The Th17-IL-9 mast cell axis in inflammatory disease
The Th17-IL-9 mast cell axis in inflammatory disease
批准号:
7895444
负责人:
RANDOLPH J. NOELLE
金额:
$31.6万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-06-15 至 2012-05-31
关键词:
AdoptedAntigen PresentationAntigensAutoimmune DiseasesCell physiologyCellsClinicalCoinConnective TissueDataDevelopmentDifferentiation and GrowthDiseaseEncephalomyelitisExperimental Autoimmune EncephalomyelitisGenesIL6 geneIL9 geneIn VitroInflammationInflammatoryInterleukin-6Interleukin-9LinkMediatingMediator of activation proteinMusNamesProductionRoleT-LymphocyteT-Lymphocyte Subsetsautocrinecell growthcytokinein vivointerleukin-23mast cellnovel strategiesparacrinepublic health relevancerecombinaseresponse
中文摘要
描述(由申请人提供):历史上,IL-9已被证明是一种th2产生的细胞因子,其功能主要归因于调节肥大细胞(MC)的生长和分化。这项研究的一个关键发现是,Th17产生的IL-9比其他任何分化的T细胞都要多得多,IL-9对Th17产生自分泌作用,而IL-9有助于Th17炎症性疾病EAE。这些发现从根本上挑战了对这种细胞因子的概念理解,并要求重新探索这种细胞因子作为th17驱动炎症的介质。因此,本R21的具体目标是1。重新探讨IL-9对T细胞功能的自分泌和旁分泌作用。似乎Th17产生il -9,而IL-9R KO Th17的分化减弱。因此,我们将定义IL-9在体外和体内对Th17分化和功能的自分泌作用。由于Th17产生如此高水平的IL-9,而IL-9是一种有效的MC生长和分化因子,我们将量化IL-9对Th17同源和非同源与MC相互作用的旁分泌作用。确定th17 - il -9肥大细胞轴是否存在,是否介导炎症?已经确定Th17是中枢神经系统炎症性疾病实验性自身免疫性脑脊髓炎(EAE)发展的核心。此外,MC与促进疾病发展有关。我们的目的是将Th17产生IL-9与MC激活导致EAE发展的关键因素因果联系起来。
英文摘要
DESCRIPTION (provided by applicant): Historically, IL-9 has been shown to be a Th2-produced cytokine whose function was mostly attributed to regulating the growth and differentiation of mast cells (MC). A key finding of this proposal is that Th17 produce far greater amounts of IL-9 then do any other differentiated T cells, that IL-9 exerts autocrine effects on Th17, and IL-9 contributes to the Th17 inflammatory disease EAE. These findings fundamentally challenge the conceptual understanding of this cytokine and warrant a re-exploration of this cytokine as a mediator of Th17-driven inflammation. Therefore, the specific aims of this R21 are 1. Re-explore the autocrine and paracrine effects of IL-9 on T cell function. It appears that Th17 produce IL9 and IL-9R KO Th17 have blunted differentiation. As such, we will define the autocrine effects of IL-9 in vitro and in vivo on Th17 differentiation and function. Because Th17 produce such high levels of IL-9 and IL-9 is a potent MC growth and differentiation factor, we will quantify the paracrine effects of IL-9 on Th17 cognate and non- cognate interactions with MC. 2. Determine if the Th17-IL-9-Mast cell axis exists and if it mediates inflammation? It is well established that Th17 are central to the development of the CNS inflammatory disease, experimental autoimmune encephalomyelitis (EAE). Furthermore, MC have been implicated in facilitating disease development. It is our intent to causally link the production of IL-9 by Th17 as a critical factor in MC activation leading to the development of EAE.
PUBLIC HEALTH RELEVANCE: We describe a new function of IL9 in mediating inflammatory diseases. Given that anti-IL9 is currently in clinical development, these studies open up the exciting possibilities of using anti-IL9 in the treatment of autoimmune disease.
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