529 research outputs found
Clinical outcome of a patient with lysosomal acid lipase deficiency and first results after initiation of treatment with Sebelipase alfa: A case report
We report on a case of very rare autosomal recessive cholesteryl ester storage disease due to lysosomal acid
lipase deficiency (LALD). LALD is caused by mutations in the lysosomal acid lipase A (LIPA) gene resulting in
cholesteryl ester accumulation in liver, spleen, and macrophages. It can lead to liver failure, accelerated
atherosclerosis and premature death. Until recently, treatment options were limited to lipid-lowering medications
to control dyslipidemia. Presently, a long-term enzyme replacement therapy with Sebelipase alfa, a recombinant
human lysosomal acid lipase, is available for patients with LALD.
Our patient's condition became conspicuous at the age of two due to a xanthogranuloma of the chin together
with increased lipid levels, elevated liver enzymes and hepatomegaly. It took another five years until our patient
was diagnosed with LALD after genetic testing. A bi-weekly therapy with intravenous Sebelipase alfa was started
at the age of 26 years. It led to normalization of lipid levels, reduction of liver enzymes and beginning regression
of hepatomegaly in the absence of adverse drug reactions after 46 infusions.
Since LALD can take a fatal course even in patients with a long-term stable condition, it is essential to identify
affected patients early and to treat them appropriately by enzyme replacement therapy. LALD should be suspected
in patients with low high-density lipoprotein cholesterol (HDL-C) and high low-density lipoprotein
cholesterol (LDL-C) in conjunction with elevated liver enzymes or hepatomegaly.
A registry for LALD patients shall help to advance our understanding of the disease as well as improve patient
care (NCT01633489)
The uncertain consequences of transferring bacterial strains between laboratories - rpoS instability as an example
Abstract\ud
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Background\ud
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Microbiological studies frequently involve exchanges of strains between laboratories and/or stock centers. The integrity of exchanged strains is vital for archival reasons and to ensure reproducible experimental results. For at least 50 years, one of the most common means of shipping bacteria was by inoculating bacterial samples in agar stabs. Long-term cultures in stabs exhibit genetic instabilities and one common instability is in rpoS. The sigma factor RpoS accumulates in response to several stresses and in the stationary phase. One consequence of RpoS accumulation is the competition with the vegetative sigma factor σ70. Under nutrient limiting conditions mutations in rpoS or in genes that regulate its expression tend to accumulate. Here, we investigate whether short-term storage and mailing of cultures in stabs results in genetic heterogeneity.\ud
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Results\ud
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We found that samples of the E. coli K-12 strain MC4100TF exchanged on three separate occasions by mail between our laboratories became heterogeneous. Reconstruction studies indicated that LB-stabs exhibited mutations previously found in GASP studies in stationary phase LB broth. At least 40% of reconstructed stocks and an equivalent proportion of actually mailed stock contained these mutations. Mutants with low RpoS levels emerged within 7 days of incubation in the stabs. Sequence analysis of ten of these segregants revealed that they harboured each of three different rpoS mutations. These mutants displayed the classical phenotypes of bacteria lacking rpoS. The genetic stability of MC4100TF was also tested in filter disks embedded in glycerol. Under these conditions, GASP mutants emerge only after a 3-week period. We also confirm that the intrinsic high RpoS level in MC4100TF is mainly due to the presence of an IS1 insertion in rssB.\ud
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Conclusions\ud
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Given that many E. coli strains contain high RpoS levels similar to MC4100TF, the integrity of such strains during transfers and storage is questionable. Variations in important collections may be due to storage-transfer related issues. These results raise important questions on the integrity of bacterial archives and transferred strains, explain variation like in the ECOR collection between laboratories and indicate a need for the development of better methods of strain transfer.We are grateful to Fundação de Amparo á Pesquisa do Estado de São Paulo (FAPESP-Brazil), who supported this study and provided a travel allowance for TF. TF was also supported by the the Australian Research Council and the US Army Research Office. We also thank K. C. Murphy and S. Kushner for respectively providing strain KM32 and plasmid pWKS130
Updated Predictions for Higgs Production at the Tevatron and the LHC
We present updated predictions for the total cross section for Higgs boson
production through gluon fusion at hadron colliders. In addition to
renormalization-group improvement at next-to-next-to-next-to-leading
logarithmic accuracy, we incorporate the two-loop electroweak corrections,
which leads to the most precise predictions at present. Numerical results are
given for Higgs masses between 115 GeV and 200 GeV at the Tevatron with
\sqrt{s}=1.96 TeV and the LHC with \sqrt{s}=7-14 TeV.Comment: 8 pages, 2 figures. v2: combined PDF+alpha_s uncertainties included;
results using NNPDF2.0 added; upgrade CTEQ6.6->CT1
РОЗВИТОК СИСТЕМИ ПОЧАТКОВОЇ ТА СЕРЕДНЬОЇ ОСВІТИ У МЕНОНІТСЬКИХ КОЛОНІЯХ КАТЕРИНОСЛАВСЬКОГО ПОВІТУ НАПРИКІНЦІ XIX – НА ПОЧАТКУ XX СТ.
Проблеми формування системи початкової освіти постійно знаходи-лись у фокусі громадської уваги менонітського соціуму, який намагався шля-хом надзвичайної концентрації інтелектуальних, фінансових та господарчих зусиль сприяти її всебічному становленню та розвитку. Ґенеза менонітсько-го віровчення, темпи та масштаб його поширення серед населення північ-них регіонів Західної Європи були об'єктивно зумовлені наявністю у пред-ставників даного релігійного руху елементарних освітянських навичок (вміння читати та писати), які були необхідні для раціонального тлумачен-ня біблійних та релігійних текстів. Поява розгалуженої освітянської системи в громадах менонітів була детермінована специфікою віровчення спільноти, її нагальними релігійними, церковними та громадськими потребами. Зазначимо, що меноніти розглядали шкільництво як один із засобів набуття «освічено-го благочестя»
Divergence Involving Global Regulatory Gene Mutations in an Escherichia coli Population Evolving under Phosphate Limitation
Many of the important changes in evolution are regulatory in nature. Sequenced bacterial genomes point to flexibility in regulatory circuits but we do not know how regulation is remodeled in evolving bacteria. Here, we study the regulatory changes that emerge in populations evolving under controlled conditions during experimental evolution of Escherichia coli in a phosphate-limited chemostat culture. Genomes were sequenced from five clones with different combinations of phenotypic properties that coexisted in a population after 37 days. Each of the distinct isolates contained a different mutation in 1 of 3 highly pleiotropic regulatory genes (hfq, spoT, or rpoS). The mutations resulted in dissimilar proteomic changes, consistent with the documented effects of hfq, spoT, and rpoS mutations. The different mutations do share a common benefit, however, in that the mutations each redirect cellular resources away from stress responses that are redundant in a constant selection environment. The hfq mutation lowers several individual stress responses as well the small RNA–dependent activation of rpoS translation and hence general stress resistance. The spoT mutation reduces ppGpp levels, decreasing the stringent response as well as rpoS expression. The mutations in and upstream of rpoS resulted in partial or complete loss of general stress resistance. Our observations suggest that the degeneracy at the core of bacterial stress regulation provides alternative solutions to a common evolutionary challenge. These results can explain phenotypic divergence in a constant environment and also how evolutionary jumps and adaptive radiations involve altered gene regulation
RRx-001 followed by platinum plus etoposide in patients with previously treated small-cell lung cancer
BACKGROUND: This exploratory single-arm phase II study evaluated the efficacy and safety of RRx-001 followed by reintroduction of platinum plus etoposide in patients with previously treated small-cell lung cancer (SCLC).
METHODS: Patients were treated with RRx-001 4 mg IV on day 1 of each week of a 21-day cycle followed at progression by re-challenge with etoposide 80-100 IV mg/m
RESULTS: Twenty-six patients were enroled and received at least one dose of RRx-001. The median number of prior lines of therapy was 2 (range 1-9) and 19 (73.1%) patients had platinum-resistant disease. In the intention-to-treat population, one patient (3.8%) had complete response and six (23.1%) had partial response on platinum plus etoposide. The estimated median and 12-month OS from enrolment were 8.6 months and 44.1%, respectively. The most common treatment-emergent adverse event from RRx-001 was mild discomfort at the infusion site (23%).
CONCLUSIONS: RRx-001 followed by re-challenge with platinum plus etoposide chemotherapy is feasible and associated with promising results.
CLINICAL TRIAL REGISTRATION: NCT02489903
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