Nevens Frederik, Trauner Michael, Manns Michael P
Department of Gastroenterology and Hepatology, University Hospital KU Leuven, Belgium; Centre of ERN RARE-LIVER.
Division of Gastroenterology and Hepatology, Department of Medicine III, Medical University of Vienna, Austria; Centre of ERN RARE-LIVER.
J Hepatol. 2023 Feb;78(2):430-441. doi: 10.1016/j.jhep.2022.10.007. Epub 2022 Oct 20.
The discovery of nuclear receptors and transporters has contributed to the development of new drugs for the treatment of cholestatic liver diseases. Particular progress has been made in the development of second-line therapies for PBC. These new drugs can be separated into compounds primarily targeting cholestasis, molecules targeting fibrogenesis and molecules with immune-mediated action. Finally, drugs aimed at symptom relief (pruritus and fatigue) are also under investigation. Obeticholic acid is currently the only approved second-line therapy for PBC. Drugs in the late phase of clinical development include peroxisome proliferator-activated receptor agonists, norursodeoxycholic acid and NADPH oxidase 1/4 inhibitors.
核受体和转运体的发现推动了治疗胆汁淤积性肝病新药的研发。原发性胆汁性胆管炎(PBC)二线治疗的研发取得了显著进展。这些新药可分为主要针对胆汁淤积的化合物、针对纤维化形成的分子以及具有免疫介导作用的分子。最后,旨在缓解症状(瘙痒和疲劳)的药物也在研究中。奥贝胆酸是目前唯一获批用于PBC的二线治疗药物。处于临床开发后期的药物包括过氧化物酶体增殖物激活受体激动剂、去氧熊胆酸和NADPH氧化酶1/4抑制剂。