Interferon-Regulatory Factor 4 Is Essential for the Developmental Program of T Helper 9 Cells

被引:485
作者
Staudt, Valerie [1 ]
Bothur, Evita [3 ]
Klein, Matthias [1 ]
Lingnau, Karen [4 ]
Reuter, Sebastian [2 ]
Grebe, Nadine [1 ]
Gerlitzki, Bastian [1 ]
Hoffmann, Markus [1 ]
Ulges, Alexander [1 ]
Taube, Christian [2 ]
Dehzad, Nina [2 ]
Becker, Marc [1 ]
Stassen, Michael [1 ]
Steinborn, Andrea [5 ]
Lohoff, Michael [3 ]
Schild, Hansjoerg [1 ]
Schmitt, Edgar [1 ]
Bopp, Tobias [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Immunol, D-55131 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Ill Med Clin, D-55131 Mainz, Germany
[3] Inst Med Mikrobiol & Krankenhaushyg, D-35043 Marburg, Germany
[4] Intercell AG, Vienna, Austria
[5] Univ Heidelberg, Dept Obstet & Gynecol, D-69115 Heidelberg, Germany
关键词
GROWTH-FACTOR-BETA; TRANSCRIPTION FACTOR; TGF-BETA; BRONCHIAL HYPERRESPONSIVENESS; MONOCLONAL-ANTIBODY; IL-9; EXPRESSION; GENE-EXPRESSION; WORM EXPULSION; FACTOR PU.1; ASTHMA;
D O I
10.1016/j.immuni.2010.07.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interferon-regulatory factor 4 (IRF4) is essential for the development of T helper 2 (Th2) and Th17 cells. Herein, we report that IRF4 is also crucial for the development and function of an interleukin-9 (IL-9)-producing CD4(+) T cell subset designated Th9. IRF4-deficient CD4(+) T cells failed to develop into IL-9-producing Th9 cells, and IRF4-specific siRNA inhibited IL-9 production in wild-type CD4(+) T cells. Chromatin-immunoprecipitation (ChIP) analyses revealed direct IRF4 binding to the II9 promoter in Th9 cells. In a Th9-dependent asthma model, neutralization of IL-9 substantially ameliorated asthma symptoms. The relevance of these findings is emphasized by the fact that the induction of IL-9 production also occurs in human CD4(+) T cells accompanied by the upregulation of IRF4. Our data clearly demonstrate the central function of IRF4 in the development of Th9 cells and underline the contribution of this T helper cell subset to the pathogenesis of asthma.
引用
收藏
页码:192 / 202
页数:11
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