23 research outputs found

    Assessment of the inherent allergenic potential of proteins in mice.

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    There is considerable interest in the design of approaches that will permit the accurate identification and characterization of proteins that have the inherent potential to induce sensitization and cause food allergy. Among the methods used currently as part of such assessments are consideration of structural similarity to, or amino acid sequence homology with, known human allergens; whether there exists immunologic cross-reactivity with known allergens; and measurement of resistance to proteolytic digestion in a simulated gastric fluid. Although such approaches provide information that will contribute to a safety assessment, they do not--either individually or collectively--provide a direct evaluation of the ability of a novel protein to cause allergic sensitization. For this reason, work is in progress to design and evaluate suitable animal models that will provide a more holistic assessment of allergenic potential. In this laboratory, the approach we have taken has been to examine the characteristics of immune responses induced in mice following parenteral (intraperitoneal) exposure to test proteins. The basis of this method is to determine simultaneously the overall immunogenic potential of proteins [measured as a function of immunoglobulin (Ig) G antibody responses] and to compare this with their ability to provoke IgE antibody production, IgE being the antibody that effects allergic sensitization. Although this approach has not yet been evaluated fully, the results available to date suggest that it will be possible to distinguish proteins that have the inherent potential to induce allergic sensitization from those that do not. In this article we summarize progress to date in the context of the scientific background against which such methods are being developed

    Анализ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠ² вибродиагностики ΠΌΠ΅Ρ‚Π°Π»Π»ΠΎΡ€Π΅ΠΆΡƒΡ‰ΠΈΡ… станков

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    ЦСль Ρ€Π°Π±ΠΎΡ‚Ρ‹ - Π²Ρ‹Ρ€Π°Π±ΠΎΡ‚ΠΊΠ° Ρ€Π΅ΠΊΠΎΠΌΠ΅Π½Π΄Π°Ρ†ΠΈΠΉ ΠΏΠΎ ΠΏΡ€ΠΈΠΌΠ΅Π½Π΅Π½ΠΈΡŽ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠ² вибродиагностики ΠΌΠ΅Ρ‚Π°Π»Π»ΠΎΡ€Π΅ΠΆΡƒΡ‰ΠΈΡ… станков Π² ΠΊΠΎΠ½ΠΊΡ€Π΅Ρ‚Π½ΠΎΠΉ Π·Π°Π΄Π°Ρ‡Π΅. ΠžΠ±ΡŠΠ΅ΠΊΡ‚ исслСдования - ΠΌΠ΅Ρ‚ΠΎΠ΄Ρ‹ ΠΈ комплСксы вибродиагностики ΠΌΠ΅Ρ‚Π°Π»Π»ΠΎΡ€Π΅ΠΆΡƒΡ‰ΠΈΡ… станков. ΠŸΡ€Π΅Π΄ΠΌΠ΅Ρ‚ исслСдования – систСматизация ΠΈ ΠΎΠ±ΠΎΠ±Ρ‰Π΅Π½ΠΈΠ΅ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠ² вибродиагностики ΠΌΠ΅Ρ‚Π°Π»Π»ΠΎΡ€Π΅ΠΆΡƒΡ‰ΠΈΡ… станков. ΠΠΊΡ‚ΡƒΠ°Π»ΡŒΠ½ΠΎΡΡ‚ΡŒ - отсутствиС простой для Ρ€Π΅Π°Π»ΠΈΠ·Π°Ρ†ΠΈΠΈ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΈΠΊΠΈ виброиспытаний. Π’ процСссС Ρ€Π°Π±ΠΎΡ‚Ρ‹ Π±Ρ‹Π»ΠΈ рассмотрСны Ρ€Π°Π·Π»ΠΈΡ‡Π½Ρ‹Π΅ ΠΌΠ΅Ρ‚ΠΎΠ΄Ρ‹ вибродиагностики ΠΌΠ΅Ρ‚Π°Π»Π»ΠΎΡ€Π΅ΠΆΡƒΡ‰ΠΈΡ… станков, сдСланы прСдлоТСния ΠΏΠΎ ΠΏΡ€ΠΈΠΌΠ΅Π½Π΅Π½ΠΈΡŽ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠ² вибродиагностики ΠΌΠ΅Ρ‚Π°Π»Π»ΠΎΡ€Π΅ΠΆΡƒΡ‰ΠΈΡ… станков Π² ΠΊΠ°ΠΆΠ΄ΠΎΠΉ ΠΊΠΎΠ½ΠΊΡ€Π΅Ρ‚Π½ΠΎΠΉ Π·Π°Π΄Π°Ρ‡Π΅, создана ΡƒΠ½ΠΈΠ²Π΅Ρ€ΡΠ°Π»ΡŒΠ½Π°Ρ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΈΠΊΠ° провСдСния вибродиагностики ΠΌΠ΅Ρ‚Π°Π»Π»ΠΎΡ€Π΅ΠΆΡƒΡ‰ΠΈΡ… станков диагностичСским комплСксом "ВиброрСгистратор-М2".The aim of the work is to develop recommendations on the application of vibration diagnostics methods for metal-cutting machine tools in a specific task. The object of research is methods and complexes of vibration diagnostics of metal cutting machines. The subject of the study is the systematization and generalization of methods of vibration diagnostics of metal-cutting machines. Actuality is the absence of a simple vibration testing technique. In the course of the work various methods of vibration diagnostics of metal cutting machines were considered, suggestions were made on the application of vibration diagnostics methods for metal cutting machines in each specific task, a universal technique for performing vibration diagnostics of metal cutting machines with the Vibroregistrator-M2

    Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans

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    Genome-wide association studies (GWAS) have identified numerous common prostate cancer (PrCa) susceptibility loci. We have fine-mapped 64 GWAS regions known at the conclusion of the iCOGS study using large-scale genotyping and imputation in 25 723 PrCa cases and 26 274 controls of European ancestry. We detected evidence for multiple independent signals at 16 regions, 12 of which contained additional newly identified significant associations. A single signal comprising a spectrum of correlated variation was observed at 39 regions; 35 of which are now described by a novel more significantly associated lead SNP, while the originally reported variant remained as the lead SNP only in 4 regions. We also confirmed two association signals in Europeans that had been previously reported only in East-Asian GWAS. Based on statistical evidence and linkage disequilibrium (LD) structure, we have curated and narrowed down the list of the most likely candidate causal variants for each region. Functional annotation using data from ENCODE filtered for PrCa cell lines and eQTL analysis demonstrated significant enrichment for overlap with bio-features within this set. By incorporating the novel risk variants identified here alongside the refined data for existing association signals, we estimate that these loci now explain ∼38.9% of the familial relative risk of PrCa, an 8.9% improvement over the previously reported GWAS tag SNPs. This suggests that a significant fraction of the heritability of PrCa may have been hidden during the discovery phase of GWAS, in particular due to the presence of multiple independent signals within the same regio

    Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

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    Genome-wide association studies (GWAS) have transformed our understanding of susceptibility to multiple myeloma (MM), but much of the heritability remains unexplained. We report a new GWAS, a meta-analysis with previous GWAS and a replication series, totalling 9974 MM cases and 247,556 controls of European ancestry. Collectively, these data provide evidence for six new MM risk loci, bringing the total number to 23. Integration of information from gene expression, epigenetic profiling and in situ Hi-C data for the 23 risk loci implicate disruption of developmental transcriptional regulators as a basis of MM susceptibility, compatible with altered B-cell differentiation as a key mechanism. Dysregulation of autophagy/apoptosis and cell cycle signalling feature as recurrently perturbed pathways. Our findings provide further insight

    Skin Sensitization Tests:The LLNA and the RhE IL-18 Potency Assay

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