Foxp3 Programs the Development and Function of CD4+CD25+ Regulatory T Cells (Reprinted from vol 4, pg 330-336, 2003)
被引:6049
作者:
Fontenot, Jason D.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Washington, Howard Hughes Med Inst, Dept Immunol, Box 357370, Seattle, WA 98195 USAUniv Washington, Howard Hughes Med Inst, Dept Immunol, Box 357370, Seattle, WA 98195 USA
Fontenot, Jason D.
[1
]
Gavin, Marc A.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Washington, Howard Hughes Med Inst, Dept Immunol, Box 357370, Seattle, WA 98195 USAUniv Washington, Howard Hughes Med Inst, Dept Immunol, Box 357370, Seattle, WA 98195 USA
Gavin, Marc A.
[1
]
Rudensky, Alexander Y.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Washington, Howard Hughes Med Inst, Dept Immunol, Box 357370, Seattle, WA 98195 USAUniv Washington, Howard Hughes Med Inst, Dept Immunol, Box 357370, Seattle, WA 98195 USA
Rudensky, Alexander Y.
[1
]
机构:
[1] Univ Washington, Howard Hughes Med Inst, Dept Immunol, Box 357370, Seattle, WA 98195 USA
CD4(+)CD25(+) regulatory T cells are essential for the active suppression of autoimmunity. Here we report that the forkhead transcription factor Foxp3 is specifically expressed in CD4+CD25+ regulatoryT cells and is required for their development.The lethal autoimmune syndrome observed in Foxp3-mutant scurfy mice and Foxp3-null mice results from a CD4+CD25+ regulatory T cell deficiency and not from a cell-intrinsic defect of (CD4+CD25)-T cells. CD4+CD25+ regulatory T cells rescue disease development and preferentially expand when transferred into neonatal Foxp3deficient mice. Furthermore, ectopic expression of Foxp3 confers suppressor function on peripheral (CD4+CD25)-T cells. Thus, Foxp3 is a critical regulator of CD4+CD25+ regulatoryT cell development and function.