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Viruses 2010, 2(8), 1589-1602; doi:10.3390/v2081589
Review

Interferon-λ in HCV Infection and Therapy  

 and
*
Department of Pathology, Yale University School of Medicine, New Haven, CT 06510, USA
* Author to whom correspondence should be addressed.
Received: 28 June 2010 / Accepted: 28 July 2010 / Published: 5 August 2010
(This article belongs to the Special Issue Antivirals Against Hepatitis C Virus)
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Abstract

Chronic infection with hepatitis C virus (HCV) is associated with significant liver disease and is therefore an important public health problem. The current standard-of-care therapy for chronic HCV infection consists of a combination of pegylated (PEG) interferon (IFN)-α and ribavirin. Although this therapy effectively generates a sustained viral response in approximately half of treated individuals, it is associated with significant hematological and neurological side effects. A new family of IFN-related proteins (IFN-λ1, 2, and 3; or alternately, IL-29, 28A, 28B, respectively) possesses properties that may make these cytokines superior to PEG-IFN-α for HCV therapy. Genetic studies have also implicated these proteins in both the natural and therapy-induced resolution of HCV infection. This review summarizes the basic aspects of IFN-λ biology, the potential role of these cytokines in HCV infection, and the outlook for their therapeutic application.
Keywords: IFN-λ; IL-28; IL-29; type III interferon; IL28B; IL-28Rα IFN-λ; IL-28; IL-29; type III interferon; IL28B; IL-28Rα
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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Pagliaccetti, N.E.; Robek, M.D. Interferon-λ in HCV Infection and Therapy  . Viruses 2010, 2, 1589-1602.

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