Impairment of the retinoic acid-inducible gene-I-IFN-β signaling pathway in chronic hepatitis B virus infection

Int J Mol Med. 2012 Dec;30(6):1498-504. doi: 10.3892/ijmm.2012.1131. Epub 2012 Sep 19.

Abstract

Chronic hepatitis B (CHB) virus infection is caused by compromised host immunity, but the precise underlying mechanism remains unclear. Retinoic acid-inducible gene I (RIG-I) triggers antiviral immunity by inducing interferon-β (IFN-β) production following viral infection. To investigate the role of the RIG-I-IFN-β signaling pathway in monocyte-derived dendritic cells (moDCs) during CHB infection, moDCs were generated by stimulating CD14+ monocytes in vitro. MoDCs from patients with CHB, acute hepatitis B (AHB) and healthy controls (HCs) were challenged with vesicular stomatitis virus (VSV) and the levels of RIG-I, IFN-β promoter stimulator 1 (IPS-1) and IFN-β in the stimulated moDCs were determined. Following 16 h of VSV stimulation, RIG-I expression was reduced by 50% in moDCs from CHB patients and by 70% in moDCs from AHB patients relative to HC moDCs, concomitant with a 20% decrease in IFN-β expression in CHB patients relative to AHB patients and HCs. Additionally, a significant correlation between the RIG-I/IPS-1 ratio and alanine aminotransferase (ALT) level was observed. To further investigate the function of RIG-I in chronic hepatitis B virus (HBV) infection, HepG2 or HepG2.2.15 (HBV-transformed) cell lines were challenged with VSV following RIG-1 transfection. IFN-β induction was suppressed in HepG2.2.15 cells, but was restored following RIG-I transfection. Taken together, these data indicate that compromised moDC function in CHB patients is attributable to an impaired RIG-I-IFN-β signaling pathway, which results in compromised host viral clearance and HBV persistence in a susceptible population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Adult
  • Case-Control Studies
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / metabolism*
  • Dendritic Cells / metabolism
  • Dendritic Cells / virology
  • Female
  • Hep G2 Cells
  • Hepatitis B virus / physiology
  • Hepatitis B, Chronic / metabolism*
  • Host-Pathogen Interactions
  • Humans
  • Immunity, Innate
  • Interferon-beta / genetics
  • Interferon-beta / metabolism*
  • Male
  • Receptors, Immunologic
  • Signal Transduction*
  • Transcriptional Activation
  • Vesiculovirus / physiology

Substances

  • Adaptor Proteins, Signal Transducing
  • MAVS protein, human
  • Receptors, Immunologic
  • Interferon-beta
  • RIGI protein, human
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases