Novel cell culture systems for the hepatitis C virus

被引:155
作者
Bartenschlager, R [1 ]
Lohmann, V [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Inst Virol, D-55131 Mainz, Germany
关键词
hepatitis C virus; HCV cell cultures; antiviral therapy; flaviviridae; HCV replication systems; HCV replicons;
D O I
10.1016/S0166-3542(01)00164-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Infections with the hepatitis C virus (HCV) are a major cause of acute and chronic liver disease. The high prevalence of the virus, the insidious course of the disease and the poor prognosis for long-term persistent infection make this pathogen a serious medical and socioeconomical problem. The identification of the viral genome similar to 10 years ago rapidly led to the delineation of the genomic organization and the structural and biochemical characterization of several virus proteins. However, studies of the viral life cycle as well as the development of antiviral drugs have been difficult because of the lack of a robust and reliable cell culture system. Numerous attempts have been undertaken in the past few years but only recently a highly efficient cell culture model could be developed. This system is based on the self replication of engineered HCV minigenomes (replicons) in a transfected human hepatoma cell line. A summary of the various HCV cell culture models with a focus on the replicon system and its use for drug development is described. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1 / 17
页数:17
相关论文
共 103 条
[1]   Hepatitis C virus and other Flaviviridae viruses enter cells via low density lipoprotein receptor [J].
Agnello, V ;
Abel, G ;
Elfahal, M ;
Knight, GB ;
Zhang, QX .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12766-12771
[2]   Crystal structure of the RNA-dependent RNA polymerase of hepatitis C virus [J].
Ago, H ;
Adachi, T ;
Yoshida, A ;
Yamamoto, M ;
Habuka, N ;
Yatsunami, K ;
Miyano, M .
STRUCTURE, 1999, 7 (11) :1417-1426
[3]   NONSTRUCTURAL PROTEIN-3 OF THE HEPATITIS-C VIRUS ENCODES A SERINE-TYPE PROTEINASE REQUIRED FOR CLEAVAGE AT THE NS3/4 AND NS4/5 JUNCTIONS [J].
BARTENSCHLAGER, R ;
AHLBORNLAAKE, L ;
MOUS, J ;
JACOBSEN, H .
JOURNAL OF VIROLOGY, 1993, 67 (07) :3835-3844
[4]   The NS3/4A proteinase of the hepatitis C virus: unravelling structure and function of an unusual enzyme and a prime target for antiviral therapy [J].
Bartenschlager, R .
JOURNAL OF VIRAL HEPATITIS, 1999, 6 (03) :165-181
[5]   Replication of hepatitis C virus [J].
Bartenschlager, R ;
Lohmann, V .
JOURNAL OF GENERAL VIROLOGY, 2000, 81 :1631-1648
[6]   An infectious molecular clone of a Japanese genotype 1b hepatitis C virus [J].
Beard, MR ;
Abell, G ;
Honda, M ;
Carroll, A ;
Gartland, M ;
Clarke, B ;
Suzuki, K ;
Lanford, R ;
Sangar, DV ;
Lemon, SM .
HEPATOLOGY, 1999, 30 (01) :316-324
[7]   Identification and properties of the RNA-dependent RNA polymerase of hepatitis C virus [J].
Behrens, SE ;
Tomei, L ;
DeFrancesco, R .
EMBO JOURNAL, 1996, 15 (01) :12-22
[8]   THE HUMAN BONE-MARROW-DERIVED B-CELL LINE CE, SUSCEPTIBLE TO HEPATITIS-C VIRUS-INFECTION [J].
BERTOLINI, L ;
IACOVACCI, S ;
PONZETTO, A ;
GORINI, G ;
BATTAGLIA, M ;
CARLONI, G .
RESEARCH IN VIROLOGY, 1993, 144 (04) :281-285
[9]   Efficient initiation of HCV RNA replication in cell culture [J].
Blight, KJ ;
Kolykhalov, AA ;
Rice, CM .
SCIENCE, 2000, 290 (5498) :1972-1974
[10]   HEPATITIS-C VIRUS IS DETECTED IN A MONOCYTE MACROPHAGE SUBPOPULATION OF PERIPHERAL-BLOOD MONONUCLEAR-CELLS OF INFECTED PATIENTS [J].
BOUFFARD, P ;
HAYASHI, PH ;
ACEVEDO, R ;
LEVY, N ;
ZELDIS, JB .
JOURNAL OF INFECTIOUS DISEASES, 1992, 166 (06) :1276-1280