胎儿祖细胞用于治疗慢性肢体缺血。

IF 1.5 Q4 CELL BIOLOGY
American journal of stem cells Pub Date : 2024-06-15 eCollection Date: 2024-01-01 DOI:10.62347/MZKI8393
Oleksandr Kukharchuk, Abhijit Bopardikar, Padma Priya Anand Baskaran, Andrii Kukharchuk, Rohit Kulkarni, Ranjit Ranbhor
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引用次数: 0

摘要

研究目的本研究探讨了胎儿祖细胞(FPCs)在治疗与慢性肢体缺血(CLI)相关的慢性不愈合伤口和溃疡方面的治疗潜力。研究旨在阐明胎儿祖细胞的作用机制,并评估其对慢性肢体缺血患者的疗效和安全性:研究人员从流产的人类胎儿肝脏、大脑和皮肤组织中分离出 FPCs,并对其进行了全面鉴定。临床前阶段的研究包括评估 FPCs 在急性脑梗塞大鼠模型中的效果。随后,进行了一项随机对照临床试验,以比较 FPCs 与标准疗法和自体骨髓单核细胞对 CLI 患者的疗效。临床试验为期 12 个月,随访期为 24-36 个月。主要结果包括伤口愈合、大截肢和小截肢的频率、疼痛减轻以及并发症的发生率。次要结果包括局部血流动力学变化以及血管生成的组织学、超微结构和免疫组化评估:结果:在动物模型中,与对照组相比,FPC 治疗明显促进了血管生成,加快了缺血性伤口的愈合。对慢性缺血性心肌梗死患者进行的临床试验表明,与对照组相比,FPC疗法在伤口完全愈合率、防止大截肢率、减轻疼痛率和改善踝肱指数方面均有大幅提高。值得注意的是,该研究未报告严重不良事件:结论:FPC疗法在促进缺血性伤口愈合、预防截肢、改善CLI患者症状和生活质量方面疗效显著。FPCs 的促血管生成和促血管生成作用可能归因于其分泌特定生长因子的能力。这些发现为细胞治疗性血管生成的发展提供了新的视角,是治疗外周动脉疾病的一种前景广阔的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fetal progenitor cells for treatment of chronic limb ischemia.

Objectives: This study investigated the therapeutic potential of fetal progenitor cells (FPCs) in the treatment of chronic non-healing wounds and ulcers associated with chronic limb ischemia (CLI). The research aimed to elucidate the mechanism of action of FPCs and evaluate their efficacy and safety in CLI patients.

Methods: The researchers isolated FPCs from aborted human fetal liver, brain, and skin tissues and thoroughly characterized them. The preclinical phase of the study involved assessing the effects of FPCs in a rat model of CLI. Subsequently, a randomized controlled clinical trial was conducted to compare the efficacy of FPCs with standard treatment and autologous bone marrow mononuclear cells in CLI patients. The clinical trial lasted 12 months, with a follow-up period of 24-36 months. The primary outcomes included wound healing, frequency of major and minor amputations, pain reduction, and the incidence of complications. Secondary outcomes involved changes in local hemodynamics and histological, ultrastructural, and immunohistochemical assessments of angiogenesis.

Results: In the animal model, FPC treatment significantly enhanced angiogenesis and accelerated healing of ischemic wounds compared to controls. The clinical trial in CLI patients demonstrated that the FPC therapy achieved substantially higher rates of complete wound closure, prevention of major amputation, pain reduction, and improvement in ankle-brachial index compared to control groups. Notably, the study reported no serious adverse events.

Conclusions: FPC therapy exhibited remarkable efficacy in promoting the healing of ischemic wounds, preventing amputation, and improving symptoms and quality of life in patients with CLI. The proangiogenic and provasculogenic effects of FPCs may be attributed to their ability to secrete specific growth factors. These findings provide new insights into the development of cellular therapeutic angiogenesis as a promising approach for the treatment of peripheral arterial diseases.

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