Abstract:To identify the clinical factors associated with acute rejection (AR) in the first year after heart transplantation (HT), we analysed 112 patients. All patients received OKT3 and standard triple-drug therapy. We analysed the following variables to determine their relationship with AR: age and gender, panel-reactive antibodies, HLA-DR mismatch, use of Sandimmune vs Neoral, diltiazem administration, and cyclosporine levels in week 2 and months 1, 2, and 3 after HT. Fifty-two patients had no AR and 49 had at leas… Show more
“…The mechanism has been explained by the finding that diltiazem increases the blood concentration of CyA by inhibiting CyA metabolism in hepatic cytochrome P450 enzymes [45][46][47]. However, our results showed that a Ca2 + channel blocker enhanced IL-12 p40 secretion from MDDCs.…”
SummaryImmune complexes (ICs) improve the capacity of priming specific CD8+ cytotoxic T cell responses of dendritic cells (DCs). ICs induce phosphorylation of mitogen-activated protein kinases (MAPK) and calcium influx, although the precise regulating mechanism still remains unclear. In the present study, we investigated the effect of a Ca2
“…The mechanism has been explained by the finding that diltiazem increases the blood concentration of CyA by inhibiting CyA metabolism in hepatic cytochrome P450 enzymes [45][46][47]. However, our results showed that a Ca2 + channel blocker enhanced IL-12 p40 secretion from MDDCs.…”
SummaryImmune complexes (ICs) improve the capacity of priming specific CD8+ cytotoxic T cell responses of dendritic cells (DCs). ICs induce phosphorylation of mitogen-activated protein kinases (MAPK) and calcium influx, although the precise regulating mechanism still remains unclear. In the present study, we investigated the effect of a Ca2
“…31 Previous studies have reported that diltiazem slows the development of CAV 32 and reduces the incidence of acute rejection. [33][34][35] Moreover, studies with heterotopic HTx models have shown that diltiazem exerts immunosuppressive and immunomodulating effects. Transmembrane calcium movement plays a critical role in lymphocyte function, and numerous investigators have demonstrated that diltiazem inhibits lymphocyte functions and depresses the immune response.…”
“…In another study, clinical factors associated with acute rejection in the first year after heart transplantation were analyzed in 112 HTX recipients. 37 The result from this study showed that diltiazem administration and cyclosporine level in the first month after HT were both independently associated with the absence of acute rejection. Both diltiazem and cyclosporine level showed a large and independent protective effect.…”
Increased resting heart rate is an independent modifiable risk factor for the development of cardiovascular disease. Numerous studies have demonstrated improved clinical outcomes with heart rate reduction in patients with coronary artery disease and heart failure, but its role in transplanted hearts is not yet established. Sinus tachycardia is more common in heart transplant recipients due to graft denervation. Although a large number of studies have recognized increased heart rate as a predictor of native coronary artery atherosclerosis and overall cardiac mortality, contradicting results have been observed in heart transplant recipients. There is no clear consensus about what the normal range of heart rate should be following heart transplantation. The aim of this article was to review the literature to evaluate whether heart rate reduction should be considered in heart transplant recipients.
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