Therapeutic potential of mesenchymal stem/stromal cell-derived secretome and vesicles for lung injury and disease

被引:82
|
作者
Liu, Airan [1 ]
Zhang, Xiwen [1 ]
He, Hongli [2 ,3 ]
Zhou, Li [2 ,3 ]
Naito, Yoshifumi [2 ,3 ]
Sugita, Shinji [2 ,3 ]
Lee, Jae-Woo [2 ,3 ]
机构
[1] Southeast Univ, Sch Med, Zhongda Hosp, Dept Crit Care Med, Nanjing, Jiangsu, Peoples R China
[2] Univ Calif San Francisco, Dept Anesthesiol, 505 Parnassus Ave,Box 0648, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Cardiovasc Res Inst, Box 0130, San Francisco, CA 94143 USA
关键词
Acute lung injury; acute respiratory distress syndrome; exosomes; extracellular vesicles; mesenchymal stem or stromal cells; microvesicles; ENDOTHELIAL PROGENITOR CELLS; RESPIRATORY-DISTRESS-SYNDROME; ALVEOLAR FLUID CLEARANCE; STEM-CELLS; BONE-MARROW; STROMAL CELLS; EXTRACELLULAR VESICLES; INTRAVENOUS DELIVERY; HORIZONTAL TRANSFER; CONDITIONED MEDIUM;
D O I
10.1080/14712598.2020.1689954
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: The acute respiratory distress syndrome (ARDS) is a devastating clinical condition common in patients with respiratory failure. Based largely on numerous preclinical studies and recent Phase I/II clinical trials, administration of stem cells, specifically mesenchymal stem or stromal cells (MSC), as a therapeutic for acute lung injury (ALI) holds great promise. However, concern for the use of stem cells, specifically the risk of iatrogenic tumor formation, remains unresolved. Accumulating evidence now suggest that stem cell-derived conditioned medium (CM) and/or extracellular vesicles (EV) might constitute compelling alternatives. Areas covered: The current review focuses on the preclinical studies testing MSC CM and/or EV as treatment for ALI and other inflammatory lung diseases. Expert opinion: Clinical application of MSC or their secreted CM may be limited by the cost of growing enough cells, the logistic of MSC storage, and the lack of standardization of what constitutes MSC CM. However, the clinical application of MSC EV remains promising, primarily due to the ability of EV to maintain the functional phenotype of the parent cell as a therapeutic. However, utilization of MSC EV will also require large-scale production, the cost of which may be prohibitive unless the potency of the EV can be increased.
引用
收藏
页码:125 / 140
页数:16
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