Preservation with α 1 -antitrypsin improves primary graft function of murine lung transplants

• Published in: The Journal of heart and lung transplantation Vol. 37; no. 8; p. 1021
• Main Authors: Götzfried, Jessica, Smirnova, Natalia F, Morrone, Carmela, Korkmaz, Brice, Yildirim, Ali Önder, Eickelberg, Oliver, Jenne, Dieter E
• Format: Journal Article
• Language: English
• Published: United States 01.08.2018
• Subjects: alpha 1-Antitrypsin - pharmacology; Animals; Bronchoalveolar Lavage Fluid - immunology; Citrates - pharmacology; Disease Models, Animal; Lung Transplantation; Male; Mice; Mice, Inbred Strains; Neutrophils - drug effects; Organ Preservation - methods; Primary Graft Dysfunction - prevention & control; Pulmonary Gas Exchange; Reperfusion Injury - prevention & control; elastase; ischemia-reperfusion injury; animal models; proteinase 3; Primary graft dysfunction; lung transplantation; alpha-1-antitrypsin
• ISSN: 1557-3117

Vascular damage and primary graft dysfunction increase with prolonged preservation times of transplanted donor lungs. Hence, storage and conservation of donated lungs in protein-free, dextran-containing electrolyte solutions, like Perfadex, is limited to about 6 hours. We hypothesized that transplanted lungs are protected against neutrophil-mediated proteolytic damage by adding α -anti-trypsin (AAT), a highly abundant human plasma proteinase inhibitor, to Perfadex. A realistic clinically oriented murine model of lung transplantation was used to simulate the ischemia-reperfusion process. Lung grafts were stored at 4°C in Perfadex solution supplemented with AAT or an AAT mutant devoid of elastase-inhibiting activity for 18 hours. We examined wild-type and proteinase 3/neutrophil elastase (PR3/NE) double-deficient mice as graft recipients. Gas exchange function and infiltrating neutrophils of the transplanted lung, as well as protein content and neutrophil numbers in the bronchoalveolar lavage fluid, were determined. AAT as a supplement to Perfadex reduced the extent of primary graft dysfunction and early neutrophil responses after extended storage for 18 hours at 4°C and 4-hour reperfusion in the recipients. Double-knockout recipients that lack elastase-like activities in neutrophils were also protected from early reperfusion injury, but not lung grafts that were perfused with a reactive center mutant of AAT devoid of elastase-inhibiting activity. PR3 and NE, the principal targets of AAT, are major triggers of post-ischemic reperfusion damage. Their effective inhibition in the graft and recipient is a promising strategy for organ usage after storage for >6 hours.