CXCR3型
原发性胆汁性肝硬化
熊去氧胆酸
医学
趋化因子
免疫学
发病机制
胆汁性肝硬化
CXCL1型
受体
肝硬化
原发性硬化性胆管炎
趋化因子受体
自身免疫性疾病
胃肠病学
免疫系统
内科学
疾病
抗体
出处
期刊:PubMed
日期:2015-01-01
卷期号:166 (2): e122-5
被引量:5
摘要
T- helper 1 (Th1) cytokines and chemokines in primary biliary cirrhosis (PBC) has been investigated in several studies. The involvement of (C-X-C motif) receptor 3 (CXCR3) and its ligands in the pathogenesis of PBC was studied in autoimmune cholangitis animal models suggesting that CXCR3 chemokines contribute to the development of PBC. In humans with PBC, interferon (IFN)γ-induced protein 10 (IP-10) and chemokine (C-X-C motif) ligand 9 (MIG) expressions, and CXCR3-positive cells were present in the portal areas of diseased livers. MIG and IP-10 were positively associated with the severity of liver fibrosis. Circulating IP-10 and MIG levels, and CXCR3-expressing cells, in PBC were increased significantly compared to controls and appeared to increase with disease progression. Furthermore, a significant reduction of these chemokines in PBC patients' serum after ursodeoxycholic acid (UDCA) treatment has been shown.
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