Capotosti Francesca
AC Immune SA, 1015 Lausanne, Switzerland.
Cells. 2025 Jun 3;14(11):834. doi: 10.3390/cells14110834.
The development of PET tracers for the detection of pathological alpha-synuclein (a-synuclein) has the potential to revolutionize the diagnosis, monitoring, and therapeutic interventions of synucleinopathies, including Parkinson's disease. The journey toward identifying effective PET imaging agents, however, has faced significant challenges due to the complexity and heterogeneity of the a-synuclein structures. Achieving the goal is further compounded by the low density of the pathological target, necessitating that the tracer exhibits a high binding potential, as well as the co-existence of other protein aggregates, requiring the tracer to be highly specific and selective for a-synuclein. In this perspective article, the challenges regarding developing PET tracers for a-synuclein are explored and summarized, together with the most significant recent advances in the field. These include the approaches used by our laboratories, leading to the publication of the first clinical PET images of a-synuclein pathology in patients with multiple system atrophy (MSA). Building on the current understanding of the different a-synuclein species and findings based on the success of PET tracers in the field of neurodegenerative diseases, future directions are considered also to achieve the imaging of a-synuclein pathology in Parkinson's patients.
开发用于检测病理性α-突触核蛋白(α-synuclein)的正电子发射断层扫描(PET)示踪剂,有可能彻底改变包括帕金森病在内的突触核蛋白病的诊断、监测和治疗干预。然而,由于α-突触核蛋白结构的复杂性和异质性,识别有效的PET成像剂的过程面临着重大挑战。病理性靶点的低密度进一步加剧了实现这一目标的难度,这就要求示踪剂具有高结合潜力,同时其他蛋白质聚集体的共存,要求示踪剂对α-突触核蛋白具有高度特异性和选择性。在这篇观点文章中,探讨并总结了开发α-突触核蛋白PET示踪剂所面临的挑战,以及该领域最近最重要的进展。这些进展包括我们实验室所采用的方法,这些方法促成了多系统萎缩(MSA)患者α-突触核蛋白病理学的首张临床PET图像的发表。基于目前对不同α-突触核蛋白种类的理解以及PET示踪剂在神经退行性疾病领域取得成功的研究结果,我们还考虑了未来的方向,以实现帕金森病患者α-突触核蛋白病理学的成像。