articleScienceMay 15, 2003GREEN OA

Regulation of Interferon Regulatory Factor-3 by the Hepatitis C Virus Serine Protease

The University of Texas Medical Branch at Galveston · The University of Texas Southwestern Medical Center

PubMed
Indexed incrossrefdatacitepubmed

Abstract

Persistent infections with hepatitis C virus (HCV) are likely to depend on viral inhibition of host defenses. We show that the HCV NS3/4A serine protease blocks the phosphorylation and effector action of interferon regulatory factor-3 (IRF-3), a key cellular antiviral signaling molecule. Disruption of NS3/4A protease function by mutation or a ketoamide peptidomimetic inhibitor relieved this blockade and restored IRF-3 phosphorylation after cellular challenge with an unrelated virus. Furthermore, dominant-negative or constitutively active IRF-3 mutants, respectively, enhanced or suppressed HCV RNA replication in hepatoma cells. Thus, the NS3/4A protease represents a dual therapeutic target, the inhibition of…

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