Cutting edge: decreased accumulation and regulatory function of CD4+ CD25high T cells in human STAT5b deficiency

AC Cohen, KC Nadeau, W Tu, V Hwa… - The Journal of …, 2006 - journals.aai.org
AC Cohen, KC Nadeau, W Tu, V Hwa, K Dionis, L Bezrodnik, A Teper, M Gaillard, J Heinrich…
The Journal of Immunology, 2006journals.aai.org
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 …
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 γ-chain cytokine receptor and perforin, and activation-induced expressions of CD154 and IFN-γ were normal. These results indicate that STAT5b propagates an important IL-2-mediated signal for the in vivo accumulation of functional regulatory T cells.
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