Using GIS to Explore the Technical and Social Aspects of Site Selection for Radioactive Waste Disposal Facilities

This working paper reviews the current situation regarding radioactive waste disposal in the UK and questions the pursuance of a purely engineering approach to gaining public support. Past histories concerning the siting of nuclear industry facilities; power stations and latterly, waste repositories, are briefly discussed and used to demonstrate that more attention needs to be paid to the geographical and social science if current proposlas for a rock laboratory, and ultimately and operational repository, at Longlands Farm near Sellafield are to succeed. The usefulness of Geographical Information Systems (GIS) and associated spatial information technologies are highlighted. Suggestions are made as to how these may be made available for public use via the Internet in adopting a more open approach to public information, consultation and participation

Measuring Confidentiality Risks in Census Data

Two trends have been on a collision course over the recent past. The first is the increasing demand by researchers for greater detail and flexibility in outputs from the decennial Census of Population. The second is the need felt by the Census Offices to demonstrate more clearly that Census data have been explicitly protected from the risk of disclosure of information about individuals. To reconcile these competing trends the authors propose a statistical measure of risks of disclosure implicit in the release of aggregate census data. The ideas of risk measurement are first developed for microdata where there is prior experience and then modified to measure risk in tables of counts. To make sure that the theoretical ideas are fully expounded, the authors develop small worked example. The risk measure purposed here is currently being tested out with synthetic and a real Census microdata. It is hoped that this approach will both refocus the census confidentiality debate and contribute to the safe use of user defined flexible census output geographies

Measuring Confidentiality Risks in Census Data

Two trends have been on a collision course over the recent past. The first is the increasing demand by researchers for greater detail and flexibility in outputs from the decennial Census of Population. The second is the need felt by the Census Offices to demonstrate more clearly that Census data have been explicitly protected from the risk of disclosure of information about individuals. To reconcile these competing trends the authors propose a statistical measure of risks of disclosure implicit in the release of aggregate census data. The ideas of risk measurement are first developed for microdata where there is prior experience and then modified to measure risk in tables of counts. To make sure that the theoretical ideas are fully expounded, the authors develop small worked example. The risk measure purposed here is currently being tested out with synthetic and a real Census microdata. It is hoped that this approach will both refocus the census confidentiality debate and contribute to the safe use of user defined flexible census output geographies

The next steps in improving the outcomes of advanced ovarian cancer

Worldwide ovarian cancer affects over 200,000 women per year. Overall survival rates are poor due to two predominate reasons. First, the majority of patients present with advanced disease creating significant difficulty with effecting disease eradication. Second, acquisition of chemotherapy resistance results in untreatable progressive disease. Advances in treatment of advanced ovarian cancer involve a spectrum of interventions including improvements in frontline debulking surgery and combination chemotherapy. Anti-angiogenic factors have been shown to have activity in frontline and recurrent disease while novel chemotherapeutic agents and targeted treatments are in development particularly for disease that is resistant to platinum-based chemotherapy. These developments aim to improve the progression-free and overall survival of women with advanced ovarian cancer

Areal interpolation and the UK’s referendum on EU membership

I show how results from the United Kingdom’s referendum on membership of the European Union can be remapped from local authority level to parliamentary constituency level through the use of a scaled Poisson regression model which incorporates demographic information from lower level geographies. I use these estimates to show how the geographic distribution of signatures to a petition for a second referendum was strongly associated with how constituencies voted in the actual referendum

Alpha/Beta Interferon Receptor Signaling Amplifies Early Proinflammatory Cytokine Production in the Lung during Respiratory Syncytial Virus Infection

Type I interferons (IFNs) are produced early upon virus infection and signal through the alpha/beta interferon (IFN-α/β) receptor (IFNAR) to induce genes that encode proteins important for limiting viral replication and directing immune responses. To investigate the extent to which type I IFNs play a role in the local regulation of inflammation in the airways, we examined their importance in early lung responses to infection with respiratory syncytial virus (RSV). IFNAR1-deficient (IFNAR1−/−) mice displayed increased lung viral load and weight loss during RSV infection. As expected, expression of IFN-inducible genes was markedly reduced in the lungs of IFNAR1−/− mice. Surprisingly, we found that the levels of proinflammatory cytokines and chemokines in the lungs of RSV-infected mice were also greatly reduced in the absence of IFNAR signaling. Furthermore, low levels of proinflammatory cytokines were also detected in the lungs of IFNAR1−/− mice challenged with noninfectious innate immune stimuli such as selected Toll-like receptor (TLR) agonists. Finally, recombinant IFN-α was sufficient to potentiate the production of inflammatory mediators in the lungs of wild-type mice challenged with innate immune stimuli. Thus, in addition to its well-known role in antiviral resistance, type I IFN receptor signaling acts as a central driver of early proinflammatory responses in the lung. Inhibiting the effects of type I IFNs may therefore be useful in dampening inflammation in lung diseases characterized by enhanced inflammatory cytokine production

Genetic dissection of maturity using RFLPs.

Several genetic regions having major effects on maturity have been identified using RFLP analysis. One such region on chromosomes 8 is important across several diverse genotypes and ccounts for up to 50% of the variation for maturity in a cross involving an inbred line (N28) and a 20-backcross generation derivative (N28E). In addition to the chromsome 8 QTL for maturity, we have evidence using the backcross-derived line approach for regions controlling maturity on chromosomes 1, 2, 3, 5, 7, and 9. Chromosome 5 appears to be especially important in both magnitude of effect and across several genetic hackground. Maturity as measured by days to pollen shed or silking may be controlled by additive or nearly dominant gene action depending on the chromosome region. The marker-trait linkages were consistent across environnments based on A662 X B73 F3 per se and testcross evaluations from three locations in one year. UMC12 (chromosome 8) and UMC54 (chromosome 5) also marked important regions for maturity in these materials

The comparative clinical course of pregnant and non-pregnant women hospitalised with influenza A(H1N1)pdm09 infection

Introduction: The Influenza Clinical Information Network (FLU-CIN) was established to gather detailed clinical and epidemiological information about patients with laboratory confirmed A(H1N1)pdm09 infection in UK hospitals. This report focuses on the clinical course and outcomes of infection in pregnancy.Methods: A standardised data extraction form was used to obtain detailed clinical information from hospital case notes and electronic records, for patients with PCR-confirmed A(H1N1)pdm09 infection admitted to 13 sentinel hospitals in five clinical 'hubs' and a further 62 non-sentinel hospitals, between 11th May 2009 and 31st January 2010.Outcomes were compared for pregnant and non-pregnant women aged 15-44 years, using univariate and multivariable techniques.Results: Of the 395 women aged 15-44 years, 82 (21%) were pregnant; 73 (89%) in the second or third trimester. Pregnant women were significantly less likely to exhibit severe respiratory distress at initial assessment (OR?=?0.49 (95% CI: 0.30-0.82)), require supplemental oxygen on admission (OR?=?0.40 (95% CI: 0.20-0.80)), or have underlying co-morbidities (p-trend <0.001). However, they were equally likely to be admitted to high dependency (Level 2) or intensive care (Level 3) and/or to die, after adjustment for potential confounders (adj. OR?=?0.93 (95% CI: 0.46-1.92). Of 11 pregnant women needing Level 2/3 care, 10 required mechanical ventilation and three died.Conclusions: Since the expected prevalence of pregnancy in the source population was 6%, our data suggest that pregnancy greatly increased the likelihood of hospital admission with A(H1N1)pdm09. Pregnant women were less likely than non-pregnant women to have respiratory distress on admission, but severe outcomes were equally likely in both groups

Regulatory T Cells Prevent Th2 Immune Responses and Pulmonary Eosinophilia during Respiratory Syncytial Virus Infection in Mice

During viral infection, inflammation and recovery are tightly controlled by competing proinflammatory and regulatory immune pathways. Respiratory syncytial virus (RSV) is the leading global cause of infantile bronchiolitis, which is associated with recurrent wheeze and asthma diagnosis in later life. Th2-driven disease has been well described under some conditions for RSV-infected mice. In the present studies, we used the Foxp3(DTR) mice (which allow specific conditional depletion of Foxp3(+) T cells) to investigate the functional effects of regulatory T cells (Tregs) during A2-strain RSV infection. Infected Treg-depleted mice lost significantly more weight than wild-type mice, indicating enhanced disease. This enhancement was characterized by increased cellularity in the bronchoalveolar lavage (BAL) fluid and notable lung eosinophilia not seen in control mice. This was accompanied by abundant CD4(+) and CD8(+) T cells exhibiting an activated phenotype and induction of interleukin 13 (IL-13)- and GATA3-expressing Th2-type CD4(+) T cells that remained present in the airways even 14 days after infection. Therefore, Treg cells perform vital anti-inflammatory functions during RSV infection, suppressing pathogenic T cell responses and inhibiting lung eosinophilia. These findings provide additional evidence that dysregulation of normal immune responses to viral infection may contribute to severe RSV disease

OX40 Ligand and Programmed Cell Death 1 Ligand 2 Expression on Inflammatory Dendritic Cells Regulates CD4 T Cell Cytokine Production in the Lung during Viral Disease

CD4-T-helper-cell (Th) differentiation is influenced by costimulatory molecules expressed on conventional dendritic cells (DCs) in regional lymph nodes and results in specific patterns of cytokine production. However, the function of costimulatory molecules on ‘inflammatory’ (CD11b+) DCs in the lung during recall responses is not fully understood, but important for development of novel interventions to limit immunopathological responses to infection. Using a mouse model in which vaccination with vaccinia virus vectors expressing the respiratory syncytial virus (RSV) fusion protein (rVVF) or attachment protein (rVVG) leads to type 1- or type 2-biased cytokine responses respectively upon RSV-challenge, we found expression of CD40 and OX40L on lung inflammatory DCs was higher in rVVF- than in rVVG-primed mice early after RSV-challenge, while the reverse was observed later in the response. Conversely, PD-L2 was higher in rVVG-primed mice throughout. Inflammatory DCs isolated at the resolution of inflammation revealed OX40L on type 1-biased DCs promoted IL-5, while on type 2-biased DCs enhanced IFNγ production by antigen-reactive Th cells. In contrast, PD-L2 promoted IFNγ production irrespective of conditions, suppressing IL-5 only if expressed on type 1-biased DCs. Thus, OX40L and PD-L2 expressed on DCs differentially regulate cytokine production during recall responses in the lung. Manipulation of these costimulatory pathways may provide a novel approach to controlling pulmonary inflammatory responses