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Characteristics of circulating adaptive immune cells in patients with colorectal cancer
Adaptive immune cells prevent solid tumor progression by targeting and killing tumor cells. However, there are no comprehensive studies on peripheral circulating adaptive immune cell characterization in colorectal cancer (CRC) patients or the effect of tumor-node-metastasis (TNM) stages on these cel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616942/ https://www.ncbi.nlm.nih.gov/pubmed/36307548 http://dx.doi.org/10.1038/s41598-022-23190-0 |
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author | Zhang, Longyi Chen, Xuya Zu, Shujin Lu, Yan |
author_facet | Zhang, Longyi Chen, Xuya Zu, Shujin Lu, Yan |
author_sort | Zhang, Longyi |
collection | PubMed |
description | Adaptive immune cells prevent solid tumor progression by targeting and killing tumor cells. However, there are no comprehensive studies on peripheral circulating adaptive immune cell characterization in colorectal cancer (CRC) patients or the effect of tumor-node-metastasis (TNM) stages on these cells. In this study, the number, phenotype, and function of different subsets of circulating adaptive immune cells in peripheral blood of CRC patients were analyzed. We found remarkable differences in CRC patients compared with those in healthy controls, including reduced absolute counts of total T cells, helper T lymphocytes (Th), cytotoxic T lymphocytes (Tc), and double-negative T lymphocytes, a decreased proportion of INF-γ(+) cells in total T cells and Th, and increased percentages of B cells, plasmablasts, and activated T cells. Compared with early-stage CRC patients, advanced-stage CRC patients showed more severe immunosenescence, which manifested as decreased proportions of CD8(+) naive T cells with strong proliferative ability and CD8(+) central memory T cells with immune surveillance function. Proportions and absolute counts of CD8(+) and CD4(+) terminally differentiated effector memory T cells were increased, indicating immunosenescence. The immune cell characteristics analyzed in this study serve as a starting point for further research to determine potential clinical implications. |
format | Online Article Text |
id | pubmed-9616942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96169422022-10-30 Characteristics of circulating adaptive immune cells in patients with colorectal cancer Zhang, Longyi Chen, Xuya Zu, Shujin Lu, Yan Sci Rep Article Adaptive immune cells prevent solid tumor progression by targeting and killing tumor cells. However, there are no comprehensive studies on peripheral circulating adaptive immune cell characterization in colorectal cancer (CRC) patients or the effect of tumor-node-metastasis (TNM) stages on these cells. In this study, the number, phenotype, and function of different subsets of circulating adaptive immune cells in peripheral blood of CRC patients were analyzed. We found remarkable differences in CRC patients compared with those in healthy controls, including reduced absolute counts of total T cells, helper T lymphocytes (Th), cytotoxic T lymphocytes (Tc), and double-negative T lymphocytes, a decreased proportion of INF-γ(+) cells in total T cells and Th, and increased percentages of B cells, plasmablasts, and activated T cells. Compared with early-stage CRC patients, advanced-stage CRC patients showed more severe immunosenescence, which manifested as decreased proportions of CD8(+) naive T cells with strong proliferative ability and CD8(+) central memory T cells with immune surveillance function. Proportions and absolute counts of CD8(+) and CD4(+) terminally differentiated effector memory T cells were increased, indicating immunosenescence. The immune cell characteristics analyzed in this study serve as a starting point for further research to determine potential clinical implications. Nature Publishing Group UK 2022-10-28 /pmc/articles/PMC9616942/ /pubmed/36307548 http://dx.doi.org/10.1038/s41598-022-23190-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhang, Longyi Chen, Xuya Zu, Shujin Lu, Yan Characteristics of circulating adaptive immune cells in patients with colorectal cancer |
title | Characteristics of circulating adaptive immune cells in patients with colorectal cancer |
title_full | Characteristics of circulating adaptive immune cells in patients with colorectal cancer |
title_fullStr | Characteristics of circulating adaptive immune cells in patients with colorectal cancer |
title_full_unstemmed | Characteristics of circulating adaptive immune cells in patients with colorectal cancer |
title_short | Characteristics of circulating adaptive immune cells in patients with colorectal cancer |
title_sort | characteristics of circulating adaptive immune cells in patients with colorectal cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616942/ https://www.ncbi.nlm.nih.gov/pubmed/36307548 http://dx.doi.org/10.1038/s41598-022-23190-0 |
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