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Insulin gene VNTR genotype associates with frequency and phenotype of the autoimmune response to proinsulin.

机译:胰岛素基因VNTR基因型与对胰岛素原的自身免疫反应的频率和表型有关。

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摘要

Immune responses to autoantigens are in part controlled by deletion of autoreactive cells through genetically regulated selection mechanisms. We have directly analyzed peripheral CD4+ proinsulin (PI) 76-90 (SLQPLALEGSLQKRG)-specific T cells using soluble fluorescent major histocompatibility complex class II tetramers. Subjects with type I diabetes and healthy controls with high levels of peripheral proinsulin-specific T cells were characterized by the presence of a disease-susceptible polymorphism in the insulin variable number of tandem repeats (INS-VNTR) gene. Conversely, subjects with a 'protective' polymorphism in the INS-VNTR gene had nearly undetectable levels of proinsulin tetramer-positive T cells. These results strongly imply a direct relationship between genetic control of autoantigen expression and peripheral autoreactivity, in which proinsulin genotype restricts the quantity and quality of the potential T-cell response. Using a modified tetramer to isolate low-avidity proinsulin-specific T cells from subjects with the susceptible genotype, transcript arrays identified several induced pro-apoptotic genes in the control, but not diabetic subjects, likely representing a second peripheral mechanism for maintenance of tolerance to self antigens.
机译:对自身抗原的免疫反应部分通过基因调控的选择机制通过自身反应性细胞的缺失来控制。我们已经使用可溶性荧光主要组织相容性复合物II类四聚体直接分析了外周CD4 +胰岛素原(PI)76-90(SLQPLALEGSLQKRG)特异性T细胞。 I型糖尿病患者和具有高水平外周胰岛素原特异性T细胞的健康对照组的特征是在胰岛素可变数目的串联重复序列(INS-VNTR)基因中存在疾病易感多态性。相反,在INS-VNTR基因中具有“保护性”多态性的受试者的胰岛素原四聚体阳性T细胞水平几乎检测不到。这些结果强烈暗示了自身抗原表达的遗传控制与周围自身反应之间的直接关系,其中胰岛素原基因型限制了潜在T细胞反应的数量和质量。使用修饰的四聚体从具有易感基因型的受试者中分离出低亲和力的胰岛素原特异性T细胞,转录本阵列可在对照组而非糖尿病受试者中鉴定出几种诱导的促凋亡基因,这可能代表了维持耐受性的第二种外围机制自身抗原。

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