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I 期临床试验:自体培养脂肪来源的基质/干细胞治疗不可再血管化的严重肢体缺血患者。

Phase I trial: the use of autologous cultured adipose-derived stroma/stem cells to treat patients with non-revascularizable critical limb ischemia.

机构信息

Service de médecine vasculaire, Pôle cardiovasculaire et métabolique, Centre hospitalo-universitaire de Toulouse, Toulouse, France; Université de Toulouse III, Paul Sabatier, Toulouse, France.

CNRS, Université Toulouse III, UPS UMR5273 STROMAlab, Toulouse, France; EFS (Etablissement Français du Sang), STROMAlab, Toulouse, France; Inserm U1031 STROMAlab, Toulouse, France; Université Toulouse III, UPS UMR5273 STROMAlab, Toulouse, France.

出版信息

Cytotherapy. 2014 Feb;16(2):245-57. doi: 10.1016/j.jcyt.2013.11.011.

Abstract

BACKGROUND AIMS

Non-revascularizable critical limb ischemia (CLI) is the most severe stage of peripheral arterial disease, with no therapeutic option. Extensive preclinical studies have demonstrated that adipose-derived stroma cell (ASC) transplantation strongly improves revascularization and tissue perfusion in ischemic limbs. This study, named ACellDREAM, is the first phase I trial to evaluate the feasibility and safety of intramuscular injections of autologous ASC in non-revascularizable CLI patients.

METHODS

Seven patients were consecutively enrolled, on the basis of the following criteria: (i) lower-limb rest pain or ulcer; (ii) ankle systolic oxygen pressure <50 or 70 mm Hg for non-diabetic and diabetic patients, respectively, or first-toe systolic oxygen pressure <30 mm Hg or 50 mm Hg for non-diabetic and diabetic patients, respectively; (iii) not suitable for revascularization. ASCs from abdominal fat were grown for 2 weeks and were then characterized.

RESULTS

More than 200 million cells were obtained, with almost total homogeneity and no karyotype abnormality. The expressions of stemness markers Oct4 and Nanog were very low, whereas expression of telomerase was undetectable in human ASCs compared with human embryonic stem cells. ASCs (10(8)) were then intramuscularly injected into the ischemic leg of patients, with no complication, as judged by an independent committee. Trans-cutaneous oxygen pressure tended to increase in most patients. Ulcer evolution and wound healing showed improvement.

CONCLUSIONS

These data demonstrate the feasibility and safety of autologous ASC transplantation in patients with objectively proven CLI not suitable for revascularization. The improved wound healing also supports a putative functional efficiency.

摘要

背景目的

不可血管重建的严重肢体缺血(CLI)是外周动脉疾病最严重的阶段,没有治疗选择。广泛的临床前研究表明,脂肪来源的基质细胞(ASC)移植可强烈改善缺血肢体的再血管化和组织灌注。这项名为 ACellDREAM 的研究是首个评估非血管重建性 CLI 患者自体 ASC 肌肉内注射的可行性和安全性的 I 期临床试验。

方法

根据以下标准连续纳入 7 名患者:(i)下肢休息痛或溃疡;(ii)踝部收缩压<50 或 70mmHg(分别适用于非糖尿病和糖尿病患者),或第一趾收缩压<30 或 50mmHg(分别适用于非糖尿病和糖尿病患者);(iii)不适合血管重建。从腹部脂肪中获取 ASC 并培养 2 周,然后进行特征分析。

结果

获得超过 2 亿个细胞,几乎完全同质,且无染色体异常。与人类胚胎干细胞相比,人类 ASC 中干性标志物 Oct4 和 Nanog 的表达非常低,而端粒酶的表达则无法检测到。然后将 10(8)个 ASC 肌肉内注射到患者的缺血肢体中,由一个独立委员会判断,没有并发症。大多数患者的经皮氧压趋于增加。溃疡的演变和伤口愈合显示出改善。

结论

这些数据表明,在客观证实的不适合血管重建的 CLI 患者中,自体 ASC 移植是可行和安全的。改善的伤口愈合也支持其具有潜在的功能效率。

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