Chen Lin-Jiao, Lv Juan, Wen Xiao-Yu, Niu Jun-Qi
Department of Hepatology, The First Hospital, Jilin University, Changchun, 130021, China.
Hepatol Int. 2013 Jul;7(3):798-804. doi: 10.1007/s12072-013-9445-0. Epub 2013 Jul 16.
Interferon-γ-inducible protein 10 (IP-10), or C-X-C motif chemokine (CXCL10), is a small cytokine belonging to the non-ELR CXC chemokine family. By binding to its specific receptor CXCR3, IP-10 recruits activated CXCR3+ T cells to the liver parenchyma and plays a pivotal role in liver disease initiation and progression. IP-10 is mainly secreted by hepatocytes and liver sinusoidal endothelium. Different IP-10 forms exert different functions: long-length IP-10 directs CXCR3+ T cell migration and is associated with inflammation, while short IP-10 is a CXCR3 antagonist, thereby playing protective role in liver injury. IP-10 levels are positively associated with the severity of liver inflammation, fibrosis stage and acute graft rejection. High IP-10 levels are closely related to anti-HCV therapy failure. Thus, IP-10 may be both a potential prognostic tool and a therapeutic target for the treatment of patients with HCV or HIV/HCV co-infection. The purpose of this review is to highlight the growing advances in basic knowledge and clinical interest of IP-10 in liver disease.
干扰素-γ诱导蛋白10(IP-10),即C-X-C基序趋化因子(CXCL10),是一种属于非ELR CXC趋化因子家族的小分子细胞因子。通过与其特异性受体CXCR3结合,IP-10将活化的CXCR3+ T细胞募集到肝实质,在肝脏疾病的起始和进展中起关键作用。IP-10主要由肝细胞和肝窦内皮细胞分泌。不同形式的IP-10发挥不同的功能:长链IP-10引导CXCR3+ T细胞迁移并与炎症相关,而短链IP-10是一种CXCR3拮抗剂,从而在肝损伤中发挥保护作用。IP-10水平与肝脏炎症的严重程度、纤维化阶段和急性移植排斥反应呈正相关。高IP-10水平与抗丙型肝炎病毒(HCV)治疗失败密切相关。因此,IP-10可能既是一种潜在的预后工具,也是治疗HCV或HIV/HCV合并感染患者的治疗靶点。本综述的目的是强调IP-10在肝脏疾病方面的基础知识和临床研究的不断进展。