Immunoregulation Section, Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Immunol Rev. 2011 Nov;244(1):188-96. doi: 10.1111/j.1600-065X.2011.01068.x.
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.
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。