Allogeneic Bone Marrow‐Derived Mesenchymal Stem Cells for Parkinson's Disease: A Randomized Trial
IF 7.6
1区 医学
Q1 CLINICAL NEUROLOGY
Mya C. Schiess, Jessika Suescun, Juan D. Martinez‐Lemus, Charles Green, Tia S. Thomas, Mohammad Shahnawaz, Emily Tharp, Nikunj B. Satani, Jerome G. Saltarrelli, Christopher Adams, Marie‐Francoise Doursout, Vanessa Thyne, Rula Abuamouneh, Elsa M. Rodarte, Sean I. Savitz, Timothy M. Ellmore
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Abstract
BackgroundNeuroinflammation contributes to Parkinson's disease (PD) progression and motor dysfunction. Allogeneic human mesenchymal stem cells (allo‐hMSCs) may reduce neuroinflammation and improve motor symptoms.ObjectivesTo evaluate the efficacy of repeated intravenous doses of 10 × 106 /kg allo‐hMSCs in improving motor symptoms in patients with PD (PwP).MethodsIn this phase 2, randomized, placebo‐controlled trial (November 2020–July 2023), mild‐to‐moderate PwP received either three allo‐hMSC infusions, one placebo followed by two allo‐hMSC infusions, or three placebo infusions at 18‐week intervals. Follow‐up lasted 88 weeks. The primary outcome was a >70% posterior probability (PP) of a difference in the proportion of participants with ≥5‐point improvement in OFF‐medication Movement Disorder Society Sponsored Revision of the Unified Parkinson's Disease Rating Scale‐Part III (MDS‐UPDRS‐III) at week 62. Bayesian analysis was conducted using R v4.2.0.ResultsForty‐five PwP were enrolled. A larger proportion of subjects achieved a ≥5‐point improvement in MDS‐UPDRS‐III in the three‐infusion arm compared with placebo at week 62 (mean difference [MD]: 5.0%, PP = 93.7%), translating to a 16.9‐point improvement in MDS‐UPDRS‐III in the three‐infusion arm compared with a 14.6‐point improvement in the placebo arm. Conversely, fewer subjects in the two‐infusion arm compared with placebo showed ≥5‐point improvement at week 62 (MD: –62.4%, PP ≥ 99.9%), translating to only a 3.9‐point improvement in MDS‐UPDRS‐III in the two‐infusion arm. However, improvement in MDS‐UPDRS‐III was seen across all treatment arms. Adverse events were mild and transient.ConclusionsThree infusions of 10 × 106 allo‐hMSCs/kg improved motor function in mild‐to‐moderate PwP, while two infusions showed less improvement than placebo. To address this discrepancy, future studies should conduct functional potency assays to understand batch‐to‐batch variability affecting clinical efficacy. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
异基因骨髓间充质干细胞治疗帕金森病:一项随机试验
神经炎症有助于帕金森病(PD)的进展和运动功能障碍。同种异体人间充质干细胞(allo‐hMSCs)可能减轻神经炎症并改善运动症状。目的评价反复静脉注射10 × 106/kg allo - hMSCs改善PD (PwP)患者运动症状的疗效。方法:在这项2期随机安慰剂对照试验(2020年11月- 2023年7月)中,轻度至中度PwP接受3次allo - hMSC输注,1次安慰剂后2次allo - hMSC输注,或3次安慰剂输注,间隔18周。随访88周。主要结局是在第62周时,在脱药运动障碍协会赞助的统一帕金森病评定量表第三部分(MDS - UPDRS - III)修订中,改善≥5分的参与者比例差异的后验概率为70%。使用R v4.2.0进行贝叶斯分析。结果纳入45例PwP。在第62周,与安慰剂组相比,三次输注组MDS‐UPDRS‐III改善≥5个点的受试者比例更大(平均差异[MD]: 5.0%, PP = 93.7%),三次输注组MDS‐UPDRS‐III改善16.9个点,而安慰剂组改善14.6个点。相反,与安慰剂组相比,两次输注组中较少的受试者在第62周表现出≥5点的改善(MD: -62.4%, PP≥99.9%),两次输注组中MDS - UPDRS - III仅改善3.9点。然而,MDS - UPDRS - III在所有治疗组均有改善。不良事件轻微且短暂。结论3次输注10 × 106 allo - hMSCs/kg可改善轻度至中度PwP患者的运动功能,而2次输注的改善效果不如安慰剂。为了解决这一差异,未来的研究应该进行功能效价测定,以了解影响临床疗效的批次间变异性。©2025作者。Wiley期刊有限责任公司代表国际帕金森和运动障碍学会出版的《运动障碍》。
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期刊介绍:
Movement Disorders publishes a variety of content types including Reviews, Viewpoints, Full Length Articles, Historical Reports, Brief Reports, and Letters. The journal considers original manuscripts on topics related to the diagnosis, therapeutics, pharmacology, biochemistry, physiology, etiology, genetics, and epidemiology of movement disorders. Appropriate topics include Parkinsonism, Chorea, Tremors, Dystonia, Myoclonus, Tics, Tardive Dyskinesia, Spasticity, and Ataxia.