Raised serum levels of interleukin-18 is associated with disease progression and may contribute to virological treatment failure in HIV-1-infected patients

Clin Exp Immunol. 2003 Jun;132(3):462-6. doi: 10.1046/j.1365-2249.2003.02179.x.

Abstract

To gain further insight into the possible role of interleukin (IL)-18 in HIV-1 infection we examined serum levels of IL-18 in various clinical and immunological stages of HIV-1 infection during cross-sectional (n = 41) and longitudinal testing (n = 20) and during HAART (n = 21, 24 months follow-up). Our main findings were that HIV-1-infected patients had significantly raised IL-18 levels comparing healthy controls, particularly in those with advanced disease, that while HAART induced a marked decline in IL-18, virological treatment failure was associated with persistently raised IL-18 levels during such therapy and that our in vitro experiments showed an IL-18-mediated up-regulation of the HIV-1 coreceptor CXCR4 and the pro-apoptotic mediator TRAIL in PBMC from HIV-1-infected patients receiving HAART. HIV-1 infection appears to be characterized by persistently raised IL-18 levels and during HAART, such a pattern was associated with virological treatment failure, possibly contributing to immunodeficiency and HIV-1 replication in these patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiretroviral Therapy, Highly Active*
  • Chemokines / biosynthesis
  • Chemokines / genetics
  • Cross-Sectional Studies
  • Disease Progression
  • Drug Resistance, Viral / immunology
  • Female
  • Gene Expression Regulation / immunology
  • HIV Infections / drug therapy
  • HIV Infections / immunology*
  • HIV-1*
  • Humans
  • Immune Tolerance
  • Interleukin-18 / blood*
  • Interleukin-18 / immunology
  • Longitudinal Studies
  • Male
  • Middle Aged
  • RNA, Messenger / genetics
  • Receptors, Chemokine / biosynthesis
  • Receptors, Chemokine / genetics
  • Treatment Failure

Substances

  • Chemokines
  • Interleukin-18
  • RNA, Messenger
  • Receptors, Chemokine