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Diverse Activity of IL-17(+) Cells in Chronic Skin and Mucosa Graft-Versus-Host Disease
Excessive inflammatory environment in a course of chronic graft-versus-host disease (cGvHD) is associated with T-cell trafficking into inflamed tissues. This study focused on the identification of IL-17-producing cells in the tissue biopsies of cGvHD patients. Forty-one biopsy specimens of cGvHD les...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732123/ https://www.ncbi.nlm.nih.gov/pubmed/31177288 http://dx.doi.org/10.1007/s00005-019-00549-2 |
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author | Klimczak, Aleksandra Suchnicki, Krzysztof Sedzimirska, Mariola Lange, Andrzej |
author_facet | Klimczak, Aleksandra Suchnicki, Krzysztof Sedzimirska, Mariola Lange, Andrzej |
author_sort | Klimczak, Aleksandra |
collection | PubMed |
description | Excessive inflammatory environment in a course of chronic graft-versus-host disease (cGvHD) is associated with T-cell trafficking into inflamed tissues. This study focused on the identification of IL-17-producing cells in the tissue biopsies of cGvHD patients. Forty-one biopsy specimens of cGvHD lesions of the skin (n = 27), gastrointestinal tract (n = 9) and oral mucosa (n = 5), examined in 24 patients, were morphologically defined according to the NIH criteria and analyzed for the presence of cellular infiltrations including: IL-17(+), FOXP3(+) and CCR6(+) cells. IL-17(+) cells were identified in 26/27 skin and in all gut and oral mucosa biopsies, being more frequent in mucosa lesions than in the skin (11/14 vs 14/26, respectively; NS: not significant). Double staining documented that CD138(+)/IL-17(+) cells were commonly seen in the gut than in the skin (5/8 vs 3/11, respectively; NS). In the skin, cells expressing trafficking receptor CCR6(+) were more frequent than IL-17(+) cells compared to the mucosa (23/26 vs 2/13, respectively; p < 0.0001). CCR6 was present on a majority of IL-17(+) cells in all examined skin biopsies but only in 6 out of 11 digestive tract biopsies (p = 0.0112). FOXP3(+) cells were identified only in five patients (with mild lesions) at least in one biopsy. In this study group, results documented that local expansion of IL-17-producing cells in the digestive tract correlate with moderate and severe clinical symptoms of cGvHD, in contrast to the skin, where IL-17(+) cells are rather scarcely present (p = 0.0301) and the course of cGvHD is slowly progressing with final organ deterioration. |
format | Online Article Text |
id | pubmed-6732123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-67321232019-09-20 Diverse Activity of IL-17(+) Cells in Chronic Skin and Mucosa Graft-Versus-Host Disease Klimczak, Aleksandra Suchnicki, Krzysztof Sedzimirska, Mariola Lange, Andrzej Arch Immunol Ther Exp (Warsz) Original Article Excessive inflammatory environment in a course of chronic graft-versus-host disease (cGvHD) is associated with T-cell trafficking into inflamed tissues. This study focused on the identification of IL-17-producing cells in the tissue biopsies of cGvHD patients. Forty-one biopsy specimens of cGvHD lesions of the skin (n = 27), gastrointestinal tract (n = 9) and oral mucosa (n = 5), examined in 24 patients, were morphologically defined according to the NIH criteria and analyzed for the presence of cellular infiltrations including: IL-17(+), FOXP3(+) and CCR6(+) cells. IL-17(+) cells were identified in 26/27 skin and in all gut and oral mucosa biopsies, being more frequent in mucosa lesions than in the skin (11/14 vs 14/26, respectively; NS: not significant). Double staining documented that CD138(+)/IL-17(+) cells were commonly seen in the gut than in the skin (5/8 vs 3/11, respectively; NS). In the skin, cells expressing trafficking receptor CCR6(+) were more frequent than IL-17(+) cells compared to the mucosa (23/26 vs 2/13, respectively; p < 0.0001). CCR6 was present on a majority of IL-17(+) cells in all examined skin biopsies but only in 6 out of 11 digestive tract biopsies (p = 0.0112). FOXP3(+) cells were identified only in five patients (with mild lesions) at least in one biopsy. In this study group, results documented that local expansion of IL-17-producing cells in the digestive tract correlate with moderate and severe clinical symptoms of cGvHD, in contrast to the skin, where IL-17(+) cells are rather scarcely present (p = 0.0301) and the course of cGvHD is slowly progressing with final organ deterioration. Springer International Publishing 2019-06-08 2019 /pmc/articles/PMC6732123/ /pubmed/31177288 http://dx.doi.org/10.1007/s00005-019-00549-2 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Klimczak, Aleksandra Suchnicki, Krzysztof Sedzimirska, Mariola Lange, Andrzej Diverse Activity of IL-17(+) Cells in Chronic Skin and Mucosa Graft-Versus-Host Disease |
title | Diverse Activity of IL-17(+) Cells in Chronic Skin and Mucosa Graft-Versus-Host Disease |
title_full | Diverse Activity of IL-17(+) Cells in Chronic Skin and Mucosa Graft-Versus-Host Disease |
title_fullStr | Diverse Activity of IL-17(+) Cells in Chronic Skin and Mucosa Graft-Versus-Host Disease |
title_full_unstemmed | Diverse Activity of IL-17(+) Cells in Chronic Skin and Mucosa Graft-Versus-Host Disease |
title_short | Diverse Activity of IL-17(+) Cells in Chronic Skin and Mucosa Graft-Versus-Host Disease |
title_sort | diverse activity of il-17(+) cells in chronic skin and mucosa graft-versus-host disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732123/ https://www.ncbi.nlm.nih.gov/pubmed/31177288 http://dx.doi.org/10.1007/s00005-019-00549-2 |
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