TY - JOUR
T1 - A Peptide to Reduce Pulmonary Edema in a Rat Model of Lung Transplantation
AU - Schossleitner, Klaudia
AU - Habertheuer, Andreas
AU - Finsterwalder, Richard
AU - Friedl, Heinz P
AU - Rauscher, Sabine
AU - Gröger, Marion
AU - Kocher, Alfred
AU - Wagner, Christine
AU - Wagner, Stephan N
AU - Fischer, Gottfried
AU - Schultz, Marcus J
AU - Wiedemann, Dominik
AU - Petzelbauer, Peter
N1 - Publisher Copyright:
© 2015 Schossleitner et al. 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 credited.
PY - 2015/11/4
Y1 - 2015/11/4
N2 - 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.
AB - 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.
KW - Animals
KW - Disease Models, Animal
KW - Lung Transplantation/adverse effects
KW - Male
KW - Membrane Proteins
KW - Microfilament Proteins
KW - Organ Preservation
KW - Peptide Fragments/pharmacology
KW - Primary Graft Dysfunction/etiology
KW - Pulmonary Edema/etiology
KW - Rats
KW - Rats, Wistar
KW - Real-Time Polymerase Chain Reaction
KW - Vascular Resistance/drug effects
KW - Ventilation
UR - https://www.scopus.com/pages/publications/84951056581
U2 - 10.1371/journal.pone.0142115
DO - 10.1371/journal.pone.0142115
M3 - Journal article
C2 - 26536466
SN - 1932-6203
VL - 10
SP - e0142115
JO - PLoS ONE
JF - PLoS ONE
IS - 11
M1 - e0142115
ER -