Targeting the Innate Immune Response to Improve Cardiac Graft Recovery after Heart Transplantation: Implications for the Donation after Cardiac Death

• Published in: International journal of molecular sciences 2016-06, Vol.17 (6), p.958-958
• Main Authors: Toldo, Stefano, Quader, Mohammed, Salloum, Fadi N, Mezzaroma, Eleonora, Abbate, Antonio
• Format: Article
• Language: English
• Subjects: Animals; Death; donation after brain death (DBD); donation after cardiac death (DCD); graft failure; Heart; Heart failure; heart transplantation; Heart Transplantation - adverse effects; Heart Transplantation - methods; Host vs Graft Reaction - immunology; Humans; Immune system; Immunity, Innate; inflammasome; innate immune response; ischemia-reperfusion injury; rejection; Review; Tissue and Organ Procurement - methods; Tissue and Organ Procurement - standards; Toll-like receptors; Transplants & implants
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms17060958

Heart transplantation (HTx) is the ultimate treatment for end-stage heart failure. The number of patients on waiting lists for heart transplants, however, is much higher than the number of available organs. The shortage of donor hearts is a serious concern since the population affected by heart failure is constantly increasing. Furthermore, the long-term success of HTx poses some challenges despite the improvement in the management of the short-term complications and in the methods to limit graft rejection. Myocardial injury occurs during transplantation. Injury initiated in the donor as result of brain or cardiac death is exacerbated by organ procurement and storage, and is ultimately amplified by reperfusion injury at the time of transplantation. The innate immune system is a mechanism of first-line defense against pathogens and cell injury. Innate immunity is activated during myocardial injury and produces deleterious effects on the heart structure and function. Here, we briefly discuss the role of the innate immunity in the initiation of myocardial injury, with particular focus on the Toll-like receptors and inflammasome, and how to potentially expand the donor population by targeting the innate immune response.