95 research outputs found

    A Soluble Form of the High Affinity IgE Receptor, Fc-Epsilon-RI, Circulates in Human Serum

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    Soluble IgE receptors are potential in vivo modulators of IgE-mediated immune responses and are thus important for our basic understanding of allergic responses. We here characterize a novel soluble version of the IgE-binding alpha-chain of Fc-epsilon-RI (sFcεRI), the high affinity receptor for IgE. sFcεRI immunoprecipitates as a protein of ∼40 kDa and contains an intact IgE-binding site. In human serum, sFcεRI is found as a soluble free IgE receptor as well as a complex with IgE. Using a newly established ELISA, we show that serum sFcεRI levels correlate with serum IgE in patients with elevated IgE. We also show that serum of individuals with normal IgE levels can be found to contain high levels of sFcεRI. After IgE-antigen-mediated crosslinking of surface FcεRI, we detect sFcεRI in the exosome-depleted, soluble fraction of cell culture supernatants. We further show that sFcεRI can block binding of IgE to FcεRI expressed at the cell surface. In summary, we here describe the alpha-chain of FcεRI as a circulating soluble IgE receptor isoform in human serum

    The design of the instrument control unit and its role within the data processing system of the ESA PLATO Mission

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    PLATO1 is an M-class mission of the European Space Agency's Cosmic Vision program, whose launch is foreseen by 2026. PLAnetary Transits and Oscillations of stars aims to characterize exoplanets and exoplanetary systems by detecting planetary transits and conducting asteroseismology of their parent stars. PLATO is the next generation planetary transit space experiment, as it will fly after CoRoT, Kepler, TESS and CHEOPS; its objective is to characterize exoplanets and their host stars in the solar neighbors. While it is built on the heritage from previous missions, the major breakthrough to be achieved by PLATO will come from its strong focus on bright targets, typically with mvv<=8. The prime science goals characterizing and distinguishing PLATO from the previous missions are: the detection and characterization of exoplanetary systems of all kinds, including both the planets and their host stars, reaching down to small, terrestrial planets in the habitable zone; the identification of suitable targets for future, more detailed characterization, including a spectroscopic search for biomarkers in nearby habitable exoplanets (e.g. ARIEL Mission scientific case, E-ELT observations from Ground); a full characterization of the planet host stars, via asteroseismic analysis: this will provide the Community with the masses, radii and ages of the host stars, from which masses, radii and ages of the detected planets will be determined

    Effects of omalizumab on basophils: Potential biomarkers in asthma and chronic spontaneous urticaria

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    Omalizumab is an anti-IgE humanized monoclonal antibody approved for the treatment of severe asthma and chronic spontaneous urticaria. Omalizumab binds free serum IgE and antagonizes its interaction with FcεRI, which is considered the main pharmacodynamic mechanism responsible for the clinical response to the treatment. The reduction of IgE serum concentration down-regulates the cellular expression of FcεRI on basophils. However, the biological events occurring on basophils during the therapy with omalizumab are multiple and complex. Here we review the current evidence regarding the specific biological effects of omalizumab on basophils in patients with asthma and chronic spontaneous urticaria. In addition to the modulation of IgE receptors, omalizumab may affect basophils homeostasis, intra-cellular signaling, cellular responsiveness/activation and cytokine release. These effects may be partially responsible for the clinical success of omalizumab and potentially provide useful biological markers for future assessment of the clinical response to the treatment. However, further investigation is required to better elucidate the role of basophils during the treatment with omalizumab

    Improved Initial Synchronisation in the presence of Frequency Offset in UMTS FDD mode

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    The UMTS-FDD system, one of the members of the ITU IMT-2000 third generation standard for terrestrial cellular systems, employs pruned Golay sequences to enable initial synchronisation of the mobile terminals to the network. In this paper a low complexity solution for initial synchronisation is proposed, which is able to counteract the performance degradation introduced by large frequency offsets occurring in the mobile station receiver. Simulation results are provided to validate the proposed solution
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