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Role of T Lymphocytes in Type 2 Diabetes and Diabetes-Associated Inflammation
Although a critical role of adaptive immune system has been confirmed in driving local and systemic inflammation in type 2 diabetes and promoting insulin resistance, the underlying mechanism is not completely understood. Inflammatory regulation has been focused on innate immunity especially macropha...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5307004/ https://www.ncbi.nlm.nih.gov/pubmed/28251163 http://dx.doi.org/10.1155/2017/6494795 |
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author | Xia, Chang Rao, Xiaoquan Zhong, Jixin |
author_facet | Xia, Chang Rao, Xiaoquan Zhong, Jixin |
author_sort | Xia, Chang |
collection | PubMed |
description | Although a critical role of adaptive immune system has been confirmed in driving local and systemic inflammation in type 2 diabetes and promoting insulin resistance, the underlying mechanism is not completely understood. Inflammatory regulation has been focused on innate immunity especially macrophage for a long time, while increasing evidence suggests T cells are crucial for the development of metabolic inflammation and insulin resistance since 2009. There was growing evidence supporting the critical implication of T cells in the pathogenesis of type 2 diabetes. We will discuss the available effect of T cells subsets in adaptive immune system associated with the procession of T2DM, which may unveil several potential strategies that could provide successful therapies in the future. |
format | Online Article Text |
id | pubmed-5307004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-53070042017-03-01 Role of T Lymphocytes in Type 2 Diabetes and Diabetes-Associated Inflammation Xia, Chang Rao, Xiaoquan Zhong, Jixin J Diabetes Res Review Article Although a critical role of adaptive immune system has been confirmed in driving local and systemic inflammation in type 2 diabetes and promoting insulin resistance, the underlying mechanism is not completely understood. Inflammatory regulation has been focused on innate immunity especially macrophage for a long time, while increasing evidence suggests T cells are crucial for the development of metabolic inflammation and insulin resistance since 2009. There was growing evidence supporting the critical implication of T cells in the pathogenesis of type 2 diabetes. We will discuss the available effect of T cells subsets in adaptive immune system associated with the procession of T2DM, which may unveil several potential strategies that could provide successful therapies in the future. Hindawi Publishing Corporation 2017 2017-01-31 /pmc/articles/PMC5307004/ /pubmed/28251163 http://dx.doi.org/10.1155/2017/6494795 Text en Copyright © 2017 Chang Xia 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 Xia, Chang Rao, Xiaoquan Zhong, Jixin Role of T Lymphocytes in Type 2 Diabetes and Diabetes-Associated Inflammation |
title | Role of T Lymphocytes in Type 2 Diabetes and Diabetes-Associated Inflammation |
title_full | Role of T Lymphocytes in Type 2 Diabetes and Diabetes-Associated Inflammation |
title_fullStr | Role of T Lymphocytes in Type 2 Diabetes and Diabetes-Associated Inflammation |
title_full_unstemmed | Role of T Lymphocytes in Type 2 Diabetes and Diabetes-Associated Inflammation |
title_short | Role of T Lymphocytes in Type 2 Diabetes and Diabetes-Associated Inflammation |
title_sort | role of t lymphocytes in type 2 diabetes and diabetes-associated inflammation |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5307004/ https://www.ncbi.nlm.nih.gov/pubmed/28251163 http://dx.doi.org/10.1155/2017/6494795 |
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