Department of Neurology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
Indian J Med Res. 2012 Aug;136(2):221-8.
BACKGROUND & OBJECTIVES: Bone marrow mononuclear cell therapy has emerged as one of the option for the treatment of Stroke. Several preclinical studies have shown that the treatment with mononuclear cell (MNCs) can reduce the infarct size and improve the functional outcome. We evaluated the feasibility, safety and clinical outcome of administering bone marrow mononuclear cell (MNCs) intravenously to patients with subacute ischaemic stroke.
In a non-randomized phase-I clinical study, 11 consecutive, eligible and consenting patients, aged 30-70 yr with ischaemic stroke involving anterior circulation within 7 to 30 days of onset of stroke were included. Bone marrow was aspirated from iliac crest and the harvested mononuclear cells were infused into antecubital vein. Outcomes measured for safety included immediate reactions after cell infusion and evidence of tumour formation at one year in whole body PET scan. Patients were followed at week 1, 4-6, 24 and 52 to determine clinical progress using National Institute of Health Stroke Scale (NIHSS), Barthel Index (BI), modified Rankin Scale (mRS), MRI, EEG and PET. Feasibility outcomes included target-dose feasibility. Favourable clinical outcome was defined as mRS score of 2 or less or BI score of 75 to 100 at six months after stem cell therapy.
Between September 2006 and April 2007, 11 patients were infused with bone-marrow mononuclear cells (mean 80 million with CD-34 + mean 0.92 million). Protocol was target-dose feasible in 9 patients (82%). FDG-PET scan at 24 and 52 wk in nine patients did not reveal evidence of tumour formation. Seven patients had favourable clinical outcome.
INTERPRETATION & CONCLUSIONS: Intravenous bone marrow mononuclear cell therapy appears feasible and safe in patients with subacute ischaemic stroke. Further, a randomized controlled trial to examine its efficacy is being conducted.
骨髓单个核细胞治疗已成为治疗中风的一种选择。几项临床前研究表明,单核细胞(MNC)治疗可减少梗死面积并改善功能结果。我们评估了将骨髓单个核细胞(MNC)静脉内给予亚急性缺血性中风患者的可行性、安全性和临床结果。
在一项非随机的 I 期临床研究中,纳入了 11 名连续、符合条件且同意的年龄在 30-70 岁的患者,这些患者在中风发作后 7-30 天内患有涉及前循环的缺血性中风。从髂嵴抽吸骨髓,收获的单核细胞注入肘前静脉。安全性评估的结果包括细胞输注后的即刻反应和在整个身体 PET 扫描中一年时肿瘤形成的证据。患者在第 1、4-6、24 和 52 周进行随访,以使用国立卫生研究院中风量表(NIHSS)、巴氏指数(BI)、改良 Rankin 量表(mRS)、MRI、EEG 和 PET 确定临床进展。可行性结果包括目标剂量可行性。有利的临床结果定义为在干细胞治疗后 6 个月时 mRS 评分<2 或 BI 评分 75-100。
在 2006 年 9 月至 2007 年 4 月期间,11 名患者输注了骨髓单个核细胞(平均输注 8000 万,CD-34+平均 92 万)。9 名患者(82%)中方案达到目标剂量。9 名患者在 24 和 52 周时的 FDG-PET 扫描未显示肿瘤形成的证据。7 名患者有良好的临床结果。
静脉内骨髓单个核细胞治疗似乎在亚急性缺血性中风患者中是可行和安全的。此外,正在进行一项随机对照试验以检查其疗效。