Protective effect of interleukin-4 -589T polymorphism on human immunodeficiency virus type 1 disease progression: relationship with virus load

J Infect Dis. 2002 Apr 15;185(8):1183-6. doi: 10.1086/339825. Epub 2002 Mar 20.

Abstract

The interleukin (IL)-4 -589T allele bears a single nucleotide polymorphism at position -589 upstream from the open-reading frame of the IL-4 gene. To determine the influence of this allele on human immunodeficiency virus (HIV) type 1 disease, disease progression and serum virus load were assessed by IL-4 genotype in 427 white patients with known seroconversion dates who were followed in the French SEROCO cohort between 1988 and 1996. Serum virus load was 0.20 log lower during the 6-24-month plateau phase after seroconversion in patients with IL-4 -589T than in those without this allele (P=.02). Kaplan-Meier analysis survival curves showed a slower progression to clinical AIDS in carriers of IL-4 -589T (P=.04). Adjustment for early serum virus load greatly diminished the strength of this association. These results suggest that IL-4 -589T protects against HIV-1 disease progression by reducing virus load.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acquired Immunodeficiency Syndrome / genetics*
  • Acquired Immunodeficiency Syndrome / virology
  • Adult
  • Female
  • HIV-1 / isolation & purification*
  • Humans
  • Interleukin-4 / genetics*
  • Male
  • Polymorphism, Genetic*
  • Receptors, CCR2
  • Receptors, Chemokine / genetics
  • Viral Load*

Substances

  • CCR2 protein, human
  • Receptors, CCR2
  • Receptors, Chemokine
  • Interleukin-4