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肝纤维化病理学:转译的成功故事 [复制链接]

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发表于 2015-2-14 21:47 |只看该作者 |倒序浏览 |打印
Gut doi:10.1136/gutjnl-2014-306842

    Recent advances in basic science

Pathobiology of liver fibrosis: a translational success story

    Youngmin A Lee,
    Michael C Wallace,
    Scott L Friedman

+ Author Affiliations

    Division of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, New York, USA

    Correspondence to Scott L Friedman, Division of Liver Diseases, Icahn School of Medicine at Mount Sinai, 1425 Madison Ave., Room 11-70C, Box 1123, New York, NY 10029-6574, USA; [email protected]

    Received 16 December 2014
    Revised 6 January 2015
    Accepted 7 January 2015
    Published Online First 13 February 2015

Abstract

Reversibility of hepatic fibrosis and cirrhosis following antiviral therapy for hepatitis B or C has advanced the prospect of developing antifibrotic therapies for patients with chronic liver diseases, especially non-alcoholic steatohepatitis. Mechanisms of fibrosis have focused on hepatic stellate cells, which become fibrogenic myofibroblasts during injury through ‘activation’, and are at the nexus of efforts to define novel drug targets. Recent studies have clarified pathways of stellate cell gene regulation and epigenetics, emerging pathways of fibrosis regression through the recruitment and amplification of fibrolytic macrophages, nuanced responses of discrete inflammatory cell subsets and the identification of the ‘ductular reaction’ as a marker of severe injury and repair. Based on our expanded knowledge of fibrosis pathogenesis, attention is now directed towards strategies for antifibrotic therapies and regulatory challenges for conducting clinical trials with these agents. New therapies are attempting to: 1) Control or cure the primary disease or reduce tissue injury; 2) Target receptor-ligand interactions and intracellular signaling; 3) Inhibit fibrogenesis; and 4) Promote resolution of fibrosis. Progress is urgently needed in validating non-invasive markers of fibrosis progression and regression that can supplant biopsy and shorten the duration of clinical trials. Both scientific and clinical challenges remain, however the past three decades of steady progress in understanding liver fibrosis have contributed to an emerging translational success story, with realistic hopes for antifibrotic therapies to treat patients with chronic liver disease in the near future.

Rank: 8Rank: 8

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62111 元 
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30437 
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2022-12-28 

才高八斗

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发表于 2015-2-14 21:47 |只看该作者

肠道DOI:10.1136/ gutjnl-2014-306842

在基础科学的最新进展

病理学肝纤维化:转译的成功故事

Youngmin李易达,
迈克尔·C·华莱士,
斯科特·L·弗里德曼

+作者所属机构

肝病科,西奈山伊坎医学院,纽约州,纽约州,美国

通讯作者斯科特·L·弗里德曼,肝病科,西奈山伊坎医学院,1425麦迪逊大道,客房11-70C,盒1123,纽约,NY10029-6574,USA; [email protected]

收到的2014年12月16日
修订后的2015年1月6日
接受2015年1月7日
网上公布的第一2015年2月13日

抽象

肝纤维化和肝硬化的抗病毒之后治疗乙型或丙型肝炎可逆性拥有先进的开发抗纤维化治疗的慢性肝病,尤其是非酒精性脂肪性肝炎的前景。纤维化机制都集中在肝星状细胞,通过“激活”受伤期间,成为纤维化肌成纤维细胞,并在努力确定新的药物靶点的关系。最近的研究阐明了星状细胞基因调控和表观遗传途径,通过纤维蛋白溶解的巨噬细胞,离散的炎性细胞亚群的细致入微的反应和“胆小管反应”作为严重伤害的标志物的识别和招募和放大新兴纤维化回归的途径修理。基于纤维化发病机制我们扩大了知识,注意力现在针对的抗纤维化治疗,并负责对这些药物临床试验的监管挑战的策略。新疗法正在尝试:1)控制或治愈原发病或减少组织损伤; 2)目标受体 - 配体的相互作用和细胞内信号传导; 3)抑制纤维化; 4)促进纤维化的分辨率。进展,迫切需要在验证纤维化进展和回归的非侵入性标记物,可以取代活检和缩短临床试验的持续时间。科学和临床的挑战依然存在,但在过去的三十年中稳步前进在了解肝纤维化促成了一个新兴的平移的成功故事,与现实的希望抗纤维化疗法来治疗慢性肝病在不久的将来。
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