Methods and efficacy of extracellular vesicles derived from mesenchymal stromal cells in animal models of disease: a preclinical systematic review protocol

被引:18
作者
Tieu, Alvin [1 ,2 ,3 ]
Slobodian, Mitchell [2 ]
Fergusson, Dean A. [2 ,4 ,5 ]
Montroy, Joshua [2 ]
Burger, Dylan [1 ,6 ,7 ]
Stewart, Duncan J. [1 ,3 ,4 ]
Shorr, Risa [8 ]
Allan, David S. [2 ,3 ,4 ]
Lalu, Manoj M. [1 ,2 ,3 ,4 ,9 ]
机构
[1] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON, Canada
[2] Ottawa Hosp, Res Inst, BLUEPRINT Translat Res Grp, Clin Epidemiol Program, Ottawa, ON, Canada
[3] Ottawa Hosp, Res Inst, Regenerat Med Program, Ottawa, ON, Canada
[4] Univ Ottawa, Ottawa Hosp, Dept Med, Ottawa, ON, Canada
[5] Univ Ottawa, Ottawa Hosp, Dept Surg, Ottawa, ON, Canada
[6] Univ Ottawa, Ottawa Hosp, Dept Nephrol, Ottawa, ON, Canada
[7] Ottawa Hosp, Res Inst, Kidney Res Ctr, Ottawa, ON, Canada
[8] Ottawa Hosp, Learning Serv, Ottawa, ON, Canada
[9] Univ Ottawa, Ottawa Hosp, Dept Anesthesiol & Pain Med, Ottawa, ON, Canada
基金
加拿大健康研究院;
关键词
Mesenchymal stromal cells; Mesenchymal stem cells; Exosomes; Microvesicles; Extracellular vesicles; Systematic review protocol; Preclinical; STEM-CELL; SEARCH FILTER; METAANALYSIS; THERAPY;
D O I
10.1186/s13643-019-1242-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Over the past decade, mesenchymal stromal cells have been increasingly investigated for their therapeutic potential in several different illnesses. However, cell therapy can be limited by potentially serious adverse events including cell embolus formation and tumorigenesis. Importantly, the protective effects of mesenchymal stromal cells are largely mediated by paracrine mechanisms including release of extracellular vesicles. This systematic review intends to synthesize the current knowledge of mesenchymal stromal cell-derived extracellular vesicles as a therapeutic option for preclinical models of disease, inflammation, or injury. Methods A systematic literature search of MEDLINE, Embase, and BIOSIS databases will be conducted. Interventional preclinical in vivo studies using extracellular vesicles derived from any tissue source of mesenchymal stromal cells will be included. Studies will be screened by abstract, and full-text by two independent reviewers. Eligible studies will undergo data extraction with subcategorization into domains based on disease. Methods utilized for extracellular vesicle characterization and isolation will be collected, as well as information on interventional traits, such as tissue source of mesenchymal stromal cells, dosage regimen, and vesicle modifications. Reported outcomes will be collected to determine which diseases studied may be impacted most from treatment with mesenchymal stromal cell-derived extracellular vesicles. Discussion This systematic review will summarize preclinical studies investigating the therapeutic efficacy of both small and large extracellular vesicles derived by mesenchymal stromal cells. Extracellular vesicles represent a possibility to harness the benefits of mesenchymal stromal cells with added benefits of reduced manufacturing costs and an improved safety profile. Hence, there has been an exponential increase in interest for developing this cell-free therapy with hundreds of preclinical studies published to date. However, a vast amount of heterogeneity between groups relates to methods of extracellular vesicle isolation, characterization, and study design. This review will capture this heterogeneity and identify the most commonly used and optimal approaches to evaluate mesenchymal stromal cell-derived extracellular vesicle treatment. A meta-analysis of outcomes within each disease domain will help elucidate which fields of research demonstrate promise for developing extracellular vesicles as a novel cell-free therapy. Summarizing this robust information on extracellular vesicles as an intervention can provide guidance for designing preclinical studies with hopes of future clinical translation.
引用
收藏
页数:8
相关论文
共 29 条
[1]   A Systematic Review of Preclinical Studies on the Therapeutic Potential of Mesenchymal Stromal Cell-Derived Microvesicles [J].
Akyurekli, Celine ;
Le, Yevgeniya ;
Richardson, Richard B. ;
Fergusson, Dean ;
Tay, Jason ;
Allan, David S. .
STEM CELL REVIEWS AND REPORTS, 2015, 11 (01) :150-160
[2]  
[Anonymous], 2014, REV MAN REVMAN VERS
[3]   A search filter for increasing the retrieval of animal studies in Embase [J].
de Vries, Rob B. M. ;
Hooijmans, Carlijn R. ;
Tillema, Alice ;
Leenaars, Marlies ;
Ritskes-Hoitinga, Merel .
LABORATORY ANIMALS, 2011, 45 (04) :268-270
[4]   METAANALYSIS IN CLINICAL-TRIALS [J].
DERSIMONIAN, R ;
LAIRD, N .
CONTROLLED CLINICAL TRIALS, 1986, 7 (03) :177-188
[5]   Bias in meta-analysis detected by a simple, graphical test [J].
Egger, M ;
Smith, GD ;
Schneider, M ;
Minder, C .
BMJ-BRITISH MEDICAL JOURNAL, 1997, 315 (7109) :629-634
[6]   The ratio of means method as an alternative to mean differences for analyzing continuous outcome variables in meta-analysis: A simulation study [J].
Friedrich, Jan O. ;
Adhikari, Neill K. J. ;
Beyene, Joseph .
BMC MEDICAL RESEARCH METHODOLOGY, 2008, 8 (1)
[7]   Mesenchymal Stromal Cells: Clinical Challenges and Therapeutic Opportunities [J].
Galipeau, Jacques ;
Sensebe, Luc .
CELL STEM CELL, 2018, 22 (06) :824-833
[8]   Mesenchymal stem cells and immunomodulation: current status and future prospects [J].
Gao, F. ;
Chiu, S. M. ;
Motan, D. A. L. ;
Zhang, Z. ;
Chen, L. ;
Ji, H-L ;
Tse, H-F ;
Fu, Q-L ;
Lian, Q. .
CELL DEATH & DISEASE, 2016, 7 :e2062-e2062
[9]   Endothelial NO-Synthase Gene-Enhanced Progenitor Cell Therapy for Pulmonary Arterial Hypertension The PHACeT Trial [J].
Granton, John ;
Langleben, David ;
Kutryk, Michael B. ;
Camack, Nancy ;
Galipeau, Jacques ;
Courtman, David W. ;
Stewart, Duncan J. .
CIRCULATION RESEARCH, 2015, 117 (07) :645-654
[10]   Membrane vesicles, current state-of-the-art: emerging role of extracellular vesicles [J].
Gyoergy, Bence ;
Szabo, Tamas G. ;
Pasztoi, Maria ;
Pal, Zsuzsanna ;
Misjak, Petra ;
Aradi, Borbala ;
Laszlo, Valeria ;
Pallinger, Eva ;
Pap, Erna ;
Kittel, Agnes ;
Nagy, Gyoergy ;
Falus, Andras ;
Buzas, Edit I. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2011, 68 (16) :2667-2688