Resonance production from jet fragmentation

Short lived resonances are sensitive to the medium properties in heavy-ion collisions. Heavy hadrons have larger probability to be produced within the quark gluon plasma phase due to their short formation times. Therefore heavy mass resonances are more likely to be affected by the medium, and the identification of early produced resonances from jet fragmentation might be a viable option to study chirality. The high momentum resonances on the away-side of a triggered di-jet are likely to be the most modified by the partonic or early hadronic medium. We will discuss first results of triggered hadron-resonance correlations in Cu+Cu heavy ion collisions.Comment: Hot Quarks Colorado 2008 Proceedings, 4 pages 5 figure

What do we learn from Resonance Production in Heavy Ion Collisions?

Resonances with their short life time and strong coupling to the dense and hot medium are suggested as a signature of the early stage of the fireball created in a heavy ion collision \cite{rap00,lut01,lut02}. The comparison of resonances with different lifetimes and quark contents may give information about time evolution and density and temperature of during the expanding of fireball medium. Resonances in elementary reactions have been measured since 1960. Resonance production in elementary collisions compared with heavy ion collisions where we expect to create a hot and dense medium may show the direct of influence of the medium on the resonances. This paper shows a selection of the recent resonance measurements from SPS and RHIC heavy ion colliders.Comment: 10 pages, 8 figures, HotQuarks 2004 conference proceeding

Resonance production in heavy ion collisions

Recent results of resonance production from RHIC at $\sqrt{s_{\rm NN}} =$ 200 GeV and SPS at $\sqrt{s_{\rm NN}} =$ 17 GeV are presented and discussed in terms of the evolution and freeze-out conditions of a hot and dense fireball medium. Yields and spectra are compared with thermal model predictions at chemical freeze-out. Deviations in the low transverse momentum region of the resonance spectrum of the hadronic decay channel, suggest a strongly interaction hadronic phase between chemical and kinetic freeze-out. Microscopic models including resonance rescattering and regeneration are able to describe the trend of the data. The magnitude of the regeneration cross sections for different inverse decay channels are discussed. Model calculations which include elastic hadronic interactions between chemical freeze-out and thermal freeze-out based on the K(892)/K and $\Lambda$(1520)/$\Lambda$ ratios suggest a time between two freeze-outs surfaces of $\Delta \tau>$ 4 fm/c. The difference in momentum distributions and yields for the $\phi$(1020) resonance reconstructed from the leptonic and hadronic decay channels at SPS energy are discussed taking into account the impact of a hadronic phase and possible medium modifications.Comment: 8 pages, 4 figures, conference proceedings (SQM2004

Role of protein adsorption on haemodialysis-induced complement activation and neutrophil defects

The present clinical study investigated the role of protein adsorption on complement activation and neutrophil functions during in vivo haemodialysis. The parameters were measured simultaneously at the arterial and venous sites of a cuprophan (CU) dialyser with or without pretreatment with human albumin, human immunoglobulins or human total plasma proteins (PLP). Leukocyte count, complement activation (C3a des arg), oxygen radical production and chemotaxis were measured at time zero and 15 min at the arterial and venous sites of the dialyser. Leukopenia observed at both sites was prevented only with PLP treatment. Complement activation was maximal at the venous site, but was not prevented by any of the treatments. Neutrophil oxygen radical production and chemotaxis were significantly decreased only at the venous site and restored to normal with any of the three treatments. Complement activation was maximal at the venous site, but was not prevented by any of the treatments. Protein adsorption on the dialyser membrane seems to modulate the bioincompatibility parameters in a different way. Depending on the functions tested, the protein fractions have different protecting effects, indicating the multifactorial mechanism implicated in the CU haemodialysis-induced leukopenia, complement activation and neutrophil defec

Thymus transplantation for complete DiGeorge syndrome: European experience

Background: Thymus transplantation is a promising strategy for the treatment of athymic complete DiGeorge syndrome (cDGS). Methods: Twelve patients with cDGS were transplanted with allogeneic cultured thymus. Objective: To confirm and extend the results previously obtained in a single centre. Results: Two patients died of pre-existing viral infections without developing thymopoeisis and one late death occurred from autoimmune thrombocytopaenia. One infant suffered septic shock shortly after transplant resulting in graft loss and the need for a second transplant. Evidence of thymopoeisis developed from 5-6 months after transplantation in ten patients. The median (range) of circulating naïve CD4 counts (x10663 /L) were 44(11-440) and 200(5-310) at twelve and twenty-four months post-transplant and T-cell receptor excision circles were 2238 (320-8807) and 4184 (1582 -24596) per106 65 T-cells. Counts did not usually reach normal levels for age but patients were able to clear pre-existing and later acquired infections. At a median of 49 months (22-80), eight have ceased prophylactic antimicrobials and five immunoglobulin replacement. Histological confirmation of thymopoeisis was seen in seven of eleven patients undergoing biopsy of transplanted tissue including five showing full maturation through to the terminal stage of Hassall body formation. Autoimmune regulator (AIRE) expression was also demonstrated. Autoimmune complications were seen in 7/12 patients. In two, early transient autoimmune haemolysis settled after treatment and did not recur. The other five suffered ongoing autoimmune problems including: thyroiditis (3); haemolysis (1), thrombocytopaenia (4) and neutropenia (1). Conclusions: This study confirms the previous reports that thymus transplantation can reconstitute T cells in cDGS but with frequent autoimmune complications in survivors

Intracranial Pressure is a Better Predictor of Mortalitythan Cerebral Perfusion Pressure

Objective: To evaluate whether elevated intracranial pressure (ICP) or depressed cerebral perfusion pressure (CPP) is a better predictor of intracranial compartment syndrome and long-term functional outcomes in blunt traumatic brain injury. Methods: This was a retrospective evaluation of data collected on 203 patients with blunt traumatic brain injury who were admitted to Miami Valley Hospital, a Level I trauma center, over a 2 years period, whose initial hospital management required an intracranial pressure monitor. Serial measurements of ICP and CPP were recorded during the patients’ hospital stay. These patients were then evaluated at 3,6,12 and 24 months post-injury to assess their outcome based on functional status, as defined by death vegetative state, severe disability, moderate disability and good recovery. Results: Utilizing an ICP cut-off value of 25 or greater and a CPP value of less than 60 at any point during the patients’ hospital course, ICP elevation consistently correlated with a higher percentage of deaths and persistent vegetative state than a depression in CPP value. Outcomes as measured by severe or moderate disability where similar in both groups. However, neither measure approached statistical significance. Conclusion: ICP appears to be a better predictor of intracranial compartment syndrome and extent of brain injury, predicting better than CPP values, the outcome of death or persistent vegetative state. This may help to predict prognosis, change management strategies and guide discussions with family, especially in the early phase of injur

On the Mechanisms of Haemodialysis-induced Neutropenia: A Study with Five New and Re-used Membranes

A prospective study was undertaken in 12 haemodialysed patients successively treated on five new as well as re-used dialyser membranes, that is cuprophane, cellulose acetate, polysulphone, polycarbonate, and polyacrylonitrile. A significant reduction of neutrophils occurred with every membrane during their first use, which improved only with cuprophane upon re-use. Thrombocytopenia was noted only when neutropenia reached very low values. Monocyte reduction occurred on cuprophane, cellulose acetate and polycarbonate, but did not improve during second use. C3d accumulation paralleled the time course of neutropenia only with cuprophane and cellulose acetate. Plasma collected at the extreme of neutropenia induced aggregation of control and predialysis cells, but did not aggregate autologous dialysed neutrophils collected at 5 min. Our data indicate that the mechanism linking complement activation to neutropenia is probably triggered by more than one facto

Dielectron Measurements in STAR

Ultrarelativistic heavy-ion collisions provide a unique environment to study the properties of strongly interacting matter. Dileptons, which are not affected by the strong interactions, are an ideal penetrating probe. We present the dielectron results for p+p and Au+Au collisions at \sqrt{s_\mathrm{NN}}} =200 GeV, as measured by the STAR experiment. We discuss the prospects of dilepton measurements with the near-future detector upgrades, and the recent lower beam energy Au+Au measurements.Comment: Resonance Workshop at UT Austin (2012), 8 pages,15 figure

Expression site attenuation mechanistically links antigenic variation and development in Trypanosoma brucei

We have discovered a new mechanism of monoallelic gene expression that links antigenic variation, cell cycle, and development in the model parasite Trypanosoma brucei. African trypanosomes possess hundreds of variant surface glycoprotein (VSG) genes, but only one is expressed from a telomeric expression site (ES) at any given time. We found that the expression of a second VSG alone is sufficient to silence the active VSG gene and directionally attenuate the ES by disruptor of telomeric silencing-1B (DOT1B)-mediated histone methylation. Three conserved expression-site-associated genes (ESAGs) appear to serve as signal for ES attenuation. Their depletion causes G1-phase dormancy and reversible initiation of the slender-to-stumpy differentiation pathway. ES-attenuated slender bloodstream trypanosomes gain full developmental competence for transformation to the tsetse fly stage. This surprising connection between antigenic variation and developmental progression provides an unexpected point of attack against the deadly sleeping sickness