Division of Translational Brain Sciences, Department of Neurology, Duke University Medical Center, Durham, NC 27710, USA; Center for Genomic and Computational Biology, Duke University Medical Center, Durham, NC 27710, USA.
Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA; Center for Advanced Genomic Technologies, Duke University Medical Center, Durham, NC 27710, USA; Viral Vector Core, Duke University Medical Center, Durham, NC 27710, USA.
Mol Ther. 2021 Mar 3;29(3):949-972. doi: 10.1016/j.ymthe.2021.01.001. Epub 2021 Jan 9.
Alzheimer's disease (AD) and Parkinson's disease (PD) are the two most prevalent age-related neurodegenerative diseases, and currently no effective clinical treatments exist for either, despite decades of clinical trials. The failure to translate preclinical findings into effective treatments is indicative of a problem in the current evaluation pipeline for potential therapeutics. At present, there are no useful animal models for AD and PD research that reflect the entire biology of the diseases, specifically, the more common non-Mendelian forms. Whereas the field continues to seek suitable rodent models for investigating potential therapeutics for these diseases, rodent models have still been used primarily for preclinical studies. Here, we advocate for a paradigm shift toward the application of human-induced pluripotent stem cell (hiPSC)-derived systems for PD and AD modeling and the development of improved human-based models in a dish for drug discovery and preclinical assessment of therapeutic targets.
阿尔茨海默病(AD)和帕金森病(PD)是两种最常见的与年龄相关的神经退行性疾病,尽管经过了几十年的临床试验,但目前两种疾病都没有有效的临床治疗方法。临床前研究结果未能转化为有效的治疗方法,表明目前对潜在治疗药物的评估方法存在问题。目前,尚无用于 AD 和 PD 研究的有用动物模型能够反映疾病的全部生物学特性,特别是更常见的非孟德尔形式。尽管该领域仍在继续寻找合适的啮齿动物模型来研究这些疾病的潜在治疗方法,但啮齿动物模型主要仍用于临床前研究。在这里,我们提倡将范式转变为应用人诱导多能干细胞(hiPSC)衍生系统进行 PD 和 AD 建模,并开发改良的基于人类的体外模型用于药物发现和治疗靶点的临床前评估。