From Mesenchymal Stromal Cells to Engineered Extracellular Vesicles: A New Therapeutic Paradigm.

EV therapeutics MSC-EVs MSCs engineered EVs extracellular vesicles mesenchymal stromal cells

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2021
Historique:
received: 06 05 2021
accepted: 29 06 2021
entrez: 19 8 2021
pubmed: 20 8 2021
medline: 20 8 2021
Statut: epublish

Résumé

Mesenchymal stromal cells (MSCs) are multipotent cells obtained from many tissues including bone marrow, adipose tissue, umbilical cord, amniotic fluid, and placenta. MSCs are the leading cell source for stem cell therapy due to their regenerative and immunomodulatory properties, their low risk of tumorigenesis and lack of ethical constraints. However, clinical applications of MSCs remain limited. MSC therapeutic development continues to pose challenges in terms of preparation, purity, consistency, efficiency, reproducibility, processing time and scalability. Additionally, there are issues with their poor engraftment and survival in sites of disease or damage that limit their capacity to directly replace damaged cells. A key recent development in MSC research, however, is the now widely accepted view that MSCs primarily exert therapeutic effects via paracrine factor secretion. One of the major paracrine effectors are extracellular vesicles (EVs). EVs represent a potential cell-free alternative to stem cell therapy but are also rapidly emerging as a novel therapeutic platform in their own right, particularly in the form of engineered EVs (EEVs) tailored to target a broad range of clinical indications. However, the development of EVs and EEVs for therapeutic application still faces a number of hurdles, including the establishment of a consistent, scalable cell source, and the development of robust GMP-compliant upstream and downstream manufacturing processes. In this review we will highlight the clinical challenges of MSC therapeutic development and discuss how EVs and EEVs can overcome the challenges faced in the clinical application of MSCs.

Identifiants

pubmed: 34409037
doi: 10.3389/fcell.2021.705676
pmc: PMC8366519
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

705676

Informations de copyright

Copyright © 2021 Johnson, Shojaee, Mitchell Crow and Khanabdali.

Déclaration de conflit d'intérêts

MS, JJ, and RK are employed by Exopharm Ltd. JMC is a contractor to Exopharm Ltd.

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Auteurs

Jancy Johnson (J)

Exopharm Ltd., Melbourne, VIC, Australia.
Department of Biochemistry and Pharmacology, University of Melbourne, Parkville, VIC, Australia.

Mozhgan Shojaee (M)

Exopharm Ltd., Melbourne, VIC, Australia.

James Mitchell Crow (J)

Exopharm Ltd., Melbourne, VIC, Australia.

Ramin Khanabdali (R)

Exopharm Ltd., Melbourne, VIC, Australia.

Classifications MeSH