51 research outputs found

    Syrian refugees in Lebanon: A turning point?

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    This paper was presented at a workshop on ‘The Long-term Challenges of Forced Migration: Local and Regional Perspectives from Lebanon, Jordan and Iraq’ organised by the LSE Middle East Centre in June 2016. It was published as part of a collected papers volume available in English and Arabic

    Les roses flamboyantes en France

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    Avec "Les roses flamboyantes en France", nous avons voulu présenter une étude systématique d'un sujet encore neuf. Près de quatre-vingt roses, réalisées entre 1380 et 1550, ont d'abord été classifiées en quatre grands types de remplage: les souffiets-mouchettes, les rose à pétales, les multiples cercles, les divers polygones. Par ailleurs, trois périodes principales ont été distinguées : entre 1380 et 1435, entre 1435 et 1480, entre 1480 et 1550. Les derniers chapitres sont consacrés aux roses appréhendées dans leur province respective, afin de mieux souligner leurs tendances et caractères propres, comme la fusion des motifs en Picardie (Amiens, Abbeville), ou encore l'harmonie des roses des Chambiges autour de Paris.Montréal Trigonix inc. 201

    The long-term challenges of forced migration: perspectives from Lebanon, Jordan and Iraq

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    "The Arab Uprisings of 2011 set events in motion that have vastly changed the Middle East and North Africa region (MENA), not only through organised protest and violent conflict, but also through migration and demographic change. The Syrian conflict has forcibly displaced more than 11 million people – half of the country’s population. 6.5 million are internally displaced, while 5 million have crossed the border to find refuge abroad, in neighbouring countries such as Turkey, Lebanon, Jordan, Iraq and Egypt, and elsewhere both regionally and globally. In a workshop held on 17–18 June 2016, the LSE Middle East Centre brought together a diverse group of people (policymakers from host states, representatives from international organisations, academics and NGOs practitioners) to explore the effects of the Syrian refugee emergency on Arab host states such as Lebanon, Jordan, and Iraq. This volume brings together a set of papers presented at the workshop. It also presents a list of key recommendations relevant for all stakeholders and agreed upon by participants.

    Evaluation of the dystrophin carboxy-terminal domain for micro-dystrophin gene therapy in cardiac and skeletal muscles in the DMDmdx rat model

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    Duchenne muscular dystrophy (DMD) is a muscle wasting disorder caused by mutations in the gene encoding dystrophin. Gene therapy using micro-dystrophin (MD) transgenes and recombinant adeno-associated virus (rAAV) vectors hold great promise. To overcome the limited packaging capacity of rAAV vectors, most MD do not include dystrophin carboxy-terminal (CT) domain. Yet, the CT domain is known to recruit α1- and β1-syntrophins and α-dystrobrevin, a part of the dystrophin-associated protein complex (DAPC), which is a signaling and structural mediator of muscle cells. In this study, we explored the impact of inclusion of the dystrophin CT domain on ΔR4-23/ΔCT MD (MD1), in DMDmdx rats, which allows for relevant evaluations at muscular and cardiac levels. We showed by LC-MS/MS that MD1 expression is sufficient to restore the interactions at a physiological level of most DAPC partners in skeletal and cardiac muscles, and that inclusion of the CT domain increases the recruitment of some DAPC partners at supra-physiological levels. In parallel, we demonstrated that inclusion of the CT domain does not improve MD1 therapeutic efficacy on DMD muscle and cardiac pathologies. Our work highlights new evidences of the therapeutic potential of MD1 and strengthens the relevance of this candidate for gene therapy of DMD

    Impact of Anti-Inflammatory Agents on the Gene Expression Profile of Stimulated Human Neutrophils: Unraveling Endogenous Resolution Pathways

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    Adenosine, prostaglandin E2, or increased intracellular cyclic AMP concentration each elicit potent anti-inflammatory events in human neutrophils by inhibiting functions such as phagocytosis, superoxide production, adhesion and cytokine release. However, the endogenous molecular pathways mediating these actions are poorly understood. In the present study, we examined their impact on the gene expression profile of stimulated neutrophils. Purified blood neutrophils from healthy donors were stimulated with a cocktail of inflammatory agonists in the presence of at least one of the following anti-inflammatory agents: adenosine A2A receptor agonist CGS 21680, prostaglandin E2, cyclic-AMP-elevating compounds forskolin and RO 20-1724. Total RNA was analyzed using gene chips and real-time PCR. Genes encoding transcription factors, enzymes and regulatory proteins, as well as secreted cytokines/chemokines showed differential expression. We identified 15 genes for which the anti-inflammatory agents altered mRNA levels. The agents affected the expression profile in remarkably similar fashion, suggesting a central mechanism limiting cell activation. We have identified a set of genes that may be part of important resolution pathways that interfere with cell activation. Identification of these pathways will improve understanding of the capacity of tissues to terminate inflammatory responses and contribute to the development of therapeutic strategies based on endogenous resolution

    Effect of angiotensin-converting enzyme inhibitor and angiotensin receptor blocker initiation on organ support-free days in patients hospitalized with COVID-19

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    IMPORTANCE Overactivation of the renin-angiotensin system (RAS) may contribute to poor clinical outcomes in patients with COVID-19. Objective To determine whether angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) initiation improves outcomes in patients hospitalized for COVID-19. DESIGN, SETTING, AND PARTICIPANTS In an ongoing, adaptive platform randomized clinical trial, 721 critically ill and 58 non–critically ill hospitalized adults were randomized to receive an RAS inhibitor or control between March 16, 2021, and February 25, 2022, at 69 sites in 7 countries (final follow-up on June 1, 2022). INTERVENTIONS Patients were randomized to receive open-label initiation of an ACE inhibitor (n = 257), ARB (n = 248), ARB in combination with DMX-200 (a chemokine receptor-2 inhibitor; n = 10), or no RAS inhibitor (control; n = 264) for up to 10 days. MAIN OUTCOMES AND MEASURES The primary outcome was organ support–free days, a composite of hospital survival and days alive without cardiovascular or respiratory organ support through 21 days. The primary analysis was a bayesian cumulative logistic model. Odds ratios (ORs) greater than 1 represent improved outcomes. RESULTS On February 25, 2022, enrollment was discontinued due to safety concerns. Among 679 critically ill patients with available primary outcome data, the median age was 56 years and 239 participants (35.2%) were women. Median (IQR) organ support–free days among critically ill patients was 10 (–1 to 16) in the ACE inhibitor group (n = 231), 8 (–1 to 17) in the ARB group (n = 217), and 12 (0 to 17) in the control group (n = 231) (median adjusted odds ratios of 0.77 [95% bayesian credible interval, 0.58-1.06] for improvement for ACE inhibitor and 0.76 [95% credible interval, 0.56-1.05] for ARB compared with control). The posterior probabilities that ACE inhibitors and ARBs worsened organ support–free days compared with control were 94.9% and 95.4%, respectively. Hospital survival occurred in 166 of 231 critically ill participants (71.9%) in the ACE inhibitor group, 152 of 217 (70.0%) in the ARB group, and 182 of 231 (78.8%) in the control group (posterior probabilities that ACE inhibitor and ARB worsened hospital survival compared with control were 95.3% and 98.1%, respectively). CONCLUSIONS AND RELEVANCE In this trial, among critically ill adults with COVID-19, initiation of an ACE inhibitor or ARB did not improve, and likely worsened, clinical outcomes. TRIAL REGISTRATION ClinicalTrials.gov Identifier: NCT0273570

    Quelles synergies entre connaissances scientifiques et empiriques ? L'exemple des cultures du safran et de la truffe

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    Dans un contexte de redéfinition des fonctions de l'agriculture dans la société, les "systèmes de connaissance agricole" doivent concevoir de nouveaux modes de collaboration entre agriculteurs, agents de développement et scientifiques, mais aussi renouveler les connaissances à produire. Peu de travaux portent sur le contenu des connaissances à construire dans ces situations. Ce texte part de l'hypothèse que des connaissances agronomiques peuvent émerger d'une synergie entre connaissances empiriques des praticiens et connaissances scientifiques. Il s'attache à explorer cette nouvelle forme de production de connaissances, à partir des cas du safran et de la truffe, deux cultures dont la maîtrise technique constitue un frein majeur à leur développement. En confrontant les données sur les connaissances des safraniers et trufficulteurs à la littérature scientifique et technique existant sur ces cultures et à la théorie agronomique, ce texte propose quatre modes de combinaison entre connaissances empiriques et scientifiques
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