Key result
Mammalian target of rapamycin inhibitors (sirolimus and everolimus) significantly reduced acute rejection, cytomegalovirus infection, and transplantation vasculopathy after heart transplantation.
Why the study?
Do mammalian target of rapamycin (mTOR) inhibitors prevent cardiac allograft vasculopathy and acute rejection in cardiac transplantation patients?
Do mammalian target of rapamycin (mTOR) inhibitors prevent cardiac allograft vasculopathy and acute rejection in cardiac transplantation patients?
mTOR inhibitors like sirolimus and everolimus show promise as antirejection agents that also prevent cardiac allograft vasculopathy and cytomegalovirus infection after heart transplantation.
May support mTOR inhibitor use to curb rejection and vasculopathy post-transplant; leaves open confirmation in randomized trials.
Purpose of review This review discusses the use of mammalian target of rapamycin inhibitors in cardiac transplantation. Recent findings Two major trials of mammalian target of rapamycin inhibitors in cardiac transplantation have been published in the past 9 months, confirming their promise as antirejection agents. More importantly, a potent preventive influence on transplantation vasculopathy has been shown. Both sirolimus and everolimus significantly reduced acute rejection and cytomegalovirus infection, and they reduced transplantation vasculopathy both early, and also at 2 years, as determined by intracoronary ultrasonography. Summary Although refinements to the use of mammalian target of rapamycin inhibitors are required to diminish the magnitude of interaction with calcineurin inhibitors and other drugs, these unique benefits will ensure their early adoption into clinical practice after heart transplantation.
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Keogh et al. (2004) conducted a review in Cardiac transplantation. Mammalian target of rapamycin inhibitors (sirolimus and everolimus) was evaluated on Acute rejection, cytomegalovirus infection, and transplantation vasculopathy. Mammalian target of rapamycin inhibitors (sirolimus and everolimus) significantly reduced acute rejection, cytomegalovirus infection, and transplantation vasculopathy after heart transplantation.
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