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Evaluation of Human MSCs Treatment Frequency on Airway Inflammation in a Mouse Model of Acute Asthma

BACKGROUND: Studies in experimental models of allergic asthma have shown that mesenchymal stem cells (MSCs) have therapeutic potential for T-helper 2 (T(H)2) cell-mediated inflammation. However, the mechanisms underlying these therapeutic effects are not fully understood and their safety has not bee...

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Autores principales: Hur, Jung, Kang, Ji Young, Kim, Young Kyoon, Lee, Sook Young, Jeon, Sora, Kim, Yourha, Jung, Chan Kwon, Rhee, Chin Kook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295606/
https://www.ncbi.nlm.nih.gov/pubmed/32537953
http://dx.doi.org/10.3346/jkms.2020.35.e188
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author Hur, Jung
Kang, Ji Young
Kim, Young Kyoon
Lee, Sook Young
Jeon, Sora
Kim, Yourha
Jung, Chan Kwon
Rhee, Chin Kook
author_facet Hur, Jung
Kang, Ji Young
Kim, Young Kyoon
Lee, Sook Young
Jeon, Sora
Kim, Yourha
Jung, Chan Kwon
Rhee, Chin Kook
author_sort Hur, Jung
collection PubMed
description BACKGROUND: Studies in experimental models of allergic asthma have shown that mesenchymal stem cells (MSCs) have therapeutic potential for T-helper 2 (T(H)2) cell-mediated inflammation. However, the mechanisms underlying these therapeutic effects are not fully understood and their safety has not been confirmed. METHODS: Using a mouse model of experimental allergic asthma, we investigated the efficacy of human adipose-derived mesenchymal stem cells (hADSCs) or human bone marrow-derived mesenchymal stem cells (hBMSCs) according to treatment frequency and timing. RESULTS: Ovalbumin (OVA)-sensitized and -challenged mice exhibited airway hyperresponsiveness (AHR), airway inflammation, and significant increases in T(H)2 cytokine levels. Both double and single human mesenchymal stem cell (hMSC) treatments significantly decreased AHR and bronchoalveolar lavage fluid counts. In addition, single treatment with hMSCs showed significant attenuation of allergic airway inflammation. However, double treatment with hMSCs during OVA -sensitization and -challenge further increased inflammatory cell infiltration, and T(H)2 cytokine levels. CONCLUSION: The results of treatment with hADSCs or hBMSCs suppresses AHR and airway inflammation. However, double hMSC treatment significantly induces eosinophilic airway inflammation and lung histological changes. Therefore, double hMSC treatment is ineffective against asthma and single injection frequency appears to be more important for the treatment of asthma. These results suggest that hMSC therapy can be used for treatment of asthma patients but that it should be used carefully.
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spelling pubmed-72956062020-06-18 Evaluation of Human MSCs Treatment Frequency on Airway Inflammation in a Mouse Model of Acute Asthma Hur, Jung Kang, Ji Young Kim, Young Kyoon Lee, Sook Young Jeon, Sora Kim, Yourha Jung, Chan Kwon Rhee, Chin Kook J Korean Med Sci Original Article BACKGROUND: Studies in experimental models of allergic asthma have shown that mesenchymal stem cells (MSCs) have therapeutic potential for T-helper 2 (T(H)2) cell-mediated inflammation. However, the mechanisms underlying these therapeutic effects are not fully understood and their safety has not been confirmed. METHODS: Using a mouse model of experimental allergic asthma, we investigated the efficacy of human adipose-derived mesenchymal stem cells (hADSCs) or human bone marrow-derived mesenchymal stem cells (hBMSCs) according to treatment frequency and timing. RESULTS: Ovalbumin (OVA)-sensitized and -challenged mice exhibited airway hyperresponsiveness (AHR), airway inflammation, and significant increases in T(H)2 cytokine levels. Both double and single human mesenchymal stem cell (hMSC) treatments significantly decreased AHR and bronchoalveolar lavage fluid counts. In addition, single treatment with hMSCs showed significant attenuation of allergic airway inflammation. However, double treatment with hMSCs during OVA -sensitization and -challenge further increased inflammatory cell infiltration, and T(H)2 cytokine levels. CONCLUSION: The results of treatment with hADSCs or hBMSCs suppresses AHR and airway inflammation. However, double hMSC treatment significantly induces eosinophilic airway inflammation and lung histological changes. Therefore, double hMSC treatment is ineffective against asthma and single injection frequency appears to be more important for the treatment of asthma. These results suggest that hMSC therapy can be used for treatment of asthma patients but that it should be used carefully. The Korean Academy of Medical Sciences 2020-05-12 /pmc/articles/PMC7295606/ /pubmed/32537953 http://dx.doi.org/10.3346/jkms.2020.35.e188 Text en © 2020 The Korean Academy of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hur, Jung
Kang, Ji Young
Kim, Young Kyoon
Lee, Sook Young
Jeon, Sora
Kim, Yourha
Jung, Chan Kwon
Rhee, Chin Kook
Evaluation of Human MSCs Treatment Frequency on Airway Inflammation in a Mouse Model of Acute Asthma
title Evaluation of Human MSCs Treatment Frequency on Airway Inflammation in a Mouse Model of Acute Asthma
title_full Evaluation of Human MSCs Treatment Frequency on Airway Inflammation in a Mouse Model of Acute Asthma
title_fullStr Evaluation of Human MSCs Treatment Frequency on Airway Inflammation in a Mouse Model of Acute Asthma
title_full_unstemmed Evaluation of Human MSCs Treatment Frequency on Airway Inflammation in a Mouse Model of Acute Asthma
title_short Evaluation of Human MSCs Treatment Frequency on Airway Inflammation in a Mouse Model of Acute Asthma
title_sort evaluation of human mscs treatment frequency on airway inflammation in a mouse model of acute asthma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295606/
https://www.ncbi.nlm.nih.gov/pubmed/32537953
http://dx.doi.org/10.3346/jkms.2020.35.e188
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