Role of GB virus C in modulating HIV disease

Expert Rev Anti Infect Ther. 2012 May;10(5):563-72. doi: 10.1586/eri.12.37.

Abstract

GB virus C (GBV-C) is a member of the Flaviviridae family and the most closely related human virus to HCV. However, GBV-C does not replicate in hepatocytes, but rather in lymphocytes. GBV-C has a worldwide distribution and is transmitted sexually, parenterally and through mother-to-child transmission. Thus, co-infection with HCV and HIV is common. Until now, no human disease has been associated with GBV-C infection. However, there are several reports of a beneficial effect of GBV-C on HIV disease progression in vivo. Different mechanisms to explain these observations have been proposed, including modification of antiviral cytokine production, HIV co-receptor expression, direct inhibition of HIV-1 entry, T-cell activation and Fas-mediated apoptosis. Further understanding of these mechanisms may open new strategies for the treatment of HIV/AIDS.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Coinfection*
  • Cytokines / immunology
  • Flaviviridae Infections / diagnosis
  • Flaviviridae Infections / immunology*
  • Flaviviridae Infections / transmission
  • Flaviviridae Infections / virology
  • GB virus C / genetics
  • GB virus C / immunology
  • GB virus C / pathogenicity
  • GB virus C / physiology*
  • Genetic Variation
  • HIV Infections / immunology*
  • HIV Infections / pathology
  • HIV Infections / virology
  • HIV-1 / genetics
  • HIV-1 / immunology
  • HIV-1 / pathogenicity
  • HIV-1 / physiology
  • Hepacivirus / immunology
  • Hepacivirus / pathogenicity
  • Hepatitis C / immunology*
  • Hepatitis C / pathology
  • Hepatitis C / virology
  • Humans
  • Lymphocyte Activation
  • RNA, Viral / blood
  • Viral Load
  • Virus Internalization
  • Virus Replication

Substances

  • Cytokines
  • RNA, Viral