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胎儿细胞移植治疗帕金森病的长期临床疗效:两例报告

Long-term clinical outcome of fetal cell transplantation for Parkinson disease: two case reports.

机构信息

Sobell Department of Motor Neuroscience, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London, England.

Department of Medicine, Hammersmith Hospital, Imperial College London, London, England.

出版信息

JAMA Neurol. 2014 Jan;71(1):83-7. doi: 10.1001/jamaneurol.2013.4749.

Abstract

IMPORTANCE

Recent advances in stem cell technologies have rekindled an interest in the use of cell replacement strategies for patients with Parkinson disease. This study reports the very long-term clinical outcomes of fetal cell transplantation in 2 patients with Parkinson disease. Such long-term follow-up data can usefully inform on the potential efficacy of this approach, as well as the design of trials for its further evaluation.

OBSERVATIONS

Two patients received intrastriatal grafts of human fetal ventral mesencephalic tissue, rich in dopaminergic neuroblasts, as restorative treatment for their Parkinson disease. To evaluate the very long-term efficacy of the grafts, clinical assessments were performed 18 and 15 years posttransplantation. Motor improvements gained gradually over the first postoperative years were sustained up to 18 years posttransplantation, while both patients have discontinued, and remained free of any, pharmacological dopaminergic therapy.

CONCLUSIONS AND RELEVANCE

The results from these 2 cases indicate that dopaminergic cell transplantation can offer very long-term symptomatic relief in patients with Parkinson disease and provide proof-of-concept support for future clinical trials using fetal or stem cell therapies.

摘要

重要性

最近干细胞技术的进步重新点燃了人们对使用细胞替代策略治疗帕金森病患者的兴趣。本研究报告了 2 例帕金森病患者接受胎儿细胞移植后的非常长期临床结果。这种长期随访数据可有效地提供该方法的潜在疗效信息,并为进一步评估该方法的临床试验设计提供信息。

观察结果

2 名患者接受了富含多巴胺能神经前体细胞的人胎儿腹侧中脑组织的纹状体内移植,作为他们帕金森病的修复治疗。为了评估移植物的非常长期疗效,在移植后 18 年和 15 年进行了临床评估。术后最初几年逐渐获得的运动改善持续到移植后 18 年,而两名患者均已停止并一直无需任何药物多巴胺治疗。

结论和相关性

这两个案例的结果表明,多巴胺能细胞移植可为帕金森病患者提供非常长期的症状缓解,并为未来使用胎儿或干细胞疗法的临床试验提供概念验证支持。

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