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Safety and Efficacy of Allogeneic Lung Spheroid Cells in a Mismatched Rat Model of Pulmonary Fibrosis

Idiopathic pulmonary fibrosis is a devastating interstitial lung disease characterized by the relentless deposition of extracellular matrix causing lung distortions and dysfunctions. The prognosis after detection is merely 3–5 years and the only two Food and Drug Administration‐approved drugs treat...

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Autores principales: Cores, Jhon, Hensley, M. Taylor, Kinlaw, Kathryn, Rikard, S. Michaela, Dinh, Phuong‐Uyen, Paudel, Dipti, Tang, Junnan, Vandergriff, Adam C., Allen, Tyler A., Li, Yazhou, Liu, Jianhua, Niu, Bo, Chi, Yuepeng, Caranasos, Thomas, Lobo, Leonard J., Cheng, Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430052/
https://www.ncbi.nlm.nih.gov/pubmed/28783251
http://dx.doi.org/10.1002/sctm.16-0374
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author Cores, Jhon
Hensley, M. Taylor
Kinlaw, Kathryn
Rikard, S. Michaela
Dinh, Phuong‐Uyen
Paudel, Dipti
Tang, Junnan
Vandergriff, Adam C.
Allen, Tyler A.
Li, Yazhou
Liu, Jianhua
Niu, Bo
Chi, Yuepeng
Caranasos, Thomas
Lobo, Leonard J.
Cheng, Ke
author_facet Cores, Jhon
Hensley, M. Taylor
Kinlaw, Kathryn
Rikard, S. Michaela
Dinh, Phuong‐Uyen
Paudel, Dipti
Tang, Junnan
Vandergriff, Adam C.
Allen, Tyler A.
Li, Yazhou
Liu, Jianhua
Niu, Bo
Chi, Yuepeng
Caranasos, Thomas
Lobo, Leonard J.
Cheng, Ke
author_sort Cores, Jhon
collection PubMed
description Idiopathic pulmonary fibrosis is a devastating interstitial lung disease characterized by the relentless deposition of extracellular matrix causing lung distortions and dysfunctions. The prognosis after detection is merely 3–5 years and the only two Food and Drug Administration‐approved drugs treat the symptoms, not the disease, and have numerous side effects. Stem cell therapy is a promising treatment strategy for pulmonary fibrosis. Current animal and clinical studies focus on the use of adipose or bone marrow‐derived mesenchymal stem cells. We, instead, have established adult lung spheroid cells (LSCs) as an intrinsic source of therapeutic lung stem cells. In the present study, we compared the efficacy and safety of syngeneic and allogeneic LSCs in immuno‐competent rats with bleomycin‐induced pulmonary inflammation in an effort to mitigate fibrosis development. We found that infusion of allogeneic LSCs reduces the progression of inflammation and fibrotic manifestation and preserves epithelial and endothelial health without eliciting significant immune rejection. Our study sheds light on potential future developments of LSCs as an allogeneic cell therapy for humans with pulmonary fibrosis. Stem Cells Translational Medicine 2017;9:1905–1916
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spelling pubmed-64300522019-04-01 Safety and Efficacy of Allogeneic Lung Spheroid Cells in a Mismatched Rat Model of Pulmonary Fibrosis Cores, Jhon Hensley, M. Taylor Kinlaw, Kathryn Rikard, S. Michaela Dinh, Phuong‐Uyen Paudel, Dipti Tang, Junnan Vandergriff, Adam C. Allen, Tyler A. Li, Yazhou Liu, Jianhua Niu, Bo Chi, Yuepeng Caranasos, Thomas Lobo, Leonard J. Cheng, Ke Stem Cells Transl Med Translational Research Articles and Reviews Idiopathic pulmonary fibrosis is a devastating interstitial lung disease characterized by the relentless deposition of extracellular matrix causing lung distortions and dysfunctions. The prognosis after detection is merely 3–5 years and the only two Food and Drug Administration‐approved drugs treat the symptoms, not the disease, and have numerous side effects. Stem cell therapy is a promising treatment strategy for pulmonary fibrosis. Current animal and clinical studies focus on the use of adipose or bone marrow‐derived mesenchymal stem cells. We, instead, have established adult lung spheroid cells (LSCs) as an intrinsic source of therapeutic lung stem cells. In the present study, we compared the efficacy and safety of syngeneic and allogeneic LSCs in immuno‐competent rats with bleomycin‐induced pulmonary inflammation in an effort to mitigate fibrosis development. We found that infusion of allogeneic LSCs reduces the progression of inflammation and fibrotic manifestation and preserves epithelial and endothelial health without eliciting significant immune rejection. Our study sheds light on potential future developments of LSCs as an allogeneic cell therapy for humans with pulmonary fibrosis. Stem Cells Translational Medicine 2017;9:1905–1916 John Wiley and Sons Inc. 2017-08-07 /pmc/articles/PMC6430052/ /pubmed/28783251 http://dx.doi.org/10.1002/sctm.16-0374 Text en © 2017 The Authors stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Translational Research Articles and Reviews
Cores, Jhon
Hensley, M. Taylor
Kinlaw, Kathryn
Rikard, S. Michaela
Dinh, Phuong‐Uyen
Paudel, Dipti
Tang, Junnan
Vandergriff, Adam C.
Allen, Tyler A.
Li, Yazhou
Liu, Jianhua
Niu, Bo
Chi, Yuepeng
Caranasos, Thomas
Lobo, Leonard J.
Cheng, Ke
Safety and Efficacy of Allogeneic Lung Spheroid Cells in a Mismatched Rat Model of Pulmonary Fibrosis
title Safety and Efficacy of Allogeneic Lung Spheroid Cells in a Mismatched Rat Model of Pulmonary Fibrosis
title_full Safety and Efficacy of Allogeneic Lung Spheroid Cells in a Mismatched Rat Model of Pulmonary Fibrosis
title_fullStr Safety and Efficacy of Allogeneic Lung Spheroid Cells in a Mismatched Rat Model of Pulmonary Fibrosis
title_full_unstemmed Safety and Efficacy of Allogeneic Lung Spheroid Cells in a Mismatched Rat Model of Pulmonary Fibrosis
title_short Safety and Efficacy of Allogeneic Lung Spheroid Cells in a Mismatched Rat Model of Pulmonary Fibrosis
title_sort safety and efficacy of allogeneic lung spheroid cells in a mismatched rat model of pulmonary fibrosis
topic Translational Research Articles and Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430052/
https://www.ncbi.nlm.nih.gov/pubmed/28783251
http://dx.doi.org/10.1002/sctm.16-0374
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