Allogeneic vs. autologous mesenchymal stem/stromal cells in their medication practice

Abstract Mesenchymal stem/stromal cell (MSC)-based therapeutics is already available for treatment of a range of diseases or medical conditions. Autologous or allogeneic MSCs obtained from self or donors have their own advantages and disadvantages in their medical practice. Therapeutic benefits of u...

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Autores principales: Chenghai Li, Hua Zhao, Linna Cheng, Bin Wang
Formato: article
Lenguaje:EN
Publicado: BMC 2021
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Acceso en línea:https://doaj.org/article/b9a0181604a0473094a7f3f403ffd713
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spelling oai:doaj.org-article:b9a0181604a0473094a7f3f403ffd7132021-11-08T11:03:37ZAllogeneic vs. autologous mesenchymal stem/stromal cells in their medication practice10.1186/s13578-021-00698-y2045-3701https://doaj.org/article/b9a0181604a0473094a7f3f403ffd7132021-11-01T00:00:00Zhttps://doi.org/10.1186/s13578-021-00698-yhttps://doaj.org/toc/2045-3701Abstract Mesenchymal stem/stromal cell (MSC)-based therapeutics is already available for treatment of a range of diseases or medical conditions. Autologous or allogeneic MSCs obtained from self or donors have their own advantages and disadvantages in their medical practice. Therapeutic benefits of using autologous vs. allogeneic MSCs are inconclusive. Transplanted MSCs within the body interact with their physical microenvironment or niche, physiologically or pathologically, and such cells in a newly established tissue microenvironment may be impacted by the pathological harmful environmental factors to alter their unique biological behaviors. Meanwhile, a temporary microenvironment/niche may be also altered by the resident or niche-surrounding MSCs. Therefore, the functional plasticity and heterogeneity of MSCs caused by different donors and subpopulations of MSCs may result in potential uncertainty in their safe and efficacious medical practice. Acknowledging a connection between MSCs’ biology and their existing microenvironment, donor-controlled clinical practice for the long-term therapeutic benefit is suggested to further consider minimizing MSCs potential harm for MSC-based individual therapies. In this review, we summarize the advantages and disadvantages of autologous vs. allogeneic MSCs in their therapeutic applications. Among other issues, we highlight the importance of better understanding of the various microenvironments that may affect the properties of niche-surrounding MSCs and discuss the clinical applications of MSCs within different contexts for treatment of different diseases including cardiomyopathy, lupus and lupus nephritis, diabetes and diabetic complications, bone and cartilage repair, cancer and tissue fibrosis.Chenghai LiHua ZhaoLinna ChengBin WangBMCarticleMesenchymal stem/stromal cellSingle-nucleotide polymorphismStem cell heterogeneityStem cell microenvironmentStem cell transplantationBiotechnologyTP248.13-248.65Biology (General)QH301-705.5BiochemistryQD415-436ENCell & Bioscience, Vol 11, Iss 1, Pp 1-21 (2021)
institution DOAJ
collection DOAJ
language EN
topic Mesenchymal stem/stromal cell
Single-nucleotide polymorphism
Stem cell heterogeneity
Stem cell microenvironment
Stem cell transplantation
Biotechnology
TP248.13-248.65
Biology (General)
QH301-705.5
Biochemistry
QD415-436
spellingShingle Mesenchymal stem/stromal cell
Single-nucleotide polymorphism
Stem cell heterogeneity
Stem cell microenvironment
Stem cell transplantation
Biotechnology
TP248.13-248.65
Biology (General)
QH301-705.5
Biochemistry
QD415-436
Chenghai Li
Hua Zhao
Linna Cheng
Bin Wang
Allogeneic vs. autologous mesenchymal stem/stromal cells in their medication practice
description Abstract Mesenchymal stem/stromal cell (MSC)-based therapeutics is already available for treatment of a range of diseases or medical conditions. Autologous or allogeneic MSCs obtained from self or donors have their own advantages and disadvantages in their medical practice. Therapeutic benefits of using autologous vs. allogeneic MSCs are inconclusive. Transplanted MSCs within the body interact with their physical microenvironment or niche, physiologically or pathologically, and such cells in a newly established tissue microenvironment may be impacted by the pathological harmful environmental factors to alter their unique biological behaviors. Meanwhile, a temporary microenvironment/niche may be also altered by the resident or niche-surrounding MSCs. Therefore, the functional plasticity and heterogeneity of MSCs caused by different donors and subpopulations of MSCs may result in potential uncertainty in their safe and efficacious medical practice. Acknowledging a connection between MSCs’ biology and their existing microenvironment, donor-controlled clinical practice for the long-term therapeutic benefit is suggested to further consider minimizing MSCs potential harm for MSC-based individual therapies. In this review, we summarize the advantages and disadvantages of autologous vs. allogeneic MSCs in their therapeutic applications. Among other issues, we highlight the importance of better understanding of the various microenvironments that may affect the properties of niche-surrounding MSCs and discuss the clinical applications of MSCs within different contexts for treatment of different diseases including cardiomyopathy, lupus and lupus nephritis, diabetes and diabetic complications, bone and cartilage repair, cancer and tissue fibrosis.
format article
author Chenghai Li
Hua Zhao
Linna Cheng
Bin Wang
author_facet Chenghai Li
Hua Zhao
Linna Cheng
Bin Wang
author_sort Chenghai Li
title Allogeneic vs. autologous mesenchymal stem/stromal cells in their medication practice
title_short Allogeneic vs. autologous mesenchymal stem/stromal cells in their medication practice
title_full Allogeneic vs. autologous mesenchymal stem/stromal cells in their medication practice
title_fullStr Allogeneic vs. autologous mesenchymal stem/stromal cells in their medication practice
title_full_unstemmed Allogeneic vs. autologous mesenchymal stem/stromal cells in their medication practice
title_sort allogeneic vs. autologous mesenchymal stem/stromal cells in their medication practice
publisher BMC
publishDate 2021
url https://doaj.org/article/b9a0181604a0473094a7f3f403ffd713
work_keys_str_mv AT chenghaili allogeneicvsautologousmesenchymalstemstromalcellsintheirmedicationpractice
AT huazhao allogeneicvsautologousmesenchymalstemstromalcellsintheirmedicationpractice
AT linnacheng allogeneicvsautologousmesenchymalstemstromalcellsintheirmedicationpractice
AT binwang allogeneicvsautologousmesenchymalstemstromalcellsintheirmedicationpractice
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