European Programme for Intervention Epidemiology Training (EPIET), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden; National Institute for Public Health and the Environment (RIVM), Bilthoven, the Netherlands.
Amsterdam UMC, University of Amsterdam, Medical Microbiology and Infection Prevention and the Netherlands Reference Laboratory of Bacterial Meningitis, Amsterdam, the Netherlands.
Vaccine. 2021 Jan 8;39(2):431-437. doi: 10.1016/j.vaccine.2020.11.018. Epub 2020 Nov 24.
In 2011, the 7-valent pneumococcal conjugate vaccine (PCV7) was replaced by the 10-valent vaccine (PCV10) in the Netherlands. We report on impact and effectiveness against invasive pneumococcal disease (IPD) in children aged under 5 years by switching from PCV7 to PCV10.
We included IPD cases between 2004 and 2019 in children aged < 5 years reported via the national surveillance system. To assess the impact of the PCV10 vaccination program we compared IPD incidence 6-8 years after PCV10 introduction (2017-2019) to the two years just before the switch to PCV10 (2009-2011). We estimated vaccine effectiveness (VE) using the indirect cohort method, comparing vaccination status (at least two vaccine doses) in IPD-cases caused by PCV10 serotypes (cases) to non-PCV10 IPD cases (controls), in children eligible for PCV10.
The overall incidence decreased from 8.7 (n = 162) in 2009-2011 to 7.3 per 100.000 (n = 127) in 2017-2019 (Incidence rate ratio (IRR) 0.83, 95%CI: 0.66; 1.05). IPD caused by the additional serotypes included in PCV10 declined by 93% (IRR 0.07, 95%CI: 0.02; 0.23). Incidence of non-PCV10 IPD showed a non-significant increase (IRR 1.25, 95%CI: 0.96; 1.63). Among 231 IPD-cases eligible for PCV10, the overall VE was 91% (95%CI: 67; 97) and did not differ by sex or age at diagnosis. Effectiveness against non-PCV10 serotype 19A IPD was non-significant with an estimate of 28% (95%CI:-179; 81).
PCV10 is highly effective in protecting against IPD in Dutch children under 5 years with limited serotype replacement after switching from PCV7 to PCV10. We found no evidence for significant cross-protection of PCV10 against 19A serotype IPD.
2011 年,荷兰用 10 价肺炎球菌结合疫苗(PCV10)替代了 7 价肺炎球菌结合疫苗(PCV7)。我们报告了从 PCV7 切换到 PCV10 后,对 5 岁以下儿童侵袭性肺炎球菌病(IPD)的影响和有效性。
我们纳入了 2004 年至 2019 年期间报告的通过国家监测系统的 5 岁以下儿童的 IPD 病例。为了评估 PCV10 疫苗接种计划的影响,我们比较了 PCV10 引入后 6-8 年(2017-2019 年)与切换到 PCV10 前两年(2009-2011 年)的 IPD 发病率。我们使用间接队列法估计疫苗效力(VE),将 PCV10 血清型引起的 IPD 病例(病例)的疫苗接种状态(至少两剂疫苗)与非 PCV10 IPD 病例(对照)进行比较,在有资格接种 PCV10 的儿童中进行比较。
总体发病率从 2009-2011 年的每 100,000 人 8.7 例(n=162)降至 2017-2019 年的每 100,000 人 7.3 例(n=127)(发病率比(IRR)0.83,95%CI:0.66;1.05)。包括在 PCV10 中的额外血清型引起的 IPD 下降了 93%(IRR 0.07,95%CI:0.02;0.23)。非 PCV10 IPD 的发病率呈非显著上升(IRR 1.25,95%CI:0.96;1.63)。在 231 例有资格接种 PCV10 的 IPD 病例中,总体 VE 为 91%(95%CI:67;97),且不因性别或诊断时的年龄而有所差异。针对非 PCV10 血清型 19A IPD 的效力无显著差异,估计为 28%(95%CI:-179;81)。
PCV10 对 5 岁以下荷兰儿童的 IPD 具有高度有效性,从 PCV7 切换到 PCV10 后,血清型替代有限。我们没有发现 PCV10 对 19A 血清型 IPD 有显著交叉保护作用的证据。