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Universal or Personalized Mesenchymal Stem Cell Therapies: Impact of Age, Sex, and Biological Source

Mesenchymal stem/stromal cells (MSCs) hold great promise for the treatment of autoimmune conditions given their immunomodulatory properties. Based on the low immunogenicity of MSCs, it is tempting to consider the expansion of MSCs from a “universal donor” in culture prior to their allogeneic applica...

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Autores principales: Carp, Diana M., Liang, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9265811/
https://www.ncbi.nlm.nih.gov/pubmed/35805161
http://dx.doi.org/10.3390/cells11132077
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author Carp, Diana M.
Liang, Yun
author_facet Carp, Diana M.
Liang, Yun
author_sort Carp, Diana M.
collection PubMed
description Mesenchymal stem/stromal cells (MSCs) hold great promise for the treatment of autoimmune conditions given their immunomodulatory properties. Based on the low immunogenicity of MSCs, it is tempting to consider the expansion of MSCs from a “universal donor” in culture prior to their allogeneic applications for immediate care. This raises the critical question of the criteria we should use to select the best “universal donor”. It is also imperative we compare the “universal” approach with a “personalized” one for clinical value. In addition to the call for MHC-matching, recent studies suggest that factors including age, sex, and biological sources of MSCs can have significant impact on therapy outcome. Here, we will review findings from these studies, which shed light on the variables that can guide the important choice of “universal” or “personalized” MSC therapy for autoimmune diseases.
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spelling pubmed-92658112022-07-09 Universal or Personalized Mesenchymal Stem Cell Therapies: Impact of Age, Sex, and Biological Source Carp, Diana M. Liang, Yun Cells Review Mesenchymal stem/stromal cells (MSCs) hold great promise for the treatment of autoimmune conditions given their immunomodulatory properties. Based on the low immunogenicity of MSCs, it is tempting to consider the expansion of MSCs from a “universal donor” in culture prior to their allogeneic applications for immediate care. This raises the critical question of the criteria we should use to select the best “universal donor”. It is also imperative we compare the “universal” approach with a “personalized” one for clinical value. In addition to the call for MHC-matching, recent studies suggest that factors including age, sex, and biological sources of MSCs can have significant impact on therapy outcome. Here, we will review findings from these studies, which shed light on the variables that can guide the important choice of “universal” or “personalized” MSC therapy for autoimmune diseases. MDPI 2022-06-30 /pmc/articles/PMC9265811/ /pubmed/35805161 http://dx.doi.org/10.3390/cells11132077 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Carp, Diana M.
Liang, Yun
Universal or Personalized Mesenchymal Stem Cell Therapies: Impact of Age, Sex, and Biological Source
title Universal or Personalized Mesenchymal Stem Cell Therapies: Impact of Age, Sex, and Biological Source
title_full Universal or Personalized Mesenchymal Stem Cell Therapies: Impact of Age, Sex, and Biological Source
title_fullStr Universal or Personalized Mesenchymal Stem Cell Therapies: Impact of Age, Sex, and Biological Source
title_full_unstemmed Universal or Personalized Mesenchymal Stem Cell Therapies: Impact of Age, Sex, and Biological Source
title_short Universal or Personalized Mesenchymal Stem Cell Therapies: Impact of Age, Sex, and Biological Source
title_sort universal or personalized mesenchymal stem cell therapies: impact of age, sex, and biological source
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9265811/
https://www.ncbi.nlm.nih.gov/pubmed/35805161
http://dx.doi.org/10.3390/cells11132077
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