Preclinical Studies of Mesenchymal Stem Cell (MSC) Administration in Chronic Obstructive Pulmonary Disease (COPD): A Systematic Review and Meta-Analysis

被引:41
作者
Liu, Xiangde [1 ]
Fang, Qiuhong [2 ]
Kim, Huijung [3 ]
机构
[1] Univ Nebraska Med Ctr, Dept Internal Med, Pulm Crit Care Sleep & Allergy Med, Omaha, NE USA
[2] Capital Med Univ, Beijing Chaoyang Hosp, Dept Pulm & Crit Care, Beijing, Peoples R China
[3] WonKwang Univ, Sanbon Med Ctr, Div Pulm & Crit Care, Seoul, South Korea
来源
PLOS ONE | 2016年 / 11卷 / 06期
关键词
ELASTASE-INDUCED EMPHYSEMA; REGULATORY T-CELLS; STROMAL CELLS; BONE-MARROW; MOUSE MODEL; ADIPOSE-TISSUE; LUNG INJURY; AIRWAY INFLAMMATION; STEM/STROMAL CELLS; GROWTH-FACTOR;
D O I
10.1371/journal.pone.0157099
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background In the last two decades, mesenchymal stem cells (MSCs) have been pre-clinically utilized in the treatment of a variety of kinds of diseases including chronic obstructive pulmonary disease (COPD). The aim of the current study was to systematically review and conduct a meta-analysis on the published pre-clinical studies of MSC administration in the treatment of COPD in animal models. Methods and Results A systematic search of electronic databases was performed. Statistical analysis was performed using the Comprehensive Meta-Analysis software (Version 3). The pooled Hedges's g with 95% confidence intervals (95% CIs) was adopted to assess the effect size. Random effect model was used due to the heterogeneity between the studies. A total of 20 eligible studies were included in the current systematic review. The overall meta-analysis showed that MSC administration was significantly in favor of attenuating acute lung injury (Hedges's g = -2.325 +/- 0.145 with 95% CI: -2.609 similar to -2.040, P < 0.001 for mean linear intercept, MLI; Hedges's g = -3.488 +/- 0.504 with 95% CI: -4.476 similar to -2.501, P < 0.001 for TUNEL staining), stimulating lung tissue repair (Hedges's g = 3.249 +/- 0.586 with 95% CI: 2.103 similar to 4.394, P < 0.001) and improving lung function (Hedges's g = 2.053 +/- 0.408 with 95% CI: 1.253 similar to 2.854, P< 0.001). The mechanism of MSC therapy in COPD is through ameliorating airway inflammation (Hedges's g = -2.956 +/- 0.371 with 95% CI: -3.683 similar to -2.229, P< 0.001) and stimulating cytokine synthesis that involves lung tissue repair (Hedges's g = 3.103 +/- 0.734 with 95% CI: 1.664 similar to 4.541, P< 0.001). Conclusion This systematic review and meta-analysis suggest a promising role for MSCs in COPD treatment. Although the COPD models may not truly mimic COPD patients, these pre-clinical studies demonstrate that MSC hold promise in the treatment of chronic lung diseases including COPD. The mechanisms of MSCs role in preclinical COPD treatment may be associated with attenuating airway inflammation as well as stimulating lung tissue repair.
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页数:17
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