Effects of PCV10 and PCV13 on pneumococcal serotype 6C disease, carriage, and antimicrobial resistance

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Lindsay R. Grant , Germaine Hanquet , Ingrid T. Sepúlveda-Pachón , Christian Theilacker , Marc Baay , Mary P.E. Slack , Luis Jodar , Bradford D. Gessner
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引用次数: 0

Abstract

Background

The cross-protection of pneumococcal conjugate vaccines (PCV) against serotype 6C is not clearly documented, although 6C represents a substantial burden of pneumococcal disease in recent years. A systematic review by the World Health Organization that covered studies through 2016 concluded that available data were insufficient to determine if either PCV10 (which contains serotype 6B but not 6A) or PCV13 (containing serotype 6A and 6B) conferred protection against 6C.

Methods

We performed a systematic review of randomized controlled trials and observational studies published between January 2010 – August 2022 (Medline/Embase), covering the direct, indirect, and overall effect of PCV10 and PCV13 against 6C invasive pneumococcal disease (IPD), non-IPD, nasopharyngeal carriage (NPC), and antimicrobial resistance (AMR).

Results

Of 2548 publications identified, 112 were included. Direct vaccine effectiveness against 6C IPD in children ranged between 70 and 85 % for ≥ 1 dose PCV13 (n = 3 studies), was 94 % in fully PCV13 vaccinated children (n = 2), and −14 % for ≥ 1 dose of PCV10 (n = 1). Compared to PCV7, PCV13 efficacy against 6C NPC in children was 66 % (n = 1). Serotype 6C IPD rates or NPC prevalence declined post-PCV13 in most studies in children (n = 5/6) and almost half of studies in adults (n = 5/11), while it increased post-PCV10 for IPD and non-IPD in all studies (n = 6/6). Changes in AMR prevalence were inconsistent.

Conclusions

In contrast to PCV10, PCV13 vaccination consistently protected against 6C IPD and NPC in children, and provided some level of indirect protection to adults, supporting that serotype 6A but not 6B provides cross-protection to 6C. Vaccine policy makers and regulators should consider the effects of serotype 6A-containing PCVs against serotype 6C disease in their decisions.

PCV10 和 PCV13 对肺炎球菌血清 6C 型疾病、携带和抗菌药耐药性的影响。
背景:肺炎球菌结合疫苗 (PCV) 对血清 6C 型的交叉保护作用尚无明确记载,尽管 6C 型是近年来肺炎球菌疾病的主要负担。世界卫生组织对截至 2016 年的研究进行了系统性回顾,得出的结论是现有数据不足以确定 PCV10(含有 6B 血清型,但不含 6A)或 PCV13(含有 6A 和 6B 血清型)是否能对 6C 产生保护作用:我们对 2010 年 1 月至 2022 年 8 月间发表的随机对照试验和观察性研究(Medline/Embase)进行了系统性回顾,内容涵盖 PCV10 和 PCV13 对 6C 侵袭性肺炎球菌疾病(IPD)、非 IPD、鼻咽带菌(NPC)和抗菌药耐药性(AMR)的直接、间接和总体影响:结果:在已确定的 2548 篇出版物中,有 112 篇被收录。接种≥1剂PCV13的儿童接种6C IPD疫苗的直接有效率在70%至85%之间(n = 3项研究),完全接种PCV13的儿童接种有效率为94%(n = 2项研究),接种≥1剂PCV10的儿童接种有效率为-14%(n = 1项研究)。与 PCV7 相比,PCV13 对儿童 6C 型鼻咽癌的有效率为 66 %(n = 1)。在大多数儿童研究(n = 5/6)和几乎一半的成人研究(n = 5/11)中,血清型 6C IPD 感染率或非 IPD 感染率在 PCV13 后有所下降,而在所有研究(n = 6/6)中,IPD 和非 IPD 感染率在 PCV10 后有所上升。AMR流行率的变化并不一致:结论:与 PCV10 相比,接种 PCV13 可持续预防儿童 6C IPD 和非 IPD,并为成人提供一定程度的间接保护,这证明血清型 6A 而非 6B 可为 6C 提供交叉保护。疫苗政策制定者和监管者在决策时应考虑含血清 6A 型 PCV 对血清 6C 型疾病的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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