Key result
Targeting the innate immune response, particularly Toll-like receptors and the inflammasome, is discussed as a potential strategy to mitigate myocardial injury and expand the heart donor pool.
Why the study?
Does targeting the innate immune response improve cardiac graft recovery after heart transplantation?
Does targeting the innate immune response improve cardiac graft recovery after heart transplantation?
Targeting the innate immune response, particularly Toll-like receptors and inflammasomes, may mitigate myocardial injury during heart transplantation and help expand the donor pool.
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.
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Toldo et al. (2016) conducted a review in End-stage heart failure requiring heart transplantation. Targeting the innate immune response was evaluated. Targeting the innate immune response, particularly Toll-like receptors and the inflammasome, is discussed as a potential strategy to mitigate myocardial injury and expand the heart donor pool.
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