Department of Medicine, Cardiovascular Division and the Interdisciplinary Stem Cell Institute, Miller School of Medicine, University of Miami, Miami, Florida 33136, USA.
J Am Coll Cardiol. 2009 Dec 8;54(24):2277-86. doi: 10.1016/j.jacc.2009.06.055.
Our aim was to investigate the safety and efficacy of intravenous allogeneic human mesenchymal stem cells (hMSCs) in patients with myocardial infarction (MI).
Bone marrow-derived hMSCs may ameliorate consequences of MI, and have the advantages of preparation ease, allogeneic use due to immunoprivilege, capacity to home to injured tissue, and extensive pre-clinical support.
We performed a double-blind, placebo-controlled, dose-ranging (0.5, 1.6, and 5 million cells/kg) safety trial of intravenous allogeneic hMSCs (Prochymal, Osiris Therapeutics, Inc., Baltimore, Maryland) in reperfused MI patients (n=53). The primary end point was incidence of treatment-emergent adverse events within 6 months. Ejection fraction and left ventricular volumes determined by echocardiography and magnetic resonance imaging were exploratory efficacy end points.
Adverse event rates were similar between the hMSC-treated (5.3 per patient) and placebo-treated (7.0 per patient) groups, and renal, hepatic, and hematologic laboratory indexes were not different. Ambulatory electrocardiogram monitoring demonstrated reduced ventricular tachycardia episodes (p=0.025), and pulmonary function testing demonstrated improved forced expiratory volume in 1 s (p=0.003) in the hMSC-treated patients. Global symptom score in all patients (p=0.027) and ejection fraction in the important subset of anterior MI patients were both significantly better in hMSCs versus placebo subjects. In the cardiac magnetic resonance imaging substudy, hMSC treatment, but not placebo, increased left ventricular ejection fraction and led to reverse remodeling.
Intravenous allogeneic hMSCs are safe in patients after acute MI. This trial provides pivotal safety and provisional efficacy data for an allogeneic bone marrow-derived stem cell in post-infarction patients. (Safety Study of Adult Mesenchymal Stem Cells [MSC] to Treat Acute Myocardial Infarction; NCT00114452).
本研究旨在探讨静脉输注同种异体人骨髓间充质干细胞(hMSC)治疗心肌梗死(MI)患者的安全性和疗效。
骨髓来源的 hMSC 可能改善 MI 的后果,且具有制备简便、因免疫豁免而可同种异体使用、归巢至损伤组织、广泛的临床前支持等优点。
我们进行了一项双盲、安慰剂对照、剂量范围(0.5、1.6 和 500 万细胞/kg)的同种异体静脉输注 hMSC(Prochymal,Osiris Therapeutics,Inc.,马里兰州巴尔的摩)治疗再灌注 MI 患者(n=53)的安全性试验。主要终点为 6 个月内治疗后出现的不良事件发生率。超声心动图和磁共振成像测定的射血分数和左心室容积为探索性疗效终点。
hMSC 治疗组(5.3 例/患者)和安慰剂治疗组(7.0 例/患者)的不良事件发生率相似,且肾功能、肝功能和血液学实验室指标无差异。动态心电图监测显示室性心动过速发作减少(p=0.025),肺功能检测显示 hMSC 治疗组用力呼气量 1 秒率(FEV1)改善(p=0.003)。所有患者的整体症状评分(p=0.027)和前壁 MI 患者亚组的射血分数均显著优于安慰剂组。心脏磁共振成像亚组研究中,hMSC 治疗而非安慰剂治疗可增加左心室射血分数并导致逆重构。
静脉输注同种异体 hMSC 治疗急性 MI 患者是安全的。这项试验为同种异体骨髓源性干细胞治疗心肌梗死后患者提供了关键的安全性和初步疗效数据。(成人间充质干细胞 [MSC] 治疗急性心肌梗死的安全性研究;NCT00114452)。