Mesenchymal stromal cell extracellular vesicles for multiple sclerosis in preclinical rodent models: A meta-analysis

被引:15
作者
Xun, Chengfeng [1 ,2 ,3 ]
Deng, Huiyin [4 ]
Zhao, Jing [1 ]
Ge, Lite [1 ,2 ,3 ]
Hu, Zhiping [1 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Neurol, Changsha, Peoples R China
[2] Hunan Normal Univ, Affiliated Hosp 2, Hunan Prov Key Lab Neurorestoratol, Changsha, Peoples R China
[3] Hunan Normal Univ, Coll Life Sci, Natl & Local Joint Engn Lab Anim Peptide Drug Dev, Changsha, Peoples R China
[4] Cent South Univ, Xiangya Hosp 3, Dept Anesthesiol, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
exosomes; extracellular vesicles; stem cells; multiple sclerosis; animal model; meta-analysis; systematic review; CENTRAL-NERVOUS-SYSTEM; STEM-CELLS; ANIMAL-MODELS; BIAS;
D O I
10.3389/fimmu.2022.972247
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IntroductionExtracellular vesicles (EVs), especially mesenchymal stem (stromal) cell-derived EVs (MSC-EVs), have gained attention as potential novel treatments for multiple sclerosis (MS). However, their effects remain incompletely understood. Thus, the purpose of this meta-analysis was to systematically review the efficacy of MSC-EVs in preclinical rodent models of MS. MethodsWe searched PubMed, EMBASE, and the Web of Science databases up to August 2021 for studies that reported the treatment effects of MSC-EVs in rodent MS models. The clinical score was extracted as an outcome. Articles were peer-reviewed by two authors based on the inclusion and exclusion criteria. This meta-analysis was conducted using Stata 15.1 and R. ResultsA total of twelve animal studies met the inclusion criteria. In our study, the MSC-EVs had a positive overall effect on the clinical score with a standardized mean difference (SMD) of -2.17 (95% confidence interval (CI)):-3.99 to -0.34, P = 0.01). A significant amount of heterogeneity was observed among the studies. ConclusionsThis meta-analysis suggests that transplantation of MSC-EVs in MS rodent models improved functional recovery. Additionally, we identified several critical knowledge gaps, such as insufficient standardized dosage units and uncertainty regarding the optimal dose of MSC-EVs transplantation in MS. These gaps must be addressed before clinical trials can begin with MSC-EVs.
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页数:14
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