Antiviral therapy for hepatitis B virus infections: new targets and technical challenges

被引:19
作者
Feld, J
Locarnini, S
机构
[1] Victorian Infect Dis Reference Lab, Melbourne, Vic 3051, Australia
[2] Univ Toronto, Toronto Hosp, Dept Med, Toronto, ON M5T 2S8, Canada
关键词
antiviral agents; antiviral targets; hepatitis B virus; non-nucleotide inhibitors; antiviral resistance;
D O I
10.1016/S1386-6532(02)00107-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
There are presently only two licensed therapies for treating liver disease caused by infection with the hepatitis B virus (HBV). These are interferon-alpha and lamivudine. Neither agent was specifically developed as an antiviral compound for treating patients infected with HBV. Both therapies are limited in the clinic by a low response rate and in the case of lamivudine, selection of drug-resistant mutants, whilst troublesome side effects limit the use of interferon-alpha. Several promising nucleoside/nucleotide analogues are undergoing clinical trials, including adefovir dipivoxil and entecavir, both of which appear to be active against lamivudine- resistant HBV. In addition to these nucleoside/nucleotide analogues, it will be important to develop new agents with different modes of action, which can be added to the antiviral cocktails that will be required to adequately suppress and hopefully eliminate HBV replication. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:267 / 283
页数:17
相关论文
共 118 条
[1]   Identification and characterization of mutations in hepatitis B virus resistant to lamivudine [J].
Allen, MI ;
Deslauriers, M ;
Andrews, CW ;
Tipples, GA ;
Walters, KA ;
Tyrrell, DLJ ;
Brown, N ;
Condreay, LD .
HEPATOLOGY, 1998, 27 (06) :1670-1677
[2]   HEPATITIS-B VIRUS-X GENE-PRODUCT ACTS AS A TRANSACTIVATOR IN-VIVO [J].
BALSANO, C ;
BILLET, O ;
BENNOUN, M ;
CAVARD, C ;
ZIDER, A ;
GRIMBER, G ;
NATOLI, G ;
BRIAND, P ;
LEVRERO, M .
JOURNAL OF HEPATOLOGY, 1994, 21 (01) :103-109
[3]   THE P-GENE PRODUCT OF HEPATITIS-B VIRUS IS REQUIRED AS A STRUCTURAL COMPONENT FOR GENOMIC RNA ENCAPSIDATION [J].
BARTENSCHLAGER, R ;
JUNKERNIEPMANN, M ;
SCHALLER, H .
JOURNAL OF VIROLOGY, 1990, 64 (11) :5324-5332
[4]   Clinical experience with famciclovir against hepatitis B virus [J].
Bartholomeusz, A ;
Groenen, LC ;
Locarnini, SA .
INTERVIROLOGY, 1997, 40 (5-6) :337-342
[5]   SECRETION OF HUMAN HEPATITIS-B VIRUS IS INHIBITED BY THE IMINO SUGAR N-BUTYLDEOXYNOJIRIMYCIN [J].
BLOCK, TM ;
LU, XY ;
PLATT, FM ;
FOSTER, GR ;
GERLICH, WH ;
BLUMBERG, BS ;
DWEK, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2235-2239
[6]   Iminosugars as possible broad spectrum anti hepatitis virus agents: the glucovirs and alkovirs [J].
Block, TM ;
Jordan, R .
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 2001, 12 (06) :317-325
[7]  
BLUM HE, 2002, MOL BIOL IMMUNOLOGY, V8, P97
[8]   Structural organization of the hepatitis B virus minichromosome [J].
Bock, CT ;
Schwinn, S ;
Locarnini, S ;
Fyfe, J ;
Manns, MP ;
Trautwein, C ;
Zentgraf, H .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 307 (01) :183-196
[9]   HEPATITIS-B VIRUS GENOME IS ORGANIZED INTO NUCLEOSOMES IN THE NUCLEUS OF THE INFECTED CELL [J].
BOCK, CT ;
SCHRANZ, P ;
SCHRODER, CH ;
ZENTGRAF, H .
VIRUS GENES, 1994, 8 (03) :215-229
[10]   THE ROLE OF ENVELOPE PROTEINS IN HEPATITIS-B VIRUS ASSEMBLY [J].
BRUSS, V ;
GANEM, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (03) :1059-1063