MSC-Derived Extracellular Vesicles to Heal Diabetic Wounds: a Systematic Review and Meta-Analysis of Preclinical Animal Studies

被引:42
作者
Bailey, Adrian J. M. [1 ,2 ,3 ]
Li, Heidi [1 ]
Kirkham, Aidan M. [2 ,3 ]
Tieu, Alvin [1 ,3 ,4 ,5 ,6 ]
Maganti, Harinad B. [2 ,3 ]
Shorr, Risa [7 ]
Fergusson, Dean A. [1 ,3 ,8 ,9 ]
Lalu, Manoj M. [1 ,3 ,4 ,5 ,6 ,10 ,11 ]
Elomazzen, Heidi [2 ]
Allan, David S. [1 ,2 ,3 ,4 ,8 ,12 ]
机构
[1] Univ Ottawa, Fac Med, Ottawa, ON, Canada
[2] Canadian Blood Serv, Stem Cells & Ctr Innovat, Ottawa, ON, Canada
[3] Ottawa Hosp Res Inst, Clin Epidemiol, Ottawa, ON, Canada
[4] Ottawa Hosp Res Inst, Regenerat Med Programs, Ottawa, ON, Canada
[5] Univ Ottawa, Dept Cellular, Ottawa, ON, Canada
[6] Univ Ottawa, Dept Mol Med, Ottawa, ON, Canada
[7] Ottawa Hosp, Lib & Informat Serv, Ottawa, ON, Canada
[8] Univ Ottawa, Ottawa Hosp, Med, Ottawa, ON, Canada
[9] Univ Ottawa, Sch Publ Hlth & Epidemiol, Ottawa, ON, Canada
[10] Univ Ottawa, Dept Anesthesiol, Ottawa, ON, Canada
[11] Univ Ottawa, Dept Pain Med, Ottawa, ON, Canada
[12] Univ Ottawa, Biochem Microbiol & Immunol, Ottawa, ON, Canada
关键词
Mesenchymal stromal cells; Extracellular vesicles; Exosomes; Diabetes; Wound healing; MESENCHYMAL STEM-CELLS; STROMAL CELLS; FOOT ULCERS; EXOSOMES; ANGIOGENESIS; EFFICACY; HYDROGEL; THERAPY; SAFETY; TOOL;
D O I
10.1007/s12015-021-10164-4
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Introduction Extracellular vesicles from mesenchymal stromal cells (MSC-EVs) have shown promise in wound healing. Their use in diabetic wounds specifically, however, remains pre-clinical and their efficacy remains uncertain less clear. A systematic review of preclinical studies is needed to determine the efficacy of MSC-EVs in the treatment of diabetic wounds to accelerate the clinical translation of this cell-based therapy. Methods PubMed and Embase were searched (to June 23, 2020). All English-language, full-text, controlled interventional studies comparing MSC-EVs to placebo or a "no treatment" arm in animal models of diabetic wounds were included. Study outcomes, including wound closure (primary outcome), scar width, blood vessel number and density, and re-epithelialisation were pooled using a random effects meta-analysis. Risk of bias (ROB) was assessed using the SYRCLE tool for pre-clinical animal studies. Results A total of 313 unique records were identified from our search, with 10 full text articles satisfying inclusion criteria (n = 136 animals). The administration of MSC-EVs improved closure of diabetic wounds compared to controls with a large observed effect (Standardized Mean Difference (SMD) 5.48, 95% Confidence Interval (CI) 3.55-8.13). Healing was further enhanced using MSC-EVs enriched in non-coding RNAs or microRNAs compared to controls (SMD 9.89, 95%CI 7.32-12.46). Other outcomes, such as blood vessel density and number, scar width, and re-epithelialisation were improved with the administration of MSC-EVs, with a large effect. ROB across studies was unclear. Conclusion MSC-EVs, particularly following enrichment for specific RNAs, are a promising treatment for diabetic wounds in pre-clinical studies and translation to the clinical domain appears warranted.
引用
收藏
页码:968 / 979
页数:12
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