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- Featured Article from the ISCT Exosomes Scientific Committee
Critical considerations for the development of potency tests for therapeutic applications of mesenchymal stromal cell-derived small extracellular vesicles
CytotherapyVol. 23Issue 5p373–380Published online: April 9, 2021- Mario Gimona
- Maria Felice Brizzi
- Andre Boon Hwa Choo
- Massimo Dominici
- Sean M. Davidson
- Johannes Grillari
- and others
Cited in Scopus: 58Mesenchymal stromal/stem cells (MSCs) have been widely tested against many diseases, with more than 1000 registered clinical trials worldwide. Despite many setbacks, MSCs have been approved for the treatment of graft-versus-host disease and Crohn disease. However, it is increasingly clear that MSCs exert their therapeutic functions in a paracrine manner through the secretion of small extracellular vesicles (sEVs) of 50–200 nm in diameter. Unlike living cells that can persist long-term, sEVs are non-living and non-replicative and have a transient presence in the body. - Short Communication
International Society for Extracellular Vesicles and International Society for Cell and Gene Therapy statement on extracellular vesicles from mesenchymal stromal cells and other cells: considerations for potential therapeutic agents to suppress coronavirus disease-19
CytotherapyVol. 22Issue 9p482–485Published online: May 16, 2020- Verena Börger
- Daniel J. Weiss
- Johnathon D. Anderson
- Francesc E. Borràs
- Benedetta Bussolati
- David R.F. Carter
- and others
Cited in Scopus: 69STATEMENT: The International Society for Cellular and Gene Therapies (ISCT) and the International Society for Extracellular Vesicles (ISEV) recognize the potential of extracellular vesicles (EVs, including exosomes) from mesenchymal stromal cells (MSCs) and possibly other cell sources as treatments for COVID-19. Research and trials in this area are encouraged. However, ISEV and ISCT do not currently endorse the use of EVs or exosomes for any purpose in COVID-19, including but not limited to reducing cytokine storm, exerting regenerative effects or delivering drugs, pending the generation of appropriate manufacturing and quality control provisions, pre-clinical safety and efficacy data, rational clinical trial design and proper regulatory oversight.