Moving Fast Toward Hepatitis B Virus Elimination

被引:8
|
作者
Bassit, Leda [1 ,2 ]
Ono, Suzane Kioko [3 ]
Schinazi, Raymond F. [1 ,2 ]
机构
[1] Emory Univ, Sch Med, Dept Pediat, Ctr AIDS Res,Lab Biochem Pharmacol, Atlanta, GA 30322 USA
[2] Childrens Healthcare Atlanta, Atlanta, GA 30329 USA
[3] Univ Sao Paulo, Sch Med, Dept Gastroenterol, Sao Paulo, SP, Brazil
来源
基金
巴西圣保罗研究基金会;
关键词
Hepatitis B; Core inhibitor; cccDNA; DAA-directly acting antiviral; Immune therapy; Hepatocellular carcinoma; IN-VITRO; ANTISENSE OLIGONUCLEOTIDE; ANTIVIRAL ACTIVITY; INTERFERON-ALPHA; CELL-CULTURE; DOUBLE-BLIND; HBV DNA; REPLICATION; EFFICACY; INHIBITION;
D O I
10.1007/978-981-16-0267-2_5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Currently, there are two safe and effective therapeutic strategies for chronic hepatitis B treatment, namely, nucleoside analogs and interferon alpha (pegylated or non-pegylated). These treatments can control viral replication and improve survival; however, they do not eliminate the virus and therefore require long-term continued therapy. In addition, there are significant concerns about virus rebound on discontinuation of therapy and the development of fibrosis and hepatocellular carcinoma despite therapy. Therefore, the search for new, more effective, and safer antiviral agents that can cure hepatitis B virus (HBV) continues. Anti-HBV drug discovery and development is fundamentally impacted by our current understanding of HBV replication, disease physiopathology, and persistence of HBV covalently closed circular DNA (cccDNA). Several HBV replication targets are the basis for novel anti-HBV drug development strategies. Many of them are already in clinical trial phase 1 or 2, while others with promising results are still in preclinical stages. As research intensifies, potential HBV curative therapies and modalities in the pipeline are now on the horizon.
引用
收藏
页码:115 / 138
页数:24
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