4.8 Article

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

Journal

IMMUNITY
Volume 33, Issue 2, Pages 192-202

Publisher

CELL PRESS
DOI: 10.1016/j.immuni.2010.07.014

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Funding

  1. Deutsche Forschungsgemeinschaft DFG [SFB TR52 TPA1, SFB 548 A6, SFB TR22, GRK 767, GRK 1043]
  2. International Graduate School of Immunotherapy
  3. Carl Zeiss Foundation
  4. Forschungszentrum Immunologie (FZI)
  5. Asthma Core Facility, JGU Mainz

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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.

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