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参与III期谷氨酸脱羧酶-明矾干预试验的1型糖尿病患者的细胞免疫和体液免疫反应。

Cellular and humoral immune responses in type 1 diabetic patients participating in a phase III GAD-alum intervention trial.

作者信息

Axelsson Stina, Chéramy Mikael, Akerman Linda, Pihl Mikael, Ludvigsson Johnny, Casas Rosaura

机构信息

Corresponding author: Mikael Chéramy,

出版信息

Diabetes Care. 2013 Nov;36(11):3418-24. doi: 10.2337/dc12-2251. Epub 2013 Jul 17.

Abstract

OBJECTIVE

GAD formulated in aluminum hydroxide (GAD-alum) has previously been shown to induce preservation of residual insulin secretion in recent-onset type 1 diabetes, but recent phase II and III GAD-alum trials failed to reach primary outcomes. The European phase III study was therefore closed after 15 months, and only a minority of patients completed the 30 months of follow-up.

RESEARCH DESIGN AND METHODS

This study aimed to characterize cellular and humoral responses in the Swedish patients (n = 148) participating in the phase III trial, receiving four (4D) or two (2D) GAD-alum doses or placebo. Serum GAD65 antibody (GADA) levels, GADA IgG1-4 subclass distribution, cytokine secretion, and proliferative responses in peripheral blood mononuclear cells (PBMCs) were analyzed.

RESULTS

The GAD65-induced cytokine profile tended to switch toward a predominant Th2-associated profile over time both in the 2D and 4D group. The groups also displayed increased GADA levels and PBMC proliferation compared with placebo, whereas GADA IgG subclass distribution changed in 4D patients.

CONCLUSIONS

Both 2D and 4D patients displayed GAD65-specifc cellular and humoral effects after GAD-alum treatment, but at different time points and magnitudes. No specific immune markers could be associated with treatment efficacy.

摘要

目的

先前研究表明,氢氧化铝配制的谷氨酸脱羧酶(GAD-明矾)可诱导新发1型糖尿病患者保留残余胰岛素分泌,但近期的II期和III期GAD-明矾试验未达到主要结局。因此,欧洲的III期研究在15个月后结束,只有少数患者完成了30个月的随访。

研究设计与方法

本研究旨在对参与III期试验的瑞典患者(n = 148)的细胞和体液反应进行特征分析,这些患者接受了四剂(4D)或两剂(2D)GAD-明矾或安慰剂。分析了血清GAD65抗体(GADA)水平、GADA IgG1-4亚类分布、细胞因子分泌以及外周血单核细胞(PBMC)的增殖反应。

结果

随着时间的推移,2D组和4D组中GAD65诱导的细胞因子谱都倾向于转向以Th2相关为主的谱型。与安慰剂相比,这两组患者的GADA水平和PBMC增殖也有所增加,而4D组患者的GADA IgG亚类分布发生了变化。

结论

2D组和4D组患者在接受GAD-明矾治疗后均表现出GAD65特异性的细胞和体液效应,但时间点和程度不同。没有特定的免疫标志物与治疗效果相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ab/3816912/1c3c27fe93ed/3418fig1.jpg

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