乙型肝炎表面抗原
医学
不利影响
肝硬化
乙型肝炎
行动方式
乙型肝炎病毒
免疫学
cccDNA
药品
内科学
肝细胞癌
药理学
病毒学
病毒
生物
生物化学
作者
Jidong Jia,Junqi Niu,Hong You,Yuanyuan Kong,Jinlin Hou
标识
DOI:10.3760/cma.j.cn501113-20210201-00055
摘要
Long term antiviral therapy with nucleos(ti)ide analogues could suppress HBV viral load thereby prevent the progression to cirrhosis and hepatocellular carcinoma. Interferon-based therapy could result in sustained virological response in a fair proportion of patients and even HBsAg loss in a small proportion of them. Novel therapies aiming at functional cure (loss of HBsAg) are under active development. Among the categories of many, HBV core protein inhibitors are safe and could suppress the HBV DNA and HBV RNA, but only with modest effect on the level of HBsAg; silencing of HBV mRNA by siRNA or antisense oligonucleotides could produce meaningful and sustainable declining in HBsAg levels; immune modulators with different mode of action showed modest effect on the reduction of HBsAg, but with noticeable adverse event (especially transaminase flares) related to the mode of action. Novel clinical trial design on the combination or sequential use of innovative molecules will ultimately lead to the functional cure of CHB in the near future.
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