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Role of CD(4)(+) T and CD(8)(+) T Lymphocytes-Mediated Cellular Immunity in Pathogenesis of Chronic Obstructive Pulmonary Disease
This work was to explore the changes of T lymphocyte subsets in peripheral blood of patients with acute exacerbation of chronic obstructive pulmonary disease (COPD) (AECOPD) and the role of cellular immunity mediated in the disease process. Eighty-six patients with AECOPD who visited Qingdao Hiser M...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242747/ https://www.ncbi.nlm.nih.gov/pubmed/35785027 http://dx.doi.org/10.1155/2022/1429213 |
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author | Xue, Weilin Ma, Jianying Li, Yue Xie, Chunxia |
author_facet | Xue, Weilin Ma, Jianying Li, Yue Xie, Chunxia |
author_sort | Xue, Weilin |
collection | PubMed |
description | This work was to explore the changes of T lymphocyte subsets in peripheral blood of patients with acute exacerbation of chronic obstructive pulmonary disease (COPD) (AECOPD) and the role of cellular immunity mediated in the disease process. Eighty-six patients with AECOPD who visited Qingdao Hiser Medical Center from June 2020 to December 2021 and 30 healthy people (controls) who underwent health examination in the same period were selected. The differences of pulmonary function (PF), arterial blood gas (ABG), blood routine inflammatory indexes, T lymphocyte and T lymphocyte subsets were compared between the two groups, and the correlation between T lymphocyte subsets and each index was analyzed. There were clear differences in PF, ABG, and PB inflammation indexes between AECOPD patients and the controls (P <0.05). Compared with the controls, the CD(4)(+) and CD(4)(+)/CD(8)(+) ratio in PB of AECOPD group were obviously decreased, and the CD(8)(+) level was clearly increased (P <0.05); Th1 of CD(4)(+) cell subsets and Tc1 of CD(8)(+) cell subsets were significantly increased, while Th2 of CD(4)(+) cell subsets and Tc2 of CD(8)(+) cell subsets were obviously decreased (P <0.05). However, CD4(+) was significantly positively correlated with lung function indexes, and significantly negatively correlated with neutrophils/lymphocytes and high-sensitivity C-reactive protein (P <0.05) and significantly positively correlated with Hs-CRP (P <0.05). In summary, CD4+ and CD8(+) T lymphocytes were involved in the occurrence and occurrence of AECOPD, the decrease of CD4(+) and the increase of CD8(+) may promote the deterioration of COPD. |
format | Online Article Text |
id | pubmed-9242747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-92427472022-06-30 Role of CD(4)(+) T and CD(8)(+) T Lymphocytes-Mediated Cellular Immunity in Pathogenesis of Chronic Obstructive Pulmonary Disease Xue, Weilin Ma, Jianying Li, Yue Xie, Chunxia J Immunol Res Research Article This work was to explore the changes of T lymphocyte subsets in peripheral blood of patients with acute exacerbation of chronic obstructive pulmonary disease (COPD) (AECOPD) and the role of cellular immunity mediated in the disease process. Eighty-six patients with AECOPD who visited Qingdao Hiser Medical Center from June 2020 to December 2021 and 30 healthy people (controls) who underwent health examination in the same period were selected. The differences of pulmonary function (PF), arterial blood gas (ABG), blood routine inflammatory indexes, T lymphocyte and T lymphocyte subsets were compared between the two groups, and the correlation between T lymphocyte subsets and each index was analyzed. There were clear differences in PF, ABG, and PB inflammation indexes between AECOPD patients and the controls (P <0.05). Compared with the controls, the CD(4)(+) and CD(4)(+)/CD(8)(+) ratio in PB of AECOPD group were obviously decreased, and the CD(8)(+) level was clearly increased (P <0.05); Th1 of CD(4)(+) cell subsets and Tc1 of CD(8)(+) cell subsets were significantly increased, while Th2 of CD(4)(+) cell subsets and Tc2 of CD(8)(+) cell subsets were obviously decreased (P <0.05). However, CD4(+) was significantly positively correlated with lung function indexes, and significantly negatively correlated with neutrophils/lymphocytes and high-sensitivity C-reactive protein (P <0.05) and significantly positively correlated with Hs-CRP (P <0.05). In summary, CD4+ and CD8(+) T lymphocytes were involved in the occurrence and occurrence of AECOPD, the decrease of CD4(+) and the increase of CD8(+) may promote the deterioration of COPD. Hindawi 2022-06-22 /pmc/articles/PMC9242747/ /pubmed/35785027 http://dx.doi.org/10.1155/2022/1429213 Text en Copyright © 2022 Weilin Xue et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Xue, Weilin Ma, Jianying Li, Yue Xie, Chunxia Role of CD(4)(+) T and CD(8)(+) T Lymphocytes-Mediated Cellular Immunity in Pathogenesis of Chronic Obstructive Pulmonary Disease |
title | Role of CD(4)(+) T and CD(8)(+) T Lymphocytes-Mediated Cellular Immunity in Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_full | Role of CD(4)(+) T and CD(8)(+) T Lymphocytes-Mediated Cellular Immunity in Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_fullStr | Role of CD(4)(+) T and CD(8)(+) T Lymphocytes-Mediated Cellular Immunity in Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_full_unstemmed | Role of CD(4)(+) T and CD(8)(+) T Lymphocytes-Mediated Cellular Immunity in Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_short | Role of CD(4)(+) T and CD(8)(+) T Lymphocytes-Mediated Cellular Immunity in Pathogenesis of Chronic Obstructive Pulmonary Disease |
title_sort | role of cd(4)(+) t and cd(8)(+) t lymphocytes-mediated cellular immunity in pathogenesis of chronic obstructive pulmonary disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242747/ https://www.ncbi.nlm.nih.gov/pubmed/35785027 http://dx.doi.org/10.1155/2022/1429213 |
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