McIntyre Lauralyn A, Moher David, Fergusson Dean A, Sullivan Katrina J, Mei Shirley H J, Lalu Manoj, Marshall John, Mcleod Malcolm, Griffin Gilly, Grimshaw Jeremy, Turgeon Alexis, Avey Marc T, Rudnicki Michael A, Jazi Mazen, Fishman Jason, Stewart Duncan J
Department of Medicine (Division of Critical Care), University of Ottawa, Ottawa, Ontario, Canada.
The Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
PLoS One. 2016 Jan 28;11(1):e0147170. doi: 10.1371/journal.pone.0147170. eCollection 2016.
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.
急性呼吸窘迫综合征(ARDS)是一种严重的临床病症,其死亡风险为30%-40%,幸存者还会有严重的长期发病率。间充质基质细胞(MSC)已成为一种潜在的新型治疗方法,因为在临床前模型中,它们已被证明可以调节炎症(ARDS的主要病理生理特征),同时增强细菌清除能力,减少器官损伤和死亡。我们对MEDLINE、EMBASE、BIOSIS和科学网进行了系统检索,以确定与患病对照组相比,研究MSC治疗急性肺损伤(ALI,人类ARDS的临床前对应病症)对死亡率(一项临床相关结果)疗效的临床前研究。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项实验)报告了死亡率并被纳入荟萃分析。与对照组相比,用MSC治疗可显著降低ALI动物的总体死亡几率(优势比0.24,95%置信区间0.18-0.34,I2 8%)。在不同类型的动物模型和ALI诱导方式中均保持了疗效;MSC的来源、源头、给药途径和制剂;以及模型的临床相关性(MSC给药时间、液体和/或抗生素的给药)。对于使用人类MSC的实验,标准MSC特征的报告和偏倚风险通常较差,尽管无统计学意义,但总体死亡率的漏斗图分析表明存在发表偏倚。我们的荟萃分析结果支持,MSC可大幅降低ALI动物模型的死亡几率,但重要的报告要素不够理想,限制了我们结论的力度。