Molecular immunity to mycobacteria: knowledge from the mutation and phenotype spectrum analysis of Mendelian susceptibility to mycobacterial diseases

Int J Infect Dis. 2011 May;15(5):e305-13. doi: 10.1016/j.ijid.2011.01.004. Epub 2011 Feb 16.

Abstract

Understanding molecular immunity against mycobacterial infection is critical for the development of effective strategies to control tuberculosis (TB), which is a major health issue in the developing world. Host immunogenetic studies represent an indispensable approach to understand the molecular mechanisms against mycobacterial infection. A superb paradigm is the identification of rare mutations causing Mendelian susceptibility to mycobacterial diseases (MSMD). Mutations in the interferon-gamma (IFN-γ) receptor genes are highly specific (although not exclusive) for mycobacterial infection. Only dominant negative mutations of STAT1 have specific susceptibility to mycobacterial infection. Mutations in the interleukin-12 (IL-12) signaling genes have phenotypes with non-specificity. Current studies highlight a complex molecular network in antimycobacterial immunity, centered on IFN-γ signaling.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Genetic Predisposition to Disease / genetics*
  • Immunity / genetics*
  • Interferon gamma Receptor
  • Interferon-gamma / genetics
  • Interleukin-12 / genetics
  • Mutation / genetics*
  • Mycobacterium / immunology*
  • Mycobacterium / pathogenicity
  • Mycobacterium Infections / genetics
  • Mycobacterium Infections / immunology*
  • Mycobacterium Infections / microbiology
  • Receptors, Interferon / genetics
  • STAT1 Transcription Factor / genetics
  • Signal Transduction / genetics
  • Tuberculosis / genetics
  • Tuberculosis / immunology*
  • Tuberculosis / microbiology
  • Tuberculosis / prevention & control

Substances

  • Receptors, Interferon
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Interleukin-12
  • Interferon-gamma