Research center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Life Sci. 2021 May 15;273:119271. doi: 10.1016/j.lfs.2021.119271. Epub 2021 Feb 27.
A growing body of evidence has shown that extracellular vesicles can be efficient as experimental therapeutics in pre-clinical models of skin wounds, but there is a significant unmet need to translate this to clinical utilization. The objectives of the current systematic review were to identify the strength of the therapeutic effects of EVs derived from stem cells in cutaneous wounds and to assess which EV-mediated mechanisms could be involved in the therapeutic response. PubMed, ISI Web of Science, and Scopus databases were systematically searched. We retrieved English-language articles published through June 2020. In vivo studies which applied stem cell-derived EVs were included for further analysis. The Risk of bias was assessed by the SYRCLE tool. We identified thirty-nine pre-clinical studies that evaluated the effects of EVs on the wound healing process. The included studies varied greatly in EVs isolation techniques, route of administration, EVs producing cells, and follow-up time. In vivo application revealed beneficial effects of EVs on accelerating wound closure and re-epithelialization in a dose-dependent manner. Elevated angiogenesis was reported in twelve eligible studies through multiple signaling pathways such as PI3K/Akt, MAPK/ERK, and JAK/STAT. The well-known signaling pathway to inhibit scar formation was TGF-β2/SMAD2. However, all included studies were not blinded enough which may have introduced bias. Therefore, the transition of EV's efficacy into the clinics is deeply rooted in the following important factors: 1) pre-clinical studies with a lower risk of bias and longer follow-up time, and 2) consistent, reproducible, and feasible manufacturing of EVs production in a large-scale commercial program.
越来越多的证据表明,细胞外囊泡在皮肤伤口的临床前模型中作为实验治疗方法非常有效,但将其转化为临床应用仍存在重大未满足的需求。本系统评价的目的是确定来源于干细胞的 EV 在皮肤伤口中的治疗效果的强度,并评估哪些 EV 介导的机制可能参与治疗反应。我们系统性地检索了 PubMed、ISI Web of Science 和 Scopus 数据库。我们检索了截至 2020 年 6 月发表的英文文章。纳入了进一步分析的应用干细胞衍生 EV 的体内研究。使用 SYRCLE 工具评估偏倚风险。我们确定了 39 项评估 EV 对伤口愈合过程影响的临床前研究。纳入的研究在 EV 分离技术、给药途径、EV 产生细胞和随访时间方面差异很大。体内应用表明 EV 以剂量依赖的方式加速伤口闭合和再上皮化具有有益作用。通过多个信号通路,如 PI3K/Akt、MAPK/ERK 和 JAK/STAT,有 12 项合格研究报道了升高的血管生成。众所周知的抑制瘢痕形成的信号通路是 TGF-β2/SMAD2。然而,所有纳入的研究都没有足够的盲法,这可能会引入偏倚。因此,EV 疗效向临床的转化深深植根于以下重要因素:1)低偏倚风险和更长随访时间的临床前研究,以及 2)在大规模商业化项目中一致、可重复和可行的 EV 生产制造。