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Long-Term Immunogenicity of an Inactivated Split-Virion 2009 Pandemic Influenza A H1N1 Virus Vaccine with or without Aluminum Adjuvant in Mice

机译:含或不含铝佐剂的灭活的2009年分离的病毒颗粒大流行性甲型H1N1流感病毒疫苗的长期免疫原性

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In 2009, a global epidemic of influenza A(H1N1) virus caused the death of tens of thousands of people. Vaccination is the most effective means of controlling an epidemic of influenza and reducing the mortality rate. In this study, the long-term immunogenicity of influenza A/California/7/2009 (H1N1) split vaccine was observed as long as 15 months (450 days) after immunization in a mouse model. Female BALB/c mice were immunized intraperitoneally with different doses of aluminum-adjuvanted vaccine. The mice were challenged with a lethal dose (10× 50% lethal dose [LD50]) of homologous virus 450 days after immunization. The results showed that the supplemented aluminum adjuvant not only effectively enhanced the protective effect of the vaccine but also reduced the immunizing dose of the vaccine. In addition, the aluminum adjuvant enhanced the IgG antibody level of mice immunized with the H1N1 split vaccine. The IgG level was correlated to the survival rate of the mice. Aluminum-adjuvanted inactivated split-virion 2009 pandemic influenza A H1N1 vaccine has good immunogenicity and provided long-term protection against lethal influenza virus challenge in mice.
机译:2009年,甲型H1N1流感全球流行,导致成千上万人死亡。接种疫苗是控制流感流行和降低死亡率的最有效手段。在这项研究中,在小鼠模型中免疫了15个月(450天)后,就观察到了甲型流感/加利福尼亚/ 7/2009(H1N1)流感疫苗的长期免疫原性。用不同剂量的铝佐剂腹膜内免疫雌性BALB / c小鼠。免疫后450天,用致死剂量(10×50%致死剂量[LD 50 ])的同源病毒攻击小鼠。结果表明,添加的铝佐剂不仅有效增强了疫苗的保护作用,而且降低了疫苗的免疫剂量。另外,铝佐剂增强了用H1N1分裂疫苗免疫的小鼠的IgG抗体水平。 IgG水平与小鼠的存活率相关。铝佐剂灭活的分裂病毒2009大流行性流感A H1N1疫苗具有良好的免疫原性,可长期抵抗小鼠致命的流感病毒。

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