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Efficacy of Mesenchymal Stromal Cell Therapy for Acute Lung Injury in Preclinical Animal Models: A Systematic Review

机译:间充质基质细胞疗法在临床前动物模型中对急性肺损伤的疗效:系统评价

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摘要

The Acute Respiratory Distress Syndrome (ARDS) is a devastating clinical condition that is associated with a 30–40% risk of death, and significant long term morbidity for those who survive. Mesenchymal stromal cells (MSC) have emerged as a potential novel treatment as in pre-clinical models they have been shown to modulate inflammation (a major pathophysiological hallmark of ARDS) while enhancing bacterial clearance and reducing organ injury and death. A systematic search of MEDLINE, EMBASE, BIOSIS and Web of Science was performed to identify pre-clinical studies that examined the efficacy MSCs as compared to diseased controls for the treatment of Acute Lung Injury (ALI) (the pre-clinical correlate of human ARDS) on mortality, a clinically relevant outcome. We assessed study quality and pooled results using random effect meta-analysis. A total of 54 publications met our inclusion criteria of which 17 (21 experiments) reported mortality and were included in the meta-analysis. Treatment with MSCs, as compared to controls, significantly decreased the overall odds of death in animals with ALI (Odds Ratio 0.24, 95% Confidence Interval 0.18–0.34, I2 8%). Efficacy was maintained across different types of animal models and means of ALI induction; MSC origin, source, route of administration and preparation; and the clinical relevance of the model (timing of MSC administration, administration of fluids and or antibiotics). Reporting of standard MSC characterization for experiments that used human MSCs and risks of bias was generally poor, and although not statistically significant, a funnel plot analysis for overall mortality suggested the presence of publication bias. The results from our meta-analysis support that MSCs substantially reduce the odds of death in animal models of ALI but important reporting elements were sub optimal and limit the strength of our conclusions.
机译:急性呼吸窘迫综合征(ARDS)是一种破坏性临床疾病,与30%至40%的死亡风险以及存活者的严重长期发病率相关。间质基质细胞(MSC)已成为一种潜在的新型治疗方法,就像在临床前模型中一样,它们已被证明可以调节炎症(ARDS的主要病理生理特征),同时增强细菌清除率并减少器官损伤和死亡。对MEDLINE,EMBASE,BIOSIS和Web of Science进行了系统搜索,以确定临床前研究,该研究检查了MSC与患病对照相比在治疗急性肺损伤(ALI)(人类ARDS的临床前相关性)方面的功效。 ),这是临床相关的结果。我们使用随机效应荟萃分析评估研究质量并汇总结果。共有54篇出版物符合我们的纳入标准,其中17篇(21个实验)报告了死亡率,并纳入了荟萃分析。与对照组相比,用MSCs治疗可显着降低ALI动物的总死亡几率(几率0.24,95%置信区间0.18-0.34,I 2 8%)。在不同类型的动物模型和ALI诱导方法中均保持了疗效; MSC的来源,来源,给药途径和制备方法;以及模型的临床相关性(MSC给药的时间,液体和/或抗生素的给药时间)。对于使用人MSC的实验进行标准MSC表征的报告和偏倚风险通常较差,尽管统计意义不大,但总死亡率的漏斗图分析表明存在出版物偏倚。我们的荟萃分析结果表明,MSCs可以大大降低ALI动物模型中的死亡几率,但重要的报告要素却不够理想,因此限制了我们的结论。

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