Preconditioning With Ozone Abrogates Acute Rejection and Prolongs Cardiac Allograft Survival in Rats

• Published in: Transplantation proceedings Vol. 40; no. 4; pp. 974 - 977
• Main Authors: Stadlbauer, T.H.W, Eisele, A, Heidt, M.C, Tillmanns, H.H, Schulz, S
• Format: Journal Article Conference Proceeding
• Language: English
• Published: New York, NY Elsevier Inc 01.05.2008; Elsevier Science
• Subjects: Animals; Biological and medical sciences; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Graft Rejection - prevention & control; Heart Transplantation - physiology; Immunosuppressive Agents - therapeutic use; Male; Medical sciences; Models, Animal; Ozone - therapeutic use; Rats; Rats, Inbred WF; Surgery; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases; Tissue, organ and graft immunology; Transplantation Conditioning - methods; Transplantation, Homologous - physiology; Heart; Graft(material); Prognosis; Rat; Acute; Rodentia; Ozone; Transplantation; Homotransplantation; Survival; Medicine; Rejection; Vertebrata; Mammalia; Treatment; Surgery; Animal; Graft; Circulatory system; Preconditioning; Prolonged
• ISSN: 0041-1345; 1873-2623
• DOI: 10.1016/j.transproceed.2008.03.036

Abstract Acute cardiac allograft rejection remains a major cause of morbidity and mortality after heart transplantation and predisposes for the development of graft vasculopathy. The aim of this study was to investigate the immunomodulatory effect of preconditioning of the donor and recipient with medical ozone (O3 /O2 ) on acute allograft rejection. Minimizing the initial ischemia-reperfusion injury may result in a reduction of graft vasculopathy and ameliorate long-term outcomes after cardiac transplantation. Lewis rats were challenged with Wistar-Furth cardiac allograft. In donor and recipient animals a medical ozone (O3 /O2 )-pneumoperitoneum was induced by single (1×) or repetitive (5×) insufflation (concentration: 50 μg/mL, 80 mL/kg body weight) of medical ozone intraperitoneally. Without immunomodulatory therapy (n = 11) cardiac allograft survival was 5.9 ± 0.9 days. Preconditioning with medical ozone alone (single bolus as well as repetitive administration, n = 7) of the donor and recipient animals prolonged cardiac allograft survival significantly to 7.6 ± 1.4 days ( P < .05), without any adjunctive immunosuppressive therapy. In this pilot study, the intraperitoneal administration of ozone in donor and recipient animals protected from ischemia-reperfusion injury, reduced the immunogenicity of the graft, and prolonged cardiac allograft survival. Further studies are warranted to elucidate the underlying mechanisms and—more important—to investigate the effect on the development of graft vasculopathy, the major obstacle to long-term graft and patient survivals.