Mesenchymal stem cell-derived exosomes for managing graft-versus-host disease: An updated view.

Exosome Graft-versus-host disease (GvHD) Mesenchymal stem cell (MSC)

Journal

Transplant immunology
ISSN: 1878-5492
Titre abrégé: Transpl Immunol
Pays: Netherlands
ID NLM: 9309923

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 12 07 2023
revised: 02 11 2023
accepted: 03 11 2023
pubmed: 8 11 2023
medline: 8 11 2023
entrez: 7 11 2023
Statut: ppublish

Résumé

Graft-versus-host disease (GvHD) is the most common complication after stem cell transplantation, and also it is one of the primary limiting factors for the use of hematopoietic stem cell transplantation (HSCT) in the treatment of hematologic cancers. GvHD, a systemic inflammatory disease, is caused by donor T cells recognizing the recipient's foreign antigens. In addition, an immune dysregulation, caused by autoreactive immune cells, complicates potent inflammatory process following HSCT. While there is no one approved treatment method for GvHD, corticosteroids are the most common first-line treatment. Exosomes are biological vesicles between 30 and 120 nm in diameter, which carry various biologically active molecules. They are known to play a key role in the paracrine effect of mesenchymal stem cells with therapeutic and tissue repair effects, including an immunosuppressive potential. Exosomes are unable to replicate themselves but because of their small size and fluid-like structure, they can pass through physiological barriers. Exosome are relatively easy to prepare and they can be quickly sterilized by a filtration process. Administration of exosomes, derived from mesenchymal stem cells, effectively reduced GvHD symptoms and significantly increased HSCT recipients' survival. Mesenchymal stem cell-derived exosome therapy reduced clinical symptoms of GvHD in patients after HSCT. Studies in patients with GvHD described that that mesenchymal stem cell-derived exosomes inhibited the release of IFN-γ and TNF-α by activated natural killer (NK cells), thereby reducing the lethal function of NK cells and inflammatory responses. Current review provides a comprehensive overview about the use of mesenchymal stem cells and their derived exosomes for the treatment of GvHD.

Identifiants

pubmed: 37935319
pii: S0966-3274(23)00174-0
doi: 10.1016/j.trim.2023.101957
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

101957

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no competing interests.

Auteurs

Zahra Shafeghat (Z)

Department of Immunology, School of medicine, Iran University of Medical Sciences, Tehran, Iran.

Maryam Dorfaki (M)

Department of Microbiology and Immunology, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran.

Shiva Dehrouyeh (S)

Department of Immunology, School of medicine, Iran University of Medical Sciences, Tehran, Iran.

Fahime Lavi Arab (FL)

Department of Immunology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Mona Roozbehani (M)

Vaccine Research Center, Iran University of Medical Sciences, Tehran, Iran.

Reza Falak (R)

Immunology Research Center, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran. Electronic address: Falak.r@iums.ac.ir.

Fatemeh Faraji (F)

Antimicrobial Resistance Research Center, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran. Electronic address: Faraji.fat@iums.ac.ir.

Reza Jafari (R)

Cellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran. Electronic address: Jafari.reza@umsu.ac.ir.

Classifications MeSH