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1型糖尿病的进展与谷氨酸脱羧酶(GAD65)自身抗体的免疫球蛋白同种型谱变化有关。芬兰儿童糖尿病研究小组。

Progression to type 1 diabetes is associated with a change in the immunoglobulin isotype profile of autoantibodies to glutamic acid decarboxylase (GAD65). Childhood Diabetes in Finland Study Group.

作者信息

Petersen J S, Kulmala P, Clausen J T, Knip M, Dyrberg T

机构信息

Novo-Nordisk A/S, Bagsvaerd, DK-2880, Denmark.

出版信息

Clin Immunol. 1999 Feb;90(2):276-81. doi: 10.1006/clim.1998.4641.

Abstract

To investigate whether type 1 diabetes in man is associated with a preferential Th1/Th2 response, and whether autoantibodies to one of the main autoantigens would reflect such a response, we characterized the immunoglobulin isotype profile to the 65-kDa isoform of glutamic acid decarboxylase (GAD65) in siblings to IDDM patients. Samples obtained from affected subjects before and at clinical onset of IDDM, from unaffected individuals at high risk and at low risk and from healthy controls were studied. The immunoglobulin isotype profile in the siblings at low risk reflected a more immature, i.e., IgM and Th2 like, i.e., IgE response compared to the progressors and siblings at high risk, with significantly higher median levels of IgM and IgE. The rank order of anti-GAD65 immunoglobulin isotypes was similar in the siblings before and at clinical onset of IDDM, IgG1 > IgG4 > IgM > IgE > IgA > IgG3 > IgG2, but markedly different in the individuals at low risk, IgG1 > IgM > IgE > IgG4 > IgG3 > IgA > IgG2. Based on these observations, we suggest that progression to clinical onset of IDDM is associated with a maturation and a decrease in the Th2 immune response against GAD65; findings which could have implications for future intervention and prediction strategies.

摘要

为了研究人类1型糖尿病是否与Th1/Th2反应偏好相关,以及针对主要自身抗原之一的自身抗体是否会反映出这种反应,我们对1型糖尿病患者的兄弟姐妹针对谷氨酸脱羧酶65-kDa异构体(GAD65)的免疫球蛋白同种型谱进行了特征分析。研究了从1型糖尿病患者发病前及临床发病时的患病个体、高风险和低风险的未患病个体以及健康对照者获取的样本。与进展期患者和高风险的兄弟姐妹相比,低风险的兄弟姐妹的免疫球蛋白同种型谱反映出更不成熟的反应,即IgM反应,以及类似Th2的反应,即IgE反应,IgM和IgE的中位水平显著更高。在1型糖尿病患者临床发病前及发病时,其兄弟姐妹中抗GAD65免疫球蛋白同种型的排序为IgG1 > IgG4 > IgM > IgE > IgA > IgG3 > IgG2,但在低风险个体中则明显不同,为IgG1 > IgM > IgE > IgG4 > IgG3 > IgA > IgG2。基于这些观察结果,我们认为进展至1型糖尿病临床发病与针对GAD65的Th2免疫反应的成熟和减弱有关;这些发现可能对未来的干预和预测策略具有重要意义。

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