IL-1 family members and STAT activators induce cytokine production by Th2, Th17, and Th1 cells

被引:329
作者
Guo, Liying [1 ]
Wei, Gang [2 ]
Zhu, Jinfang [1 ]
Liao, Wei [2 ]
Leonard, Warren J. [2 ]
Zhao, Keji [2 ]
Paul, William [1 ]
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Lab Mol Immunol, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
IL-33; TSLP; IL-18; STAT5; T1ST2; INTERFERON-GAMMA PRODUCTION; RECEPTOR ACCESSORY PROTEIN; CD4(+) T-CELLS; NF-KAPPA-B; EXPRESSION; DIFFERENTIATION; INTERLEUKIN-13; T1/ST2; TRANSCRIPTION; REQUIREMENT;
D O I
10.1073/pnas.0906988106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Expression of T1ST2, the IL-33R, by Th2 cells requires GATA3. Resting Th2 cells express little GATA3, which is increased by IL-33 and a STAT5 activator, in turn increasing T1ST2 from its low-level expression on resting Th2 cells. Th2 cells that have upregulated T1ST2 produce IL-13, but not IL-4, in response to IL-33 plus a STAT5 activator in an antigen-independent, NF-kappa B-dependent, cyclosporin A (CsA)-resistant manner. Similarly, Th17 cells produce IL-17A in response to IL-1 beta and a STAT3 activator and Th1 cells produce IFN gamma in response to IL-18 and a STAT4 inducer. Thus, each effector Th cell produces cytokines without antigenic stimulation in response to an IL-1 family member and a specific STAT activator, implying an innate mechanism through which memory CD4 T cells are recruited by an induced cytokine environment.
引用
收藏
页码:13463 / 13468
页数:6
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