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AS03B 佐剂的裂解病毒颗粒和未佐剂的全病毒颗粒 H1N1(2009)流感疫苗的免疫反应和反应原性预测因子。

Predictors of immune response and reactogenicity to AS03B-adjuvanted split virion and non-adjuvanted whole virion H1N1 (2009) pandemic influenza vaccines.

机构信息

Department of Statistics, Modelling and Economics, Health Protection Services, Health Protection Agency, Colindale, London NW9 5EQ, UK.

出版信息

Vaccine. 2011 Oct 19;29(45):7913-9. doi: 10.1016/j.vaccine.2011.08.076. Epub 2011 Aug 27.

DOI:10.1016/j.vaccine.2011.08.076
PMID:21875635
Abstract

In 2009, 943 children aged 6 months to 10 years were randomised to receive two doses of an oil-in water AS03B-adjuvanted split virion or a non-adjuvanted whole virion H1N1 (2009) vaccine. The large numbers allowed investigation of possible predictors of immune response and reactogenicity. We used regression analysis to examine the effect of variables including past receipt of seasonal vaccine, antipyretics post-vaccination, interval between doses and pre-existing antibodies to H1N1 (2009) on immunogenicity. We also examined the relationship between immunogenicity and reactogenicity and whether prior infection or underlying conditions affected reactogenicity. For both vaccines, haemagglutination-inhibition titres were 60% higher in children with fever ≥38 °C after vaccination and 29% lower in those previously given seasonal vaccine. Early use of antipyretics did not affect immunogenicity. Post-vaccination titres were higher with longer intervals between doses and in those with evidence of prior infection, but reactogenicity in the latter was unaffected. In the adjuvanted vaccine group, reactions were more common in children with atopy. Both vaccines were safe and immunogenic in those with prior infection. Reduction in the interval between doses for earlier protection would be at the cost of reduced immunogenicity. The effect of seasonal vaccine on immunogenicity merits further investigation.

摘要

2009 年,943 名 6 个月至 10 岁的儿童被随机分为两组,分别接种两剂 AS03B 佐剂的油包水裂解病毒或非佐剂的全病毒 H1N1(2009)疫苗。大量的参与者数量允许我们研究免疫反应和不良反应的可能预测因素。我们使用回归分析来检查变量的影响,包括过去接种季节性疫苗、接种后使用退烧药、剂量间隔和对 H1N1(2009)的预先存在的抗体,以研究其对免疫原性的影响。我们还检查了免疫原性和不良反应之间的关系,以及先前的感染或潜在疾病是否影响不良反应。对于这两种疫苗,接种后体温≥38°C 的儿童的血凝抑制滴度均高出 60%,而先前接种过季节性疫苗的儿童则低 29%。早期使用退烧药不会影响免疫原性。剂量间隔时间较长和有先前感染证据的儿童的接种后滴度较高,但后者的不良反应不受影响。在佐剂疫苗组中,过敏的儿童更容易出现反应。对于有先前感染的儿童,两种疫苗均安全且具有免疫原性。为了更早地提供保护而缩短剂量间隔会降低免疫原性。季节性疫苗对免疫原性的影响值得进一步研究。

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