TH17 deficiency in human disease

J Allergy Clin Immunol. 2012 Jun;129(6):1429-35; quiz 1436-7. doi: 10.1016/j.jaci.2012.03.034. Epub 2012 May 1.

Abstract

The differentiation of naive T cells into distinct subsets of effector T cells is critical for effective immunity against a wide variety of infectious agents in the environment. Activation of innate immune responses by Candida species through pattern-recognition receptors directs the subsequent development of naive T cells into T(H)17 cells, which are essential for effective mucosal immunity against fungi. Thorough analyses of cohorts of patients with unusual susceptibility to chronic mucocutaneous candidiasis resulting from T(H)17 deficiency have confirmed the role of T(H)17 cells and T(H)17 cytokines in human host defense against Candida species and have provided valuable insights into the complex process of T(H)17 cell development.

Publication types

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

MeSH terms

  • Candidiasis, Chronic Mucocutaneous / genetics
  • Candidiasis, Chronic Mucocutaneous / immunology*
  • Cell Differentiation / immunology
  • Cytokines / immunology
  • Guanine Nucleotide Exchange Factors / genetics
  • Humans
  • Immunity, Innate*
  • Job Syndrome / genetics
  • Job Syndrome / immunology
  • Mutation
  • STAT1 Transcription Factor / genetics
  • STAT3 Transcription Factor / genetics
  • Th17 Cells / cytology
  • Th17 Cells / immunology*
  • Th17 Cells / metabolism

Substances

  • Cytokines
  • DOCK8 protein, human
  • Guanine Nucleotide Exchange Factors
  • STAT1 Transcription Factor
  • STAT3 Transcription Factor