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Development of Mucosal PNAd(+) and MAdCAM-1(+) Venules during Disease Course in Ulcerative Colitis
PNAd and MAdCAM-1 addressins on venules are of importance in T-cell homing and potential therapeutic targets in ulcerative colitis (UC). Normally, PNAd(+) high endothelial venules (HEVs) are only present in lymphoid organs, whereas small numbers of MAdCAM-1(+) venules can be seen in non-lymphoid tis...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226824/ https://www.ncbi.nlm.nih.gov/pubmed/32268498 http://dx.doi.org/10.3390/cells9040891 |
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author | Roosenboom, Britt van Lochem, Ellen G. Meijer, Jos Smids, Carolijn Nierkens, Stefan Brand, Eelco C. van Erp, Liselot W. Kemperman, Larissa G.J.M. Groenen, Marcel J.M. Horjus Talabur Horje, Carmen S. Wahab, Peter J. |
author_facet | Roosenboom, Britt van Lochem, Ellen G. Meijer, Jos Smids, Carolijn Nierkens, Stefan Brand, Eelco C. van Erp, Liselot W. Kemperman, Larissa G.J.M. Groenen, Marcel J.M. Horjus Talabur Horje, Carmen S. Wahab, Peter J. |
author_sort | Roosenboom, Britt |
collection | PubMed |
description | PNAd and MAdCAM-1 addressins on venules are of importance in T-cell homing and potential therapeutic targets in ulcerative colitis (UC). Normally, PNAd(+) high endothelial venules (HEVs) are only present in lymphoid organs, whereas small numbers of MAdCAM-1(+) venules can be seen in non-lymphoid tissue. We aimed to study their presence in the intestinal mucosa of UC patients at diagnosis and during follow-up, and their correlation with disease activity. Colonic biopsy specimens of 378 UC patients were analyzed by immunohistochemistry for CD3, CD20, ERG, MECA-79 (PNAd) and MECA-376 (MAdCAM-1) and compared to healthy controls (HC). The proportion of PNAd(+)HEVs in UC at diagnosis was 4.9% (IQR 2.0%–8.3%), while none were detected in HC. During follow-up, PNAd(+)HEVs completely disappeared in remission (n = 93), whereas the proportion in active disease was similar to baseline (n = 285, p = 0.39). The proportion of MAdCAM-1(+)venules in UC at baseline was 5.8% (IQR 2.6–10.0). During follow-up, the proportion in remission was comparable to diagnosis, but upregulated (7.5% (IQR 4.4–10.9), p = 0.001) in active disease. In conclusion, PNAd(+)HEVs appear in UC during active inflammation which could thus serve as a marker for disease activity, whereas MAdCAM-1(+)venules remain present after inflammation is resolved and increase after subsequent flares, reflecting chronicity and potentially serving as a therapeutic target. |
format | Online Article Text |
id | pubmed-7226824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72268242020-05-18 Development of Mucosal PNAd(+) and MAdCAM-1(+) Venules during Disease Course in Ulcerative Colitis Roosenboom, Britt van Lochem, Ellen G. Meijer, Jos Smids, Carolijn Nierkens, Stefan Brand, Eelco C. van Erp, Liselot W. Kemperman, Larissa G.J.M. Groenen, Marcel J.M. Horjus Talabur Horje, Carmen S. Wahab, Peter J. Cells Article PNAd and MAdCAM-1 addressins on venules are of importance in T-cell homing and potential therapeutic targets in ulcerative colitis (UC). Normally, PNAd(+) high endothelial venules (HEVs) are only present in lymphoid organs, whereas small numbers of MAdCAM-1(+) venules can be seen in non-lymphoid tissue. We aimed to study their presence in the intestinal mucosa of UC patients at diagnosis and during follow-up, and their correlation with disease activity. Colonic biopsy specimens of 378 UC patients were analyzed by immunohistochemistry for CD3, CD20, ERG, MECA-79 (PNAd) and MECA-376 (MAdCAM-1) and compared to healthy controls (HC). The proportion of PNAd(+)HEVs in UC at diagnosis was 4.9% (IQR 2.0%–8.3%), while none were detected in HC. During follow-up, PNAd(+)HEVs completely disappeared in remission (n = 93), whereas the proportion in active disease was similar to baseline (n = 285, p = 0.39). The proportion of MAdCAM-1(+)venules in UC at baseline was 5.8% (IQR 2.6–10.0). During follow-up, the proportion in remission was comparable to diagnosis, but upregulated (7.5% (IQR 4.4–10.9), p = 0.001) in active disease. In conclusion, PNAd(+)HEVs appear in UC during active inflammation which could thus serve as a marker for disease activity, whereas MAdCAM-1(+)venules remain present after inflammation is resolved and increase after subsequent flares, reflecting chronicity and potentially serving as a therapeutic target. MDPI 2020-04-06 /pmc/articles/PMC7226824/ /pubmed/32268498 http://dx.doi.org/10.3390/cells9040891 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Roosenboom, Britt van Lochem, Ellen G. Meijer, Jos Smids, Carolijn Nierkens, Stefan Brand, Eelco C. van Erp, Liselot W. Kemperman, Larissa G.J.M. Groenen, Marcel J.M. Horjus Talabur Horje, Carmen S. Wahab, Peter J. Development of Mucosal PNAd(+) and MAdCAM-1(+) Venules during Disease Course in Ulcerative Colitis |
title | Development of Mucosal PNAd(+) and MAdCAM-1(+) Venules during Disease Course in Ulcerative Colitis |
title_full | Development of Mucosal PNAd(+) and MAdCAM-1(+) Venules during Disease Course in Ulcerative Colitis |
title_fullStr | Development of Mucosal PNAd(+) and MAdCAM-1(+) Venules during Disease Course in Ulcerative Colitis |
title_full_unstemmed | Development of Mucosal PNAd(+) and MAdCAM-1(+) Venules during Disease Course in Ulcerative Colitis |
title_short | Development of Mucosal PNAd(+) and MAdCAM-1(+) Venules during Disease Course in Ulcerative Colitis |
title_sort | development of mucosal pnad(+) and madcam-1(+) venules during disease course in ulcerative colitis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226824/ https://www.ncbi.nlm.nih.gov/pubmed/32268498 http://dx.doi.org/10.3390/cells9040891 |
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