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Rationale and study design of the Adaptive study of IL-2 dose on regulatory T cells in type 1 diabetes (DILT1D): a non-randomised open label adaptive dose finding trial

机译:IL-2剂量对1型糖尿病调节性T细胞(DILT1D)的适应性研究的理论基础和研究设计:一项非随机开放标签适应性剂量寻找试验

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摘要

IntroductionCD4 T regulatory cells (Tregs) are crucial for the maintenance of self-tolerance and are deficient in many common autoimmune diseases such as type 1 diabetes (T1D). Interleukin 2 (IL-2) plays a major role in the activation and function of Tregs and treatment with ultra-low dose (ULD) IL-2 could increase Treg function to potentially halt disease progression in T1D. However, prior to embarking on large phase II/III clinical trials it is critical to develop new strategies for determining the mechanism of action of ULD IL-2 in participants with T1D. In this mechanistic study we will combine a novel trial design with a clinical grade Treg assay to identify the best doses of ULD IL-2 to induce targeted increases in Tregs.
机译:简介CD4 T调节细胞(Tregs)对于维持自我耐受至关重要,并且缺乏许多常见的自身免疫性疾病,例如1型糖尿病(T1D)。白细胞介素2(IL-2)在Treg的激活和功能中起主要作用,超低剂量(ULD)IL-2的治疗可能会增加Treg功能,从而可能阻止T1D中疾病的发展。但是,在着手进行大型II / III期临床试验之前,至关重要的是,开发新的策略来确定T1D参与者中ULD IL-2的作用机制。在这项机理研究中,我们将新颖的试验设计与临床级Treg测定结合起来,以鉴定最佳剂量的ULD IL-2来诱导Treg的靶向增加。

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