Epidemic Intelligence Service and.
National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Pediatrics. 2020 Mar;145(3). doi: 10.1542/peds.2019-0836. Epub 2020 Feb 13.
Most countries use 3-dose pneumococcal conjugate vaccine (PCV) schedules; a 4-dose (3 primary and 1 booster) schedule is licensed for US infants. We evaluated the invasive pneumococcal disease (IPD) breakthrough infection incidence in children receiving 2 vs 3 primary PCV doses with and without booster doses (2 + 1 vs 3 + 1; 2 + 0 vs 3 + 0).
We used 2001-2016 Active Bacterial Core surveillance data to identify breakthrough infections (vaccine-type IPD in children receiving ≥1 7-valent pneumococcal conjugate vaccine [PCV7] or 13-valent pneumococcal conjugate vaccine [PCV13] dose) among children aged <5 years. We estimated schedule-specific IPD incidence rates (IRs) per 100 000 person-years and compared incidence by schedule (2 + 1 vs 3 + 1; 2 + 0 vs 3 + 0) using rate differences (RDs) and incidence rate ratios.
We identified 71 PCV7 and 49 PCV13 breakthrough infections among children receiving a schedule of interest. PCV13 breakthrough infection rates were higher in children aged <1 year receiving the 2 + 0 (IR: 7.8) vs 3 + 0 (IR: 0.6) schedule (incidence rate ratio: 12.9; 95% confidence interval: 4.1-40.4); PCV7 results were similar. Differences in PCV13 breakthrough infection rates by schedule in children aged <1 year were larger in 2010-2011 (2 + 0 IR: 18.6; 3 + 0 IR: 1.4; RD: 16.6) vs 2012-2016 (2 + 0 IR: 3.6; 3 + 0 IR: 0.2; RD: 3.4). No differences between schedules were detected in children aged ≥1 year for PCV13 breakthrough infections.
Fewer PCV breakthrough infections occurred in the first year of life with 3 primary doses. Differences in breakthrough infection rates by schedule decreased as vaccine serotypes decreased in circulation.
大多数国家使用 3 剂型肺炎球菌结合疫苗(PCV)接种方案;4 剂型(3 剂基础免疫和 1 剂加强免疫)方案已获美国婴儿使用许可。我们评估了接受 2 剂与 3 剂基础 PCV 接种且有无加强免疫(2+1 与 3+1;2+0 与 3+0)的儿童中侵袭性肺炎球菌病(IPD)突破性感染的发生率。
我们使用 2001-2016 年主动细菌性核心监测数据,在年龄<5 岁的儿童中识别接受≥1 剂 7 价肺炎球菌结合疫苗(PCV7)或 13 价肺炎球菌结合疫苗(PCV13)后出现的突破性感染(疫苗型 IPD)。我们通过比较方案特异性发病率(IR)(每 10 万人年)来估计方案特异性 IPD 发生率,并使用率差(RD)和发病率比(IRR)比较不同方案的发病率。
我们在接受研究方案的儿童中发现 71 例 PCV7 和 49 例 PCV13 突破性感染。2+0 方案(IR:7.8)与 3+0 方案(IR:0.6)相比,1 岁以下儿童中 PCV13 突破性感染率更高(IRR:12.9;95%置信区间:4.1-40.4);PCV7 结果相似。2010-2011 年(2+0IR:18.6;3+0IR:1.4;RD:16.6)与 2012-2016 年(2+0IR:3.6;3+0IR:0.2;RD:3.4)相比,1 岁以下儿童中 PCV13 突破性感染率的方案差异更大。年龄≥1 岁的儿童中,PCV13 突破性感染率在不同方案之间无差异。
3 剂基础免疫接种后,1 岁以下儿童中 PCV 突破性感染的发生率更低。随着疫苗血清型在人群中的流行率降低,方案间突破性感染率的差异减小。