寄主(生物学)
药品
病毒学
宿主因子
甲型肝炎病毒
病毒
乙型肝炎病毒
生物
肝炎病毒
医学
药理学
遗传学
作者
Bingyi Zhang,Dan-Ping Chai,Yicheng Wu,Lipeng Qiu,Yongyong Zhang,Zihong Ye,Xiaoping Yu
出处
期刊:Current Drug Targets
[Bentham Science]
日期:2019-11-13
卷期号:20 (16): 1636-1651
被引量:5
标识
DOI:10.2174/1389450120666190729115646
摘要
Hepatitis B is a very harmful and epidemic disease caused by hepatitis B virus (HBV). Although an effective anti-HBV vaccine is available, chronic infection poses still a huge health burden in the whole world. The present anti-HBV drugs including nucleoside analogues and interferonalpha have their limitations without exception. There is no effective drug and therapeutic method that can really and truly cure hepatitis B so far. The variability of HBV genome results in that a significant number of patients develop drug resistance during the long-term use of anti-HBV drugs. Hence, it is urgently needed to discover novel targets and develop new drugs against hepatitis B.The review aims to provide the theory support for designing of the anti-HBV innovative drugs by offering a summary of the current situation of antiviral potential targets.Since HBV is obligate intracellular parasite, and as such it depends on host cellular components and functions to replicate itself. The targeting both virus and host might be a novel therapeutic option for hepatitis B. Accordingly, we analyse the advances in the study of the potential drug targets for anti-HBV infection, focusing on targeting virus genome, on targeting host cellular functions and on targeting virus-host proteins interactions, respectively. Meanwhile, the immune targets against chronic hepatitis B are also emphasized. In short, the review provides a summary of antiviral therapeutic strategies to target virus factors, host factors and immune factors for future designing of the innovative drug against HBV infection.
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