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Detection of GAD65 Autoreactive T-Cells by HLA Class I Tetramers in Type 1 Diabetic Patients

机译:HLA I类四聚体在1型糖尿病患者中检测GAD65自反应性T细胞

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摘要

Type 1 diabetes (T1D) is an autoimmune disease, in which pancreatic β cells are destroyed in genetically predisposed individuals. While the direct contribution of autoantibodies to the disease pathogenesis is controversial, it is generally recognised that the mechanism of β cell destruction is mediated by autoreactive T cells that had escaped the thymic selection. We aimed to design a method to detect circulating CD8+ T cells autoreactive against an epitope of the glutamic acid decarboxylase autoantigen, isoform 65 (GAD65) ex vivo in T1D patients by using HLA class I tetramers. Low frequencies of GAD65 peptide-specific CD8+ cytotoxic T lymphocytes were detected in peripheral blood lymphocytes (PBMC) of normal controls after GAD65 peptide-specific stimulation. Conversely, their frequencies were significantly higher than in controls in PBMC of T1D patients after GAD65 peptide stimulation. These preliminary data are encouraging in order to develop a reliable assay to be employed in large-scale screening studies.
机译:1型糖尿病(T1D)是一种自身免疫性疾病,其中遗传上易患个体的胰腺β细胞被破坏。尽管自身抗体对疾病发病机理的直接贡献是有争议的,但通常认为β细胞破坏的机制是由逃避胸腺选择的自身反应性T细胞介导的。我们旨在设计一种方法,通过使用HLA I类四聚体,在T1D患者体内检测对谷氨酸脱羧酶自身抗原同工型65(GAD65)抗原决定簇自身反应的循环CD8 + T细胞。 GAD65肽特异性刺激后,正常对照组的外周血淋巴细胞(PBMC)中检测到GAD65肽特异性CD8 +细胞毒性T淋巴细胞的频率较低。相反,在GAD65肽刺激后,T1D患者的PBMC中它们的频率显着高于对照组。这些初步数据令人鼓舞,以便开发出可用于大规模筛选研究的可靠测定方法。

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