Stempeutics Research Pvt Ltd, Akshay Tech Park, No, 72 & 73, 2nd Floor, EPIP Zone, Phase I-Area, Whitefield, Bangalore 560066, India.
J Transl Med. 2013 Jun 10;11:143. doi: 10.1186/1479-5876-11-143.
Peripheral vascular disease of the lower extremities comprises a clinical spectrum that extends from no symptoms to presentation with critical limb ischemia (CLI). Bone marrow derived Mesenchymal Stem Cells (BM- MSCs) may ameliorate the consequences of CLI due to their combinatorial potential for inducing angiogenesis and immunomodulatory environment in situ. The primary objective was to determine the safety of BM- MSCs in patients with CLI.
Prospective, double blind randomized placebo controlled multi-center study was conducted in patients with established CLI as per Rutherford classification in category II-4, III-5, or III-6 with infra-inguinal arterial occlusive disease and were not suitable for or had failed revascularization treatment. The primary end point was incidence of treatment - related adverse events (AE). Exploratory efficacy end points were improvement in rest pain, increase in Ankle Brachial Pressure Index (ABPI), ankle pressure, healing of ulcers, and amputation rates. Twenty patients (BM-MSC: Placebo = 1:1) were administered with allogeneic BM-MSCs at a dose of 2 million cells/kg or placebo (PlasmaLyte A) at the gastrocnemius muscle of the ischemic limb.
Improvement was observed in the rest pain scores in both the arms. Significant increase in ABPI and ankle pressure was seen in BM-MSC arm compared to the placebo group. Incidence of AEs in the BM-MSC arm was 13 vs. 45 in the placebo arm where as serious adverse events (SAE) were similar in both the arms (5 in BM-MSC and 4 in the placebo group). SAEs resulted in death, infected gangrene, amputations in these patients. It was observed that the SAEs were related to disease progression and not related to stem cells.
BM-MSCs are safe when injected IM at a dose of 2 million cells/kg body weight. Few efficacy parameters such as ABPI and ankle pressure showed positive trend warranting further studies.
NIH website (http://www.clinicaltrials.gov/ct2/show/NCT00883870).
下肢外周血管疾病包括一个从无症状到出现临界肢体缺血(CLI)的临床谱。骨髓来源的间充质干细胞(BM-MSCs)由于其在原位诱导血管生成和免疫调节环境的组合潜力,可能改善 CLI 的后果。主要目的是确定 BM-MSCs 在 CLI 患者中的安全性。
前瞻性、双盲、随机、安慰剂对照多中心研究纳入了根据 Rutherford 分类为 II-4、III-5 或 III-6 期的下肢动脉闭塞性疾病患者,这些患者存在 CLI,不适合或已经失败了血管重建治疗。主要终点是治疗相关不良事件(AE)的发生率。探索性疗效终点是静息痛的改善、踝肱血压指数(ABPI)的增加、踝压、溃疡的愈合和截肢率。20 名患者(BM-MSC:安慰剂=1:1)在缺血肢体的腓肠肌内给予 200 万细胞/kg 的同种异体 BM-MSCs 或安慰剂(PlasmaLyte A)。
两支手臂的静息痛评分都有改善。与安慰剂组相比,BM-MSC 组的 ABPI 和踝压显著增加。BM-MSC 组的 AE 发生率为 13 例,安慰剂组为 45 例,而严重不良事件(SAE)在两组相似(BM-MSC 组 5 例,安慰剂组 4 例)。SAE 导致这些患者死亡、感染性坏疽和截肢。观察到这些 SAE 与疾病进展有关,与干细胞无关。
当以 200 万细胞/kg 体重的剂量肌内注射 BM-MSCs 时,BM-MSCs 是安全的。一些疗效参数,如 ABPI 和踝压,显示出积极的趋势,需要进一步研究。