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Unusual patterns of igG avidity in some young children following two doses of the adjuvanted pandemic H1N1 (2009) influenza virus vaccine

机译:两次辅助大流行H1N1(2009)流感病毒疫苗的幼儿的IgG流行的异常模式

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During the 2009-2010 H1N1 influenza pandemic, an adjuvanted monovalent vaccine containing 25% of the normal antigen dose and AS03 adjuvant was widely used in Canada. This vaccine was found to be well-tolerated and immunogenic in young children (D. W. Scheifele et al., Pediatr. Infect. Dis. J. 30:402- 407, 2011). We report here additional analyses to further characterize the humoral response to this vaccine. We measured standard hemagglutination inhibition (HAI) and microneutralization (MN) titers, as well as influenza virus-specific IgG avidity and subclass distribution by enzyme-linked immunosorbent assay in 73 subjects. Sera were collected before (day 0) and 3 weeks after each dose of vaccine (days 21 and 42). Most children (55/73) had undetectable HAI andMNtiters at day 0 (presumed to be antigen naive) and mounted good responses at days 21 and 42. The majority of these children (43/55) had the expected pattern of an increasing IgG avidity index (AI) after each dose of vaccine (not detected [ND], 0.30, and 2.97 at days 0, 21, and 42, respectively). The avidity responses in the remaining children (12/55) were quite different, with AIs increasing abruptly after the first dose and then declining after the second dose of vaccine (ND, 8.83, and 7.15, respectively). These children also had higher concentrations of influenza virus-specific IgG1 and IgG3 antibodies at day 21. Although the antibody titers were similar, some antigen-naive children demonstrated an unusual pattern of avidity maturation after two immunizations with AS03-adjuvanted, low-dose influenza virus vaccine. These data suggest the presence of subtle differences in the quality of the antibodies produced by some subjects in response to this vaccine.
机译:在2009-2010 H1N1流感大流行期间,加拿大广泛使用了含有25%正常抗原剂量和AS03辅助的辅助单价疫苗。发现这种疫苗在幼儿中具有耐受性和免疫原性(D. W. Scheifele等人,Pediatr.Infect。J.30:402-407,2011)。我们在这里报告了其他分析,以进一步表征对该疫苗的体液反应。我们通过73名受试者在73名受试者中测量了标准的血液凝集抑制(HAI)和微中性化(MN)滴度,以及通过酶联免疫吸附测定法,以及通过酶连接的免疫吸附测定法。每次疫苗(第21和42天)之前(第0天)和3周收集血清。大多数儿童(55/73)在第0天(假定是抗原天真)的HAI和MNTITER,并在第21和42天安装了良好的反应每剂量的疫苗(分别在第0、21和42天分别检测到[ND],0.30和2.97)之后的索引(AI)。其余儿童(12/55)中的亲和力反应完全不同,第一次剂量后AIS突然增加,然后在第二剂疫苗后(ND,8.83和7.15)下降。这些儿童在第21天的流感病毒特异性IgG1和IgG3抗体的浓度较高。尽管抗体滴度相似,但在两种抗原的儿童中,有两种抗原的儿童在两种AS03-辅助,低剂量的流感疫苗的疫苗后表现出异常的流行病。病毒疫苗。这些数据表明,某些受试者对这种疫苗产生的抗体质量存在细微差异。

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