Liver fibrosis: mechanisms of immune-mediated liver injury

被引:127
|
作者
Xu, Ruonan [1 ]
Zhang, Zheng [1 ]
Wang, Fu-Sheng [1 ]
机构
[1] Beijing 302 Hosp, Liver Dis Res Ctr Biol Therapy, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
cirrhosis; hepatic stellate cell; liver fibrosis; HEPATIC STELLATE CELLS; COMPENSATED CIRRHOSIS; FIBROTIC HUMAN; TGF-BETA; COMPLEMENT; INHIBITOR; APOPTOSIS; EXPRESS; MATRIX; MICE;
D O I
10.1038/cmi.2011.53
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Liver fibrosis and its end-stage consequence, cirrhosis, represent the final common pathway of virtually all chronic liver diseases. Research into hepatic stellate cell activation, imbalance of the extracellular matrix synthesis and degradation and the contribution of cytokines and chemokines has further elucidated the mechanisms underlying fibrosis. Furthermore, clarification of changes in host adaptive and innate immune systems has accelerated our understanding of the association between liver inflammation and fibrosis. Continued elucidation of the mechanisms of hepatic fibrosis has provided a comprehensive model of fibrosis progression and regression. This review summarizes the current concepts of improvements that have been made in the field of fibrosis. Cellular & Molecular Immunology (2012) 9, 296-301; doi: 10.1038/cmi.2011.53; published online 12 December 2011
引用
收藏
页码:296 / 301
页数:6
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