Institute for Immunology, University Medical Center of the Johannes Gutenberg-University Mainz, 55131 Mainz, Germany.
Immunity. 2010 Aug 27;33(2):192-202. doi: 10.1016/j.immuni.2010.07.014. Epub 2010 Jul 30.
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 Il9 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.
干扰素调节因子 4(IRF4)对于辅助性 T 细胞 2(Th2)和 Th17 细胞的发育是必需的。在此,我们报告称,IRF4 对于白细胞介素-9(IL-9)产生的 CD4(+) T 细胞亚群(称为 Th9)的发育和功能也是至关重要的。IRF4 缺陷型 CD4(+) T 细胞无法发育成为产生 IL-9 的 Th9 细胞,而 IRF4 特异性 siRNA 抑制野生型 CD4(+) T 细胞中 IL-9 的产生。染色质免疫沉淀(ChIP)分析显示,IRF4 直接结合 Th9 细胞中 Il9 启动子。在 Th9 依赖性哮喘模型中,中和 IL-9 可显著改善哮喘症状。这些发现的相关性在于,在人 CD4(+) T 细胞中也会发生 IL-9 产生的诱导,同时伴随着 IRF4 的上调。我们的数据清楚地表明了 IRF4 在 Th9 细胞发育中的核心作用,并强调了该辅助性 T 细胞亚群对哮喘发病机制的贡献。