Hepatitis C virus: current understanding and prospects for future therapies

被引:61
作者
Rosen, HR [1 ]
Gretch, DR
机构
[1] Vet Adm Med Ctr, Div Gastroenterol & Hepatol, Portland, OR 97207 USA
[2] Univ Washington, Viral Hepatitis Lab, Seattle, WA 98195 USA
来源
MOLECULAR MEDICINE TODAY | 1999年 / 5卷 / 09期
关键词
D O I
10.1016/S1357-4310(99)01523-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis C virus (HCV) is the leading cause of chronic liver disease worldwide and the leading indication for liver transplantation. The hallmark of the disease is its propensity to evolve into chronicity, probably because viral heterogeneity allows the virus to escape immune-mediated neutratization. Treatment with interferon alpha (IFN-alpha) has been disappointing, but higher and more frequent doses, and combination therapies, including nucleoside analogs, might lead to improved suppression of HCV RNA levels. Molecular analysis of HCV before and during treatment has indicated that high viral RNA levels and the presence of HCV genotype 1 are independent predictors of poor treatment outcome, New antiviral agents in development include inhibitors of HCV replicative enzymes, such as protease, helicase and polymerase, as well as several genetic approaches, such as ribozymes and antisense oligonucleotides. The main hindrance to drug development for hepatitis C is the lack of a small animal model or a productive tissue culture system for assessing drug action.
引用
收藏
页码:393 / 399
页数:7
相关论文
共 53 条
[1]   THE NATURAL-HISTORY OF COMMUNITY-ACQUIRED HEPATITIS-C IN THE UNITED-STATES [J].
ALTER, MJ ;
MARGOLIS, HS ;
KRAWCZYNSKI, K ;
JUDSON, FN ;
MARES, A ;
ALEXANDER, WJ ;
HU, PY ;
MILLER, JK ;
GERBER, MA ;
SAMPLINER, RE ;
MEEKS, EL ;
BEACH, MJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (27) :1899-1905
[2]   RISK-FACTORS FOR ACUTE NON-A, NON-B HEPATITIS IN THE UNITED-STATES AND ASSOCIATION WITH HEPATITIS-C VIRUS-INFECTION [J].
ALTER, MJ ;
HADLER, SC ;
JUDSON, FN ;
MARES, A ;
ALEXANDER, WJ ;
HU, PY ;
MILLER, JK ;
MOYER, LA ;
FIELDS, HA ;
BRADLEY, DW ;
MARGOLIS, HS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1990, 264 (17) :2231-2235
[3]  
Andreone P, 1996, LIVER, V16, P207
[4]   Molecular targets in inhibition of hepatitis C virus replication [J].
Bartenschlager, R .
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1997, 8 (04) :281-301
[5]  
Benvegnù L, 1998, CANCER-AM CANCER SOC, V83, P901, DOI 10.1002/(SICI)1097-0142(19980901)83:5<901::AID-CNCR15>3.0.CO
[6]  
2-Z
[7]   Interactions between alcohol and hepatitis viruses in the liver [J].
Brechot, C ;
Nalpas, B ;
Feitelson, MA .
CLINICS IN LABORATORY MEDICINE, 1996, 16 (02) :273-+
[8]   GENETIC-HETEROGENEITY OF HEPATITIS-C VIRUS - QUASI-SPECIES AND GENOTYPES [J].
BUKH, J ;
MILLER, RH ;
PURCELL, RH .
SEMINARS IN LIVER DISEASE, 1995, 15 (01) :41-63
[9]   CHARACTERIZATION OF KUNJIN VIRUS RNA-DEPENDENT RNA-POLYMERASE - REINITIATION OF SYNTHESIS INVITRO [J].
CHU, PWG ;
WESTAWAY, EG .
VIROLOGY, 1987, 157 (02) :330-337
[10]   Routes of infection, viremia, and liver disease in blood donors found to have hepatitis C virus infection [J].
ConryCantilena, C ;
VanRaden, M ;
Gibble, J ;
Melpolder, J ;
Shakil, AO ;
Viladomiu, L ;
Cheung, L ;
DiBisceglie, A ;
Hoofnagle, J ;
Shih, JW ;
Kaslow, R ;
Ness, P ;
Alter, HJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (26) :1691-1696