Immune Complex Stimulation of TNFalpha

TNFα 的免疫复合物刺激

• 批准号: 6873752
• 负责人: KATHLEEN E SULLIVAN
• 金额: $ 31.82万
• 依托单位: CHILDREN'S HOSP OF PHILADELPHIA
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-04-15 至 2008-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6873752
• 关键词: acetylation; antibody receptor; biological signal transduction; chromatin; clinical research; gene mutation; genetic polymorphism; histones; human subject; immune complex; interferon gamma; macrophage; molecular pathology; monocyte; nucleosomes; systemic lupus erythematosus; tissue /cell culture; transcription factor; transfection; tumor necrosis factor alpha

DESCRIPTION (provided by applicant): Systemic lupus erythematosus (SLE) is an autoimmune/inflammatory disorder in which multiple susceptibility genes have been identified. The genes implicated in SLE fall into four categories: [1] antigen presentation, [2] immune complex clearance, [3] dysregulated antibody production, and [4] dysregulated T cell function. FcgammaR plays a dominant role in the uptake of immune complexes in SLE patients who are hypocomplementemic. These receptors are widely expressed on hematopoietic cells and mediate inflammatory responses to IgG and IgG-immune complexes in addition to acting as receptors for their clearance. Inflammatory responses include phagocytosis, antibody-dependent cell-mediated cytotoxicity, release of cytokines, and release of reactive oxygen intermediates. Regulation of FcgammaR responses depends upon the balance achieved by signals transduced by activating receptors and signals transduced by inhibitory receptors. Our preliminary data suggest that macrophage responses to immune complexes are highly dependent on maturational status and milieu. We hypothesize that FcgammaR polymorphisms associated with decreased binding result in impaired clearance of immune complexes, particularly in SLE patients with active disease and hypocomplementemia. These circulating immune complexes deposit in end organs and incite an inflammatory response. The precise nature of the response depends critically on the prior experience or exposures of the responding cells, maturational status, and milieu. This sensitivity to environmental cues is probably required by a system that mediates both uptake, in which an inflammatory response is undesirable, and response to infection, in which an inflammatory response is desirable. To investigate the role of FcgammaR in SLE, we will determine the role of FcgammaR polymorphisms in the susceptibility to SLE. In specific aim 2, we will define the signaling pathways important in the responses to immune complexes and transcription factors relevant for the response of the TNFalpha gene to immune complexes. In the third aim, we will define the role of chromatin in the regulation of responses to immune complexes.

描述（由申请人提供）：系统性红斑狼疮（SLE）是一种自身免疫性/炎症性疾病，其中已鉴定出多种易感基因。与SLE有关的基因分为四类：[1]抗原呈递，[2]免疫复合物清除，[3]抗体产生失调，[4] T细胞功能失调。Fc γ R在低补体血症的SLE患者的免疫复合物摄取中起主导作用。这些受体在造血细胞上广泛表达，除了作为清除IgG和IgG-免疫复合物的受体外，还介导对IgG和IgG-免疫复合物的炎症反应。炎症反应包括吞噬作用、抗体依赖性细胞介导的细胞毒性、细胞因子的释放和活性氧中间体的释放。Fc γ R应答的调节取决于通过活化受体转导的信号和抑制性受体转导的信号实现的平衡。我们的初步数据表明，巨噬细胞对免疫复合物的反应高度依赖于成熟状态和环境。我们推测FcgammaR多态性与结合减少相关，导致免疫复合物清除受损，特别是在活动性疾病和低补体血症的SLE患者中。这些循环免疫复合物存款在终末器官中并引起炎症反应。反应的确切性质主要取决于反应细胞的先前经历或暴露、成熟状态和环境。这种对环境线索的敏感性可能是介导摄取（其中炎症反应是不希望的）和对感染的反应（其中炎症反应是希望的）的系统所需要的。为了研究Fc γ R在SLE中的作用，我们将确定Fc γ R多态性在SLE易感性中的作用。在具体目标2中，我们将定义在对免疫复合物的应答中重要的信号传导途径和与TNF α基因对免疫复合物的应答相关的转录因子。在第三个目标中，我们将定义染色质在调节免疫复合物反应中的作用。