Pees Anna, Grotegerd Ann-Kathrin, Bleher Daniel, Herfert Kristina, Vasdev Neil
Azrieli Centre for Neuro-Radiochemistry, Brain Health Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, Canada.
Werner Siemens Imaging Center, Department of Preclinical Imaging and Radiopharmacy, University of Tuebingen, Tuebingen, Germany.
Eur J Nucl Med Mol Imaging. 2026 Jan 21. doi: 10.1007/s00259-025-07695-0.
The development of positron emission tomography (PET) tracers targeting α-synuclein (α-syn) aggregates remains a major challenge in PET imaging of neurodegenerative diseases. This review provides a comprehensive overview of the recent advances, key obstacles, and aims to give future directions for the development of α-syn PET tracers. The first part of the review focuses on the experimental strategies to develop potential α-syn PET ligands. We overview the differences between various types of α-syn fibrils, including preformed fibrils and patient-derived fibrils, and methods such as solid-state nuclear magnetic resonance and cryogenic electron microscopy used for structure elucidation of the fibrils. Furthermore, the review summarizes the techniques for the assessment of ligand binding to α-syn, such as fibril binding assays (competition and saturation binding assays), macro- and microautoradiography, and alternative methods like surface plasmon resonance and biolayer interferometry. Determination of pharmacokinetics and metabolism are likewise important steps in α-syn tracer development, and hurdles and merits of in vitro and in vivo methods are contemplated, in the context of translation to in vivo evaluation in fibril-inoculated and transgenic animal models. Finally, off-target binding of tracer candidates is described, which still remains one of the major pitfalls of α-syn-targeting PET tracers. The second part of the review overviews all small molecule α-syn PET tracers developed since 2022, highlighting their progress, current limitations, and future directions for achieving clinically viable α-syn PET imaging agents.
开发针对α-突触核蛋白(α-syn)聚集体的正电子发射断层扫描(PET)示踪剂仍然是神经退行性疾病PET成像中的一项重大挑战。本综述全面概述了近期的进展、关键障碍,并旨在为α-syn PET示踪剂的开发提供未来方向。综述的第一部分重点关注开发潜在α-syn PET配体的实验策略。我们概述了各种类型的α-syn原纤维之间的差异,包括预形成的原纤维和患者来源的原纤维,以及用于原纤维结构解析的固态核磁共振和低温电子显微镜等方法。此外,综述总结了评估配体与α-syn结合的技术,如原纤维结合测定(竞争和饱和结合测定)、宏观和微观放射自显影,以及表面等离子体共振和生物层干涉测量等替代方法。确定药代动力学和代谢同样是α-syn示踪剂开发中的重要步骤,在向原纤维接种和转基因动物模型的体内评估转化的背景下,考虑了体外和体内方法的障碍和优点。最后,描述了候选示踪剂的脱靶结合,这仍然是靶向α-syn的PET示踪剂的主要缺陷之一。综述的第二部分概述了自2022年以来开发的所有小分子α-syn PET示踪剂,突出了它们的进展、当前局限性以及实现临床上可行的α-syn PET成像剂的未来方向。