Journal List > J Bacteriol Virol > v.45(2) > 1034172

Cho: The Applications of Hepatitis C Virus (HCV) Replication System in Developing Anti-HCV Reagents

Abstract

Hepatitis C virus (HCV) is known to be a major cause of chronic hepatitis, liver cirrhosis and hepatocarcinoma. Therapeutic reagents are improving, but are still limited, and the protective vaccine against HCV is not available yet. However, the research of HCV life cycle and pathogenesis has been difficult due to obstacles, which are the lack of effective cell culture systems and small-animal models. Recently, breathtaking progress in terms of HCV replication system has been made using various forms of HCV clones and human hepatocarcinoma 7 cell lines (huh 7). The establishment of complete cell-culture system for HCV replication gave researchers opportunities to study the entire viral life cycle including entry, assembly, release of viral particles and the interaction with host cells. In fact, these efforts now appear to move into the identification and the development of innovative anti-HCV reagents. In this review, we go over the biological characters of HCV, a variety of in vitro cell culture, in vivo animal models of HCV infection, HCV immune-pathogenesis and the application of HCVcc system in terms of developing anti-HCV reagents.

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Figure 1.
Establishment of infectious HCV cell culture system with J6/JFH1 (HCVcc). (A) The experimental outline of HCVcc. (B) Immunohistochemical expression of HCV NS5A protein (dark spots) in cytoplasm of huh 7.5 cells. ∗(B) is modified from Cho et al. (24).
jbv-45-171f1.tif
Table 1.
In vitro and in vivo models to investigate HCV pathogenesis
In vitro models References
Transient expression systems (9)
Infection of primary hepatocytes (10)
Retroviral pseudoparticles displaying functional HCV (11)
Replicons (subgenomic/full-length; selectable/transient) (12), (13)
Recombinant infectious cell culture system (14), (15)
In vivo models  
Chimpanzee (Pan troglodytes) (16), (17)
Tree shrew (18)
Transgenic mice (19)
Immunodeficient/xenograft mice (16), (20)
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