Cutting edge: Decreased accumulation and regulatory function of CD4+ CD25(high) T cells in human STAT5b deficiency

J Immunol. 2006 Sep 1;177(5):2770-4. doi: 10.4049/jimmunol.177.5.2770.

Abstract

We show that STAT5b is important for the in vivo accumulation of CD4+ CD25(high) T cells with regulatory cell function. A patient homozygous for a missense A630P STAT5b mutation displayed immune dysregulation and decreased numbers of CD4+ CD25(high) T cells. STAT5b(A630P/A630P) CD4+ CD25(high) T cells had low expression of forkhead box P3 and an impaired ability to suppress the proliferation of or to kill CD4+ CD25- T cells. Expression of CD25, a component of the high-affinity IL-2R, was also reduced in response to IL-2 or after in vitro propagation. The impact of the STAT5b mutation was selective in that IL-2-mediated up-regulation of the common gamma-chain cytokine receptor and perforin, and activation-induced expressions of CD154 and IFN-gamma were normal. These results indicate that STAT5b propagates an important IL-2-mediated signal for the in vivo accumulation of functional regulatory T cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alanine / genetics
  • Alanine / metabolism
  • CD4-Positive T-Lymphocytes / cytology*
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism*
  • Cell Proliferation
  • Cells, Cultured
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Lymphocyte Activation / immunology
  • Male
  • Mutation / genetics
  • Receptors, Interleukin-2 / metabolism*
  • STAT5 Transcription Factor / deficiency*
  • STAT5 Transcription Factor / genetics
  • STAT5 Transcription Factor / metabolism*

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Receptors, Interleukin-2
  • STAT5 Transcription Factor
  • STAT5B protein, human
  • Alanine