Preclinical Studies of MSC-Derived Extracellular Vesicles to Treat or Prevent Graft Versus Host Disease: a Systematic Review of the Literature

被引:18
作者
Gupta, Manika [1 ,2 ]
Tieu, Alvin [2 ,3 ]
Slobodian, Mitchell [3 ]
Shorr, Risa [4 ]
Burger, Dylan [2 ,5 ]
Lalu, Manoj M. [2 ,3 ]
Allan, David S. [1 ,2 ,3 ]
机构
[1] Ottawa Hosp, Dept Med, Blood & Marrow Transplantat, 501 Smyth Rd,Box 704, Ottawa, ON K1H 8L6, Canada
[2] Univ Ottawa, Fac Med, Ottawa, ON, Canada
[3] Ottawa Hosp Res Inst, Clin Epidmiol, Ottawa, ON, Canada
[4] Ottawa Hosp, Lib Serv, Ottawa, ON, Canada
[5] Ottawa Hosp Res Inst, Chron Dis Programs, Ottawa, ON, Canada
基金
加拿大健康研究院;
关键词
Graft versus host disease; Extracellular vesicles; Preclinical; Systematic review; Mesenchymal stromal cells; MESENCHYMAL STROMAL CELLS; STEM-CELLS; INTERNATIONAL BLOOD; RISK-FACTORS; EXOSOMES; RESISTANT; GVHD;
D O I
10.1007/s12015-020-10058-x
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Introduction Treating and preventing graft-versus-host disease (GVHD) after allogeneic hematopoietic cell transplant (HCT) remains a significant challenge. The use of mesenchymal stromal cell-derived extracellular vesicles (MSC-EVs) appears promising and a systematic review of preclinical studies is needed to accelerate the design of translational studies. Methods We identified 4 eligible studies from a systematic review performed on December 1, 2018. In brief, eligible studies included the treatment or prevention of GVHD in animal models and the use of MSC-EVs. Study design and outcome data were extracted and reporting was evaluated using the SYRCLE tool to identify potential bias. Results Two studies assessed the efficacy of MSC-EVs in treatment of GVHD and 2 studies address prevention. Mice treated with MSC-EVs showed improved median survival, GVHD clinical scores and histology scores as compared to untreated mice with GVHD. Prophylactic treatment with MSC-EVs attenuated GVHD severity and improved median survival as compared to no treatment or saline. Conclusion Our systematic review provides important insight regarding the potential of MSC-EVs to treat or prevent GVHD. Although few studies were identified, improved survival and attenuated histologic findings of GVHD were observed in mice after MSC-EV administration for the treatment and prevention of GVHD. Dosing of EVs and route of administration remain inconsistent, however, and scalability of EV isolation for clinical studies remains a challenge. Standardized outcome reporting is needed to pool results for metanalysis.
引用
收藏
页码:332 / 340
页数:9
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