A role for TSLP in the development of inflammation in an asthma model

被引:396
作者
Al-Shami, A
Spolski, R
Kelly, J
Keane-Myers, A
Leonard, WJ [1 ]
机构
[1] NHLBI, Lab Mol Immunol, NIH, Bethesda, MD 20892 USA
[2] NIAID, Lab Allerg Dis, NIH, Rockville, MD 20852 USA
关键词
D O I
10.1084/jem.20050199
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thymic stromal lymphopoietin (TSLP) is a cytokine that promotes CD4(+) T cell homeostasis. We now demonstrate that TSLP is required to mount a normal CD4(+) T cell-mediated inflammatory response. TSLP acts directly on naive, but not, memory CD4(+) T cells, and promotes their proliferation in response to antigen. In addition, TSLP exerts an effect indirectly through DCs to promote Th2 differentiation of CD4(+) T cells. Correspondingly, TSLP receptor (TSLPR) knockout (KO) mice exhibit strong Th1 responses, with high levels of interleukin (IL)-12, interferon-gamma, and immunoglobulin (Ig) G2a, but low production of IL- 4, - 5, - 10, - 13, and IgE; moreover, CD4(+) T cells from these animals proliferate less well in response to antigen. Furthermore, TSLPR KO mice fail to develop an inflammatory lung response to inhaled antigen unless supplemented with wild-type CD4(+) T cells. This underscores an important role for this cytokine in the development of inflammatory and/or allergic responses in vivo.
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收藏
页码:829 / 839
页数:11
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