Transcriptional regulation of Th2 differentiation by inducible costimulator

被引:128
作者
Nurieva, RI
Duong, J
Kishikawa, H
Dianzani, U
Rojo, JM
Ho, IC
Flavell, RA
Dong, C [1 ]
机构
[1] Univ Washington, Sch Med, Dept Immunol, Seattle, WA 98195 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[3] A Avogadro Univ Eastern Piedmont, Interdisciplinary Res Ctr Autoimmune Dis, I-28100 Novara, Italy
[4] A Avogadro Univ Eastern Piedmont, Dept Med Sci, I-28100 Novara, Italy
[5] CSIC, Ctr Invest Biol, Dept Immunol, E-28006 Madrid, Spain
[6] Brigham & Womens Hosp, Dept Med, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[7] Yale Univ, Sch Med, Howard Hughes Med Inst, Div Immunobiol, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1074-7613(03)00144-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Helper T (Th) cell differentiation is accompanied by complex transcriptional changes. Although costimulatory receptors are important in Th differentiation, the underlying mechanisms are poorly understood. Here we examine the transcriptional mechanisms by which ICOS regulates Th2 differentiation and selective IL-4 expression by effector T cells. We found impaired expression of c-Maf transcription factor functionally associated with the IL-4 defect in ICOS-/- cells. c-Maf expression in effector cells was regulated by IL-4 levels during Th differentiation. ICOS costimulation potentiated the T cell receptor (TcR)-mediated initial IL-4 production, possibly through the enhancement of NFATc1 expression. These data indicate that ICOS, by enhancing TcR signals at an early stage of T cell activation, regulates IL-4 transcription and T cell function in effector cells.
引用
收藏
页码:801 / 811
页数:11
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