Antiviral treatment of chronic hepatitis B virus infections:: the past, the present and the future

被引:63
作者
Ferir, Geoffrey [1 ]
Kaptein, Suzanne [1 ]
Neyts, Johan [1 ]
De Clercq, Erik [1 ]
机构
[1] Rega Inst, B-3000 Louvain, Belgium
关键词
D O I
10.1002/rmv.554
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A decade ago, standard therapy against chronic hepatitis B virus infections only consisted of lamivudine or IFN-alpha. Treatment with lamivudine and IFN has been compounded by, respectively, the emergence of drug-resistant virus strains and the appearance of serious side effects. In the last 10 years, hepatitis B treatment has made much progress. Several treatments are now licensed for the treatment of patients with chronic hepatitis B and others are under development. Here, we provide an overview of the potential and mode of action of anti-HBV agents that are currently available, and/or may become available in the near future. Foremost among these newer compounds are adefovir dipivoxil, entecavir and telbivudine. Copyright (c) 2007 John Wiley & Sons, Ltd.
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页码:19 / 34
页数:16
相关论文
共 132 条
[1]  
BALAKRISHNA PS, 1996, ANTIMICROB AGENTS CH, V40, P380
[2]   THE AMINO-TERMINAL DOMAIN OF THE HEPADNAVIRAL P-GENE ENCODES THE TERMINAL PROTEIN (GENOME-LINKED PROTEIN) BELIEVED TO PRIME REVERSE TRANSCRIPTION [J].
BARTENSCHLAGER, R ;
SCHALLER, H .
EMBO JOURNAL, 1988, 7 (13) :4185-4192
[3]  
BEASLEY RP, 1988, CANCER, V61, P1942, DOI 10.1002/1097-0142(19880515)61:10<1942::AID-CNCR2820611003>3.0.CO
[4]  
2-J
[5]   Anti-hepatitis B virus efficacy of tendovir disoproxil fumarate in HIV-infected patients [J].
Benhamou, Y ;
Fleury, H ;
Trimoulet, P ;
Pellegrin, I ;
Urbinelli, R ;
Katlama, C ;
Rozenbaum, W ;
Le Teuff, G ;
Trylesinski, A ;
Piketty, C .
HEPATOLOGY, 2006, 43 (03) :548-555
[6]   Tenofovir diphosphate is a poor substrate and a weak inhibitor of rat DNA polymerases α,δ, and ε [J].
Birkus, G ;
Hájek, M ;
Kramata, P ;
Votruba, I ;
Holy, A ;
Otová, B .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (05) :1610-1613
[7]  
BORROTOESODA K, 2006, 41 ANN M EASL AUSTR
[8]   In vitro activity of 2,4-diamino-6-[2-(phosphonomethoxy)ethoxy]-pyrimidine against multidrug-resistant hepatitis B virus mutants [J].
Brunelle, M. N. ;
Lucifora, J. ;
Neyts, J. ;
Villet, S. ;
Holy, A. ;
Trepo, C. ;
Zoulim, F. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (06) :2240-2243
[9]   Susceptibility to antivirals of a human HBV strain with mutations conferring resistance to both lamivudine and adefovir [J].
Brunelle, MN ;
Jacquard, AC ;
Pichoud, C ;
Durantel, D ;
Carrouée-Durantel, S ;
Villeneuve, JP ;
Trépo, C ;
Zoulim, F .
HEPATOLOGY, 2005, 41 (06) :1391-1398
[10]   Antiviral L-nucleosides specific for hepatitis B virus infection [J].
Bryant, ML ;
Bridges, EG ;
Placidi, L ;
Faraj, A ;
Loi, AG ;
Pierra, C ;
Dukhan, D ;
Gosselin, G ;
Imbach, JL ;
Hernandez, B ;
Juodawlkis, A ;
Tennant, B ;
Korba, B ;
Cote, P ;
Marion, P ;
Cretton-Scott, E ;
Schinazi, RF ;
Sommadossi, JP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (01) :229-235