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SUMMARY An interface-capturing method based on mass fraction is developed to solve the Riemann problem in multi-component compressible flow. Equations of mass fraction with modified form, which is derived from conservative equations of mass, are employed here to capture the interface. By introducing mass fraction into Euler equations system, as well as other conservative coefficients, a quasi-conservative numerical model is created. Numerical examples show that the mass fraction model performs well not only in multi-component fluids modeled by simple stiffened gas equation of state (EOS) but also in that modeled by complex Mie-Grüneisen EOS. Moreover, the mass fraction model is applied to Riemann problem with piecewise EOS; the expression of which depends on density. It is found that the mass fraction model can well adapt to the analytic change in piecewise EOS and produce accuracy solutions with fewer unknown quantities, and the model can be easily extended to m-component fluid mixture by using only m + 4 equations with no additional conditions. Copyright © 2013 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

Sj16, a 16-kDa protein produced by Schistosoma japonicum, has been demonstrated to have anti-inflammatory effect. However, the possible mechanism of these phenomena has not been discovered. Here, we tried to touch it with arthritis rats' model induced by injection of complete Freund's adjuvant (CFA). A set of pathogenic characters were observed in CFA-treated rat, including local and systematic read-out, which showed the model successfully set up. After administration of rSj16 (recombinant Sj16) in vivo, paw swelling reduced significantly and in a dose-dependent manner, the level of TNF-α, IL-1β and NO decreased and IL-10 in the serum increased. In vitro, rSj16 reversed the augmented surface expression of CD80, CD86, CD54 and OX6 induced by lipopolysaccharide (LPS) in bone marrow-derived DCs (BMDCs), whereas endocytotic capacity of rSj16-treated dendritic cell (DC) was profoundly increased. IL-12p70 released from rSj16-treated BMDC was decreased but IL-10 increased. Further, following incubation with rSj16 primed BMDCs, the sensitized T cells exhibited increased production of anti-inflammatory IL-10 and IL-4 and decreased production of IL-12p70 and IFN-γ. Collectively, these results implied that rSj16 alleviated CFA-induced arthritis, and the possible mechanisms may be its interruption of maturation and function of DCs. rSj16 could be a potential therapeutic agent against rheumatoid arthritis. [ABSTRACT FROM AUTHOR]

An absorbing fictitious boundary condition (FBC) is presented to generate an iterative domain decomposition method (DDM) for analyzing waveguide problems. The FBC for connecting the subdomains on a fictitious boundary is developed according to the actual field distribution in the waveguide to ensure the propagation of waves between adjacent subdomains. Numerical experiments demonstrate that the proposed iterative algorithm can acquire a convergent solution accurately. © 2001 John Wiley & Sons, Inc. Microwave Opt Technol Lett 30: 252–254, 2001. [ABSTRACT FROM AUTHOR]

Various proteins are expressed during different stages of schistosome development that are essential for cercarial penetration of vertebrate skin and evasion of host immune response. CD4+CD25+ regulatory T cells are important in modulating immune responses towards helminth infections. Schistosoma japonicum protein Sj16 present in the secretions of schistosomula has been shown to have anti-inflammatory effects; however, it is uncertain whether Sj16 can induce CD4+CD25+ regulatory T cells to participate in the regulation of early infection. In this study, we demonstrate a relationship between recombinant Sj16 (rSj16) and the induction of CD4+CD25+ Foxp3+ regulatory T cells. An increase in CD4+CD25+ T cells was observed both in splenic cells from mice injected with rSj16 and the cells pretreated with rSj16, respectively. The induced CD4+CD25+ T cells suppressed CD4+CD25− T-cell proliferation; furthermore, IFN-γ and IL-10 released from rSj16-stimulated cells contribute to this suppression. Additionally, rSj16-treated bone marrow dendritic cells (BMDCs) demonstrate an immature phenotype and play a role in the conversion of CD4+CD25− T cells into suppressive CD4+CD25+ regulatory T cells. Our study identified a new CD4+CD25+ T-cell population that induced by rSj16 and suggests that an IFN-γ-biased microenvironment during early infection of schistosome may favour the establishment of infection. [ABSTRACT FROM AUTHOR]