Viruses 2010, 2(8), 1782-1803; doi:10.3390/v2081782
Review

Last Stop Before Exit – Hepatitis C Assembly and Release as Antiviral Drug Targets

1,* email, 1,2email and 1email
Received: 15 June 2010; in revised form: 16 July 2010 / Accepted: 4 August 2010 / Published: 24 August 2010
(This article belongs to the Special Issue Antivirals Against Hepatitis C Virus)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Chronic Hepatitis C infection is a global health problem. While primary infection is often inapparent, it becomes chronic in most cases. Chronic infection with Hepatitis C virus (HCV) frequently leads to liver cirrhosis or liver cancer. Consequently, HCV infection is one of the leading causes for liver transplantation in industrialized countries. Current treatment is not HCV specific and is only effective in about half of the infected patients. This situation underlines the need for new antivirals against HCV. To develop new and more efficient drugs, it is essential to specifically target the different steps of the viral life cycle. Of those steps, the targeting of HCV assembly has the potential to abolish virus production. This review summarizes the advances in our understanding of HCV particle assembly and the identification of new antiviral targets of potential interest in this late step of the HCV life cycle.
Keywords: Hepatitis C; assembly; release; antivirals
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MDPI and ACS Style

Tews, B.A.; Popescu, C.-I.; Dubuisson, J. Last Stop Before Exit – Hepatitis C Assembly and Release as Antiviral Drug Targets. Viruses 2010, 2, 1782-1803.

AMA Style

Tews BA, Popescu C-I, Dubuisson J. Last Stop Before Exit – Hepatitis C Assembly and Release as Antiviral Drug Targets. Viruses. 2010; 2(8):1782-1803.

Chicago/Turabian Style

Tews, Birke Andrea; Popescu, Costin-Ioan; Dubuisson, Jean. 2010. "Last Stop Before Exit – Hepatitis C Assembly and Release as Antiviral Drug Targets." Viruses 2, no. 8: 1782-1803.

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