13,793 research outputs found

    Reply to Comment on "A local realist model for correlations of the singlet state"

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    The general conclusion of Seevinck and Larsson is that our model exploits the so-called coincidence-time loophole and produces sinusoidal (quantum-like) correlations but does not model the singlet state because it does not violate the relevant Bell inequality derived by Larsson and Gill, since in order to obtain the sinusoidal correlations the probability of coincidences in our model goes to zero. In this reply, we refute their arguments that lead to this conclusion and demonstrate that our model can reproduce results of photon and ion-trap experiments with frequencies of coincidences that are not in conflict with the observations.Comment: Corrected typo

    T-cell activation by organic dust in vitro

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    AbstractInhalation of swine dust causes intense airway inflammation with a multifold increase of inflammatory cells and lymphocyte activation as assessed by bronchoalveolar lavage. To further investigate the mechanism for lymphocyte activation the present in vitro study focuses on the lymphocyte response to swine dust in whole blood.Various concentrations of phytohaemagglutinin (PHA) (final concentrations: 3·16, 10·0, 3·16 and 100 μ g ml−1) and swine dust (final cocentrations: 10·0, 31·6, 100 and 316 μ g ml−1) were added to heparinized whole blood from healthy donors. The blood samples were incubated in duplicate, using the homologous unstimulated blood as control, for 4, 24, 48 and 72 h in a water bath at 37°C. The cells were stained with fluorochrome conjugated monoclonal antibodies. For analysis of T-cell activation CD3 was doublestained together with the activation markers CD69, CD25 and HLADR. Cell count percentages were analysed by flow cytometry. Soluble IL-2sR α in plasma was analysed using commercial sandwich ELISA techniqe.At baseline CD69, CD25 and HLA-DR were expressed in < 1%, approx 5% and < 1% of the T-cells respectively. We found a dose response relationship between swine dust exposure and the expression of all three T-cell activation markers which appeared at different time-points. Maximal expression of CD69 (8%,P <0·05) and CD25 (15%, P<0·001) was found after 24 h of activation. HLA-DR was significantly expressed after 48 h (8%) and maximally expressed after 72 h of activation (13%,P <0·05). The soluble IL-2sR α in plasma was maximally expressed after 24–48 h (1200 pg ml−1and 1500 pg ml−1, respectively.In conclusion, T-cells were activated by swine dustin vitro . Thus, our previous findings of T-cell activation following swine dust exposure, in vivo may be an effect of the dust either directly on T-cells or on other cells which in turn contribute to the T-cell activation

    USE OF NET CAGES FOR FISH FARMING IN SWEDISH CONDITIONS

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    Effects by 8-bromo-cyclicAMP on basal and organic dust-induced release of interleukin-6 and interleukin-8 in A549 human airway epithelial cells

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    AbstractInhalation of organic dust from a swine-confinement building leads to an intense inflammatory reaction with an increased number of inflammatory cells and mediators in the upper and lower respiratory tract of previously unexposed subjects. In vitro the dust induces cytokine release from epithelial cells and alveolar macrophages. It is known that intracellular cyclic AMP (cAMP) contributes to the regulation of inflammatory responses. We therefore investigated whether 8-Bromo-cAMP, a cell membrane-permeable cAMP analogue, would influence release of the cytokines interleukin-6 (IL-6) and IL-8 in a human airway epithelial cell line, A549, exposed to a suspension of the organic dust, and to a supernatant prepared by centrifugation (at low g-force) of a suspension of dust. The large particulate matter was thus sedimented, leaving bacteria, whole and cell wall constituents in the supernatant. Cytokine release was measured with enzyme-linked immunosorbent assay (ELISA). The cytokine release induced by a supernatant was 23% (IL-6) and 27% (IL-8) of the release induced by a dust suspension. 8-Bromo-cAMP (1mM) doubled basal IL-6 release and IL-6 release induced by a dust supernatant (P<0.01), and increased IL-6 release induced by a dust suspension by 19% (P<0.05). 8-Bromo-cAMP did not affect basal IL-8 release, partially inhibited (28%) the release of IL-8 induced by a dust suspension (P<0.01), but increased IL-8 release induced by a dust supernatant by 13% (P<0.05). In summary, expression of the cytokines IL-6 and IL-8 is differentially regulated by 8-Bromo-cAMP, both with regard to basal and dust-induced release. The results indicate that 8-Bromo-cAMP attenuated IL-8 release by affecting signaling transductions induced by the particulate fraction
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