TNFSF15在肠道炎症反应中的作用。

Tanya Kadiyska, Ivan Tourtourikov, Ana-Maria Popmihaylova, Hilda Kadian, Ani Chavoushian
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引用次数: 11

摘要

胃肠道疾病,特别是克罗恩病、溃疡性结肠炎、憩室病和原发性胆汁性肝硬化,都以消化道的复杂炎症为特征。其病理是多因素的,危险因素包括遗传和环境因素。炎症性肠病(IBDs)遗传成分的最新进展表明,肿瘤坏死因子超家族成员15 (TNFSF15)包含许多危险等位基因,不仅与IBD有关,还与憩室病和原发性胆汁性肝硬化等其他疾病有关。TNFSF15中的这些风险等位基因及其基因产物表达的改变可以作为这些疾病之间的共同点,至少可以解释导致免疫反应失调和随后的慢性炎症的一些潜在过程。在这里,我们的目标是概述TNFSF15基因如何参与不同群体T细胞的增殖和细胞命运,并随后控制促炎性和抗炎性细胞因子。此外,我们总结了目前已知的TNFSF15控制区变异,它们如何与上述每种疾病相关,以及这些变异如何通过改变TNFSF15表达来解释所述疾病的自身免疫病理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Role of <i>TNFSF15</i> in the intestinal inflammatory response.

Role of TNFSF15 in the intestinal inflammatory response.

Gastrointestinal diseases, specifically Crohn's disease, ulcerative colitis, diverticular disease, and primary biliary cirrhosis are all characterized by complicated inflammation of the digestive tract. Their pathology is multifactorial, and risk factors encompass both genetic and environmental factors. Recent advances in the genetic component of inflammatory bowel diseases (IBDs) have revealed that the tumor necrosis factor superfamily member 15 (TNFSF15) contains a number of risk alleles associated not only with IBD but also with other diseases such as diverticular disease and primary biliary cirrhosis. These risk alleles in TNFSF15 and the altered expression of its gene product can serve as the common ground between these disorders by explaining at least some of the underlying processes that lead to a dysregulated immune response and subsequent chronic inflammation. Here, we aim to outline how the TNFSF15 gene is involved in the proliferation and cell fate of different populations of T cells and subsequently in the control of both pro- and anti-inflammatory cytokines. Furthermore, we summarize what is currently known of TNFSF15 control region variants, how they are associated with each mentioned disease, and how these variants can explain the autoimmune pathology of said diseases through altered TNFSF15 expression.

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