Influenza Centre, Department of Clinical Science, University of Bergen.
K. G. Jebsen Centre for Influenza Vaccine Research, Department of Clinical Science, University of Bergen, Bergen, Norway.
Clin Infect Dis. 2019 Jan 18;68(3):382-392. doi: 10.1093/cid/ciy487.
The 2009 influenza pandemic was caused by the A/H1N1pdm09 virus, which was subsequently included in the seasonal vaccine, up to 2016/2017, as the A/H1N1 strain. This provided a unique opportunity to investigate the antibody response to H1N1pdm09 over time.
Healthcare workers (HCWs) were immunized with the AS03-adjuvanted H1N1pdm09 vaccine in 2009 (N = 250), and subsequently vaccinated with seasonal vaccines containing H1N1pdm09 for 4 seasons (repeated group), <4 seasons (occasional group), or no seasons (single group). Blood samples were collected pre and at 21 days and 3, 6, and 12 months after each vaccination, or annually (pre-season) from 2010 in the single group. The H1N1pdm09-specific antibodies were measured by the hemagglutination inhibition (HI) assay.
Pandemic vaccination robustly induced HI antibodies that persisted above the 50% protective threshold (HI titers ≥ 40) over 12 months post-vaccination. Previous seasonal vaccination and the duration of adverse events after the pandemic vaccination influenced the decision to vaccinate in subsequent seasons. During 2010/2011-2013/2014, antibodies were boosted after each seasonal vaccination, although no significant difference was observed between the repeated and occasional groups. In the single group without seasonal vaccination, 32% of HCWs seroconverted (≥4-fold increase in HI titers) during the 4 subsequent years, most of whom had HI titers <40 prior to seroconversion. When excluding these seroconverted HCWs, HI titers gradually declined from 12 to 60 months post-pandemic vaccination.
Pandemic vaccination elicited durable antibodies, supporting the incorporation of adjuvant. Our findings support the current recommendation of annual influenza vaccination in HCWs.
NCT01003288.
2009 年流感大流行是由 A/H1N1pdm09 病毒引起的,该病毒随后被纳入季节性疫苗中,直至 2016/2017 年,作为 A/H1N1 株。这为研究 H1N1pdm09 的抗体反应随时间的变化提供了一个独特的机会。
2009 年,医护人员(HCWs)接种了 AS03 佐剂的 H1N1pdm09 疫苗(N=250),随后接种了含有 H1N1pdm09 的季节性疫苗 4 个季节(重复组)、<4 个季节(偶尔组)或无季节(单一组)。每次接种前和接种后 21 天以及 3、6 和 12 个月采集血液样本,或从 2010 年开始,单一组每年(季节前)采集。通过血凝抑制(HI)试验测量 H1N1pdm09 特异性抗体。
大流行疫苗接种强烈诱导 HI 抗体,在接种后 12 个月内持续高于 50%的保护阈值(HI 滴度≥40)。以前的季节性疫苗接种和大流行疫苗接种后的不良反应持续时间影响了随后季节接种疫苗的决定。在 2010/2011 年至 2013/2014 年期间,每次季节性疫苗接种后抗体都得到了增强,尽管重复组和偶尔组之间没有观察到显著差异。在没有季节性疫苗接种的单一组中,在随后的 4 年中,有 32%的 HCWs 发生了血清转化(HI 滴度增加≥4 倍),其中大多数在血清转化前 HI 滴度<40。当排除这些血清转化的 HCWs 时,HI 滴度从大流行疫苗接种后 12 至 60 个月逐渐下降。
大流行疫苗接种引发了持久的抗体,支持佐剂的加入。我们的研究结果支持目前建议 HCWs 每年接种流感疫苗。
NCT01003288。