Newcastle disease (ND) and avian influenza (AI) are common in the poultry industry. The objective of this study was to evaluate the effect of oral administration of ginseng stem-and-leaf saponins (GSLS) on the humoral immune responses of chickens to inactivated ND and AI vaccines. In experiment 1, oral administration of GSLS at a dose of 5 mg/kg of BW for 7 d on the immune response in chickens intramuscularly injected with inactivated ND vaccine was evaluated. Results showed that GSLS significantly increased the antibody level against ND in the serum of chickens. In experiment 2, the same regimen of GSLS was administered to chickens inoculated with inactivated AI vaccines, and an enhanced serum antibody response to AI vaccination was also observed. Considering the safety of GSLS, because no adverse effect was found throughout the experiments, GSLS may be a promising oral adjuvant to improve immunization in poultry.

We develop from scratch a comprehensive linear stability eigenvalue code based on a finite element method, namely, the drift Alfvén energetic particle stability (DAEPS) code, to investigate the physics of various stable and unstable modes observed in toroidal fusion plasmas, which has the advantage of accurate calculation of the mode characteristics near marginal stability. The DAEPS code is dedicated to providing a thorough understanding of low frequency modes in collisionless plasmas, e.g., shear Alfvén wave SAW and drift Alfvén wave physics with an energetic particle (EP) effect. DAEPS can calculate the linear frequency and growth rate for these modes by keeping correct asymptotic behavior in ballooning space. In this work, we demonstrate that the DAEPS code is able to analyze linear electromagnetic modes excited by circulating particles, including the thermal particle excited beta-induced Alfvén eigenmode and EP excited toroidicity-induced Alfvén eigenmode, where the verifications are performed successfully with other codes and theories, where the finite orbit width is discovered to play an important stabilizing role, which are usually ignored by traditional theory.

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We aimed to assess the immunogenicity of a single half-dose of AS03-adjuvanted monovalent 2009 pandemic H1N1 vaccine in healthy adults. Healthy subjects age 20-60 years were prospectively enrolled in a cohort receiving intramuscular administration of a single half-dose (1.875 μg of hemagglutinin [HA]) of adjuvanted 2009 pandemic H1N1 influenza vaccine. Data from participants enrolled in a concomitant study of immunogenicity following a full-dose (3.75 μg of HA) are presented concurrently. Sera for assessment of hemagglutination-inhibiting (HAI) antibody to the vaccine strain were obtained before and 14 or 21 days after vaccination. Ninety-seven participants received a half-dose and 50 received a full-dose of vaccine. In the half-dose cohort, Food and Drug Administration criteria for immunogenicity regarding seroprotection and seroconversion rates were met for subjects aged 20-45 years, but not for those aged 46-60 years. There was no statistically significant difference in the proportion of individuals achieving a post-vaccination HAI titre of ≥1:40, the geometric mean titres of post-vaccination antibody, or the proportion of individuals with a four-fold or greater increase in antibody levels between the two cohorts. Participants 46-60 years of age were significantly less likely to be seroprotected at day 21 than those 20-45 years old in both cohorts. Immunogenicity of a half dose of adjuvanted pH1N1 influenza vaccine was adequate in subjects aged 20-45 years. Dose reduction is a possible strategy for expanding the availability in the event of vaccine shortage in this age group.