Abstract

The nucleoside analogue Ribavirin significantly increases patient response to IFN-α treatment of HCV, by directly inhibiting viral replication. Recent studies indicate that Ribavirin also regulates immunity and we propose that Ribavirin enhances specific interferon sensitive gene (ISG) expression by amplifying the IFN-α-JAK/STAT pathway. We found that IFN-α-induced STAT1 and STAT3 phosphorylation was increased in hepatocytes co-treated with Ribavirin and IFN-α, compared to IFN-α alone. Ribavirin specifically enhanced IFN-α induced mRNA and protein of the anti-viral mediator MxA, which co-localised with HCV core protein. These novel findings indicate for the first time that Ribavirin, in addition to its viral incorporation, also enhances IFN-α-JAK/STAT signalling, leading to a novel MxA-mediated immuno-modulatory mechanism that may enhance IFN-α anti-viral activity against HCV.

Highlights

  • In combination with the anti-viral cytokine interferon (IFN)-a, Ribavirin is used to treat chronic Hepatitis C Virus (HCV) infection

  • We found that Ribavirin enhanced IFN-a-induced phosphorylation of STAT1 and STAT3 and myxovirus resistance gene A (MxA) expression in Huh7 hepatocytes, revealing a novel mechanism of immune regulation by Ribavirin

  • We found that Ribavirin amplified IFN-a-induced STAT1 and STAT3 phosphorylation and that this combined treatment increased MxA expression, but had no effect on PKR or 2959-OAS, indicating that Ribavirin amplification of JAK/STAT signalling enhances the anti-viral protein MxA

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Summary

Introduction

In combination with the anti-viral cytokine interferon (IFN)-a, Ribavirin is used to treat chronic Hepatitis C Virus (HCV) infection. In addition to its effect on viral replication, this nucleoside analogue is thought to have immune modulatory properties, including the regulation of macrophage and T helper (Th) cell produced cytokines, modulation of the Th1/Th2 subset balance and the enhancement of IFN sensitive gene (ISG) expression, suggesting an effect on the JAK/STAT pathway [10,11,12,13,14,15]. Anti-viral responses to IFN-a are mediated by a number of key proteins induced through activation of the JAK/STAT pathway, including double-stranded RNA-activated protein kinase (PKR) and 2959-oligoadenylate synthethase (2959-OAS), which block translation and degrade viral RNA, respectively. Mx proteins were initially discovered in influenza A resistant mice and are thought to mediate innate immunity against numerous RNA viruses, including

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