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Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease
Graft versus host disease (GvHD) is a life-threating complication of allogeneic hematopoietic stem cell transplantation, which is initially treated with high dose corticosteroids. Approximately 50% of acute GvHD cases are resistant to steroid treatment, and two-year mortality rates in those steroid-...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577186/ https://www.ncbi.nlm.nih.gov/pubmed/34764962 http://dx.doi.org/10.3389/fimmu.2021.761616 |
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author | Kelly, Kilian Rasko, John E. J. |
author_facet | Kelly, Kilian Rasko, John E. J. |
author_sort | Kelly, Kilian |
collection | PubMed |
description | Graft versus host disease (GvHD) is a life-threating complication of allogeneic hematopoietic stem cell transplantation, which is initially treated with high dose corticosteroids. Approximately 50% of acute GvHD cases are resistant to steroid treatment, and two-year mortality rates in those steroid-resistant patients exceed 80%. Chronic GvHD necessitates prolonged corticosteroid use, which is typically associated with limited efficacy and troublesome adverse effects. No agent has yet been established as an optimal second line therapy for either acute or chronic GvHD, but mesenchymal stromal cells (MSCs) have shown substantial promise. MSCs promote an immunosuppressive and immunoregulatory environment via multifactorial mechanisms, including: secretion of proteins/peptides/hormones; transfer of mitochondria; and transfer of exosomes or microvesicles containing RNA and other molecules. A large number of clinical studies have investigated MSCs from various sources as a treatment for acute and/or chronic GvHD. MSCs are generally safe and well tolerated, and most clinical studies have generated encouraging efficacy results, but response rates have varied. Confounding factors include variability in MSC donor types, production methodology and dose regimens, as well as variations in study design. It is well-established that extensive culture expansion of primary donor-derived MSCs leads to marked changes in functionality, and that there is a high level of inter-donor variability in MSC properties. However, recent manufacturing innovations may be capable of overcoming these problems. Further adequately powered prospective studies are required to confirm efficacy and establish the place of MSC therapy in the treatment of this condition. |
format | Online Article Text |
id | pubmed-8577186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85771862021-11-10 Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease Kelly, Kilian Rasko, John E. J. Front Immunol Immunology Graft versus host disease (GvHD) is a life-threating complication of allogeneic hematopoietic stem cell transplantation, which is initially treated with high dose corticosteroids. Approximately 50% of acute GvHD cases are resistant to steroid treatment, and two-year mortality rates in those steroid-resistant patients exceed 80%. Chronic GvHD necessitates prolonged corticosteroid use, which is typically associated with limited efficacy and troublesome adverse effects. No agent has yet been established as an optimal second line therapy for either acute or chronic GvHD, but mesenchymal stromal cells (MSCs) have shown substantial promise. MSCs promote an immunosuppressive and immunoregulatory environment via multifactorial mechanisms, including: secretion of proteins/peptides/hormones; transfer of mitochondria; and transfer of exosomes or microvesicles containing RNA and other molecules. A large number of clinical studies have investigated MSCs from various sources as a treatment for acute and/or chronic GvHD. MSCs are generally safe and well tolerated, and most clinical studies have generated encouraging efficacy results, but response rates have varied. Confounding factors include variability in MSC donor types, production methodology and dose regimens, as well as variations in study design. It is well-established that extensive culture expansion of primary donor-derived MSCs leads to marked changes in functionality, and that there is a high level of inter-donor variability in MSC properties. However, recent manufacturing innovations may be capable of overcoming these problems. Further adequately powered prospective studies are required to confirm efficacy and establish the place of MSC therapy in the treatment of this condition. Frontiers Media S.A. 2021-10-26 /pmc/articles/PMC8577186/ /pubmed/34764962 http://dx.doi.org/10.3389/fimmu.2021.761616 Text en Copyright © 2021 Kelly and Rasko https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Kelly, Kilian Rasko, John E. J. Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease |
title | Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease |
title_full | Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease |
title_fullStr | Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease |
title_full_unstemmed | Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease |
title_short | Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease |
title_sort | mesenchymal stromal cells for the treatment of graft versus host disease |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577186/ https://www.ncbi.nlm.nih.gov/pubmed/34764962 http://dx.doi.org/10.3389/fimmu.2021.761616 |
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