严重肢体缺血
细胞疗法
遗传增强
干细胞疗法
血运重建
祖细胞
医学
旁分泌信号
血管生成
缺血
内皮祖细胞
临床试验
干细胞
生物信息学
内科学
基因
移植
受体
生物
细胞生物学
心肌梗塞
生物化学
作者
О. С. Осипова,Shoraan Saaya,А. А. Карпенко,Suren M. Zakian,Edouard Aboian
出处
期刊:VASA
[Hogrefe Publishing Group]
日期:2019-11-01
卷期号:48 (6): 461-471
被引量:12
标识
DOI:10.1024/0301-1526/a000787
摘要
Summary. Cell therapy is proposed for indirect revascularization for the patient’s incurable by endovascular or surgical revascularization. The therapy with stem cells (SCs) or progenitor cells is assumed to be more efficient as compared with protein or gene therapy not only because of their direct vasculogenic properties, but also thanks to their paracrine effect via secretion of manifold biologically active substances. This review gives an overview of the potential of SC-based therapy for critical limb ischemia (CLI), putative mechanism underlying cell therapy, and comparison of cell therapy to angiogenesis gene therapy in CLI treatment. Human trial data and meta-analysis, as well as some problems of clinical trials and considerations for future SC-based therapy in CLI are also discussed.
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