Discovery of Small Molecule Therapeutics for Treatment of Chronic HBV Infection

被引:44
作者
Feng, Song [1 ]
Gao, Lu [1 ]
Han, Xingchun [1 ]
Hu, Taishan [1 ]
Hu, Yimin [1 ]
Liu, Haixia [1 ]
Thomas, Andrew W. [1 ]
Yan, Zhipeng [1 ]
Yang, Song [1 ]
Young, John A. T. [1 ]
Yun, Hongying [1 ]
Zhu, Wei [1 ]
Shen, Hong C. [1 ]
机构
[1] Roche Pharma Res & Early Dev, Roche Innovat Ctr Shanghai, Bldg 5,720 Cailun Rd, Shanghai 201203, Peoples R China
来源
ACS INFECTIOUS DISEASES | 2018年 / 4卷 / 03期
关键词
HBV chronic infection; small molecule HBV inhibitors; HBsAg; HBV DNA; HBV cccDNA; capsid; nucleos(t)ides; immunomodulators; HBV polymerase inhibitors; interferon; HEPATITIS-B-VIRUS; CLOSED CIRCULAR DNA; TAUROCHOLATE COTRANSPORTING POLYPEPTIDE; RIBONUCLEASE H ACTIVITY; CAPSID ASSEMBLY INHIBITORS; PRIMARY HUMAN HEPATOCYTES; HBEAG-POSITIVE PATIENTS; DEMETHYLASE; INHIBITOR; LIVER-TARGETED PRODRUG; LARGE ENVELOPE PROTEIN;
D O I
10.1021/acsinfecdis.7b00144
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The chronic infection of hepatitis B virus (HBV) inflicts 250 million people worldwide representing a major public health threat. A significant sub population of patients eventually develop cirrhosis and hepatocellular carcinoma (HCC). Unfortunately, none of the current standard therapies for chronic hepatitis B (CHB) result in a satisfactory clinical cure rate. Driven by a highly unmet medical need, multiple pharmaceutical companies and research institutions have been engaged in drug discovery and development to improve the CHB functional cure rate, defined by sustainable viral suppression and HBsAg clearance after a finite treatment. This Review summarizes the recent advances in the discovery and development of novel anti-HBV small molecules. It is believed that an improved CHB functional cure rate may be accomplished via the combination of molecules with distinct MoAs. Thus, certain molecules may evolve into key components of a suitable combination therapy leading to superior outcome of clinical efficacy in the future.
引用
收藏
页码:257 / 277
页数:41
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