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Changes in γδT Cells in Peripheral Blood of Patients with Ulcerative Colitis Exacerbations

The role of γδT cells in ulcerative colitis (UC) is well confirmed in experimental animals and demonstrated in many clinical observations. Recent investigations have indicated that UC is associated with several forms of immune imbalance, such as an imbalance between effector T cells and regulatory T...

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Autores principales: Gryglewski, Andrzej, Richter, Piotr, Szczepanik, Marian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295081/
https://www.ncbi.nlm.nih.gov/pubmed/34287711
http://dx.doi.org/10.1007/s00005-021-00620-x
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author Gryglewski, Andrzej
Richter, Piotr
Szczepanik, Marian
author_facet Gryglewski, Andrzej
Richter, Piotr
Szczepanik, Marian
author_sort Gryglewski, Andrzej
collection PubMed
description The role of γδT cells in ulcerative colitis (UC) is well confirmed in experimental animals and demonstrated in many clinical observations. Recent investigations have indicated that UC is associated with several forms of immune imbalance, such as an imbalance between effector T cells and regulatory T cells. However, little is known about the cellular aspect of clinical colitis exacerbations. We observed 140 patients with histologically confirmed UC over the course of 8 years. We investigated the percentage of γδT and αβT cells in peripheral blood of patients and also the expression of various surface markers (CD25, CD54, CD62L). Patients were assembled into stable colitis and exacerbated colitis groups. The percentage of γδT and αβT cells was evaluated by Ortho Cytorone Absolute flow cytometer. In patients with exacerbated colitis we observed a decrease of γδT cells in peripheral blood and an increased ratio of αβT/γδT. Additionally, we found that exacerbation results in a significant increase of percentage of γδTCD25, γδTCD54 and γδTCD62L lymphocytes in peripheral blood when compared to patients with stable colitis. Exacerbation of ulcerative colitis results in a decreased percentage of γδT cells in peripheral blood with increase of CD25, CD54 and CD62L expressing γδT cells. This may represent the effect of cell activation and migration, similar to that observed after the surgical trauma. We hope that this observation may help to predict exacerbations in colitis patients.
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spelling pubmed-82950812021-07-23 Changes in γδT Cells in Peripheral Blood of Patients with Ulcerative Colitis Exacerbations Gryglewski, Andrzej Richter, Piotr Szczepanik, Marian Arch Immunol Ther Exp (Warsz) Original Article The role of γδT cells in ulcerative colitis (UC) is well confirmed in experimental animals and demonstrated in many clinical observations. Recent investigations have indicated that UC is associated with several forms of immune imbalance, such as an imbalance between effector T cells and regulatory T cells. However, little is known about the cellular aspect of clinical colitis exacerbations. We observed 140 patients with histologically confirmed UC over the course of 8 years. We investigated the percentage of γδT and αβT cells in peripheral blood of patients and also the expression of various surface markers (CD25, CD54, CD62L). Patients were assembled into stable colitis and exacerbated colitis groups. The percentage of γδT and αβT cells was evaluated by Ortho Cytorone Absolute flow cytometer. In patients with exacerbated colitis we observed a decrease of γδT cells in peripheral blood and an increased ratio of αβT/γδT. Additionally, we found that exacerbation results in a significant increase of percentage of γδTCD25, γδTCD54 and γδTCD62L lymphocytes in peripheral blood when compared to patients with stable colitis. Exacerbation of ulcerative colitis results in a decreased percentage of γδT cells in peripheral blood with increase of CD25, CD54 and CD62L expressing γδT cells. This may represent the effect of cell activation and migration, similar to that observed after the surgical trauma. We hope that this observation may help to predict exacerbations in colitis patients. Springer International Publishing 2021-07-21 2021 /pmc/articles/PMC8295081/ /pubmed/34287711 http://dx.doi.org/10.1007/s00005-021-00620-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Gryglewski, Andrzej
Richter, Piotr
Szczepanik, Marian
Changes in γδT Cells in Peripheral Blood of Patients with Ulcerative Colitis Exacerbations
title Changes in γδT Cells in Peripheral Blood of Patients with Ulcerative Colitis Exacerbations
title_full Changes in γδT Cells in Peripheral Blood of Patients with Ulcerative Colitis Exacerbations
title_fullStr Changes in γδT Cells in Peripheral Blood of Patients with Ulcerative Colitis Exacerbations
title_full_unstemmed Changes in γδT Cells in Peripheral Blood of Patients with Ulcerative Colitis Exacerbations
title_short Changes in γδT Cells in Peripheral Blood of Patients with Ulcerative Colitis Exacerbations
title_sort changes in γδt cells in peripheral blood of patients with ulcerative colitis exacerbations
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295081/
https://www.ncbi.nlm.nih.gov/pubmed/34287711
http://dx.doi.org/10.1007/s00005-021-00620-x
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