Cargando…
Therapeutic potential of mesenchymal stem/stromal cells (MSCs)-based cell therapy for inflammatory bowel diseases (IBD) therapy
Recently, mesenchymal stem/stromal cells (MSCs) therapy has become an emerging therapeutic modality for the treatment of inflammatory bowel disease (IBD), given their immunoregulatory and pro-survival attributes. MSCs alleviate dysregulated inflammatory responses through the secretion of a myriad of...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881387/ https://www.ncbi.nlm.nih.gov/pubmed/36707899 http://dx.doi.org/10.1186/s40001-023-01008-7 |
_version_ | 1784879099006681088 |
---|---|
author | Saadh, Mohamed J. Mikhailova, Maria V. Rasoolzadegan, Soheil Falaki, Mojgan Akhavanfar, Roozbeh Gonzáles, José Luis Arias Rigi, Amir Kiasari, Bahman Abedi |
author_facet | Saadh, Mohamed J. Mikhailova, Maria V. Rasoolzadegan, Soheil Falaki, Mojgan Akhavanfar, Roozbeh Gonzáles, José Luis Arias Rigi, Amir Kiasari, Bahman Abedi |
author_sort | Saadh, Mohamed J. |
collection | PubMed |
description | Recently, mesenchymal stem/stromal cells (MSCs) therapy has become an emerging therapeutic modality for the treatment of inflammatory bowel disease (IBD), given their immunoregulatory and pro-survival attributes. MSCs alleviate dysregulated inflammatory responses through the secretion of a myriad of anti-inflammatory mediators, such as interleukin 10 (IL-10), transforming growth factor-β (TGFβ), prostaglandin E2 (PGE2), tumor necrosis factor-stimulated gene-6 (TSG-6), etc. Indeed, MSC treatment of IBD is largely carried out through local microcirculation construction, colonization and repair, and immunomodulation, thus alleviating diseases severity. The clinical therapeutic efficacy relies on to the marked secretion of various secretory molecules from viable MSCs via paracrine mechanisms that are required for gut immuno-microbiota regulation and the proliferation and differentiation of surrounding cells like intestinal epithelial cells (IECs) and intestinal stem cells (ISCs). For example, MSCs can induce IECs proliferation and upregulate the expression of tight junction (TJs)-associated protein, ensuring intestinal barrier integrity. Concerning the encouraging results derived from animal studies, various clinical trials are conducted or ongoing to address the safety and efficacy of MSCs administration in IBD patients. Although the safety and short-term efficacy of MSCs administration have been evinced, the long-term efficacy of MSCs transplantation has not yet been verified. Herein, we have emphasized the illumination of the therapeutic capacity of MSCs therapy, including naïve MSCs, preconditioned MSCs, and also MSCs-derived exosomes, to alleviate IBD severity in experimental models. Also, a brief overview of published clinical trials in IBD patients has been delivered. |
format | Online Article Text |
id | pubmed-9881387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98813872023-01-28 Therapeutic potential of mesenchymal stem/stromal cells (MSCs)-based cell therapy for inflammatory bowel diseases (IBD) therapy Saadh, Mohamed J. Mikhailova, Maria V. Rasoolzadegan, Soheil Falaki, Mojgan Akhavanfar, Roozbeh Gonzáles, José Luis Arias Rigi, Amir Kiasari, Bahman Abedi Eur J Med Res Review Recently, mesenchymal stem/stromal cells (MSCs) therapy has become an emerging therapeutic modality for the treatment of inflammatory bowel disease (IBD), given their immunoregulatory and pro-survival attributes. MSCs alleviate dysregulated inflammatory responses through the secretion of a myriad of anti-inflammatory mediators, such as interleukin 10 (IL-10), transforming growth factor-β (TGFβ), prostaglandin E2 (PGE2), tumor necrosis factor-stimulated gene-6 (TSG-6), etc. Indeed, MSC treatment of IBD is largely carried out through local microcirculation construction, colonization and repair, and immunomodulation, thus alleviating diseases severity. The clinical therapeutic efficacy relies on to the marked secretion of various secretory molecules from viable MSCs via paracrine mechanisms that are required for gut immuno-microbiota regulation and the proliferation and differentiation of surrounding cells like intestinal epithelial cells (IECs) and intestinal stem cells (ISCs). For example, MSCs can induce IECs proliferation and upregulate the expression of tight junction (TJs)-associated protein, ensuring intestinal barrier integrity. Concerning the encouraging results derived from animal studies, various clinical trials are conducted or ongoing to address the safety and efficacy of MSCs administration in IBD patients. Although the safety and short-term efficacy of MSCs administration have been evinced, the long-term efficacy of MSCs transplantation has not yet been verified. Herein, we have emphasized the illumination of the therapeutic capacity of MSCs therapy, including naïve MSCs, preconditioned MSCs, and also MSCs-derived exosomes, to alleviate IBD severity in experimental models. Also, a brief overview of published clinical trials in IBD patients has been delivered. BioMed Central 2023-01-27 /pmc/articles/PMC9881387/ /pubmed/36707899 http://dx.doi.org/10.1186/s40001-023-01008-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Saadh, Mohamed J. Mikhailova, Maria V. Rasoolzadegan, Soheil Falaki, Mojgan Akhavanfar, Roozbeh Gonzáles, José Luis Arias Rigi, Amir Kiasari, Bahman Abedi Therapeutic potential of mesenchymal stem/stromal cells (MSCs)-based cell therapy for inflammatory bowel diseases (IBD) therapy |
title | Therapeutic potential of mesenchymal stem/stromal cells (MSCs)-based cell therapy for inflammatory bowel diseases (IBD) therapy |
title_full | Therapeutic potential of mesenchymal stem/stromal cells (MSCs)-based cell therapy for inflammatory bowel diseases (IBD) therapy |
title_fullStr | Therapeutic potential of mesenchymal stem/stromal cells (MSCs)-based cell therapy for inflammatory bowel diseases (IBD) therapy |
title_full_unstemmed | Therapeutic potential of mesenchymal stem/stromal cells (MSCs)-based cell therapy for inflammatory bowel diseases (IBD) therapy |
title_short | Therapeutic potential of mesenchymal stem/stromal cells (MSCs)-based cell therapy for inflammatory bowel diseases (IBD) therapy |
title_sort | therapeutic potential of mesenchymal stem/stromal cells (mscs)-based cell therapy for inflammatory bowel diseases (ibd) therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881387/ https://www.ncbi.nlm.nih.gov/pubmed/36707899 http://dx.doi.org/10.1186/s40001-023-01008-7 |
work_keys_str_mv | AT saadhmohamedj therapeuticpotentialofmesenchymalstemstromalcellsmscsbasedcelltherapyforinflammatoryboweldiseasesibdtherapy AT mikhailovamariav therapeuticpotentialofmesenchymalstemstromalcellsmscsbasedcelltherapyforinflammatoryboweldiseasesibdtherapy AT rasoolzadegansoheil therapeuticpotentialofmesenchymalstemstromalcellsmscsbasedcelltherapyforinflammatoryboweldiseasesibdtherapy AT falakimojgan therapeuticpotentialofmesenchymalstemstromalcellsmscsbasedcelltherapyforinflammatoryboweldiseasesibdtherapy AT akhavanfarroozbeh therapeuticpotentialofmesenchymalstemstromalcellsmscsbasedcelltherapyforinflammatoryboweldiseasesibdtherapy AT gonzalesjoseluisarias therapeuticpotentialofmesenchymalstemstromalcellsmscsbasedcelltherapyforinflammatoryboweldiseasesibdtherapy AT rigiamir therapeuticpotentialofmesenchymalstemstromalcellsmscsbasedcelltherapyforinflammatoryboweldiseasesibdtherapy AT kiasaribahmanabedi therapeuticpotentialofmesenchymalstemstromalcellsmscsbasedcelltherapyforinflammatoryboweldiseasesibdtherapy |