首页> 外文期刊>The Pediatric infectious disease journal >T-cell responses in children to internal influenza antigens, 1 year after immunization with pandemic H1N1 influenza vaccine, and response to revaccination with seasonal trivalent-inactivated influenza vaccine
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T-cell responses in children to internal influenza antigens, 1 year after immunization with pandemic H1N1 influenza vaccine, and response to revaccination with seasonal trivalent-inactivated influenza vaccine

机译:大流行H1N1流感疫苗免疫后1年,儿童对内部流感抗原的T细胞反应以及季节性三价灭活流感疫苗对疫苗接种的反应

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Background: During seasonal influenza epidemics, 5-15% of the population are affected with an illness having a nontrivial mortality, morbidity and economic burden. Inactivated influenza vaccines are routinely used to prevent influenza infection, primarily by inducing humoral immunity. In addition, trivalent-inactivated influenza vaccines have previously been shown to boost influenza-specific T-cell responses in a small percentage of adults. We investigate here the influenza-specific T-cell response, in children, 1 year after pandemic H1N1 vaccination and the ability to boost the T-cell response with trivalent-inactivated influenza immunization. Methods: Peripheral blood mononuclear cells (PBMCs) were isolated from children previously vaccinated with pandemic H1N1 vaccine, pre-and postseasonal 2010-2011 trivalent influenza vaccine (TIV) vaccination. Samples were analyzed by interferon-gamma enzyme-linked immunosorbent spot for reactogenicity toward internal influenza antigens (nucleoprotein, matrix protein 1 and nonstructural protein 1). Results: Basal ex vivo T-cell responses to nucleoprotein, matrix protein 1 and nonstructural protein 1 measured by interferon-gamma enzyme-linked immunosorbent spot assay were significantly higher in those children who had previously received an AS0 3B-adjuvanted split virion pandemic vaccine 12 months earlier rather than a nonadjuvanted whole virion vaccine. Boosting of these responses, 21 days after 2010/2011 seasonal TIV vaccination was observed regardless of age or prior pandemic vaccination regime, although boosting was greater in those groups with the lowest initial response. Conclusions: We show here that children previously vaccinated with the 2009 pandemic H1N1 vaccine have measurable T-cell responses 1 year after vaccination. The magnitudes of these responses are dependent on both age of vaccine and type of pandemic H1N1 vaccine used. After 2010/2011 seasonal TIV vaccination, these T-cell responses undergo a small but significant boost.
机译:背景:在季节性流感流行期间,有5-15%的人口患有死亡率,发病率和经济负担均不低的疾病。灭活的流感疫苗通常主要通过诱导体液免疫来预防流感的感染。此外,先前已显示三价灭活的流感疫苗可在少数成年人中增强流感特异性T细胞反应。我们在这里调查大流行H1N1疫苗接种1年后儿童的流感特异性T细胞反应,以及通过三价灭活流感免疫增强T细胞反应的能力。方法:从以前接种过大流行H1N1疫苗,季节性和2010-2011年三价流感疫苗(TIV)接种的儿童中分离外周血单个核细胞(PBMC)。通过干扰素-γ酶联免疫吸附点分析样品对内部流感抗原(核蛋白,基质蛋白1和非结构蛋白1)的反应原性。结果:在以前接受过AS0 3B辅助分裂病毒粒子大流行疫苗的儿童中,通过干扰素-γ酶联免疫斑点法检测的基础离体T细胞对核蛋白,基质蛋白1和非结构蛋白1的基础应答显着更高。而不是非佐剂的完整病毒粒子疫苗。在2010/2011年季节性TIV疫苗接种后21天,无论年龄大小或以前的大流行疫苗接种方案如何,这些反应的加强作用都得到了加强,尽管最初反应最低的那些组的加强作用更大。结论:我们在这里表明,以前接种过2009大流行H1N1疫苗的儿童在接种疫苗1年后可测量的T细胞反应。这些反应的强度取决于疫苗的年龄和所用大流行H1N1疫苗的类型。在2010/2011年度季节性TIV疫苗接种后,这些T细胞反应得到了小幅但显着的增强。

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