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Dysregulation of Group 3 Innate Lymphoid Cells in the Pathogenesis of Inflammatory Bowel Disease
PURPOSE OF REVIEW: Here, we review recent literature indicating a role of innate lymphoid cells in human inflammatory bowel disease with a focus on the plastic population of ILC3. RECENT FINDINGS: Many studies suggest an involvement of ILC3 in human intestinal inflammation. ILC3 present the most abu...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028403/ https://www.ncbi.nlm.nih.gov/pubmed/27645534 http://dx.doi.org/10.1007/s11882-016-0652-3 |
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author | Forkel, Marianne Mjösberg, Jenny |
author_facet | Forkel, Marianne Mjösberg, Jenny |
author_sort | Forkel, Marianne |
collection | PubMed |
description | PURPOSE OF REVIEW: Here, we review recent literature indicating a role of innate lymphoid cells in human inflammatory bowel disease with a focus on the plastic population of ILC3. RECENT FINDINGS: Many studies suggest an involvement of ILC3 in human intestinal inflammation. ILC3 present the most abundant ILC subtype in the human intestine at steady state. In IBD, this composition is skewed towards ILCs showing an ILC1 phenotype and cytokine profile. This change is likely due to the microenvironment causing skewing of the functionally plastic ILC subsets. Interactions between ILCs and other cells are important to keep homeostasis and intestinal barrier integrity. SUMMARY: The knowledge about the involvement of ILCs in IBD is rapidly increasing, and with the help of mouse models, new pathways and functions of ILCs are continuously unraveled. In the majority of human studies, a potential role for ILCs in Crohn’s disease is found. However, less data is available for a possible role in ulcerative colitis. Results from mice are obtained from diverse model systems, and more research in this field is needed to clarify and integrate the current knowledge in order to improve treatment strategies for IBD patients. |
format | Online Article Text |
id | pubmed-5028403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-50284032016-10-09 Dysregulation of Group 3 Innate Lymphoid Cells in the Pathogenesis of Inflammatory Bowel Disease Forkel, Marianne Mjösberg, Jenny Curr Allergy Asthma Rep Immune Deficiency and Dysregulation (DP Huston and C Kuo, Section Editors) PURPOSE OF REVIEW: Here, we review recent literature indicating a role of innate lymphoid cells in human inflammatory bowel disease with a focus on the plastic population of ILC3. RECENT FINDINGS: Many studies suggest an involvement of ILC3 in human intestinal inflammation. ILC3 present the most abundant ILC subtype in the human intestine at steady state. In IBD, this composition is skewed towards ILCs showing an ILC1 phenotype and cytokine profile. This change is likely due to the microenvironment causing skewing of the functionally plastic ILC subsets. Interactions between ILCs and other cells are important to keep homeostasis and intestinal barrier integrity. SUMMARY: The knowledge about the involvement of ILCs in IBD is rapidly increasing, and with the help of mouse models, new pathways and functions of ILCs are continuously unraveled. In the majority of human studies, a potential role for ILCs in Crohn’s disease is found. However, less data is available for a possible role in ulcerative colitis. Results from mice are obtained from diverse model systems, and more research in this field is needed to clarify and integrate the current knowledge in order to improve treatment strategies for IBD patients. Springer US 2016-09-19 2016 /pmc/articles/PMC5028403/ /pubmed/27645534 http://dx.doi.org/10.1007/s11882-016-0652-3 Text en © The Author(s) 2016 Open Access This 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 | Immune Deficiency and Dysregulation (DP Huston and C Kuo, Section Editors) Forkel, Marianne Mjösberg, Jenny Dysregulation of Group 3 Innate Lymphoid Cells in the Pathogenesis of Inflammatory Bowel Disease |
title | Dysregulation of Group 3 Innate Lymphoid Cells in the Pathogenesis of Inflammatory Bowel Disease |
title_full | Dysregulation of Group 3 Innate Lymphoid Cells in the Pathogenesis of Inflammatory Bowel Disease |
title_fullStr | Dysregulation of Group 3 Innate Lymphoid Cells in the Pathogenesis of Inflammatory Bowel Disease |
title_full_unstemmed | Dysregulation of Group 3 Innate Lymphoid Cells in the Pathogenesis of Inflammatory Bowel Disease |
title_short | Dysregulation of Group 3 Innate Lymphoid Cells in the Pathogenesis of Inflammatory Bowel Disease |
title_sort | dysregulation of group 3 innate lymphoid cells in the pathogenesis of inflammatory bowel disease |
topic | Immune Deficiency and Dysregulation (DP Huston and C Kuo, Section Editors) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028403/ https://www.ncbi.nlm.nih.gov/pubmed/27645534 http://dx.doi.org/10.1007/s11882-016-0652-3 |
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