Stem cell Derived Extracellular Vesicles to Alleviate ischemia-reperfusion Injury of Transplantable Organs. A Systematic Review

被引:5
作者
Blondeel, Joris [1 ,2 ]
Gilbo, Nicholas [1 ,3 ]
De Bondt, Stijn [4 ]
Monbaliu, Diethard [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Lab Abdominal Transplantat, Leuven, Belgium
[2] Univ Hosp Leuven, Dept Abdominal Transplant Surg & Coordinat, Herestraat 49, B-3000 Leuven, Belgium
[3] CHU Liege, Dept Abdominal Surg & Transplantat, Liege, Belgium
[4] Katholieke Univ Leuven, Fac Med, Leuven, Belgium
关键词
MESENCHYMAL STROMAL CELLS; ALVEOLAR FLUID CLEARANCE; ISCHEMIA/REPERFUSION INJURY; LIVER-TRANSPLANTATION; CARDIAC DEATH; OXIDATIVE STRESS; EXOSOMES; PROTECT; KIDNEY; MICROVESICLES;
D O I
10.1007/s12015-023-10573-7
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background The possible beneficial effects of stem cell-derived EV on ischemia-reperfusion injury (IRI) in organ transplantation have been frequently investigated; however, the source of EV, as well as the methods of isolation and administration vary widely. We conducted a systematic review to summarize current pre-clinical evidence on stem cell-derived EV therapy for IRI of transplantable organs. Methods PubMed, Embase and Web of Science were searched from inception until August 19th, 2022, for studies on stem cell-derived EV therapy for IRI after heart, kidney, liver, pancreas, lung and intestine transplantation. The Systematic Review Center for Laboratory animal Experiments (SYRCLE) guidelines were followed to assess potential risk of bias. Results The search yielded 4153 unique articles, of which 96 were retained. We identified 32 studies on cardiac IRI, 38 studies on renal IRI, 21 studies on liver IRI, four studies on lung IRI and one study on intestinal IRI. Most studies used rodent models of transient ischemic injury followed by in situ reperfusion. In all studies, EV therapy was associated with improved outcome albeit to a variable degree. EV-therapy reduced organ injury and improved function while displaying anti-inflammatory-, immunomodulatory- and pro-regenerative properties. Conclusion A multitude of animal studies support the potential of stem cell-derived EV-therapy to alleviate IRI after solid organ transplantation but suffer from low reporting quality and wide methodological variability. Future studies should focus on determining optimal stem cell source, dosage, and timing of treatment, as well as long-term efficacy in transplant models.
引用
收藏
页码:2225 / 2250
页数:26
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