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TIM‐3 as a potential exhaustion marker in CD4(+) T cells of COVID‐19 patients

BACKGROUND: COVID‐19 causes a range of clinical symptoms from mild to critical and can be life‐threatening. Up to now, it has led to many deaths. We aimed to evaluate exhausted markers on CD4(+) T cells of COVID‐19 patients. METHODS: In this study, we evaluated 44 patients with confirmed COVID‐19 di...

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Autores principales: Modabber, Zahra, Shahbazi, Mehdi, Akbari, Roghayeh, Bagherzadeh, Mojgan, Firouzjahi, Alireza, Mohammadnia‐Afrouzi, Mousa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8589347/
https://www.ncbi.nlm.nih.gov/pubmed/34499819
http://dx.doi.org/10.1002/iid3.526
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author Modabber, Zahra
Shahbazi, Mehdi
Akbari, Roghayeh
Bagherzadeh, Mojgan
Firouzjahi, Alireza
Mohammadnia‐Afrouzi, Mousa
author_facet Modabber, Zahra
Shahbazi, Mehdi
Akbari, Roghayeh
Bagherzadeh, Mojgan
Firouzjahi, Alireza
Mohammadnia‐Afrouzi, Mousa
author_sort Modabber, Zahra
collection PubMed
description BACKGROUND: COVID‐19 causes a range of clinical symptoms from mild to critical and can be life‐threatening. Up to now, it has led to many deaths. We aimed to evaluate exhausted markers on CD4(+) T cells of COVID‐19 patients. METHODS: In this study, we evaluated 44 patients with confirmed COVID‐19 disease and 16 healthy individuals. Patients were divided into moderate/severe and critical groups. Peripheral blood mononuclear cells (PBMCs) were isolated and stained by anti‐human CD39, PD‐1, TIM‐3, and anti‐human CD4. The percentage of each CD4(+) subpopulation was calculated by flow cytometry. Furthermore, we collected clinical information and laboratory data of both control and patient groups. RESULTS: We detected overexpression of TIM‐3 on CD4(+) T cells in both critical and moderate/severe patients than in healthy individuals (HIs; p < .01 and p < .0001, respectively). CD4(+) TIM‐3(+) CD39(+) lymphocytes were significantly higher in the critical patients than in HI (p < .05). Both Patient groups showed lymphopenia in comparison with HI, but CD4(+) lymphocytes did not show any significant difference between study subjects. The increased amount of C‐reactive protein, erythrocyte sedimentation rate, creatinine, blood urea nitrogen, and neutrophil count was observed in patients compared to HI. CONCLUSION: T cell exhaustion occurs during COVID‐19 disease and TIM‐3 is the most important exhausted marker on CD4(+) T cells.
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spelling pubmed-85893472021-11-19 TIM‐3 as a potential exhaustion marker in CD4(+) T cells of COVID‐19 patients Modabber, Zahra Shahbazi, Mehdi Akbari, Roghayeh Bagherzadeh, Mojgan Firouzjahi, Alireza Mohammadnia‐Afrouzi, Mousa Immun Inflamm Dis Original Articles BACKGROUND: COVID‐19 causes a range of clinical symptoms from mild to critical and can be life‐threatening. Up to now, it has led to many deaths. We aimed to evaluate exhausted markers on CD4(+) T cells of COVID‐19 patients. METHODS: In this study, we evaluated 44 patients with confirmed COVID‐19 disease and 16 healthy individuals. Patients were divided into moderate/severe and critical groups. Peripheral blood mononuclear cells (PBMCs) were isolated and stained by anti‐human CD39, PD‐1, TIM‐3, and anti‐human CD4. The percentage of each CD4(+) subpopulation was calculated by flow cytometry. Furthermore, we collected clinical information and laboratory data of both control and patient groups. RESULTS: We detected overexpression of TIM‐3 on CD4(+) T cells in both critical and moderate/severe patients than in healthy individuals (HIs; p < .01 and p < .0001, respectively). CD4(+) TIM‐3(+) CD39(+) lymphocytes were significantly higher in the critical patients than in HI (p < .05). Both Patient groups showed lymphopenia in comparison with HI, but CD4(+) lymphocytes did not show any significant difference between study subjects. The increased amount of C‐reactive protein, erythrocyte sedimentation rate, creatinine, blood urea nitrogen, and neutrophil count was observed in patients compared to HI. CONCLUSION: T cell exhaustion occurs during COVID‐19 disease and TIM‐3 is the most important exhausted marker on CD4(+) T cells. John Wiley and Sons Inc. 2021-09-09 /pmc/articles/PMC8589347/ /pubmed/34499819 http://dx.doi.org/10.1002/iid3.526 Text en © 2021 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Modabber, Zahra
Shahbazi, Mehdi
Akbari, Roghayeh
Bagherzadeh, Mojgan
Firouzjahi, Alireza
Mohammadnia‐Afrouzi, Mousa
TIM‐3 as a potential exhaustion marker in CD4(+) T cells of COVID‐19 patients
title TIM‐3 as a potential exhaustion marker in CD4(+) T cells of COVID‐19 patients
title_full TIM‐3 as a potential exhaustion marker in CD4(+) T cells of COVID‐19 patients
title_fullStr TIM‐3 as a potential exhaustion marker in CD4(+) T cells of COVID‐19 patients
title_full_unstemmed TIM‐3 as a potential exhaustion marker in CD4(+) T cells of COVID‐19 patients
title_short TIM‐3 as a potential exhaustion marker in CD4(+) T cells of COVID‐19 patients
title_sort tim‐3 as a potential exhaustion marker in cd4(+) t cells of covid‐19 patients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8589347/
https://www.ncbi.nlm.nih.gov/pubmed/34499819
http://dx.doi.org/10.1002/iid3.526
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