Diabetes Research Center, Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium.
Expert Rev Clin Immunol. 2013 Dec;9(12):1173-83. doi: 10.1586/1744666X.2013.856757.
Type 1 diabetes is an incurable disease associated with risk of serious acute and chronic complications. It is caused by a marked loss in insulin-producing beta cells. Immune intervention at clinical onset can transiently suppress a further decline in residual functional beta cell mass, particularly in young patients with a higher residual insulin producing capacity at start of treatment. It might achieve a higher effect during the preclinical phase when the beta cell mass is not yet severely affected. Such prevention trials can be prepared by identifying individuals at very high risk to develop diabetes within 3 years and presenting signs of declining, yet relatively preserved, functional beta cell mass. This article reviews biomarker screening strategies to select these participants and discusses developments that can facilitate rapid and straightforward conclusions from novel clinical studies.
1 型糖尿病是一种不可治愈的疾病,与严重的急性和慢性并发症的风险相关。它是由胰岛素产生的β细胞明显丧失引起的。在临床发病时进行免疫干预可以暂时抑制残余功能性β细胞量的进一步下降,特别是在开始治疗时具有更高残余胰岛素产生能力的年轻患者中。在β细胞量尚未受到严重影响的临床前阶段,它可能会产生更高的效果。可以通过识别在 3 年内有极高风险发展为糖尿病且出现功能β细胞量下降但相对保留的迹象的个体,来准备这种预防试验。本文回顾了生物标志物筛选策略,以选择这些参与者,并讨论了有助于从新的临床研究中快速得出直接结论的进展。