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TL1A 和 DR3,一种 TNF 家族配体-受体对,可促进淋巴细胞共刺激、黏膜增生和自身免疫炎症。

TL1A and DR3, a TNF family ligand-receptor pair that promotes lymphocyte costimulation, mucosal hyperplasia, and autoimmune inflammation.

机构信息

Immunoregulation Section, Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Immunol Rev. 2011 Nov;244(1):188-96. doi: 10.1111/j.1600-065X.2011.01068.x.

Abstract

DR3 (TNFRSF25) is a member of the tumor necrosis factor receptor (TNFR) superfamily expressed primarily on lymphocytes and is a receptor for the TNF family cytokine TL1A (TNFSF15). DR3 costimulates T-cell activation, but it is unique among these receptors in that it signals through an intracytoplasmic death domain and the adapter protein TRADD (TNFR-associated death domain). TL1A costimulates T cells to produce a wide variety of cytokines and can promote expansion of activated and regulatory T cells in vivo. Studies in mice deficient in DR3 or TL1A or in animals treated with antibodies that block the activity of TL1A have revealed a specific role for DR3 in enhancing effector T-cell proliferation at the site of tissue inflammation in autoimmune disease models. DR3 appears to be required in autoimmune disease models dependent on a variety of different T-cell subsets and also invariant natural killer T (iNKT) cells. Chronic expression of TL1A induces a distinct interleukin-13-dependent pathology in the small intestine marked by goblet cell hyperplasia and other features associated with allergic and anti-parasitic responses. These studies suggest that TL1A may be a viable target for therapies designed to inhibit the T-cell-dependent component of diverse autoimmune diseases.

摘要

DR3(TNFRSF25)是肿瘤坏死因子受体(TNFR)超家族的成员,主要表达于淋巴细胞上,是 TNF 家族细胞因子 TL1A(TNFSF15)的受体。DR3 共刺激 T 细胞活化,但它在这些受体中是独特的,因为它通过细胞内死亡结构域和衔接蛋白 TRADD(TNFR 相关死亡结构域)信号传导。TL1A 共刺激 T 细胞产生多种细胞因子,并能促进体内激活和调节性 T 细胞的扩增。在缺乏 DR3 或 TL1A 的小鼠或用阻断 TL1A 活性的抗体处理的动物中进行的研究表明,DR3 在增强自身免疫疾病模型中组织炎症部位效应 T 细胞增殖方面具有特定作用。DR3 似乎是自身免疫疾病模型所必需的,这些模型依赖于多种不同的 T 细胞亚群和不变自然杀伤 T(iNKT)细胞。TL1A 的慢性表达在小肠中诱导一种独特的白细胞介素-13 依赖性病理学,其特征为杯状细胞增生和与过敏和抗寄生虫反应相关的其他特征。这些研究表明,TL1A 可能是一种有前途的治疗靶点,旨在抑制多种自身免疫疾病中依赖于 T 细胞的成分。

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