 /pmc/articles/PMC7987341/ /pubmed/33752798 http://dx.doi.org/10.7554/eLife.64909 Text en © 2021, Chioh et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Chioh, Florence WJ Fong, Siew-Wai Young, Barnaby E Wu, Kan-Xing Siau, Anthony Krishnan, Shuba Chan, Yi-Hao Carissimo, Guillaume Teo, Louis LY Gao, Fei Tan, Ru San Zhong, Liang Koh, Angela S Tan, Seow-Yen Tambyah, Paul A Renia, Laurent Ng, Lisa FP Lye, David C Cheung, Christine Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation |
title | Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation |
title_full | Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation |
title_fullStr | Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation |
title_full_unstemmed | Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation |
title_short | Convalescent COVID-19 patients are susceptible to endothelial dysfunction due to persistent immune activation |
title_sort | convalescent covid-19 patients are susceptible to endothelial dysfunction due to persistent immune activation |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987341/ https://www.ncbi.nlm.nih.gov/pubmed/33752798 http://dx.doi.org/10.7554/eLife.64909 |
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