Influence of GBV-C infection on the endogenous activation of the IFN system in HIV-1 co-infected patients

Cell Mol Biol (Noisy-le-grand). 2006 May 15;52(1):3-8.

Abstract

Background: GB virus C (GBV-C) co-infection is associated with a better prognosis in HIV-infected persons. Since interferon activation can be one of the possible mechanisms involved in GBV-C-driven protection against HIV, we compared the endogenous activation of the interferon system in PBMC from GBV-C-positive and -negative patients infected with HIV-1.

Methods: The expression of interferon related genes was analyzed in 20 GBV-C positive and 20 GBV-C-negative HIV-infected patients, comparable in terms of CD4 cell counts and HIV viral loads. The levels of mRNA for interferon-related genes (2-5-OAS, MxA, interferon AR-1 and PKR) in PBMC were measured by real time RT-PCR, using B-actin as internal control.

Results: The endogenous levels of all the Interferon-related genes in HIV/GBV-C co-infected patients were higher than in HIV mono-infected subjects. The difference was statistically significant for PKR mRNA. Direct positive correlation was found between PKR and all the other interferon-related genes, suggesting a coordinated activation of the interferon system.

Conclusions: Enhanced activation of the interferon system occurs in GBV-C-positive, as compared to GBV-C-negative patients harbouring HIV-1. These data may be relevant to understand the GBV-C-driven protection against HIV, suggesting that the endogenous activation of the interferon system can contribute to the control of HIV replication.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2',5'-Oligoadenylate Synthetase / metabolism
  • Adult
  • Aged
  • Aged, 80 and over
  • Blood Cells / metabolism
  • Blood Cells / virology
  • Female
  • Flaviviridae Infections / complications*
  • Flaviviridae Infections / immunology
  • GB virus C*
  • GTP-Binding Proteins / metabolism
  • HIV Infections / complications*
  • HIV Infections / immunology
  • HIV-1*
  • Hepatitis, Viral, Human / complications*
  • Hepatitis, Viral, Human / immunology
  • Humans
  • Interferons / metabolism*
  • Male
  • Membrane Proteins / metabolism
  • Middle Aged
  • Myxovirus Resistance Proteins
  • RNA, Messenger / metabolism
  • Receptor, Interferon alpha-beta
  • Receptors, Interferon / metabolism
  • eIF-2 Kinase / metabolism

Substances

  • MX1 protein, human
  • Membrane Proteins
  • Myxovirus Resistance Proteins
  • RNA, Messenger
  • Receptors, Interferon
  • Receptor, Interferon alpha-beta
  • Interferons
  • eIF-2 Kinase
  • OAS1 protein, human
  • 2',5'-Oligoadenylate Synthetase
  • GTP-Binding Proteins