HBV life cycle and novel drug targets

被引:90
作者
Grimm, Daniel [1 ]
Thimme, Robert [1 ]
Blum, Hubert E. [1 ]
机构
[1] Univ Freiburg, Dept Med 2, Freiburg, Germany
关键词
HBV life cycle; HEPATITIS-B-VIRUS; BONE-MARROW-TRANSPLANTATION; SURFACE-ANTIGEN; THERAPEUTIC VACCINATION; INTERFERON-LAMBDA; IMMUNE-RESPONSES; VIRAL-HEPATITIS; IFN-LAMBDA; IN-VIVO; REPLICATION;
D O I
10.1007/s12072-011-9261-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
With up to 400 million affected people worldwide, chronic hepatitis B virus (HBV) infection is still a major health care problem. During the last decade, several novel therapeutic approaches have been developed and evaluated. In most regions of the world, interferon-alpha, and nucleos(t)ide analogues (NUCs) are currently approved. Despite major improvements, none of the existing therapies is optimal since viral clearance is rarely achieved. Recently, a better understanding of the HBV life cycle and the development of novel model systems of HBV infection have led to the development of novel antiviral strategies and drug targets. This review will focus on current and potential future drug targets in the HBV life cycle and strategies to modulate the virus-host interaction.
引用
收藏
页码:644 / 653
页数:10
相关论文
共 93 条
[1]  
Akbar Sk. Md. Fazle, 2004, Current Drug Targets - Inflammation and Allergy, V3, P305, DOI 10.2174/1568010043343787
[2]   Nitazoxanide - A review of its use in the treatment of gastrointestinal infections [J].
Anderson, Vanessa R. ;
Curran, Monique P. .
DRUGS, 2007, 67 (13) :1947-1967
[3]   IFN-λ:: Novel antiviral cytokines [J].
Ank, Nina ;
West, Hans ;
Paludan, Soren R. .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2006, 26 (06) :373-379
[4]   Type III IFNs: New layers of complexity in innate antiviral immunity [J].
Ank, Nina ;
Paludan, Soren R. .
BIOFACTORS, 2009, 35 (01) :82-87
[5]   SPECIFIC EXPRESSION OF HEPATITIS-B SURFACE-ANTIGEN (HBSAG) IN TRANSGENIC MICE [J].
BABINET, C ;
FARZA, H ;
MORELLO, D ;
HADCHOUEL, M ;
POURCEL, C .
SCIENCE, 1985, 230 (4730) :1160-1163
[6]   Rational design of a potent, long-lasting form of interferon:: A 40 kDa branched polyethylene glycol-conjugated interferon α-2a for the treatment of hepatitis C [J].
Bailon, P ;
Palleroni, A ;
Schaffer, CA ;
Spence, CL ;
Fung, WJ ;
Porter, JE ;
Ehrlich, GK ;
Pan, W ;
Xu, ZX ;
Modi, MW ;
Farid, A ;
Berthold, W .
BIOCONJUGATE CHEMISTRY, 2001, 12 (02) :195-202
[7]   Viral Hepatitis B: Established and emerging therapies [J].
Balsano, Clara ;
Alisi, Anna .
CURRENT MEDICINAL CHEMISTRY, 2008, 15 (09) :930-939
[8]   6-[2-phosphonomethoxy)alkoxy]-2,4-diaminopyrimidines:: A new class of acyclic pyrimidine nucleoside phosphonates with antiviral activity [J].
Balzarini, J ;
Pannecouque, C ;
Naesens, L ;
Andrei, G ;
Snoeck, R ;
De Clercq, E ;
Hocková, D ;
Holy, A .
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 2004, 23 (8-9) :1321-1327
[9]  
Bertoletti Antonio, 2009, Expert Rev Gastroenterol Hepatol, V3, P561, DOI 10.1586/egh.09.48
[10]   Small-Molecule Effectors of Hepatitis B Virus Capsid Assembly Give Insight into Virus Life Cycle [J].
Bourne, Christina ;
Lee, Sejin ;
Venkataiah, Bollu ;
Lee, Angela ;
Korba, Brent ;
Finn, M. G. ;
Zlotnick, Adam .
JOURNAL OF VIROLOGY, 2008, 82 (20) :10262-10270