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使用传统血清学方法和口腔液来评估 2-16 岁儿童在连续每年接种 LAIV 后的免疫原性。

Use of traditional serological methods and oral fluids to assess immunogenicity in children aged 2-16 years after successive annual vaccinations with LAIV.

机构信息

Virus Reference Department, Public Health England (Colindale), London, UK.

Virus Reference Department, Public Health England (Colindale), London, UK.

出版信息

Vaccine. 2020 Mar 10;38(12):2660-2670. doi: 10.1016/j.vaccine.2020.02.024. Epub 2020 Feb 15.

Abstract

BACKGROUND

The UK introduced quadrivalent live attenuated influenza vaccine (qLAIV) for children in 2013/2014. The impact of annual vaccination on effectiveness and immunogenicity is being assessed.

METHOD

A phase III/IV open-label study of the immunogenicity of annual vaccination with qLAIV (Fluenz™) was conducted over three consecutive years (2014/15-2016/17) in 254, 249 and 162 children respectively. Serum responses to vaccine components were measured by Haemagglutination Inhibition (HAI) and anti-A(H1N1)pdm09 Neuraminidase (NAI) assays, stratified according to previous receipt of AS03-adjuvanted A(H1N1)pdm09 pandemic vaccine in 2009/10. Antibody levels to the A(H1N1)pdm09 and H3N2 vaccine components in oral fluids (OF) were explored using an ELISA.

FINDINGS

More paired pre- and post-vaccination oral fluids (96%) than paired sera (87%) were obtained. Geometric mean titre rises using HAI assays were limited, with maximum rises seen in year one for both influenza B strains when 39% and 43% of subjects seroconverted (95% confidence interval 33-46% and 36-50%, respectively) and year two for influenza H3N2, when 40% (33-46%) individuals seroconverted. Prior pandemic vaccine receipt resulted in higher pre- and post-vaccination A(H1N1)pdm09 HAI titres and lower pre-and post-vaccination NAI (N1 neuraminidase) titres in all three years. OF results were congruent with HAI results; assay specificity compared to HAI was 88.1 and 71.6 percent, and sensitivity was 86.4 and 74.8 percent respectively for A(H1N1)pdm09 and H3N2.

CONCLUSION

In all three study years, vaccination with qLAIV resulted in poor antibody responses. However, OFs are an alternative specimen type that allows self sampling, can easily be obtained from children, and their analysis leads to similar conclusions as classic serology by HAI. Their suitability for seroprevalence studies should be investigated. We demonstrated a sustained effect from prior receipt of the AS03-adjuvanted A(H1N1)pdm09 vaccine, even after repeat vaccination with qLAIV indicating that early exposure to influenza antigens has a significant long lasting effect.

摘要

背景

英国于 2013/2014 年为儿童引入了四价活减毒流感疫苗(qLAIV)。目前正在评估每年接种疫苗对其有效性和免疫原性的影响。

方法

2014/15 年至 2016/17 年连续三年开展了一项针对 qLAIV(Fluenz™)年度接种免疫原性的 III/IV 期开放标签研究,分别纳入 254、249 和 162 例儿童。通过血凝抑制(HAI)和抗 A(H1N1)pdm09 神经氨酸酶(NAI)检测,按 2009/10 年是否接种过含 AS03 的 A(H1N1)pdm09 大流行疫苗对血清应答进行分层。采用 ELISA 检测口服液(OF)中 A(H1N1)pdm09 和 H3N2 疫苗成分的抗体水平。

结果

与配对血清(87%)相比,获得了更多的配对预接种和接种后口服液(96%)。流感 B 株的 HAI 检测结果显示,抗体几何平均滴度升高有限,当 39%和 43%的受试者出现血清转化率(95%置信区间 33-46%和 36-50%)时,最大的上升发生在第一年,当 40%(33-46%)个体出现血清转化率时,最大的上升发生在第二年。所有三年的研究中,以前接种大流行疫苗导致更高的接种前和接种后的 A(H1N1)pdm09 HAI 滴度和更低的接种前和接种后的 NAI(N1 神经氨酸酶)滴度。OF 结果与 HAI 结果一致;与 HAI 相比,检测的特异性分别为 88.1%和 71.6%,敏感性分别为 86.4%和 74.8%,用于 A(H1N1)pdm09 和 H3N2。

结论

在所有三年的研究中,qLAIV 疫苗接种均导致抗体应答较差。然而,口服液是一种替代的标本类型,允许自我采样,很容易从儿童中获得,并且它们的分析结果与经典的 HAI 血清学相似。应研究它们用于血清流行率研究的适用性。我们证明了以前接种过含 AS03 的 A(H1N1)pdm09 疫苗的持续效果,即使在重复接种 qLAIV 后也是如此,这表明早期接触流感抗原具有显著的长期影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7054836/fbfd99ece1b0/gr1.jpg

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