Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Sep 10:8:997.
doi: 10.3389/fbioe.2020.00997. eCollection 2020.

Mesenchymal Stem Cell-Derived Extracellular Vesicles: Opportunities and Challenges for Clinical Translation

Affiliations
Review

Mesenchymal Stem Cell-Derived Extracellular Vesicles: Opportunities and Challenges for Clinical Translation

Marie Maumus et al. Front Bioeng Biotechnol. .

Abstract

Extracellular vesicles (EVs), including exosomes and microvesicles, derived from mesenchymal stem/stromal cells (MSCs) exert similar effects as their parental cells, and are of interest for various therapeutic applications. EVs can act through uptake by the target cells followed by release of their cargo inside the cytoplasm, or through interaction of membrane-bound ligands with receptors expressed on target cells to stimulate downstream intracellular pathways. EV-based therapeutics may be directly used as substitutes of intact cells or after modification for targeted drug delivery. However, for the development of EV-based therapeutics, several production, isolation, and characterization requirements have to be met and the quality of the final product has to be tested before its clinical implementation. In this review, we discuss the challenges associated with the development of EV-based therapeutics and the regulatory specifications for their successful clinical translation.

Keywords: clinical translation; extracellular vesicles; mesenchymal stem cells; regenerative medicine; therapy.

PubMed Disclaimer

References

    1. Abbasi-Malati Z., Roushandeh A. M., Kuwahara Y., Roudkenar M. H. (2018). Mesenchymal stem cells on horizon: a new arsenal of therapeutic agents. Stem Cell Rev. 14 484–499. 10.1007/s12015-018-9817-x - DOI - PubMed
    1. Agrahari V., Agrahari V., Burnouf P. A., Chew C. H., Burnouf T. (2019). Extracellular microvesicles as new industrial therapeutic frontiers. Trends Biotechnol. 37 707–729. 10.1016/j.tibtech.2018.11.012 - DOI - PubMed
    1. Baglio S. R., Rooijers K., Koppers-Lalic D., Verweij F. J., Perez Lanzon M., Zini N., et al. (2015). Human bone marrow- and adipose-mesenchymal stem cells secrete exosomes enriched in distinctive miRNA and tRNA species. Stem Cell Res. Ther. 6:127. 10.1186/s13287-015-0116-z - DOI - PMC - PubMed
    1. Bai L., Shao H., Wang H., Zhang Z., Su C., Dong L., et al. (2017). Effects of mesenchymal stem cell-derived exosomes on experimental autoimmune uveitis. Sci. Rep. 7:4323. 10.1038/s41598-017-04559-y - DOI - PMC - PubMed
    1. Bari E., Ferrarotti I., Di Silvestre D., Grisoli P., Barzon V., Balderacchi A., et al. (2019a). Adipose mesenchymal extracellular vesicles as alpha-1-antitrypsin physiological delivery systems for lung regeneration. Cells 8:965. 10.3390/cells8090965 - DOI - PMC - PubMed