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1型糖尿病中的CD8 + T细胞。

CD8+ T cells in type 1 diabetes.

作者信息

Tsai Sue, Shameli Afshin, Santamaria Pere

机构信息

Julia McFarlane Diabetes Research Centre (JMDRC), Department of Microbiology and Infectious Diseases, Canada.

出版信息

Adv Immunol. 2008;100:79-124. doi: 10.1016/S0065-2776(08)00804-3.

DOI:10.1016/S0065-2776(08)00804-3
PMID:19111164
Abstract

Type 1 diabetes (T1D), an autoimmune disease once thought to be mediated exclusively by beta cell-specific CD4+ T cells, is now recognized as one in which autoreactive CD8+ T cells play a fundamental role. In the nonobese diabetic (NOD) mouse model, CD8+ T effector cells take centre stage in the destruction of pancreatic beta cells and contribute to sustaining islet inflammation. Recent investigations have elucidated the mechanisms underlying the activation, homing, and beta cell destructive properties of this type of cells. Another important area is the development and testing of novel preemptive or therapeutic "vaccines" that, by targeting effector and/or regulatory autoreactive CD8+ T cell specificities may be able to induce immunological tolerance to beta cells. In humans, our understanding of the role of CD8+ T cells in T1D is also growing, through genetic linkage analyses, as well as epitope identification and characterization of disease-relevant CD8+ T cell responses in patient blood samples. The following review discusses these important advances and how they can converge towards the goal of developing an antigen-specific immunotherapy for T1D.

摘要

1型糖尿病(T1D)是一种曾被认为仅由β细胞特异性CD4 + T细胞介导的自身免疫性疾病,现在被认为是一种自身反应性CD8 + T细胞起关键作用的疾病。在非肥胖糖尿病(NOD)小鼠模型中,CD8 + T效应细胞在胰腺β细胞破坏中占据核心地位,并有助于维持胰岛炎症。最近的研究阐明了这类细胞的激活、归巢和β细胞破坏特性的潜在机制。另一个重要领域是新型预防性或治疗性“疫苗”的开发和测试,这些“疫苗”通过靶向效应和/或调节性自身反应性CD8 + T细胞特异性,可能能够诱导对β细胞的免疫耐受。在人类中,通过遗传连锁分析以及患者血液样本中疾病相关CD8 + T细胞反应的表位鉴定和表征,我们对CD8 + T细胞在T1D中的作用的理解也在不断加深。以下综述讨论了这些重要进展以及它们如何朝着开发针对T1D的抗原特异性免疫疗法的目标汇聚。

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1
CD8+ T cells in type 1 diabetes.1型糖尿病中的CD8 + T细胞。
Adv Immunol. 2008;100:79-124. doi: 10.1016/S0065-2776(08)00804-3.
2
The good turned ugly: immunopathogenic basis for diabetogenic CD8+ T cells in NOD mice.美好走向丑恶:非肥胖糖尿病(NOD)小鼠中致糖尿病CD8 + T细胞的免疫致病基础。
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CD8(+) T cells specific for beta cells encounter their cognate antigens in the islets of NOD mice.对β细胞具有特异性的CD8(+) T细胞在非肥胖糖尿病(NOD)小鼠的胰岛中遇到其同源抗原。
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Beta cells cannot directly prime diabetogenic CD8 T cells in nonobese diabetic mice.在非肥胖糖尿病小鼠中,β细胞不能直接启动致糖尿病的CD8 T细胞。
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Identification of an MHC class I-restricted autoantigen in type 1 diabetes by screening an organ-specific cDNA library.通过筛选器官特异性cDNA文库鉴定1型糖尿病中一种MHC I类限制性自身抗原。
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"Humanized" HLA transgenic NOD mice to identify pancreatic beta cell autoantigens of potential clinical relevance to type 1 diabetes.“人源化” HLA转基因NOD小鼠,用于鉴定与1型糖尿病具有潜在临床相关性的胰腺β细胞自身抗原。
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Selective destruction of mouse islet beta cells by human T lymphocytes in a newly-established humanized type 1 diabetic model.在新建立的人源化 1 型糖尿病模型中,人 T 淋巴细胞对小鼠胰岛β细胞的选择性破坏。
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Methods Mol Biol. 2010;602:119-34. doi: 10.1007/978-1-60761-058-8_8.

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