Cell Therapy for Parkinson's Disease: New Hope from Reprogramming Technologies

被引:17
作者
Chen, Zhiguo [1 ,2 ,3 ,4 ]
机构
[1] Capital Med Univ, Xuanwu Hosp, Cell Therapy Ctr, Beijing 100053, Peoples R China
[2] Minist Educ, Key Lab Neurodegenerat, Beijing 100053, Peoples R China
[3] Beijing Inst Brain Disorders, Ctr Neural Injury & Repair, Beijing, Peoples R China
[4] Beijing Inst Brain Disorders, Ctr Parkinsons Dis, Beijing, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
cell therapy; Parkinson's disease; reprogramming; dopaminergic neurons; clinical trials; PLURIPOTENT STEM-CELLS; DIRECT CONVERSION; MOUSE FIBROBLASTS; DOPAMINE NEURONS; GENE-THERAPY; DOUBLE-BLIND; OPEN-LABEL; FOLLOW-UP; TRANSPLANTATION; GENERATION;
D O I
10.14336/AD.2014.1201
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Parkinson's disease (PD) is a neurodegenerative disease with the major pathology being the progressive loss of dopaminergic (DA) midbrain neurons in the substantia nigra. As early as in the 1980s, open-label clinical trials employing fetal ventral mesencephalon (fVM) tissues have demonstrated significant efficacy for PD treatment, which led to two NIH-sponsored double-blind placebo-controlled clinical trials. However, both trials showed only mild outcome. Retrospective analysis revealed several possible reasons that include patient selection, heterogeneity of grafts, immune recognition of grafts, lack of standardization of transplantation procedure and uneven distribution of grafts. Recent years have seen advances in reprogramming technologies which may provide solutions to the problems associated with fVM tissues. Induced pluripotent stem cells (iPSCs) and induced neural stem cells (iNSCs) hold promise for generating clinical grade DA neural cells that are safe, homogeneous, scalable and standardizable. These new technologies may bring back clinical trials using cell therapy for PD treatment in the future.
引用
收藏
页码:499 / 503
页数:5
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