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Mesenchymal Stem Cell Therapy for Aging Frailty

Chronic diseases and degenerative conditions are strongly linked with the geriatric syndrome of frailty and account for a disproportionate percentage of the health care budget. Frailty increases the risk of falls, hospitalization, institutionalization, disability, and death. By definition, frailty s...

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Autores principales: Schulman, Ivonne Hernandez, Balkan, Wayne, Hare, Joshua M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249304/
https://www.ncbi.nlm.nih.gov/pubmed/30498696
http://dx.doi.org/10.3389/fnut.2018.00108
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author Schulman, Ivonne Hernandez
Balkan, Wayne
Hare, Joshua M.
author_facet Schulman, Ivonne Hernandez
Balkan, Wayne
Hare, Joshua M.
author_sort Schulman, Ivonne Hernandez
collection PubMed
description Chronic diseases and degenerative conditions are strongly linked with the geriatric syndrome of frailty and account for a disproportionate percentage of the health care budget. Frailty increases the risk of falls, hospitalization, institutionalization, disability, and death. By definition, frailty syndrome is characterized by declines in lean body mass, strength, endurance, balance, gait speed, activity and energy levels, and organ physiologic reserve. Collectively, these changes lead to the loss of homeostasis and capability to withstand stressors and resulting vulnerabilities. There is a strong link between frailty, inflammation, and the impaired ability to repair tissue injury due to decreases in endogenous stem cell production. Although exercise and nutritional supplementation provide benefit to frail patients, there are currently no specific therapies for frailty. Bone marrow-derived allogeneic mesenchymal stem cells (MSCs) provide therapeutic benefits in heart failure patients irrespective of age. MSCs contribute to cellular repair and tissue regeneration through their multilineage differentiation capacity, immunomodulatory, and anti-inflammatory effects, homing and migratory capacity to injury sites, and stimulatory effect on endogenous tissue progenitors. The advantages of using MSCs as a therapeutic strategy include standardization of isolation and culture expansion techniques and safety in allogeneic transplantation. Based on this evidence, we performed a randomized, double-blinded, dose-finding study in elderly, frail individuals and showed that intravenously delivered allogeneic MSCs are safe and produce significant improvements in physical performance measures and inflammatory biomarkers. We thus propose that frailty can be treated and the link between frailty and chronic inflammation offers a potential therapeutic target, addressable by cell therapy.
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spelling pubmed-62493042018-11-29 Mesenchymal Stem Cell Therapy for Aging Frailty Schulman, Ivonne Hernandez Balkan, Wayne Hare, Joshua M. Front Nutr Nutrition Chronic diseases and degenerative conditions are strongly linked with the geriatric syndrome of frailty and account for a disproportionate percentage of the health care budget. Frailty increases the risk of falls, hospitalization, institutionalization, disability, and death. By definition, frailty syndrome is characterized by declines in lean body mass, strength, endurance, balance, gait speed, activity and energy levels, and organ physiologic reserve. Collectively, these changes lead to the loss of homeostasis and capability to withstand stressors and resulting vulnerabilities. There is a strong link between frailty, inflammation, and the impaired ability to repair tissue injury due to decreases in endogenous stem cell production. Although exercise and nutritional supplementation provide benefit to frail patients, there are currently no specific therapies for frailty. Bone marrow-derived allogeneic mesenchymal stem cells (MSCs) provide therapeutic benefits in heart failure patients irrespective of age. MSCs contribute to cellular repair and tissue regeneration through their multilineage differentiation capacity, immunomodulatory, and anti-inflammatory effects, homing and migratory capacity to injury sites, and stimulatory effect on endogenous tissue progenitors. The advantages of using MSCs as a therapeutic strategy include standardization of isolation and culture expansion techniques and safety in allogeneic transplantation. Based on this evidence, we performed a randomized, double-blinded, dose-finding study in elderly, frail individuals and showed that intravenously delivered allogeneic MSCs are safe and produce significant improvements in physical performance measures and inflammatory biomarkers. We thus propose that frailty can be treated and the link between frailty and chronic inflammation offers a potential therapeutic target, addressable by cell therapy. Frontiers Media S.A. 2018-11-15 /pmc/articles/PMC6249304/ /pubmed/30498696 http://dx.doi.org/10.3389/fnut.2018.00108 Text en Copyright © 2018 Schulman, Balkan and Hare. http://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 Nutrition
Schulman, Ivonne Hernandez
Balkan, Wayne
Hare, Joshua M.
Mesenchymal Stem Cell Therapy for Aging Frailty
title Mesenchymal Stem Cell Therapy for Aging Frailty
title_full Mesenchymal Stem Cell Therapy for Aging Frailty
title_fullStr Mesenchymal Stem Cell Therapy for Aging Frailty
title_full_unstemmed Mesenchymal Stem Cell Therapy for Aging Frailty
title_short Mesenchymal Stem Cell Therapy for Aging Frailty
title_sort mesenchymal stem cell therapy for aging frailty
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249304/
https://www.ncbi.nlm.nih.gov/pubmed/30498696
http://dx.doi.org/10.3389/fnut.2018.00108
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