Treatment of chronic hepatitis B: current challenges and future directions

被引:32
作者
Chin, R
Locarnini, S
机构
[1] Royal Melbourne Hosp, Ctr Clin Res Excellence Infect Dis, Melbourne, Vic 3051, Australia
[2] Victorian Infect Dis Reference Lab, Melbourne, Vic 3051, Australia
关键词
D O I
10.1002/rmv.393
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The clinical management of chronic hepatitis B infection has entered a new era with the introduction and widespread use of oral nucleoside analogues such as lamivudine and nucleotides such as adefovir dipivoxil. From this, new challenges have now emerged in terms of preventing antiviral drug resistance, promoting viral clearance and improving long-term survival. For example, the natural history of nucleoside or nucleotide analogue-associated hepatitis B virus resistant mutants has yet to be determined. Furthermore, the increasing prevalence of HBeAg negative disease with its reduced response to current therapies represents an ongoing challenge to attempts to improve standard of care. There is increasing recognition of the pivotal role that viral load and genotype, and their complex interactions with the host immune response, play in determining the outcome of these treatment interventions. The purpose of this paper is to highlight several key factors that should be considered in the context of future clinical research and management of chronic hepatitis B. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:255 / 272
页数:18
相关论文
共 150 条
  • [21] In vitro antihepadnaviral activities of combinations of penciclovir, lamivudine, and adefovir
    Colledge, D
    Civitico, G
    Locarnini, S
    Shaw, T
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (03) : 551 - 560
  • [22] Colledge D, 1997, HEPATOLOGY, V26, P216
  • [23] CONDRA JH, 1997, SCI MED, V4, P2
  • [24] DANE DS, 1970, LANCET, V1, P695
  • [25] DARWIN CR, 1975, ORIGIN SPECIES MEANS
  • [26] Molecular modeling and biochemical characterization reveal the mechanism of hepatitis B virus polymerase resistance to lamivudine (3TC) and emtricitabine (FTC)
    Das, K
    Xiong, XF
    Yang, HL
    Westland, CE
    Gibbs, CS
    Sarafianos, SG
    Arnold, E
    [J]. JOURNAL OF VIROLOGY, 2001, 75 (10) : 4771 - 4779
  • [27] Acyclic nucleoside phosphonates in the chemotherapy of DNA virus and retrovirus infections
    De Clercq, E
    [J]. INTERVIROLOGY, 1997, 40 (5-6) : 295 - 303
  • [28] de Man R, 2000, HEPATOLOGY, V32, p376A
  • [29] A randomized, placebo-controlled study to evaluate the efficacy of 12-month famciclovir treatment in patients with chronic hepatitis B e antigen-positive hepatitis B
    de Man, RA
    Marcellin, P
    Habal, F
    Desmond, P
    Wright, T
    Rose, T
    Jurewicz, R
    Young, C
    [J]. HEPATOLOGY, 2000, 32 (02) : 413 - 417
  • [30] Lamivudine as initial treatment for chronic hepatitis B in the United States
    Dienstag, JL
    Schiff, ER
    Wright, TL
    Perrillo, RP
    Hann, HWL
    Goodman, Z
    Crowther, L
    Condreay, LD
    Woessner, M
    Rubin, M
    Brown, NA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (17) : 1256 - 1263