Aghayan Amir Hossein, Mirazimi Yasin, Fateh Kosar, Keshtkar Abbasali, Rafiee Mohammad, Atashi Amir
Student Research Committee, Department of Medical Laboratory Sciences, School of Paramedical Sciences, Zanjan University of Medical Sciences, Zanjan, Iran.
Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Stem Cell Rev Rep. 2024 Aug;20(6):1480-1500. doi: 10.1007/s12015-024-10741-3. Epub 2024 May 30.
Sepsis is a life-threatening disorder with no definitive cure. Preclinical studies suggest that extracellular vesicles derived from mesenchymal stromal cells (EV-MSCs) can mitigate inflammatory conditions, potentially leading to increased survival and reduced organ dysfunction during sepsis. Our aim to conduct this systematic review and meta-analysis is assessing the EV-MSCs therapeutic efficacy in sepsis.
PubMed, Embase, Scopus, WOS and ProQuest databases and also Google Scholar search engine were searched for published articles. We used hazard ratio (HR) and standardized mean difference (SMD) as effect sizes to evaluate the therapeutic effect of EV-MSCs on survival rate and determine their effect on reducing organ dysfunction, respectively. Finally, we employed GRADE tool for preclinical animal studies to evaluate certainty of the evidence.
30 studies met the inclusion criteria for our article. Our meta-analysis results demonstrate that animals treated with MSC-EVs have better survival rate than untreated animals (HR = 0.33; 95% CI: 0.27-0.41). Our meta-analysis suggests that EV-MSCs can reduce organ dysfunctions in sepsis, such as the lung, kidney, and liver. Additionally, EV-MSCs decrease pro-inflammatory mediators like TNF-α, IL-1β, and IL-6.
Our results indicate that EV-MSCs can be as promising therapy for sepsis management in animal models and leading to increased survival rate and reduced organ dysfunction. Furthermore, our study introduces a novel tool for risk of bias assessment and provides recommendations based on various analysis. Future studies with aiming to guide clinical translation can utilize the results of this article to establish stronger evidence for EV-MSC effectiveness.
脓毒症是一种危及生命的疾病,尚无确切的治愈方法。临床前研究表明,间充质基质细胞衍生的细胞外囊泡(EV-MSCs)可以减轻炎症状态,可能会提高脓毒症期间的生存率并减少器官功能障碍。我们进行这项系统评价和荟萃分析的目的是评估EV-MSCs在脓毒症中的治疗效果。
检索了PubMed、Embase、Scopus、WOS和ProQuest数据库以及谷歌学术搜索引擎中的已发表文章。我们使用风险比(HR)和标准化均数差(SMD)作为效应量,分别评估EV-MSCs对生存率的治疗效果以及确定其对减少器官功能障碍的作用。最后,我们采用GRADE工具对临床前动物研究进行证据确定性评估。
30项研究符合我们文章的纳入标准。我们的荟萃分析结果表明,接受MSC-EVs治疗的动物比未治疗的动物有更好的生存率(HR = 0.33;95%CI:0.27 - 0.41)。我们的荟萃分析表明,EV-MSCs可以减少脓毒症中的器官功能障碍,如肺、肾和肝脏。此外,EV-MSCs可降低促炎介质如TNF-α、IL-1β和IL-6。
我们的结果表明,EV-MSCs可能是动物模型中脓毒症管理的一种有前景的治疗方法,可提高生存率并减少器官功能障碍。此外,我们的研究引入了一种新的偏倚风险评估工具,并基于各种分析提供了建议。旨在指导临床转化的未来研究可以利用本文的结果来为EV-MSC的有效性建立更有力的证据。