The aim of this double-blinded, placebo-controlled pilot study was to evaluate the safety and efficacy of reparixin to suppress IRI and inflammation in patients undergoing on-pump coronary artery bypass grafting (CABG). Patients received either reparixin or placebo (n=16 in each group)

after induction of anaesthesia until 8h after cardiopulmonary bypass (CPB). We compared markers of systemic and pulmonary inflammation, surrogates of myocardial IRI and clinical outcomes using Mann-Whitney U- and Fisher’s exact tests. Thirty- and 90-day mortality was 0% in both groups. No side effects were observed in the treatment group. Surgical selleck products revision, pleural and pericardial effusion, infection and atrial fibrillation rates were not different between groups. Reparixin significantly reduced the proportion of neutrophil granulocytes in blood at the beginning [49%, interquartile range (IQR)=45-57 versus 58%, IQR=53-66, P=0035], end (71%, IQR=67-76 versus 79%, IQR=71-83, P=0023) and 1h after CPB (73%, IQR=71-75 versus 77%, IQR=72-80, P=0035). Reparixin patients required a lesser positive fluid balance during surgery (2575ml, IQR=2027-3080

versus 3200ml, IQR=2928-3778, P=0029) and during ICU stay (2603ml, IQR=1023-4288 versus 4200ml, IQR=2313-8160, Mekinist P=0021). Numerically, more control patients required noradrenaline 011g/kg/min (50 versus 19%, P=0063) and dobutamine (50 versus 25%, P=014). Therefore, administration of reparixin in CABG patients appears to be feasible and safe. It concurrently attenuated postoperative granulocytosis in peripheral blood.”
“BACKGROUND: HER-2/neu, overexpressed in breast cancer, is a source of immunogenic peptides that include GP2 and E75. Phase 2 testing of E75 as an adjuvant vaccine has suggested a clinical

benefit. GP2, derived from the transmembrane portion of HER-2/neu, has differing Elacridar binding characteristics and may be more immunogenic than E75. Results of the first phase 1 trial of GP2 peptide vaccine are presented. METHODS: Disease-free, lymph node-negative, human leukocyte antigen (HLA)-A2(+) breast cancer patients were enrolled. This dose escalation trial included 4 groups to determine safety and optimal GP2 peptide/granulocyte-macrophage colony-stimulating factor (GM-CSF) dose. Toxicities were monitored. Immunologic response was assessed ex vivo via the HLA-A2:immunoglobulin dimer assay to detect GP2-specific CD8(+) T cells (and E75-specific CD8+ T cells to assess epitope spreading) and in vivo via delayed type hypersensitivity (DTH) reaction (medians/ranges). RESULTS: Eighteen patients were enrolled. All toxicities were grade <= 2. Eight (88.9%) of 9 patients in the first 3 dose groups required GM-CSF dose reductions for local reactions >= 100 mm or grade >= 2 systemic toxicity. GM-CSF dose was reduced to 125 jig for the final dose group.