SHP 1 Regulates Conventional T cell Resistance to Regulatory T Cell Suppression

SHP 1 调节传统 T 细胞对调节性 T 细胞抑制的抵抗

• 批准号: 9081482
• 负责人: Emily R Mercadante
• 金额: $ 3.21万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-07-01 至 2017-06-25
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9081482
• 关键词: Address; Affect; Antigens; Autoimmune Diseases; Autoimmune Process; Autoimmunity; CD4 Positive T Lymphocytes; CD8B1 gene; Cell Lineage; Cells; Clinical Trials; Data; Disease model; Equilibrium; Exhibits; Genetic Models; Goals; Health; Hematopoietic; Homeostasis; Human; IL2RA gene; Immune; Immune response; Immune system; Immunotherapy; In Vitro; Inflammation; Life; Light; Malignant Neoplasms; Mediating; Modeling; Molecular; Molecular Target; Mus; Mutation; Outcome; PTPN6 gene; Pathway interactions; Patients; Phase I Clinical Trials; Phenotype; Phosphatidylinositols; Phosphotransferases; Play; Population; Predisposition; Protein Tyrosine Phosphatase; Proteins; RNA Splicing; Receptor Signaling; Regulatory T-Lymphocyte; Research; Resistance; Role; Signal Pathway; Signaling Molecule; Solid; Stibogluconate Sodium; T-Cell Proliferation; T-Cell Receptor; T-Lymphocyte; Testing; Therapeutic Intervention; Time; Tumor Immunity; Work; antitumor effect; cancer therapy; clinically relevant; improved; in vivo; inhibitor/antagonist; insight; leukemia; melanoma; molecular drug target; mouse model; prevent; receptor-mediated signaling; response; targeted treatment; tumor; tumor growth; tumor microenvironment

DESCRIPTION (provided by applicant): The goal of this proposal is to understand the molecular mechanism that governs conventional T (Tcon) cell resistance to regulatory T cell (Treg)-mediated suppression and identify potential molecular targets for use in immunotherapy. Research over the past decade has demonstrated that Treg cells are a crucial component for a healthy immune system. Once activated through their T cell receptor (TCR), Treg cells can suppress a wide range of immune cells. It is becoming evident that in many autoimmune diseases, Treg cells remain functional, yet fail to control Tcon cells. At the same time, Treg cell hinder anti-tumor immunity by creating a suppressive tumor microenvironment. Therefore, it is important to understand what determines if a Treg cell is able to successfully suppress its target, and how this plays a role in both autoimmune disease and cancer. My research focuses on the Src homology 2 domain- containing protein tyrosine phosphatase 1 (SHP-1), a well-characterized negative regulator of TCR-mediated signaling. Using three different genetic models of SHP-1 deficiency, I have recently found that SHP-1 regulates the susceptibility of Tcon cells to suppression, such that SHP-1-deficient Tcon cells display increased resistance to wt Treg-mediated suppression. In preliminary data, I have shown that Tcon cells derived from motheaten mice, which lack SHP-1 expression in all hematopoietic cells, are resistant to Treg-mediated suppression. I also observed a comparable resistance in Tcon cells from two different mouse models, carrying a T cell specific deletion of SHP-1, indicating that the SHP-1-dependent resistance to suppression is a T cell-intrinsic effect. Moreover, treatment of mice with sodium stibogluconate (SSG), a pharmacological SHP-1 inhibitor, also rendered Tcon cells resistant to Treg-mediated suppression, further reinforcing the role of SHP-1 in regulating Tcon cell susceptibility to Treg suppression. Interestingly, SSG is in phase I clinical trials for solid tumo immunotherapy, yet its anti-tumor mechanism remains unclear. The proposed study will shed light on how SSG might be augmenting Tcon cells' ability to resist Treg-mediated suppression and mount a more effective anti-tumor response. This proposal will address the role of SHP-1 in CD4+ and CD8+ T cell susceptibility to Treg mediated suppression both at the level of intracellular signaling pathways as well as in vivo in models of autoimmune disease, inflammation, and anti-tumor immunity. From these studies, I will identify possible molecular drug targets, the modulation of which would either induce Tcon cell susceptibility to Treg-suppression for treatment of autoimmune disease, or allow Tcon cells to resist Treg suppression for treatment of cancer.

描述（由申请人提供）：本提案的目的是了解控制常规T（Tcon）细胞对调节性T细胞（Treg）介导的抑制的耐药性的分子机制，并确定用于免疫治疗的潜在分子靶点。过去十年的研究表明，Treg细胞是健康免疫系统的重要组成部分。一旦通过其T细胞受体（TCR）激活，Treg细胞可以抑制广泛的免疫细胞。越来越明显的是，在许多自身免疫性疾病中，Treg细胞保持功能性，但不能控制Tcon细胞。同时，Treg细胞通过创造抑制性肿瘤微环境来阻碍抗肿瘤免疫。因此，重要的是要了解是什么决定了Treg细胞是否能够成功抑制其靶点，以及这在自身免疫性疾病和癌症中如何发挥作用。我的研究集中在Src同源2结构域包含蛋白酪氨酸磷酸酶1（SHP-1），一个良好的表征TCR介导的信号负调节。使用SHP-1缺陷的三种不同遗传模型，我最近发现SHP-1调节Tcon细胞对抑制的敏感性，使得SHP-1缺陷的Tcon细胞显示对wt Treg介导的抑制的抗性增加。在初步的数据中，我已经表明，Tcon细胞来源于飞蛾，缺乏SHP-1在所有造血细胞的表达，是耐Treg介导的抑制。我还观察到来自两种不同小鼠模型的Tcon细胞具有相当的抗性，携带SHP-1的T细胞特异性缺失，表明SHP-1依赖性抑制抗性是T细胞内在效应。此外，用SHP-1药理学抑制剂葡萄糖酸锑钠（SSG）治疗小鼠，也使Tcon细胞对Treg介导的抑制产生抗性，进一步加强了SHP-1在调节Tcon细胞对Treg抑制的敏感性中的作用。有趣的是，SSG正在进行实体瘤免疫治疗的I期临床试验，但其抗肿瘤机制仍不清楚。这项研究将揭示SSG如何增强Tcon细胞抵抗Treg介导的抑制的能力，并产生更有效的抗肿瘤反应。该提案将解决SHP-1在CD 4+和CD 8 + T细胞对Treg介导的抑制的易感性中的作用，在细胞内信号传导途径的水平以及在自身免疫性疾病、炎症和抗肿瘤免疫的模型中的体内。从这些研究中，我将确定可能的分子药物靶点，其调节将诱导Tcon细胞对Treg抑制的易感性以治疗自身免疫性疾病，或允许Tcon细胞抵抗Treg抑制以治疗癌症。