Department of Public Health and Caring Sciences, Uppsala University, Dag Hammarskjöldsväg 20, 75185, Uppsala, Sweden.
BioArctic AB, Stockholm, Sweden.
Pharm Res. 2022 Jul;39(7):1481-1496. doi: 10.1007/s11095-022-03277-z. Epub 2022 May 2.
Positron emission tomography (PET), a medical imaging technique allowing for studies of the living human brain, has gained an important role in clinical trials of novel drugs against Alzheimer's disease (AD). For example, PET data contributed to the conditional approval in 2021 of aducanumab, an antibody directed towards amyloid-beta (Aβ) aggregates, by showing a dose-dependent reduction in brain amyloid after treatment. In parallel to clinical studies, preclinical studies in animal models of Aβ pathology may also benefit from PET as a tool to detect target engagement and treatment effects of anti-Aβ drug candidates. PET is associated with a high level of translatability between species as similar, non-invasive protocols allow for longitudinal rather than cross-sectional studies and can be used both in a preclinical and clinical setting. This review focuses on the use of preclinical PET imaging in genetically modified animals that express human Aβ, and its present and potential future role in the development of drugs aimed at reducing brain Aβ levels as a therapeutic strategy to halt disease progression in AD.
正电子发射断层扫描(PET)是一种能够对活体人脑进行研究的医学成像技术,在针对阿尔茨海默病(AD)的新型药物的临床试验中发挥了重要作用。例如,PET 数据有助于 2021 年批准针对淀粉样蛋白-β(Aβ)聚集体的抗体 aducanumab,因为它表明治疗后大脑淀粉样蛋白呈剂量依赖性减少。与临床研究平行,Aβ 病理学动物模型的临床前研究也可能受益于 PET,因为它是一种检测抗 Aβ 候选药物的靶标结合和治疗效果的工具。PET 具有较高的跨物种可翻译性,因为相似的、非侵入性的方案允许进行纵向而非横断面研究,并且可以在临床前和临床环境中使用。这篇综述重点介绍了在表达人 Aβ 的基因修饰动物中使用临床前 PET 成像,以及其目前和潜在的未来在开发旨在降低大脑 Aβ 水平的药物中的作用,作为阻止 AD 疾病进展的治疗策略。