Department of Neurology, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Department of Anesthesiology, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Mov Disord. 2021 Aug;36(8):1825-1834. doi: 10.1002/mds.28582. Epub 2021 Mar 27.
Neuroinflammation plays a key role in PD pathogenesis, and allogeneic bone marrow-derived mesenchymal stem cells can be used as an immunomodulatory therapy.
The objective of this study was to prove the safety and tolerability of intravenous allogeneic bone marrow-derived mesenchymal stem cells in PD patients.
This was a 12-month single-center open-label dose-escalation phase 1 study of 20 subjects with mild/moderate PD assigned to a single intravenous infusion of 1 of 4 doses: 1, 3, 6, or 10 × 10 allogeneic bone marrow-derived mesenchymal stem cells/kg, evaluated 3, 12, 24, and 52 weeks postinfusion. Primary outcome safety measures included transfusion reaction, study-related adverse events, and immunogenic responses. Secondary outcomes included impact on peripheral markers, PD progression, and changes in brain perfusion.
There were no serious adverse reactions related to the infusion and no responses to donor-specific human leukocyte antigens. Most common treatment-emergent adverse events were dyskinesias (20%, n = 4) with 1 emergent and 3 exacerbations; and hypertension (20%, n = 4) with 3 transient episodes and 1 requiring medical intervention. One possibly related serious adverse event occurred in a patient with a 4-year history of lymphocytosis who developed asymptomatic chronic lymphocytic leukemia. Peripheral inflammation markers appear to be reduced at 52 weeks in the highest dose including, tumor necrosis factor-α (P < 0.05), chemokine (C-C motif) ligand 22 (P < 0.05), whereas brain-derived neurotrophic factor (P < 0.05) increased. The highest dose seems to have demonstrated the most significant effect at 52 weeks, reducing the OFF state UPDRS motor, -14.4 (P < 0.01), and total, -20.8 (P < 0.05), scores.
A single intravenous infusion of allogeneic bone marrow-derived mesenchymal stem cells at doses of 1, 3, 6, or 10 × 10 allogeneic bone marrow-derived mesenchymal stem cells/kg is safe, well tolerated, and not immunogenic in mild/moderate PD patients. © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
神经炎症在 PD 发病机制中起关键作用,同种异体骨髓间充质干细胞可作为一种免疫调节疗法。
本研究旨在证明静脉内同种异体骨髓间充质干细胞在 PD 患者中的安全性和耐受性。
这是一项为期 12 个月的单中心、开放性、剂量递增 1 期研究,共纳入 20 例轻度/中度 PD 患者,接受单次静脉内输注 4 种剂量之一:1、3、6 或 10×106 同种异体骨髓间充质干细胞/kg,在输注后 3、12、24 和 52 周进行评估。主要安全性评估指标包括输注反应、与研究相关的不良事件和免疫原性反应。次要结局包括对周围标志物、PD 进展和脑灌注变化的影响。
无与输注相关的严重不良反应,也无针对供体特异性人白细胞抗原的反应。最常见的治疗后不良事件是运动障碍(20%,n=4),其中 1 例新发,3 例恶化;高血压(20%,n=4),其中 3 例短暂发作,1 例需要医疗干预。1 例可能与疾病相关的严重不良事件发生在 1 例有 4 年淋巴细胞增多症病史的患者中,该患者发展为无症状慢性淋巴细胞白血病。在最高剂量组,外周炎症标志物在 52 周时似乎降低,包括肿瘤坏死因子-α(P<0.05)、趋化因子(C-C 基序)配体 22(P<0.05),而脑源性神经营养因子(P<0.05)升高。最高剂量组在 52 周时似乎显示出最显著的效果,降低了运动障碍部分统一帕金森病评定量表(UPDRS)的运动评分(-14.4,P<0.01)和总评分(-20.8,P<0.05)。
在轻度/中度 PD 患者中,单次静脉内输注 1、3、6 或 10×106 同种异体骨髓间充质干细胞/kg 的同种异体骨髓间充质干细胞是安全的、耐受良好的,且不会引起免疫原性。