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Modulating the distribution and fate of exogenously delivered MSCs to enhance therapeutic potential: knowns and unknowns

Mesenchymal stem/stromal cells (MSCs) are undergoing intensive translational research for several debilitating conditions, including critical illnesses such as ARDS and sepsis. MSCs exert diverse biologic effects via their interaction with host tissues, via mechanisms that require the MSC to be in c...

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Autores principales: Masterson, Claire H., Curley, Gerard F., Laffey, John G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658643/
https://www.ncbi.nlm.nih.gov/pubmed/31346794
http://dx.doi.org/10.1186/s40635-019-0235-4
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author Masterson, Claire H.
Curley, Gerard F.
Laffey, John G.
author_facet Masterson, Claire H.
Curley, Gerard F.
Laffey, John G.
author_sort Masterson, Claire H.
collection PubMed
description Mesenchymal stem/stromal cells (MSCs) are undergoing intensive translational research for several debilitating conditions, including critical illnesses such as ARDS and sepsis. MSCs exert diverse biologic effects via their interaction with host tissues, via mechanisms that require the MSC to be in close proximity to the area of injury. Fully harnessing the therapeutic potential of advanced medicinal therapeutic products such as MSCs and their successful translation to clinical use requires a detailed understanding of MSC distribution and persistence in the injured tissues. Key aspects include understanding MSC distribution within the body, the response of the host to MSC administration, and the ultimate fate of exogenously administered MSCs within the host. Factors affecting this interaction include the MSC tissue source, the in vitro MSC culture conditions, the route of MSC administration and the specific issues relating to the target disease state, each of which remains to be fully characterised. Understanding these factors may generate strategies to modify MSC distribution and fate that may enhance their therapeutic effect. This review will examine our understanding of the mechanisms of action of MSCs, the early and late phase distribution kinetics of MSCs following in vivo administration, the ultimate fate of MSCs following administration and the potential importance of these MSC properties to their therapeutic effects. We will critique current cellular imaging and tracking methodologies used to track exogenous MSCs and their suitability for use in patients, discuss the insights they provide into the distribution and fate of MSCs after administration, and suggest strategies by which MSC biodistribution and fate may be modulated for therapeutic effect and clinical use. In conclusion, a better understanding of patterns of biodistribution and of the fate of MSCs will add important additional safety data regarding MSCs, address regulatory requirements, and may uncover strategies to increase the distribution and/or persistence of MSC at the sites of injury, potentially increasing their therapeutic potential for multiple disorders.
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spelling pubmed-66586432019-08-07 Modulating the distribution and fate of exogenously delivered MSCs to enhance therapeutic potential: knowns and unknowns Masterson, Claire H. Curley, Gerard F. Laffey, John G. Intensive Care Med Exp Review Mesenchymal stem/stromal cells (MSCs) are undergoing intensive translational research for several debilitating conditions, including critical illnesses such as ARDS and sepsis. MSCs exert diverse biologic effects via their interaction with host tissues, via mechanisms that require the MSC to be in close proximity to the area of injury. Fully harnessing the therapeutic potential of advanced medicinal therapeutic products such as MSCs and their successful translation to clinical use requires a detailed understanding of MSC distribution and persistence in the injured tissues. Key aspects include understanding MSC distribution within the body, the response of the host to MSC administration, and the ultimate fate of exogenously administered MSCs within the host. Factors affecting this interaction include the MSC tissue source, the in vitro MSC culture conditions, the route of MSC administration and the specific issues relating to the target disease state, each of which remains to be fully characterised. Understanding these factors may generate strategies to modify MSC distribution and fate that may enhance their therapeutic effect. This review will examine our understanding of the mechanisms of action of MSCs, the early and late phase distribution kinetics of MSCs following in vivo administration, the ultimate fate of MSCs following administration and the potential importance of these MSC properties to their therapeutic effects. We will critique current cellular imaging and tracking methodologies used to track exogenous MSCs and their suitability for use in patients, discuss the insights they provide into the distribution and fate of MSCs after administration, and suggest strategies by which MSC biodistribution and fate may be modulated for therapeutic effect and clinical use. In conclusion, a better understanding of patterns of biodistribution and of the fate of MSCs will add important additional safety data regarding MSCs, address regulatory requirements, and may uncover strategies to increase the distribution and/or persistence of MSC at the sites of injury, potentially increasing their therapeutic potential for multiple disorders. Springer International Publishing 2019-07-25 /pmc/articles/PMC6658643/ /pubmed/31346794 http://dx.doi.org/10.1186/s40635-019-0235-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Masterson, Claire H.
Curley, Gerard F.
Laffey, John G.
Modulating the distribution and fate of exogenously delivered MSCs to enhance therapeutic potential: knowns and unknowns
title Modulating the distribution and fate of exogenously delivered MSCs to enhance therapeutic potential: knowns and unknowns
title_full Modulating the distribution and fate of exogenously delivered MSCs to enhance therapeutic potential: knowns and unknowns
title_fullStr Modulating the distribution and fate of exogenously delivered MSCs to enhance therapeutic potential: knowns and unknowns
title_full_unstemmed Modulating the distribution and fate of exogenously delivered MSCs to enhance therapeutic potential: knowns and unknowns
title_short Modulating the distribution and fate of exogenously delivered MSCs to enhance therapeutic potential: knowns and unknowns
title_sort modulating the distribution and fate of exogenously delivered mscs to enhance therapeutic potential: knowns and unknowns
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658643/
https://www.ncbi.nlm.nih.gov/pubmed/31346794
http://dx.doi.org/10.1186/s40635-019-0235-4
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