61 research outputs found

    Strangeness production in antiproton-nucleus annihilation

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    The results of the microscopic transport calculations of pˉ\bar p-nucleus interactions within a GiBUU model are presented. The dominating mechanism of hyperon production is the strangeness exchange processes KˉNYπ\bar K N \to Y \pi and KˉNΞK\bar K N \to \Xi K. The calculated rapidity spectra of Ξ\Xi hyperons are significantly shifted to forward rapidities with respect to the spectra of S=1S=-1 hyperons. We argue that this shift should be a sensitive test for the possible exotic mechanisms of pˉ\bar p-nucleus annihilation. The production of the double Λ\Lambda-hypernuclei by Ξ\Xi^- interaction with a secondary target is calculated.Comment: Proceedings of the 12th Int. Workshop on Meson Production, Properties and Interaction (MESON-2012), Cracow, 31.05-05.06.201

    How to measure the parity of the Θ+\Theta^+ in pp\vec p\vec p collisions

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    Triggered by a recent paper by Thomas, Hicks and Hosaka, we investigate which observables can be used to determine the parity of the Θ+\Theta^+ from the reaction ppΣ+Θ+\vec p\vec p \to \Sigma^+\Theta^+ near its production threshold. In particular, we show that the sign of the spin correlation coefficient AxxA_{xx} for small excess energies yields the negative of the parity of the Θ+\Theta^+. The argument relies solely on the Pauli principle and parity conservation and is therefore model--independent.Comment: References completed, discussion on possible influence of background added; conclusions unchange

    Toward polarized antiprotons: Machine development for spin-filtering experiments

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    The paper describes the commissioning of the experimental equipment and the machine studies required for the first spin-filtering experiment with protons at a beam kinetic energy of 49.349.3\,MeV in COSY. The implementation of a low-β\beta insertion made it possible to achieve beam lifetimes of τb=8000\tau_{\rm{b}}=8000\,s in the presence of a dense polarized hydrogen storage-cell target of areal density dt=(5.5±0.2)×1013atoms/cm2d_{\rm t}=(5.5\pm 0.2)\times 10^{13}\,\mathrm{atoms/cm^{2}}. The developed techniques can be directly applied to antiproton machines and allow for the determination of the spin-dependent pˉp\bar{p}p cross sections via spin filtering

    Polarizing a stored proton beam by spin flip?

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    We discuss polarizing a proton beam in a storage ring, either by selective removal or by spin flip of the stored ions. Prompted by recent, conflicting calculations, we have carried out a measurement of the spin flip cross section in low-energy electron-proton scattering. The experiment uses the cooling electron beam at COSY as an electron target. The measured cross sections are too small for making spin flip a viable tool in polarizing a stored beam. This invalidates a recent proposal to use co-moving polarized positrons to polarize a stored antiproton beam.Comment: 18 pages, 6 figure

    Search for a dark photon in the π0e+eγ\pi^0 \to e^+e^-\gamma decay

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    The presently world largest data sample of pi0 --> gamma e+e- decays containing nearly 5E5 events was collected using the WASA detector at COSY. A search for a dark photon U produced in the pi0 --> gamma U --> gamma e+e- decay from the pp-->pp\pi^0 reaction was carried out. An upper limit on the square of the U-gamma mixing strength parameter epsilon^2 of 5e-6 at 90% CL was obtained for the mass range 20 MeV <M_U< 100 MeV. This result together with other recent experimental limits significantly reduces the M_U vs. \epsilon^2 parameter space preferred by the measured value of the muon anomalous magnetic moment.Comment: 16 pages, 8 figures; improved analysis extending the exclusion region to 20 MeV<M_U< 100 MeV; implemented changes requested by referee

    Coherent \pi^\circ photoproduction from ^4He

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    Differential cross sections and beam asymmetries for coherent \pi^\circ photoproduction from ^4He in the \Delta energy-range have been measured with high statistical and systematic precisions using both decay photons for identifying the process.The experiment was performed at the MAinz MIcrotron using the TAPS photon spectrometer and the Glasgow/Mainz tagged photon facility. The differential cross sections are in excellent agreement with predictions based on the DWIA if an appropriate parametrization of the \Delta-nuclear interaction is applied. The beam asymmetries are interpreted in terms of degrees of linear polarization of collimated coherent bremsstrahlung. The expected increase of the degree of linear polarization with decreasing collimation angle is confirmed. Agreement with calculations is obtained on a few-percent level of precision in the maxima of the coherent peaks.Comment: 22 pages, 6 figure

    The Use of a Mobile Laboratory Unit in Support of Patient Management and Epidemiological Surveillance during the 2005 Marburg Outbreak in Angola

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    A mobile laboratory unit (MLU) was deployed to Uige, Angola as part of the World Health Organization response to an outbreak of viral hemorrhagic fever caused by Marburg virus (MARV). Utilizing mainly quantitative real-time PCR assays, this laboratory provided specific MARV diagnostics in the field. The MLU operated for 88 consecutive days allowing MARV-specific diagnostic response in <4 hours from sample receiving. Most cases were found among females in the child-bearing age and in children less than five years of age including a high number of paediatric cases implicating breastfeeding as potential transmission route. Oral swabs were identified as a useful alternative specimen source to the standard whole blood/serum specimens for patients refusing blood draw. There was a high concordance in test results between the MLU and the reference laboratory in Luanda operated by the US Centers for Disease Control and Prevention. The MLU was an important outbreak response asset providing valuable support in patient management and epidemiological surveillance. Field laboratory capacity should be expanded and made an essential part of any future outbreak investigation

    Mucosal Immunization of Cynomolgus Macaques with the VSVΔG/ZEBOVGP Vaccine Stimulates Strong Ebola GP-Specific Immune Responses

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    (ZEBOV) produces a lethal viral hemorrhagic fever in humans and non-human primates.We demonstrate that the VSVΔG/ZEBOVGP vaccine given 28 days pre-challenge either intranasally (IN), orally (OR), or intramuscularly (IM) protects non-human primates against a lethal systemic challenge of ZEBOV, and induces cellular and humoral immune responses. We demonstrated that ZEBOVGP-specific T-cell and humoral responses induced in the IN and OR groups, following an immunization and challenge, produced the most IFN-γ and IL-2 secreting cells, and long term memory responses.We have shown conclusively that mucosal immunization can protect from systemic ZEBOV challenge and that mucosal delivery, particularly IN immunization, seems to be more potent than IM injection in the immune parameters we have tested. Mucosal immunization would be a huge benefit in any emergency mass vaccination campaign during a natural outbreak, or following intentional release, or for mucosal immunization of great apes in the wild

    Inhibition of Lassa Virus Glycoprotein Cleavage and Multicycle Replication by Site 1 Protease-Adapted α1-Antitrypsin Variants

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    The virus family Arenaviridae includes several hemorrhagic fever causing agents such as Lassa, Guanarito, Junin, Machupo, and Sabia virus that pose a major public health concern to the human population in West African and South American countries. Current treatment options to control fatal outcome of disease are limited to the ribonucleoside analogue ribavirin, although its use has some significant limitations. The lack of effective treatment alternatives emphasizes the need for novel antiviral therapeutics to counteract these life-threatening infections. Maturation cleavage of the viral envelope glycoprotein by the host cell proprotein convertase site 1 protease (S1P) is critical for infectious virion production of several pathogenic arenaviruses. This finding makes this protease an attractive target for the development of novel anti-arenaviral therapeutics. We demonstrate here that highly selective S1P-adapted α1-antitrypsins have the potential to efficiently inhibit glycoprotein processing, which resulted in reduced Lassa virus replication. Our findings suggest that S1P should be considered as an antiviral target and that further optimization of modified α1-antitrypsins could lead to potent and specific S1P inhibitors with the potential for treatment of certain viral hemorrhagic fevers

    Ebola Virion Attachment and Entry into Human Macrophages Profoundly Effects Early Cellular Gene Expression

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    Zaire ebolavirus (ZEBOV) infections are associated with high lethality in primates. ZEBOV primarily targets mononuclear phagocytes, which are activated upon infection and secrete mediators believed to trigger initial stages of pathogenesis. The characterization of the responses of target cells to ZEBOV infection may therefore not only further understanding of pathogenesis but also suggest possible points of therapeutic intervention. Gene expression profiles of primary human macrophages exposed to ZEBOV were determined using DNA microarrays and quantitative PCR to gain insight into the cellular response immediately after cell entry. Significant changes in mRNA concentrations encoding for 88 cellular proteins were observed. Most of these proteins have not yet been implicated in ZEBOV infection. Some, however, are inflammatory mediators known to be elevated during the acute phase of disease in the blood of ZEBOV-infected humans. Interestingly, the cellular response occurred within the first hour of Ebola virion exposure, i.e. prior to virus gene expression. This observation supports the hypothesis that virion binding or entry mediated by the spike glycoprotein (GP1,2) is the primary stimulus for an initial response. Indeed, ZEBOV virions, LPS, and virus-like particles consisting of only the ZEBOV matrix protein VP40 and GP1,2 (VLPVP40-GP) triggered comparable responses in macrophages, including pro-inflammatory and pro-apoptotic signals. In contrast, VLPVP40 (particles lacking GP1,2) caused an aberrant response. This suggests that GP1,2 binding to macrophages plays an important role in the immediate cellular response
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