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Absolute Requirement of Macrophages for the Development and Activation of β-Cell Cytotoxic CD8+ T-Cells in T-Cell Receptor Transgenic NOD Mice

机译:巨噬细胞对T细胞受体转基因NOD小鼠中β细胞细胞毒性CD8 + T细胞的发育和激活的绝对要求

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The development of autoimmune diabetes in NOD mice results from selective destruction of β-cells by a T- cell-dependent autoimmune process. However, the mechanisms that control the generation of β-cell cyto- toxic T-cells inv vivo are poorly understood. We recently established 8.3-T-cell receptor (TCR)-β transgenic NOD mice that show a selective acceleration of the Recruitment of CD8+ T-cells into the islets of prediabetic Animals, resulting in rapid β-cell restruction and early Onset of diabetes. This study was initiated to deter- Mine the role of macrophages in the development and Activation of diabetogenic CD8+ T-cells in 8.3-TCR-β Transgenic NOD mice.
机译:NOD小鼠中自身免疫性糖尿病的发展是由依赖T细胞的自身免疫过程选择性破坏β细胞引起的。但是,对于体内控制β细胞细胞毒性T细胞生成的机制了解甚少。我们最近建立了8.3-T细胞受体(TCR)-β转基因NOD小鼠,该小鼠表现出选择性加速CD8 + T细胞向糖尿病前动物胰岛的募集,从而导致快速的β细胞重建和糖尿病的早期发作。这项研究的开始是为了确定巨噬细胞在8.3-TCR-β转基因NOD小鼠中糖尿病形成CD8 + T细胞的发育和激活中的作用。

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