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A Peptide to Reduce Pulmonary Edema in a Rat Model of Lung Transplantation

BACKGROUND: Despite significant advances in organ preservation, surgical techniques and perioperative care, primary graft dysfunction is a serious medical problem in transplantation medicine in general and a specific problem in patients undergoing lung transplantation. As a result, patients develop...

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Autores principales: Schossleitner, Klaudia, Habertheuer, Andreas, Finsterwalder, Richard, Friedl, Heinz P., Rauscher, Sabine, Gröger, Marion, Kocher, Alfred, Wagner, Christine, Wagner, Stephan N., Fischer, Gottfried, Schultz, Marcus J., Wiedemann, Dominik, Petzelbauer, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633234/
https://www.ncbi.nlm.nih.gov/pubmed/26536466
http://dx.doi.org/10.1371/journal.pone.0142115
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author Schossleitner, Klaudia
Habertheuer, Andreas
Finsterwalder, Richard
Friedl, Heinz P.
Rauscher, Sabine
Gröger, Marion
Kocher, Alfred
Wagner, Christine
Wagner, Stephan N.
Fischer, Gottfried
Schultz, Marcus J.
Wiedemann, Dominik
Petzelbauer, Peter
author_facet Schossleitner, Klaudia
Habertheuer, Andreas
Finsterwalder, Richard
Friedl, Heinz P.
Rauscher, Sabine
Gröger, Marion
Kocher, Alfred
Wagner, Christine
Wagner, Stephan N.
Fischer, Gottfried
Schultz, Marcus J.
Wiedemann, Dominik
Petzelbauer, Peter
author_sort Schossleitner, Klaudia
collection PubMed
description BACKGROUND: Despite significant advances in organ preservation, surgical techniques and perioperative care, primary graft dysfunction is a serious medical problem in transplantation medicine in general and a specific problem in patients undergoing lung transplantation. As a result, patients develop lung edema, causing reduced tissue oxygenation capacity, reduced lung compliance and increased requirements for mechanical ventilatory support. Yet, there is no effective strategy available to protect the grafted organ from stress reactions induced by ischemia/reperfusion and by the surgical procedure itself. METHODS: We assessed the effect of a cingulin-derived peptide, XIB13 or a random peptide in an established rat model of allogeneic lung transplantation. Donor lungs and recipients received therapeutic peptide at the time of transplantation and outcome was analyzed 100min and 28 days post grafting. RESULTS: XIB13 improved blood oxygenation and reduced vascular leak 100min post grafting. Even after 28 days, lung edema was significantly reduced by XIB13 and lungs had reduced fibrotic or necrotic zones. Moreover, the induction of an allogeneic T cell response was delayed indicating a reduced antigen exchange between the donor and the host. CONCLUSIONS: In summary, we provide a new tool to strengthen endothelial barrier function thereby improving outcomes in lung transplantation.
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spelling pubmed-46332342015-11-13 A Peptide to Reduce Pulmonary Edema in a Rat Model of Lung Transplantation Schossleitner, Klaudia Habertheuer, Andreas Finsterwalder, Richard Friedl, Heinz P. Rauscher, Sabine Gröger, Marion Kocher, Alfred Wagner, Christine Wagner, Stephan N. Fischer, Gottfried Schultz, Marcus J. Wiedemann, Dominik Petzelbauer, Peter PLoS One Research Article BACKGROUND: Despite significant advances in organ preservation, surgical techniques and perioperative care, primary graft dysfunction is a serious medical problem in transplantation medicine in general and a specific problem in patients undergoing lung transplantation. As a result, patients develop lung edema, causing reduced tissue oxygenation capacity, reduced lung compliance and increased requirements for mechanical ventilatory support. Yet, there is no effective strategy available to protect the grafted organ from stress reactions induced by ischemia/reperfusion and by the surgical procedure itself. METHODS: We assessed the effect of a cingulin-derived peptide, XIB13 or a random peptide in an established rat model of allogeneic lung transplantation. Donor lungs and recipients received therapeutic peptide at the time of transplantation and outcome was analyzed 100min and 28 days post grafting. RESULTS: XIB13 improved blood oxygenation and reduced vascular leak 100min post grafting. Even after 28 days, lung edema was significantly reduced by XIB13 and lungs had reduced fibrotic or necrotic zones. Moreover, the induction of an allogeneic T cell response was delayed indicating a reduced antigen exchange between the donor and the host. CONCLUSIONS: In summary, we provide a new tool to strengthen endothelial barrier function thereby improving outcomes in lung transplantation. Public Library of Science 2015-11-04 /pmc/articles/PMC4633234/ /pubmed/26536466 http://dx.doi.org/10.1371/journal.pone.0142115 Text en © 2015 Schossleitner 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Schossleitner, Klaudia
Habertheuer, Andreas
Finsterwalder, Richard
Friedl, Heinz P.
Rauscher, Sabine
Gröger, Marion
Kocher, Alfred
Wagner, Christine
Wagner, Stephan N.
Fischer, Gottfried
Schultz, Marcus J.
Wiedemann, Dominik
Petzelbauer, Peter
A Peptide to Reduce Pulmonary Edema in a Rat Model of Lung Transplantation
title A Peptide to Reduce Pulmonary Edema in a Rat Model of Lung Transplantation
title_full A Peptide to Reduce Pulmonary Edema in a Rat Model of Lung Transplantation
title_fullStr A Peptide to Reduce Pulmonary Edema in a Rat Model of Lung Transplantation
title_full_unstemmed A Peptide to Reduce Pulmonary Edema in a Rat Model of Lung Transplantation
title_short A Peptide to Reduce Pulmonary Edema in a Rat Model of Lung Transplantation
title_sort peptide to reduce pulmonary edema in a rat model of lung transplantation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633234/
https://www.ncbi.nlm.nih.gov/pubmed/26536466
http://dx.doi.org/10.1371/journal.pone.0142115
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