生物材料和细胞外囊泡治疗心肌梗死的协同作用:临床前研究的系统综述。

IF 9.6
Ying He, Zhaoxu Huang, Jie Liang, Hao Ji, Zhaoxia Pu
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引用次数: 0

摘要

细胞外囊泡(EVs)联合生物材料在治疗心肌梗死(MI)方面显示出前景,有可能减轻炎症、氧化应激和细胞凋亡,同时改善心功能。然而,系统的评价是必要的。这项荟萃分析利用了PubMed、Web of Science、Scopus、EMBASE和Ovid医学从成立到2025年5月的数据。使用GetData Graph Digitizer 2.26和Review Manager 5.4软件对相关结果进行分析。使用sycle偏倚风险工具和CAMARADES检查表评估研究质量。我们测量了12项指标,包括心功能、纤维化、细胞凋亡和炎症。荟萃分析包括33项研究。与EV单药治疗相比,EV与生物材料联合治疗可显著改善多项心脏功能和结构参数。其中包括:射血分数(SMD = 1.79;P < 0.00001);分数缩短(SMD = 1.61;P < 0.00001);心肌纤维化(SMD = -1.83; = 0.002页);IL-6 (SMD = -2.55;p = 0.01)和TNF-α (SMD = -1.18;p = 0.01),以及细胞凋亡水平(SMD = -3.72;P < 0.0001),明显降低。其中,心肌内注射msc源性EVs联合水凝胶是应用最广泛的联合疗法。电动汽车联合生物材料增强心肌梗死模型的心脏恢复,没有明显的安全性问题,突出了其潜在的治疗效益。意义声明:心肌梗死(MI)是导致死亡和疾病负担的主要原因之一。在过去的20年里,细胞外囊泡(EVs)经历了一段非凡的旅程,现在正处于成为下一代无细胞治疗工具的边缘。本研究旨在通过荟萃分析作图方法,定量分析生物材料联合ev与单独ev治疗心肌梗死的疗效和安全性。这是第一个综合荟萃分析,总结了各种生物材料联合EV治疗的有效性和安全性,突出了生物材料在推进该领域的作用。它为研究人员探索基于ev的治疗的临床转化提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synergistic effects of biomaterials and extracellular vesicles in treating myocardial infarction: A systematic review of preclinical studies.

Extracellular vesicles (EVs) combined with biomaterials have shown promise in treating myocardial infarction (MI), with potential to alleviate inflammation, oxidative stress, and apoptosis while improving cardiac function. However, systematic evaluation is needed. This meta-analysis utilized data from PubMed, Web of Science, Scopus, EMBASE, and Ovid medicine from their inception to May 2025. Relevant outcomes were analyzed using GetData Graph Digitizer 2.26 and Review Manager 5.4 software. The quality of studies was assessed using the SYRCLE risk of bias tool and CAMARADES checklist. We measured 12 indicators across cardiac function, fibrosis, apoptosis, and inflammation. The meta-analysis included 33 studies. Compared to EV monotherapy, the combination of EVs with biomaterials significantly improved several cardiac functions and structural parameters. These include: Ejection Fraction (SMD = 1.79; p < 0.00001); Fractional Shortening (SMD = 1.61; p < 0.00001); Myocardial Fibrosis (SMD = -1.83; p = 0.002); Additionally, IL-6 (SMD = -2.55; p = 0.01) and TNF-α (SMD = -1.18; p = 0.01), as well as apoptosis levels (SMD = -3.72; p < 0.0001), were markedly reduced. Among them, intramyocardial injection of MSC-derived EVs combined with hydrogel is the most widely used combination therapy. EVs combined with biomaterials enhance cardiac recovery in MI models with no significant safety issues, highlighting their potential therapeutic benefits. STATEMENT OF SIGNIFICANCE: Myocardial infarction (MI) is one of the leading causes of death and disease burden. Over the past 20 years, extracellular vesicles (EVs) have undergone a remarkable journey and are now poised on the brink of becoming the next generation of cell-free therapeutic tools. Our study aims to quantitatively analyze the efficacy and safety of combining biomaterials with EVs compared to EVs alone in MI through a meta-analytical mapping approach. This is the comprehensive meta-analysis summarizing the effectiveness and safety of various biomaterials combined with EV therapy, highlighting the role of biomaterials in advancing the field. It provides valuable insights for researchers exploring the clinical translation of EV-based therapies.

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