The costimulatory molecule ICOS regulates the expression of c-Maf and IL-21 in the development of follicular T helper cells and TH-17 cells

被引:588
|
作者
Bauquet, Aurelie T. [1 ]
Jin, Hulin [1 ]
Paterson, Alison M. [2 ]
Mitsdoerffer, Meike [1 ]
Ho, I-Cheng [3 ,4 ]
Sharpe, Arlene H. [2 ]
Kuchroo, Vijay K. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Rheumatol Allergy & Immunol, Boston, MA 02115 USA
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
COMMON VARIABLE IMMUNODEFICIENCY; DEPENDENT IMMUNE-RESPONSES; INDUCIBLE COSTIMULATOR; AUTOIMMUNE ENCEPHALOMYELITIS; MULTIPLE-SCLEROSIS; GERMINAL-CENTERS; MESSENGER-RNA; CUTTING EDGE; IN-VIVO; B-CELLS;
D O I
10.1038/ni.1690
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The inducible costimulatory molecule ICOS has been suggested to be important in the development of interleukin 17 (IL-17)producing helper T cells (T-H-17 cells) and of follicular helper T cells (T-FH cells). Here we show that ICOS-deficient mice had no defect in T-H-17 differentiation but had fewer T-H-17 cells after IL-23 stimulation and fewer TFH cells. We also show that TFH cells produced IL-17 and that TFH cells in ICOS-deficient mice were defective in IL-17 production. Both T-H-17 and TFH cells had higher expression of the transcription factor c-Maf. Genetic loss of c-Maf resulted in a defect in IL-21 production and fewer T-H-17 and T-FH cells. Thus our data suggest that ICOS-induced c-Maf regulates IL-21 production that in turn regulates the expansion of T-H-17 and T-FH cells.
引用
收藏
页码:167 / 175
页数:9
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