Benaroya Research Institute, Seattle, WA
Diabetes. 2021 May;70(5):1029-1037. doi: 10.2337/db20-1112. Epub 2021 Apr 30.
The 2019 report of a randomized, placebo-controlled clinical trial demonstrating that immune therapy can delay the onset of clinical type 1 diabetes (T1D) in antibody-positive relatives by a median of 2 years stands out as a landmark in the decades-long effort to prevent T1D. With this important step achieved, it is now time to consider what is needed to bring disease-modifying therapy for prevention or delay of T1D to clinical use from this point. Long considered a chicken and egg problem (why screen for T1D risk when we have no therapy, and how can we develop therapies without more screening), we now have the opportunity to break this impasse. The purpose of this article is to place this clinical trial result in context, highlighting key foundational studies leading to this accomplishment, addressing the current gaps, and suggesting that a key next step for prevention of T1D is to screen and monitor relatives for T1D risk in the context of clinical care.
2019 年的一项随机、安慰剂对照临床试验报告表明,免疫疗法可以将抗体阳性的糖尿病前期患者的临床 1 型糖尿病(T1D)发病时间中位数延迟 2 年,这是预防 T1D 长达数十年努力中的一个里程碑。随着这一重要步骤的实现,现在是时候考虑从这一点出发,将预防或延迟 T1D 的疾病修正疗法推向临床应用所需的条件。长期以来,这一直被认为是一个先有鸡还是先有蛋的问题(当我们没有治疗方法时,为什么要筛查 T1D 风险,而如果没有更多的筛查,我们又如何开发治疗方法),但现在我们有机会打破这种僵局。本文的目的是将这一临床试验结果置于背景之中,重点介绍导致这一成就的关键基础研究,探讨当前的差距,并提出预防 T1D 的关键下一步是在临床护理的背景下对 T1D 风险进行筛查和监测。