Interferon-stimulated genes and their role in controlling hepatitis C virus

J Hepatol. 2013 Dec;59(6):1331-41. doi: 10.1016/j.jhep.2013.07.033. Epub 2013 Aug 8.

Abstract

Infections with the hepatitis C virus (HCV) are a major cause of chronic liver disease. While the acute phase of infection is mostly asymptomatic, this virus has the high propensity to establish persistence and in the course of one to several decades liver disease can develop. HCV is a paradigm for the complex interplay between the interferon (IFN) system and viral countermeasures. The virus induces an IFN response within the infected cell and is rather sensitive against the antiviral state triggered by IFNs, yet in most cases HCV persists. Numerous IFN-stimulated genes (ISGs) have been reported to suppress HCV replication, but in only a few cases we begin to understand the molecular mechanisms underlying antiviral activity. It is becoming increasingly clear that blockage of viral replication is mediated by the concerted action of multiple ISGs that target different steps of the HCV replication cycle. This review briefly summarizes the activation of the IFN system by HCV and then focuses on ISGs targeting the HCV replication cycle and their possible mode of action.

Keywords: Hepatitis C virus; Interferon; Interferon-stimulated genes.

Publication types

  • Review

MeSH terms

  • 2',5'-Oligoadenylate Synthetase / physiology
  • Antigens, Differentiation / physiology
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases / physiology
  • Hepacivirus / isolation & purification
  • Hepacivirus / physiology*
  • Humans
  • Interferons / physiology*
  • Oxidoreductases Acting on CH-CH Group Donors
  • Proteins / physiology
  • Receptors, Immunologic
  • Toll-Like Receptors / physiology
  • Virus Replication
  • eIF-2 Kinase / physiology

Substances

  • Antigens, Differentiation
  • Proteins
  • Receptors, Immunologic
  • Toll-Like Receptors
  • leu-13 antigen
  • Interferons
  • Oxidoreductases Acting on CH-CH Group Donors
  • RSAD2 protein, human
  • eIF-2 Kinase
  • 2',5'-Oligoadenylate Synthetase
  • RIGI protein, human
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases