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

Expert Opin Biol Ther

Departments of Anesthesiology and Cardiovascular Research Institute, University of California, San Francisco, CA, USA.

Published: February 2020

AI Article Synopsis

  • Acute respiratory distress syndrome (ARDS) is a serious condition often seen in respiratory failure patients, and using mesenchymal stem cells (MSC) shows potential as a treatment for acute lung injury (ALI).
  • Concerns about MSC therapy include the risk of tumor development and the challenges of producing and standardizing MSC-derived products, like conditioned medium (CM) and extracellular vesicles (EV).
  • While MSC EVs have promising therapeutic potential due to their ability to retain the functionality of parent MSCs, their widespread use is hindered by high production costs and the need for large-scale manufacturing.

Article Abstract

: 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.: The current review focuses on the preclinical studies testing MSC CM and/or EV as treatment for ALI and other inflammatory lung diseases.: 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981051PMC
http://dx.doi.org/10.1080/14712598.2020.1689954DOI Listing

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