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Efficacy of Mesenchymal Stromal Cell Therapy for Acute Lung Injury in Preclinical Animal Models: A Systematic Review
The Acute Respiratory Distress Syndrome (ARDS) is a devastating clinical condition that is associated with a 30–40% risk of death, and significant long term morbidity for those who survive. Mesenchymal stromal cells (MSC) have emerged as a potential novel treatment as in pre-clinical models they hav...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731557/ https://www.ncbi.nlm.nih.gov/pubmed/26821255 http://dx.doi.org/10.1371/journal.pone.0147170 |
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author | McIntyre, Lauralyn A. Moher, David Fergusson, Dean A. Sullivan, Katrina J. Mei, Shirley H. J. Lalu, Manoj Marshall, John Mcleod, Malcolm Griffin, Gilly Grimshaw, Jeremy Turgeon, Alexis Avey, Marc T. Rudnicki, Michael A. Jazi, Mazen Fishman, Jason Stewart, Duncan J. |
author_facet | McIntyre, Lauralyn A. Moher, David Fergusson, Dean A. Sullivan, Katrina J. Mei, Shirley H. J. Lalu, Manoj Marshall, John Mcleod, Malcolm Griffin, Gilly Grimshaw, Jeremy Turgeon, Alexis Avey, Marc T. Rudnicki, Michael A. Jazi, Mazen Fishman, Jason Stewart, Duncan J. |
author_sort | McIntyre, Lauralyn A. |
collection | PubMed |
description | The Acute Respiratory Distress Syndrome (ARDS) is a devastating clinical condition that is associated with a 30–40% risk of death, and significant long term morbidity for those who survive. Mesenchymal stromal cells (MSC) have emerged as a potential novel treatment as in pre-clinical models they have been shown to modulate inflammation (a major pathophysiological hallmark of ARDS) while enhancing bacterial clearance and reducing organ injury and death. A systematic search of MEDLINE, EMBASE, BIOSIS and Web of Science was performed to identify pre-clinical studies that examined the efficacy MSCs as compared to diseased controls for the treatment of Acute Lung Injury (ALI) (the pre-clinical correlate of human ARDS) on mortality, a clinically relevant outcome. We assessed study quality and pooled results using random effect meta-analysis. A total of 54 publications met our inclusion criteria of which 17 (21 experiments) reported mortality and were included in the meta-analysis. Treatment with MSCs, as compared to controls, significantly decreased the overall odds of death in animals with ALI (Odds Ratio 0.24, 95% Confidence Interval 0.18–0.34, I(2) 8%). Efficacy was maintained across different types of animal models and means of ALI induction; MSC origin, source, route of administration and preparation; and the clinical relevance of the model (timing of MSC administration, administration of fluids and or antibiotics). Reporting of standard MSC characterization for experiments that used human MSCs and risks of bias was generally poor, and although not statistically significant, a funnel plot analysis for overall mortality suggested the presence of publication bias. The results from our meta-analysis support that MSCs substantially reduce the odds of death in animal models of ALI but important reporting elements were sub optimal and limit the strength of our conclusions. |
format | Online Article Text |
id | pubmed-4731557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47315572016-02-04 Efficacy of Mesenchymal Stromal Cell Therapy for Acute Lung Injury in Preclinical Animal Models: A Systematic Review McIntyre, Lauralyn A. Moher, David Fergusson, Dean A. Sullivan, Katrina J. Mei, Shirley H. J. Lalu, Manoj Marshall, John Mcleod, Malcolm Griffin, Gilly Grimshaw, Jeremy Turgeon, Alexis Avey, Marc T. Rudnicki, Michael A. Jazi, Mazen Fishman, Jason Stewart, Duncan J. PLoS One Research Article The Acute Respiratory Distress Syndrome (ARDS) is a devastating clinical condition that is associated with a 30–40% risk of death, and significant long term morbidity for those who survive. Mesenchymal stromal cells (MSC) have emerged as a potential novel treatment as in pre-clinical models they have been shown to modulate inflammation (a major pathophysiological hallmark of ARDS) while enhancing bacterial clearance and reducing organ injury and death. A systematic search of MEDLINE, EMBASE, BIOSIS and Web of Science was performed to identify pre-clinical studies that examined the efficacy MSCs as compared to diseased controls for the treatment of Acute Lung Injury (ALI) (the pre-clinical correlate of human ARDS) on mortality, a clinically relevant outcome. We assessed study quality and pooled results using random effect meta-analysis. A total of 54 publications met our inclusion criteria of which 17 (21 experiments) reported mortality and were included in the meta-analysis. Treatment with MSCs, as compared to controls, significantly decreased the overall odds of death in animals with ALI (Odds Ratio 0.24, 95% Confidence Interval 0.18–0.34, I(2) 8%). Efficacy was maintained across different types of animal models and means of ALI induction; MSC origin, source, route of administration and preparation; and the clinical relevance of the model (timing of MSC administration, administration of fluids and or antibiotics). Reporting of standard MSC characterization for experiments that used human MSCs and risks of bias was generally poor, and although not statistically significant, a funnel plot analysis for overall mortality suggested the presence of publication bias. The results from our meta-analysis support that MSCs substantially reduce the odds of death in animal models of ALI but important reporting elements were sub optimal and limit the strength of our conclusions. Public Library of Science 2016-01-28 /pmc/articles/PMC4731557/ /pubmed/26821255 http://dx.doi.org/10.1371/journal.pone.0147170 Text en © 2016 McIntyre et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article McIntyre, Lauralyn A. Moher, David Fergusson, Dean A. Sullivan, Katrina J. Mei, Shirley H. J. Lalu, Manoj Marshall, John Mcleod, Malcolm Griffin, Gilly Grimshaw, Jeremy Turgeon, Alexis Avey, Marc T. Rudnicki, Michael A. Jazi, Mazen Fishman, Jason Stewart, Duncan J. Efficacy of Mesenchymal Stromal Cell Therapy for Acute Lung Injury in Preclinical Animal Models: A Systematic Review |
title | Efficacy of Mesenchymal Stromal Cell Therapy for Acute Lung Injury in Preclinical Animal Models: A Systematic Review |
title_full | Efficacy of Mesenchymal Stromal Cell Therapy for Acute Lung Injury in Preclinical Animal Models: A Systematic Review |
title_fullStr | Efficacy of Mesenchymal Stromal Cell Therapy for Acute Lung Injury in Preclinical Animal Models: A Systematic Review |
title_full_unstemmed | Efficacy of Mesenchymal Stromal Cell Therapy for Acute Lung Injury in Preclinical Animal Models: A Systematic Review |
title_short | Efficacy of Mesenchymal Stromal Cell Therapy for Acute Lung Injury in Preclinical Animal Models: A Systematic Review |
title_sort | efficacy of mesenchymal stromal cell therapy for acute lung injury in preclinical animal models: a systematic review |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731557/ https://www.ncbi.nlm.nih.gov/pubmed/26821255 http://dx.doi.org/10.1371/journal.pone.0147170 |
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