Xu Mingjiang, Chang Binxia, Mathews Stephanie, Gao Bin
Laboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health (NIAAA/NIH), 5625 Fishers Lane, Bethesda, MD, 20892, USA.
Hepatol Int. 2014 Sep;8 Suppl 2(Suppl 2):475-80. doi: 10.1007/s12072-014-9516-x. Epub 2014 Mar 8.
Alcoholic liver disease (ALD) represents a spectrum of disorders, ranging from simple steatosis to severe alcoholic hepatitis and cirrhosis. The severe form of ALD comprises multiple problems in the liver, including inflammation, hepatocellular damage, fibrosis, and impaired liver regeneration, and likely requires combinational therapies. In this review, we discuss recently identified therapeutic targets that inhibit inflammation, ameliorate hepatocyte death, and promote liver repair in ALD, with a focus on our recent studies on the immunosuppressive drug prednisolone and the hepatoprotective cytokine interleukin-22. Clinical trials examining prednisolone plus interleukin-22 therapy for severe alcoholic hepatitis are currently under consideration.
酒精性肝病(ALD)表现为一系列病症,从单纯性脂肪变性到严重的酒精性肝炎和肝硬化。严重形式的ALD在肝脏中存在多种问题,包括炎症、肝细胞损伤、纤维化和肝脏再生受损,可能需要联合治疗。在本综述中,我们讨论了最近确定的治疗靶点,这些靶点可抑制ALD中的炎症、改善肝细胞死亡并促进肝脏修复,重点关注我们最近对免疫抑制药物泼尼松龙和肝保护细胞因子白细胞介素-22的研究。目前正在考虑进行关于泼尼松龙加白细胞介素-22治疗严重酒精性肝炎的临床试验。