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TIM-3: An emerging target in the liver diseases.
Scandinavian Journal of Immunology ( IF 4.1 ) Pub Date : 2020-02-05 , DOI: 10.1111/sji.12825
Lizhen Zhao 1 , Guoyi Yu 2 , Qi Han 1 , Congxian Cui 3 , Bei Zhang 1
Affiliation  

T cell immunoglobulin domain and mucin domain-containing molecule 3 (TIM-3) is found expression in the surface of terminally differentiated T cells and belongs to the TIM family of type Ⅰ transmembrane proteins. It binds to the ligand Galectin-9 and mediates T cell apoptosis. As the research progresses, TIM-3 is also expressed in Th17, NK, monocyte, which binds to ligand and induce immune peripheral tolerance in both mice and man. Numerous researches have demonstrated that TIM-3 influences liver diseases, including liver-associated chronic viral infection, liver fibrosis, liver cancer et al and suggest new approaches to intervention. Currently, targeted therapy of TIM-3 is a new treatment in the field of immunization. Although many studies have proven that TIM-3 has an inhibitory effect in vivo, the specific mechanism is not clear. Herein, we summarize the important role of TIM-3 in the regulation of liver disease and prospects for future clinical research. TIM-3 will provide new targets for improving clinical liver disease.

中文翻译:

TIM-3:肝脏疾病中的新兴靶标。

发现T细胞免疫球蛋白结构域和含粘蛋白结构域的分子3(TIM-3)在终末分化T细胞表面表达,属于Ⅰ型跨膜蛋白TIM家族。它与配体Galectin-9结合并介导T细胞凋亡。随着研究的进展,TIM-3也表达于Th17,NK,单核细胞中,它与配体结合并在小鼠和人体内诱导免疫性外周耐受。大量研究表明,TIM-3影响肝脏疾病,包括肝脏相关的慢性病毒感染,肝纤维化,肝癌等,并提出了新的干预方法。当前,TIM-3的靶向疗法是免疫领域中的新疗法。尽管许多研究已经证明TIM-3在体内具有抑制作用,但具体机制尚不清楚。在这里 我们总结了TIM-3在调节肝脏疾病中的重要作用以及未来临床研究的前景。TIM-3将为改善临床肝病提供新的靶标。
更新日期:2020-02-05
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