7 research outputs found

    Encoding and decoding plantation society : wistful memories of Stuart Hall and Norman Girvan

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    Abstract in Portuguese by Deborah Hickling included.Two giants of Caribbean thought have recently departed: Stuart Hall (1932 - 2014), cultural scholar, and Norman Girvan (1941 - 2014), economist. Hall held professorial posts at the University of Birmingham and the Open University in the UK, and retained close links with Jamaica. He studied ethnicity, issues of Caribbean diaspora, critical examinations of Marxism, media and communications, and the ideas of the New Left and post-modernism. Girvan, a professor at the University of the West Indies, was a strong critic of the dependence of the Caribbean and other post-colonial nations on economic and technological structures and thinking locked into a colonial paradigm. He also worked in regional and international bodies to achieve closer regional alignment in the Caribbean and strategies for regional economic transformation. This tribute explores the contributions of both scholars to the fields of cultural studies and political economy, and particularly celebrates their significance to the Caribbean and Latin American region.peer-reviewe

    Basic science232. Certolizumab pegol prevents pro-inflammatory alterations in endothelial cell function

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    Background: Cardiovascular disease is a major comorbidity of rheumatoid arthritis (RA) and a leading cause of death. Chronic systemic inflammation involving tumour necrosis factor alpha (TNF) could contribute to endothelial activation and atherogenesis. A number of anti-TNF therapies are in current use for the treatment of RA, including certolizumab pegol (CZP), (Cimzia ®; UCB, Belgium). Anti-TNF therapy has been associated with reduced clinical cardiovascular disease risk and ameliorated vascular function in RA patients. However, the specific effects of TNF inhibitors on endothelial cell function are largely unknown. Our aim was to investigate the mechanisms underpinning CZP effects on TNF-activated human endothelial cells. Methods: Human aortic endothelial cells (HAoECs) were cultured in vitro and exposed to a) TNF alone, b) TNF plus CZP, or c) neither agent. Microarray analysis was used to examine the transcriptional profile of cells treated for 6 hrs and quantitative polymerase chain reaction (qPCR) analysed gene expression at 1, 3, 6 and 24 hrs. NF-κB localization and IκB degradation were investigated using immunocytochemistry, high content analysis and western blotting. Flow cytometry was conducted to detect microparticle release from HAoECs. Results: Transcriptional profiling revealed that while TNF alone had strong effects on endothelial gene expression, TNF and CZP in combination produced a global gene expression pattern similar to untreated control. The two most highly up-regulated genes in response to TNF treatment were adhesion molecules E-selectin and VCAM-1 (q 0.2 compared to control; p > 0.05 compared to TNF alone). The NF-κB pathway was confirmed as a downstream target of TNF-induced HAoEC activation, via nuclear translocation of NF-κB and degradation of IκB, effects which were abolished by treatment with CZP. In addition, flow cytometry detected an increased production of endothelial microparticles in TNF-activated HAoECs, which was prevented by treatment with CZP. Conclusions: We have found at a cellular level that a clinically available TNF inhibitor, CZP reduces the expression of adhesion molecule expression, and prevents TNF-induced activation of the NF-κB pathway. Furthermore, CZP prevents the production of microparticles by activated endothelial cells. This could be central to the prevention of inflammatory environments underlying these conditions and measurement of microparticles has potential as a novel prognostic marker for future cardiovascular events in this patient group. Disclosure statement: Y.A. received a research grant from UCB. I.B. received a research grant from UCB. S.H. received a research grant from UCB. All other authors have declared no conflicts of interes

    Measurement of the W±ZW^{\pm}Z boson pair-production cross section in pppp collisions at s=13\sqrt{s}=13 TeV with the ATLAS Detector

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    The production of W±ZW^{\pm}Z events in proton--proton collisions at a centre-of-mass energy of 13 TeV is measured with the ATLAS detector at the LHC. The collected data correspond to an integrated luminosity of 3.2 fb1^{-1}. The W±ZW^{\pm}Z candidates are reconstructed using leptonic decays of the gauge bosons into electrons or muons. The measured inclusive cross section in the detector fiducial region for leptonic decay modes is σW±Zνfid.=63.2±3.2\sigma_{W^\pm Z \rightarrow \ell^{'} \nu \ell \ell}^{\textrm{fid.}} = 63.2 \pm 3.2 (stat.) ±2.6\pm 2.6 (sys.) ±1.5\pm 1.5 (lumi.) fb. In comparison, the next-to-leading-order Standard Model prediction is 53.42.8+3.653.4^{+3.6}_{-2.8} fb. The extrapolation of the measurement from the fiducial to the total phase space yields σW±Ztot.=50.6±2.6\sigma_{W^{\pm}Z}^{\textrm{tot.}} = 50.6 \pm 2.6 (stat.) ±2.0\pm 2.0 (sys.) ±0.9\pm 0.9 (th.) ±1.2\pm 1.2 (lumi.) pb, in agreement with a recent next-to-next-to-leading-order calculation of 48.21.0+1.148.2^{+1.1}_{-1.0} pb. The cross section as a function of jet multiplicity is also measured, together with the charge-dependent W+ZW^+Z and WZW^-Z cross sections and their ratio

    Search for Scalar Diphoton Resonances in the Mass Range 6560065-600 GeV with the ATLAS Detector in pppp Collision Data at s\sqrt{s} = 8 TeVTeV

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    A search for scalar particles decaying via narrow resonances into two photons in the mass range 65–600 GeV is performed using 20.3fb120.3\text{}\text{}{\mathrm{fb}}^{-1} of s=8TeV\sqrt{s}=8\text{}\text{}\mathrm{TeV} pppp collision data collected with the ATLAS detector at the Large Hadron Collider. The recently discovered Higgs boson is treated as a background. No significant evidence for an additional signal is observed. The results are presented as limits at the 95% confidence level on the production cross section of a scalar boson times branching ratio into two photons, in a fiducial volume where the reconstruction efficiency is approximately independent of the event topology. The upper limits set extend over a considerably wider mass range than previous searches
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