十价和十三价肺炎球菌结合疫苗在加拿大魁北克省预防血清型 19A 侵袭性肺炎球菌疾病的效果。加拿大免疫研究网络 (CIRN) 研究

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Geneviève Deceuninck , Nicholas Brousseau , Brigitte Lefebvre , Caroline Quach , Bruce Tapiero , Yen-Giang Bui , Michael Desjardins , Philippe De Wals
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引用次数: 0

摘要

加拿大魁北克省于 2004 年开始为儿童实施 2+1 剂肺炎球菌结合疫苗 (PCV) 计划。PCV7、PCV10、PCV13 和 PCV10/PCV13 混合接种计划依次实施,不进行补种。我们采用间接队列法估算了 2009-2023 年间 5 岁儿童接种 19A 血清型侵入性肺炎球菌疾病 (IPD) 疫苗的效果。分析共纳入了 248 例 19A 型 IPD 病例和 457 例 IPD 对照病例。PCV10 ≥1剂的调整后疫苗效力(VEa)为57% [95 %CI: -1 %,82 %],PCV13为62% [16 %,83 %]。PCV10 接种 3 次的 VEa 为 69 % [17 %,88 %],PCV13 为 76 % [39 %,90 %],2 次 PCV10 + 1 次 PCV13 接种的 VEa 为 86 % [64 %,95 %]。与其他两种方案相比,仅 PCV10 方案提供的保护程度往往较低。PCV10 + PCV13混合方案对19A IPD的保护作用至少与3剂PCV-13相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effectiveness of the ten- and thirteen-valent pneumococcal conjugate vaccines to prevent serotype 19A invasive pneumococcal disease in Quebec, Canada. A Canadian immunization research network (CIRN) study
In the province of Quebec, Canada, a 2 + 1 dose pneumococcal conjugate vaccine (PCV) program for children was implemented in 2004. PCV7, PCV10, PCV13 and a mixed PCV10/PCV13 schedule were sequentially used without catch-up. The effectiveness of vaccination schedules to prevent serotype 19A invasive pneumococcal disease (IPD) in <5-year-old children was estimated by the indirect cohort method during 2009–2023. A total of 248 19A IPD cases and 457 IPD controls were included in the analysis. Adjusted vaccine effectiveness (VEa) for ≥1 dose was 57 % [95 %CI: −1 %,82 %] for PCV10 and 62 % [16 %,83 %] for PCV13. VEa for 3 doses was 69 % [17 %,88 %] for PCV10, 76 % [39 %,90 %] for PCV13 and 86 % [64 %,95 %] for the 2PCV10 + 1PCV13 schedule. Protection provided by the PCV10-only schedule tended to be of lower magnitude compared to the two other schedules. The mixed PCV10 + PCV13 schedule showed a protection against 19A IPD at least comparable to that of 3 PCV-13 doses.
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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