Phase I trial of hES cell-derived dopaminergic neurons for Parkinson’s disease

多巴胺能 帕金森病 疾病 耐受性 移植 壳核 临床试验 细胞疗法 不利影响 肿瘤科 医学 生物 干细胞 多巴胺 内科学 遗传学
作者
Viviane Tabar,Harini Sarva,Andrés M. Lozano,Alfonso Fasano,Suneil K. Kalia,Kenny Kwok Hei Yu,Cameron Brennan,Yilong Ma,Shichun Peng,David Eidelberg,M. Tomishima,Stefan Irion,W. Stemple,N. Abid,Antoine Lampron,Lorenz Studer,Claire Henchcliffe
出处
期刊:Nature [Nature Portfolio]
卷期号:641 (8064): 978-983 被引量:102
标识
DOI:10.1038/s41586-025-08845-y
摘要

Parkinson's disease is a progressive neurodegenerative condition with a considerable health and economic burden1. It is characterized by the loss of midbrain dopaminergic neurons and a diminished response to symptomatic medical or surgical therapy as the disease progresses2. Cell therapy aims to replenish lost dopaminergic neurons and their striatal projections by intrastriatal grafting. Here, we report the results of an open-label phase I clinical trial (NCT04802733) of an investigational cryopreserved, off-the-shelf dopaminergic neuron progenitor cell product (bemdaneprocel) derived from human embryonic stem (hES) cells and grafted bilaterally into the putamen of patients with Parkinson's disease. Twelve patients were enrolled sequentially in two cohorts-a low-dose (0.9 million cells, n = 5) and a high-dose (2.7 million cells, n = 7) cohort-and all of the participants received one year of immunosuppression. The trial achieved its primary objectives of safety and tolerability one year after transplantation, with no adverse events related to the cell product. At 18 months after grafting, putaminal 18Fluoro-DOPA positron emission tomography uptake increased, indicating graft survival. Secondary and exploratory clinical outcomes showed improvement or stability, including improvement in the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part III OFF scores by an average of 23 points in the high-dose cohort. There were no graft-induced dyskinesias. These data demonstrate safety and support future definitive clinical studies.
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