German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany; Rheinische Friedrich-Wilhelms-Universität Bonn, 53127 Bonn, Germany.
Istituto di Ricerche Farmacologiche Mario Negri IRCCS, 20156 Milan, Italy.
Curr Opin Pharmacol. 2019 Feb;44:28-38. doi: 10.1016/j.coph.2019.02.002. Epub 2019 Mar 14.
Prion diseases are devastating neurodegenerative disorders for which no drugs are available. The successful development of therapeutics depends on drug screening platforms and preclinical models that recapitulate key molecular and pathological features of the disease. Innovative experimental tools have been developed over the last few years that might facilitate drug discovery, including cell-free prion replication assays and prion-infected flies. However, there is still room for improvement. Animal models of genetic prion disease are few, and only partially recapitulate the complexity of the human disorder. Moreover, we still lack a human cell culture model suitable for high-content anti-prion drug screening. This review provides an overview of the models currently used in prion research, and discusses their promise and limitations for drug discovery.
朊病毒病是一种具有破坏性的神经退行性疾病,目前尚无可用的药物。治疗药物的成功开发取决于能够重现疾病关键分子和病理特征的药物筛选平台和临床前模型。在过去的几年中,已经开发出了一些创新性的实验工具,这些工具可能有助于药物发现,包括无细胞朊病毒复制测定和感染朊病毒的果蝇。然而,仍有改进的空间。遗传性朊病毒病的动物模型很少,并且仅部分重现了人类疾病的复杂性。此外,我们仍然缺乏适合高通量抗朊病毒药物筛选的人细胞培养模型。本文综述了目前在朊病毒研究中使用的模型,并讨论了它们在药物发现方面的潜力和局限性。