Zhao Liangtao, Tang Haolan, Cheng Zhangjun
Hepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing 210009, China.
School of Medicine, Southeast University, Nanjing 210009, China.
Pharmaceuticals (Basel). 2024 Dec 20;17(12):1724. doi: 10.3390/ph17121724.
Liver fibrosis is a progressive scarring process primarily caused by chronic inflammation and injury, often closely associated with viral hepatitis, alcoholic liver disease, metabolic dysfunction-associated steatotic liver disease (MASLD), drug-induced liver injury, and autoimmune liver disease (AILD). Currently, there are very few clinical antifibrotic drugs available, and effective targeted therapy is lacking. Recently, emerging antifibrotic drugs and immunomodulators have shown promising results in animal studies, and some have entered clinical research phases. This review aims to systematically review the molecular mechanisms underlying liver fibrosis, focusing on advancements in drug treatments for hepatic fibrosis. Furthermore, since liver fibrosis is a progression or endpoint of many diseases, it is crucial to address the etiological treatment and secondary prevention for liver fibrosis. We will also review the pharmacological treatments available for common hepatitis leading to liver fibrosis.
肝纤维化是一种主要由慢性炎症和损伤引起的进行性瘢痕形成过程,通常与病毒性肝炎、酒精性肝病、代谢功能障碍相关脂肪性肝病(MASLD)、药物性肝损伤和自身免疫性肝病(AILD)密切相关。目前,临床可用的抗纤维化药物非常少,且缺乏有效的靶向治疗方法。最近,新兴的抗纤维化药物和免疫调节剂在动物研究中显示出了有前景的结果,一些已进入临床研究阶段。本综述旨在系统回顾肝纤维化的分子机制,重点关注肝纤维化药物治疗的进展。此外,由于肝纤维化是许多疾病的进展或终点,因此解决肝纤维化的病因治疗和二级预防至关重要。我们还将回顾可用于导致肝纤维化的常见肝炎的药物治疗方法。