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Difference in Presence and Number of CD83(+) Dendritic Cells in Patients with Ulcerative Colitis and Crohn’s Disease
Different pathophysiological models provide insight into the important role of CD83(+) dendritic cells (DCs) in the pathogenesis of Crohn’s disease (CD) and ulcerative colitis (UC). There were 154 subjects included in this study: 60 with UC, 19 with CD and 75 in the control group. Colonic biopsy was...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308349/ https://www.ncbi.nlm.nih.gov/pubmed/32572123 http://dx.doi.org/10.1038/s41598-020-67149-5 |
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author | Despalatović, Bruna Rošić Babić, Marija Bratanić, Andre Tonkić, Ante Vilović, Katarina |
author_facet | Despalatović, Bruna Rošić Babić, Marija Bratanić, Andre Tonkić, Ante Vilović, Katarina |
author_sort | Despalatović, Bruna Rošić |
collection | PubMed |
description | Different pathophysiological models provide insight into the important role of CD83(+) dendritic cells (DCs) in the pathogenesis of Crohn’s disease (CD) and ulcerative colitis (UC). There were 154 subjects included in this study: 60 with UC, 19 with CD and 75 in the control group. Colonic biopsy was performed in all subjects. Specimens were incubated with a primary anti-CD83 antibody. Intraepithelial DCs per 100 enterocytes were counted. The results were analysed according to demographic data, type of IBD and histological inflammation pattern. The odds ratio for CD83(+) DCs=0 in the UC group was 3.4 times higher than that in the control group (OR = 3.4; 95% CI: 1.63–7.14; p = 0.001), and the odds ratio for CD83(+) DCs ≥1 in the CD group was 5.3 times higher than that in the UC group (OR = 5.3; 95% CI: 1.4–20.2; p = 0.014). The odds ratio for CD83(+) DCs=0 in the acute inflammation group was 2.7 times higher than that in the group without inflammation (OR = 2.7; 95% CI: 1.2–5.9; p = 0.011). In the group of patients with CD and acute inflammation (n = 11), there was only one subject without CD83(+) DCs (p = 0,024). These results suggest an association of CD83(+) DCs with the type of IBD and the histological inflammation pattern. |
format | Online Article Text |
id | pubmed-7308349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73083492020-06-23 Difference in Presence and Number of CD83(+) Dendritic Cells in Patients with Ulcerative Colitis and Crohn’s Disease Despalatović, Bruna Rošić Babić, Marija Bratanić, Andre Tonkić, Ante Vilović, Katarina Sci Rep Article Different pathophysiological models provide insight into the important role of CD83(+) dendritic cells (DCs) in the pathogenesis of Crohn’s disease (CD) and ulcerative colitis (UC). There were 154 subjects included in this study: 60 with UC, 19 with CD and 75 in the control group. Colonic biopsy was performed in all subjects. Specimens were incubated with a primary anti-CD83 antibody. Intraepithelial DCs per 100 enterocytes were counted. The results were analysed according to demographic data, type of IBD and histological inflammation pattern. The odds ratio for CD83(+) DCs=0 in the UC group was 3.4 times higher than that in the control group (OR = 3.4; 95% CI: 1.63–7.14; p = 0.001), and the odds ratio for CD83(+) DCs ≥1 in the CD group was 5.3 times higher than that in the UC group (OR = 5.3; 95% CI: 1.4–20.2; p = 0.014). The odds ratio for CD83(+) DCs=0 in the acute inflammation group was 2.7 times higher than that in the group without inflammation (OR = 2.7; 95% CI: 1.2–5.9; p = 0.011). In the group of patients with CD and acute inflammation (n = 11), there was only one subject without CD83(+) DCs (p = 0,024). These results suggest an association of CD83(+) DCs with the type of IBD and the histological inflammation pattern. Nature Publishing Group UK 2020-06-22 /pmc/articles/PMC7308349/ /pubmed/32572123 http://dx.doi.org/10.1038/s41598-020-67149-5 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Despalatović, Bruna Rošić Babić, Marija Bratanić, Andre Tonkić, Ante Vilović, Katarina Difference in Presence and Number of CD83(+) Dendritic Cells in Patients with Ulcerative Colitis and Crohn’s Disease |
title | Difference in Presence and Number of CD83(+) Dendritic Cells in Patients with Ulcerative Colitis and Crohn’s Disease |
title_full | Difference in Presence and Number of CD83(+) Dendritic Cells in Patients with Ulcerative Colitis and Crohn’s Disease |
title_fullStr | Difference in Presence and Number of CD83(+) Dendritic Cells in Patients with Ulcerative Colitis and Crohn’s Disease |
title_full_unstemmed | Difference in Presence and Number of CD83(+) Dendritic Cells in Patients with Ulcerative Colitis and Crohn’s Disease |
title_short | Difference in Presence and Number of CD83(+) Dendritic Cells in Patients with Ulcerative Colitis and Crohn’s Disease |
title_sort | difference in presence and number of cd83(+) dendritic cells in patients with ulcerative colitis and crohn’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308349/ https://www.ncbi.nlm.nih.gov/pubmed/32572123 http://dx.doi.org/10.1038/s41598-020-67149-5 |
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