Congenital defects in the interferon-gamma/interleukin-12 pathway

Curr Opin Pediatr. 2004 Feb;16(1):3-8. doi: 10.1097/00008480-200402000-00003.

Abstract

Purpose of review: The aim of this review is to highlight the most recent and relevant advances in the interferon-gamma/interleukin-12 pathway, a pivotal player of the immune system, and their repercussions on basic and clinical aspects of science.

Recent findings: Newly described mutations are helping us to dissect the interferon-gamma/interleukin-12 pathway and its role in genetic infectious susceptibility and autoimmunity, and to reevaluate the pathophysiologic mechanisms involved in dominant and recessively inherited mutations.

Summary: The interferon-gamma/interleukin-12 pathway plays a central role in immune control of both environmental and autochthonous challenges, as reflected in human mutations and animal models. Besides being crucial for mycobacterial control, the interferon-gamma/interleukin-12 pathway is also involved in the pathogenesis of autoimmune disease, as well as tumor development and control. Genotype-phenotype correlations have been established for certain mutants in this pathway, some of which have therapeutic implications.

Publication types

  • Review

MeSH terms

  • Congenital Abnormalities / genetics
  • Congenital Abnormalities / metabolism
  • Congenital Abnormalities / physiopathology*
  • DNA-Binding Proteins / deficiency
  • Humans
  • Interferon-gamma / metabolism*
  • Interleukin-12 / metabolism*
  • Mutation
  • Receptors, Interleukin / genetics
  • Receptors, Interleukin / physiology
  • Receptors, Interleukin-12
  • STAT1 Transcription Factor
  • Signal Transduction*
  • Trans-Activators / deficiency

Substances

  • DNA-Binding Proteins
  • Receptors, Interleukin
  • Receptors, Interleukin-12
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Trans-Activators
  • Interleukin-12
  • Interferon-gamma