Division of Paediatrics and Diabetes Research Centre, Department of Clinical and Experimental Medicine, Linköping University, Sweden.
Clin Immunol. 2010 Oct;137(1):31-40. doi: 10.1016/j.clim.2010.06.001. Epub 2010 Jun 30.
We have previously shown that two injections of 20 μg GAD-alum to recent onset type 1 diabetic children induced GADA levels in parallel to preservation of insulin secretion. Here we investigated if boosted GADA induced changes in IgG1, 2, 3 and 4 subclass distributions or affected GAD(65) enzyme activity. We further studied the specific effect of GAD-alum through analyses of IA-2A, tetanus toxoid and total IgE antibodies. Serum from children receiving GAD-alum or placebo was collected pre-treatment and after 3, 9, 15 and 21 months. At 3 months a reduced percentage of IgG1 and increased IgG3/IgG4 were detected in GAD-alum treated. Further, IA-2A, IgE and tetanus toxoid antibodies, as well as GAD(65) enzyme activity, were unaffected confirming the specific effect of treatment. In the GAD-alum group, higher pre-treatment GADA were associated to more pronounced C-peptide preservation. The induced IgG3/IgG4 and reduced IgG1 suggest a Th2 deviation of the immune response.
我们之前的研究表明,对近期发病的 1 型糖尿病患儿进行两剂 20μg GAD 铝佐剂注射,可在保持胰岛素分泌的同时诱导 GADA 水平升高。在此,我们研究了增强的 GADA 是否会引起 IgG1、2、3 和 4 亚类分布的变化,或影响 GAD(65)酶活性。我们通过分析 IA-2A、破伤风类毒素和总 IgE 抗体进一步研究了 GAD 铝佐剂的特定作用。在接受 GAD 铝佐剂或安慰剂治疗的儿童中,于治疗前和治疗后 3、9、15 和 21 个月采集血清。在 3 个月时,发现 GAD 铝佐剂治疗组 IgG1 的百分比降低,而 IgG3/IgG4 增加。此外,IA-2A、IgE 和破伤风类毒素抗体以及 GAD(65)酶活性不受影响,这证实了治疗的特异性。在 GAD 铝佐剂组中,较高的治疗前 GADA 与更明显的 C 肽保存相关。诱导的 IgG3/IgG4 和降低的 IgG1 提示免疫反应存在 Th2 偏移。