Hong Xupeng, Kim Elena S, Guo Haitao
Department of Microbiology and Immunology, Georgetown University Medical Center, Washington, DC.
Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN.
Hepatology. 2017 Dec;66(6):2066-2077. doi: 10.1002/hep.29479. Epub 2017 Nov 6.
Hepatitis B virus (HBV) infection represents a significant public health burden worldwide. Although current therapeutics manage to control the disease progression, lifelong treatment and surveillance are required because drug resistance develops during treatment and reactivations frequently occur following medication cessation. Thus, the occurrence of hepatocellular carcinoma is decreased, but not eliminated. One major reason for failure of HBV treatment is the inability to eradicate or inactivate the viral covalently closed circular DNA (cccDNA), which is a stable episomal form of the viral genome decorated with host histones and nonhistone proteins. Accumulating evidence suggests that epigenetic modifications of cccDNA contribute to viral replication and the outcome of chronic HBV infection. Here, we summarize current progress on HBV epigenetics research and the therapeutic implications for chronic HBV infection by learning from the epigenetic therapies for cancer and other viral diseases, which may open a new venue to cure chronic hepatitis B. (Hepatology 2017;66:2066-2077).
乙型肝炎病毒(HBV)感染是全球一项重大的公共卫生负担。尽管目前的治疗方法能够控制疾病进展,但由于治疗期间会产生耐药性且停药后常出现病毒再激活,因此需要终身治疗和监测。这样一来,肝细胞癌的发生率虽有所降低,但并未消除。HBV治疗失败的一个主要原因是无法根除或灭活病毒共价闭合环状DNA(cccDNA),它是病毒基因组的一种稳定的游离形式,由宿主组蛋白和非组蛋白修饰。越来越多的证据表明,cccDNA的表观遗传修饰有助于病毒复制及慢性HBV感染的转归。在此,我们通过借鉴癌症和其他病毒疾病的表观遗传疗法,总结HBV表观遗传学研究的当前进展及其对慢性HBV感染的治疗意义,这可能为治愈慢性乙型肝炎开辟新途径。(《肝脏病学》2017年;66卷:2066 - 2077页)