Polymorphism of the tumor necrosis factor beta gene in systemic lupus erythematosus

We investigated the Nco I restriction fragment length polymorphism (RFLP) of the tumor necrosis factor beta (TNFB) gene in 173 patients with systemic lupus erythematosus (SLE), 192 unrelated healthy controls, and eleven panel families, all of German origin. The phenotype frequency of the TNFB*I allele was significantly increased in patients compared to controls (63.6% vs 47.1%, RR = 1.96, p <0.002). The results of a two-point haplotype statistical analysis between TNFB and HLA alleles show that there is linkage disequilibrium between TNFB*I and HLA-A1, Cw7, B8, DR3, DQ2, and C4A DE. The frequency of TNFB*I was compared in SLE patients and controls in the presence or absence of each of these alleles. TNFB*I is increased in patients over controls only in the presence of the mentioned alleles. Therefore, the whole haplotypeA1, Cw7, B8, TNFB* I, C4A DE, DR3, DQ2 is increased in patients and it cannot be determined which of the genes carried by this haplotype is responsible for the susceptibility to SLE. In addition, two-locus associations were analyzed in 192 unrelated healthy controls for TNFB and class I alleles typed by serology, and for TNFB and class II alleles typed by polymerase chain reaction/oligonucleotide probes. We found positive linkage disequilibrium between TNFB*I and the following alleles: HLA-A24, HLA-B8, DRBI*0301, DRBI*ll04, DRBI*1302, DQAI*0501, DQBI*0201, DQBI*0604, and DPBI*OIO1. TNFB*2 is associated with HLA-B7, DRBI*1501, and DQB I *0602

More Flexible Damping Systems for Blades and Vanes

The blades and the vanes of aero engines are subject to very high thermo-mechanical loads. In some cases, an additional damping system is necessary to reach the lifetime goals. Commonly, damping systems based on energy dissipation due to friction are used, e.g. under platform dampers for blades and spring dampers for the vanes. These damping systems have some limitations: under platform dampers work well mostly for just one mode family, their effectiveness is limited relative to rotational speed (because of the associated contact forces) and is dependent on the excitation order. The spring dampers work well for more than one mode family but their effectiveness is limited concerning the available contact force (just one value). Additionally, the use of the spring dampers requires a significant, sometimes suboptimal design change of the vane cluster. In this paper, some alternative damping systems are introduced and analyzed. All these new systems offer additional possibilities for damping and give more design flexibility. Two of them: insert damping and rocking damping are also based on frictional energy dissipation. The third one, impulse mistuning, adopts a special kind of absorption and is based on the so called targeted energy transfer. The analytical results for the insert damping systems were presented previously in Borufka et al. (2009), while in this paper the experimental validation by shaker tests is shown. The rocking damping was not presented so far – to the knowledge of the authors. Impulse mistuning was first presented in: Hartung and Retze (2011) and Hartung et al. (2016). In this work, an overview of such damping systems and some additional information on the experimental validation of some impulse mistuning systems are presented

Production and characterization of monoclonal antibodies to the extracellular domain of PO

Seven monoclonal antibodies were raised against the immunoglobulin-like extracellular domain of PO (POED), the major protein of peripheral nervous system myelin. Mice were immunized with purified recombinant rat PO-ED. After fusion, 7 clones (POI-P07) recognizing either recombinant, rat, mouse, or human PO-ED were selected by ELlS A and were characterized by Western blot, immunohistochemistry, and a competition assay. Antibodies belonged to the IgG or IgM class, and P04-P07, reacted with PO in fresh-frozen and paraffin-embedded sections of human or rat peripheral nerve, but not with myelin proteins of the central nervous system of either species. Epitope specificity of the antibodies was determined by a competition enzyme-linked immunosorbent assay (ELISA) and a direct ELlS A using short synthetic peptides spanning the entire extracellular domain of PO. These assays showed that POl and P02 exhibiting the same reaction pattern in Western blot and immunohistochemistry reacted with different distant epitopes of PO. Furthermore, the monoclonal antibodies P05 and P06 recognized 2 different epitopes in close proximity within the neuritogenic extracellular sequence of PO. This panel of monoclonal antibodies, each binding to a different epitope of the extracellular domain of PO, will be useful for in vitro and in vivo studies designed to explore the role of PO during myelination and in demyelinating diseases of the peripheral nervous system

Nonlinear transport of Bose-Einstein condensates through mesoscopic waveguides

We study the coherent flow of interacting Bose-condensed atoms in mesoscopic waveguide geometries. Analytical and numerical methods, based on the mean-field description of the condensate, are developed to study both stationary as well as time-dependent propagation processes. We apply these methods to the propagation of a condensate through an atomic quantum dot in a waveguide, discuss the nonlinear transmission spectrum and show that resonant transport is generally suppressed due to an interaction-induced bistability phenomenon. Finally, we establish a link between the nonlinear features of the transmission spectrum and the self-consistent quasi-bound states of the quantum dot.Comment: 23 pages, 16 figure