Current and Future Anti-Fibrotic Therapies for Chronic Liver Disease

被引:143
|
作者
Rockey, Don C. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USA
关键词
Fibrosis; Cirrhosis; Stellate cell; Extracellular matrix; Myofibroblast; Liver biopsy; Complication; Portal hypertension;
D O I
10.1016/j.cld.2008.07.011
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Chronic injury results in a wound healing response that eventually leads to fibrosis. The response is generalized, with features common among multiple organ systems. In the liver, various different types of injury lead to fibrogenesis, implying a common pathogenesis. Although several specific therapies for patients who have different liver diseases have been successfully developed, including antiviral therapies for those who have hepatitis B and hepatitis C virus infection, specific and effective antifibrotic therapy remains elusive. Over the past 2 decades, great advances in the understanding of fibrosis have been made and multiple mechanisms underlying hepatic fibrogenesis uncovered. Elucidation of these mechanisms has been of fundamental importance in highlighting novel potential therapies. Preclinical studies have indicated several putative therapies that might abrogate fibrogenesis. This article emphasizes mechanisms underlying fibrogenesis and reviews available and future therapeutics.
引用
收藏
页码:939 / +
页数:25
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