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The role of CD8 + T lymphocytes in chronic obstructive pulmonary disease: a systematic review
OBJECTIVE AND DESIGN: This systematic review aims to establish the role of CD8 + T lymphocytes in COPD. METHODS: Forty-eight papers published in the last 15 years were identified for inclusion. RESULTS: CD8 + T-cells are increased in the lungs of patients with COPD (17 studies, 16 positive) whereas...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806561/ https://www.ncbi.nlm.nih.gov/pubmed/33037881 http://dx.doi.org/10.1007/s00011-020-01408-z |
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author | Williams, Maya Todd, Ian Fairclough, Lucy C. |
author_facet | Williams, Maya Todd, Ian Fairclough, Lucy C. |
author_sort | Williams, Maya |
collection | PubMed |
description | OBJECTIVE AND DESIGN: This systematic review aims to establish the role of CD8 + T lymphocytes in COPD. METHODS: Forty-eight papers published in the last 15 years were identified for inclusion. RESULTS: CD8 + T-cells are increased in the lungs of patients with COPD (17 studies, 16 positive) whereas in the circulation, findings were inconclusive. Activation of CD8 + T-cells was enhanced in lungs (four studies, three positive) but cell phenotype was unclear. There was substantial evidence of a higher proportion of type 1 CD8 + (Tc1) cells in COPD (11 studies, 9 positive), though the population of type 2 (Tc2) cells was also increased (5 studies, 4 positive). CD8 + T-cells in COPD exhibited greater expression of cytotoxic proteins (five studies, five positive). Studies assessed a variety of questions so evidence was insufficient to draw firm conclusions. The role of CD8 + T-cells at acute exacerbation of COPD and also their contribution to alveolar destruction can only be hypothesised at this stage. CONCLUSIONS: Not only is the number of CD8 + T-cells increased in COPD, these cells have increased capacity to exert effector functions and are likely to contribute to disease pathogenesis. Several mechanisms highlighted show promise for future investigation to consolidate current knowledge. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00011-020-01408-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7806561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-78065612021-01-21 The role of CD8 + T lymphocytes in chronic obstructive pulmonary disease: a systematic review Williams, Maya Todd, Ian Fairclough, Lucy C. Inflamm Res Review OBJECTIVE AND DESIGN: This systematic review aims to establish the role of CD8 + T lymphocytes in COPD. METHODS: Forty-eight papers published in the last 15 years were identified for inclusion. RESULTS: CD8 + T-cells are increased in the lungs of patients with COPD (17 studies, 16 positive) whereas in the circulation, findings were inconclusive. Activation of CD8 + T-cells was enhanced in lungs (four studies, three positive) but cell phenotype was unclear. There was substantial evidence of a higher proportion of type 1 CD8 + (Tc1) cells in COPD (11 studies, 9 positive), though the population of type 2 (Tc2) cells was also increased (5 studies, 4 positive). CD8 + T-cells in COPD exhibited greater expression of cytotoxic proteins (five studies, five positive). Studies assessed a variety of questions so evidence was insufficient to draw firm conclusions. The role of CD8 + T-cells at acute exacerbation of COPD and also their contribution to alveolar destruction can only be hypothesised at this stage. CONCLUSIONS: Not only is the number of CD8 + T-cells increased in COPD, these cells have increased capacity to exert effector functions and are likely to contribute to disease pathogenesis. Several mechanisms highlighted show promise for future investigation to consolidate current knowledge. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00011-020-01408-z) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-10-10 2021 /pmc/articles/PMC7806561/ /pubmed/33037881 http://dx.doi.org/10.1007/s00011-020-01408-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Williams, Maya Todd, Ian Fairclough, Lucy C. The role of CD8 + T lymphocytes in chronic obstructive pulmonary disease: a systematic review |
title | The role of CD8 + T lymphocytes in chronic obstructive pulmonary disease: a systematic review |
title_full | The role of CD8 + T lymphocytes in chronic obstructive pulmonary disease: a systematic review |
title_fullStr | The role of CD8 + T lymphocytes in chronic obstructive pulmonary disease: a systematic review |
title_full_unstemmed | The role of CD8 + T lymphocytes in chronic obstructive pulmonary disease: a systematic review |
title_short | The role of CD8 + T lymphocytes in chronic obstructive pulmonary disease: a systematic review |
title_sort | role of cd8 + t lymphocytes in chronic obstructive pulmonary disease: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806561/ https://www.ncbi.nlm.nih.gov/pubmed/33037881 http://dx.doi.org/10.1007/s00011-020-01408-z |
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