Association of the interferon-gamma receptor variant (Val14Met) with systemic lupus erythematosus

Immunogenetics. 1999 Apr;49(4):266-71. doi: 10.1007/s002510050492.

Abstract

Genetic factors seem to play a significant role in susceptibility to systemic lupus erythematosus (SLE). The purpose of this study was to investigate whether the amino acid polymorphism (Val14Met) found within the IFN-gamma receptor gene (IFNGR1) plays a prominent role in susceptibility to SLE. We found Val14Met located at the COOH terminal of the signal peptide of the IFN-gamma receptor. There was a significant difference in this polymorphism frequency between SLE patients and healthy populations. To clarify whether this amino acid substitution resulted in the alteration of the receptor function, we evaluated the induction of HLA-DR antigen expression on B cells by IFN-gamma stimulation. There was also a significant difference in the induction of HLA-DR by IFN-gamma stimulation between B cells. Furthermore, an intracellular cytokine assay indicated that the Th1/Th2 balance of Th cells bearing the variant receptor shifted to Th2. The genetic polymorphism found within the IFN-gamma receptor gene (Val14Met) may result in a shift to Th2, and this shift may increase susceptibility to SLE.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Amino Acid Sequence
  • Base Sequence
  • DNA, Complementary
  • Female
  • Genetic Variation*
  • Humans
  • Interferon gamma Receptor
  • Interferon-gamma / analysis
  • Interleukin-4 / analysis
  • Lupus Erythematosus, Systemic / genetics*
  • Lupus Erythematosus, Systemic / immunology
  • Male
  • Methionine / genetics
  • Middle Aged
  • Molecular Sequence Data
  • Receptors, Interferon / genetics*
  • Valine / genetics

Substances

  • DNA, Complementary
  • Receptors, Interferon
  • Interleukin-4
  • Interferon-gamma
  • Methionine
  • Valine