Alternatively activated dendritic cells regulate CD4+ T-cell polarization in vitro and in vivo

被引:95
作者
Cook, Peter C. [1 ]
Jones, Lucy H. [1 ]
Jenkins, Stephen J. [1 ]
Wynn, Thomas A. [2 ]
Allen, Judith E. [1 ]
MacDonald, Andrew S. [1 ]
机构
[1] Univ Edinburgh, Inst Immunol & Infect Res, Ctr Immun Infect & Evolut, Sch Biol Sci, Edinburgh EH9 3JT, Midlothian, Scotland
[2] NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
基金
英国医学研究理事会; 英国惠康基金;
关键词
antigen presenting cells; T lymphocytes; innate immunity; adaptive immunity; IL-12; PRODUCTION; INTERLEUKIN (IL)-4; LECTIN RECEPTORS; IMMUNE-RESPONSES; TH2; INDUCTION; INFLAMMATION; EXPRESSION; MOUSE; MACROPHAGES; CHITINASE;
D O I
10.1073/pnas.1121231109
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
Interleukin-4 is a cytokine widely known for its role in CD4(+) T cell polarization and its ability to alternatively activate macrophage populations. In contrast, the impact of IL-4 on the activation and function of dendritic cells (DCs) is poorly understood. We report here that DCs respond to IL-4 both in vitro and in vivo by expression of multiple alternative activation markers with a different expression pattern to that of macrophages. We further demonstrate a central role for DC IL-4R alpha expression in the optimal induction of IFN gamma responses in vivo in both Th1 and Th2 settings, through a feedback loop in which IL-4 promotes DC secretion of IL-12. Finally, we reveal a central role for RELM alpha during T-cell priming, establishing that its expression by DCs is critical for optimal IL-10 and IL-13 promotion in vitro and in vivo. Together, these data highlight the significant impact that IL-4 and RELM alpha can have on DC activation and function in the context of either bacterial or helminth pathogens.
引用
收藏
页码:9977 / 9982
页数:6
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