Diabetes Centre, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
First Faculty of Medicine, Charles University, 14021 Prague, Czech Republic.
Int J Mol Sci. 2024 Sep 23;25(18):10184. doi: 10.3390/ijms251810184.
Autologous cell therapy (ACT) is primarily used in diabetic patients with chronic limb-threatening ischemia (CLTI) who are not candidates for standard revascularization. According to current research, this therapy has been shown in some studies to be effective in improving ischemia parameters, decreasing the major amputation rate, and in foot ulcer healing. This review critically evaluates the efficacy of ACT in patients with no-option CLTI, discusses the use of mononuclear and mesenchymal stem cells, and compares the route of delivery of ACT. In addition to ACT, we also describe the use of new revascularization strategies, e.g., nanodiscs, microbeads, and epigenetics, that could enhance the therapeutic effect. The main aim is to summarize new findings on subcellular and molecular levels with the clinical aspects of ACT.
自体细胞治疗(ACT)主要用于因慢性肢体缺血性疾病(CLTI)而无法进行标准血运重建的糖尿病患者。根据目前的研究,该治疗在一些研究中已被证明可有效改善缺血参数、降低主要截肢率并促进足部溃疡愈合。本综述批判性地评估了 ACT 在无选择 CLTI 患者中的疗效,讨论了单核细胞和间充质干细胞的应用,并比较了 ACT 的给药途径。除了 ACT,我们还描述了新的血运重建策略的应用,例如纳米盘、微球和表观遗传学,这些策略可以增强治疗效果。主要目的是总结 ACT 在亚细胞和分子水平上的新发现与临床方面的联系。