Differential requirements for IL-4/STAT6 signalling in CD4 T-cell fate determination and Th2-immune effector responses

被引:33
作者
Forbes, Elizabeth [1 ]
van Panhuys, Nicholas [2 ]
Min, Booki [3 ]
Le Gros, Graham [1 ]
机构
[1] Malaghan Inst Med Res, Wellington 6242, New Zealand
[2] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[3] Lerner Res Inst, Dept Immunol, Cleveland, OH USA
关键词
Th2; IL-4; STAT6; differentiation; effector response; ACTIVATED PROTEIN-KINASE; ANTIGEN-PRESENTING CELLS; TH2; IMMUNE-RESPONSES; VIVO IL-4 RESPONSES; IN-VIVO; DENDRITIC CELLS; CUTTING EDGE; NIPPOSTRONGYLUS-BRASILIENSIS; AIRWAYS HYPERREACTIVITY; EXPERIMENTAL ASTHMA;
D O I
10.1038/icb.2009.101
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Improved analytical tools have revealed that the development and expression of a Th2 immune response can be broken down into distinct stages with respect to the cytokine microenvironment that is required. Although IL-4 and its STAT6-signalling pathway are critical for the expression of Th2 effector immune responses in peripheral tissues such as the skin, lung and gut, IL-4 and STAT6 signalling are not required for the initial generation of IL-4-producing Th2 cells in the lymph node. This finding reveals that we have yet to identify the key cytokine or microenvironment that stimulates the development of this most intriguing CD4(+) T-helper subset and emphasises the tissue specificity and timing of IL-4/STAT6-dependent Th2 effector responses. Immunology and Cell Biology (2010) 88, 240-243; doi: 10.1038/icb.2009.101; published online 15 December 2009
引用
收藏
页码:240 / 243
页数:4
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