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The Immunological Basis of Inflammatory Bowel Disease

Inflammatory bowel diseases (IBDs) are chronic ailments, Crohn's disease and ulcerative colitis being the most important. These diseases present an inflammatory profile and they differ according to pathophysiology, the affected area in the gastrointestinal tract, and the depth of the inflammati...

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Autores principales: Silva, Francesca A. R., Rodrigues, Bruno L., Ayrizono, Maria de Lourdes S., Leal, Raquel F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5192315/
https://www.ncbi.nlm.nih.gov/pubmed/28070181
http://dx.doi.org/10.1155/2016/2097274
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author Silva, Francesca A. R.
Rodrigues, Bruno L.
Ayrizono, Maria de Lourdes S.
Leal, Raquel F.
author_facet Silva, Francesca A. R.
Rodrigues, Bruno L.
Ayrizono, Maria de Lourdes S.
Leal, Raquel F.
author_sort Silva, Francesca A. R.
collection PubMed
description Inflammatory bowel diseases (IBDs) are chronic ailments, Crohn's disease and ulcerative colitis being the most important. These diseases present an inflammatory profile and they differ according to pathophysiology, the affected area in the gastrointestinal tract, and the depth of the inflammation in the intestinal wall. The immune characteristics of IBD arise from abnormal responses of the innate and adaptive immune system. The number of Th17 cells increases in the peripheral blood of IBD patients, while Treg cells decrease, suggesting that the Th17/Treg proportion plays an important role in the development and maintenance of inflammation. The purpose of this review was to determine the current state of knowledge on the immunological basis of IBD. Many studies have shown the need for further explanation of the development and maintenance of the inflammatory process.
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spelling pubmed-51923152017-01-09 The Immunological Basis of Inflammatory Bowel Disease Silva, Francesca A. R. Rodrigues, Bruno L. Ayrizono, Maria de Lourdes S. Leal, Raquel F. Gastroenterol Res Pract Review Article Inflammatory bowel diseases (IBDs) are chronic ailments, Crohn's disease and ulcerative colitis being the most important. These diseases present an inflammatory profile and they differ according to pathophysiology, the affected area in the gastrointestinal tract, and the depth of the inflammation in the intestinal wall. The immune characteristics of IBD arise from abnormal responses of the innate and adaptive immune system. The number of Th17 cells increases in the peripheral blood of IBD patients, while Treg cells decrease, suggesting that the Th17/Treg proportion plays an important role in the development and maintenance of inflammation. The purpose of this review was to determine the current state of knowledge on the immunological basis of IBD. Many studies have shown the need for further explanation of the development and maintenance of the inflammatory process. Hindawi Publishing Corporation 2016 2016-12-14 /pmc/articles/PMC5192315/ /pubmed/28070181 http://dx.doi.org/10.1155/2016/2097274 Text en Copyright © 2016 Francesca A. R. Silva et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Silva, Francesca A. R.
Rodrigues, Bruno L.
Ayrizono, Maria de Lourdes S.
Leal, Raquel F.
The Immunological Basis of Inflammatory Bowel Disease
title The Immunological Basis of Inflammatory Bowel Disease
title_full The Immunological Basis of Inflammatory Bowel Disease
title_fullStr The Immunological Basis of Inflammatory Bowel Disease
title_full_unstemmed The Immunological Basis of Inflammatory Bowel Disease
title_short The Immunological Basis of Inflammatory Bowel Disease
title_sort immunological basis of inflammatory bowel disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5192315/
https://www.ncbi.nlm.nih.gov/pubmed/28070181
http://dx.doi.org/10.1155/2016/2097274
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