Antifibrotic Therapies in the Liver

被引:73
作者
Mehal, W. Z. [1 ,2 ]
Schuppan, D. [3 ,4 ,5 ]
机构
[1] Yale Univ, Sect Digest Dis, 333 Cedar St,1080 LMP, New Haven, CT 06520 USA
[2] West Haven Vet Med Ctr, West Haven, CT USA
[3] Johannes Gutenberg Univ Mainz, Med Ctr, Dept Med, Inst Translat Immunol, Mainz, Germany
[4] Johannes Gutenberg Univ Mainz, Med Ctr, Res Ctr Immunotherapy, Mainz, Germany
[5] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Div Gastroenterol, Boston, MA 02215 USA
基金
欧洲研究理事会; 美国国家卫生研究院;
关键词
cirrhosis; collagen; fibroblast; fibrosis; liver; macrophage; myofibroblast; progression; regression; stellate cells; therapy; HEPATIC STELLATE CELLS; IDIOPATHIC PULMONARY-FIBROSIS; PLACEBO-CONTROLLED TRIAL; GROWTH-FACTOR-BETA; SINUSOIDAL ENDOTHELIAL-CELLS; ACTIVATES LATENT TGF-BETA-1; PRECISION-CUT LIVER; TGF-BETA; LYSYL OXIDASE; NONALCOHOLIC STEATOHEPATITIS;
D O I
10.1055/s-0035-1550055
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Significant progress has been made in understanding the principles underlying the development of liver fibrosis. This includes appreciating its dynamic nature, the importance of active fibrolysis in fibrosis regression, and the plasticity of cell populations endowing them with fibrogenic or fibrolytic properties. This is complemented by an increasing array of therapeutic targets with known roles in the progression or regression of fibrosis. With a key role for fibrosis in determining clinical outcomes and encouraging data from recently Food and Drug Administration-approved antifibrotics for pulmonary fibrosis, the development and validation of antifibrotic therapies has taken center stage in translational hepatology. In addition to summarizing the recent progress in antifibrotic therapies, the authors discuss some of the challenges ahead, such as achieving a better understanding of the interindividual heterogeneity of the fibrotic response, how to match interventions with the ideal patient population, and the development of better noninvasive methods to assess the dynamics of fibrogenesis and fibrolysis. Together, these advances will permit a better targeting and dose titration of individualized therapies. Finally, the authors discuss combination therapy with different antifibrotics as possibly the most potent approach for treating fibrosis in the liver.
引用
收藏
页码:184 / 198
页数:15
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