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19A 型肺炎链球菌:全球流行病学。

Streptococcus pneumoniae serotype 19A: worldwide epidemiology.

机构信息

a Pfizer Inc , Collegeville , PA , USA.

b Pfizer Ltd , Shanghai , People's Republic of China.

出版信息

Expert Rev Vaccines. 2017 Oct;16(10):1007-1027. doi: 10.1080/14760584.2017.1362339. Epub 2017 Aug 28.

Abstract

Streptococcus pneumoniae causes mucosal and invasive diseases with high morbidity and mortality. Introduction of the 7-valent pneumococcal conjugate vaccine (PCV7) into routine infant immunization programs worldwide resulted in serotype 19A becoming a leading cause of the remaining pneumococcal disease burden in vaccinated and nonvaccinated individuals. This article reviews the impact of the latest generation PCVs (10-valent PCV, PCV10, and 13-valent PCV, PCV13) on serotype 19A. Areas covered: This article covers immune responses elicited by PCV7, PCV10 and PCV13 against serotype 19A and their impact on nasopharyngeal (NP) carriage and disease in vaccinated and unvaccinated populations using data from surveillance systems, randomized controlled trials, and observational studies. Expert commentary: As expected from a PCV containing serotype 19A, PCV13 elicits significantly higher functional immune responses against serotype 19A than PCV7 and PCV10. Higher responses are likely to be linked to both direct impact in vaccinated populations and reductions in 19A NP carriage in children, thus inducing herd protection and reducing 19A invasive pneumococcal disease (IPD) in nonvaccinated children and adults. In contrast, PCV7 and PCV10 have shown mixed evidence of direct short-lived cross-protection and little to no impact on 19A carriage, resulting in continued transmission and disease.

摘要

肺炎链球菌可引起高发病率和高死亡率的黏膜和侵袭性疾病。全球将 7 价肺炎球菌结合疫苗(PCV7)纳入常规婴儿免疫计划后,血清型 19A 成为接种和未接种人群中剩余肺炎球菌疾病负担的主要原因。本文综述了最新一代 PCVs(10 价 PCV、PCV10 和 13 价 PCV、PCV13)对血清型 19A 的影响。

涵盖领域

本文涵盖了 PCV7、PCV10 和 PCV13 对血清型 19A 产生的免疫反应及其对疫苗接种和未接种人群鼻咽(NP)携带和疾病的影响,使用了来自监测系统、随机对照试验和观察性研究的数据。

专家评论

正如包含血清型 19A 的 PCV 所预期的那样,PCV13 对血清型 19A 产生的功能性免疫反应明显高于 PCV7 和 PCV10。更高的反应可能与疫苗接种人群的直接影响以及儿童中 19A NP 携带的减少有关,从而诱导群体保护并减少非疫苗接种儿童和成人的 19A 侵袭性肺炎球菌病(IPD)。相比之下,PCV7 和 PCV10 显示出直接短期交叉保护的混合证据,对 19A 携带的影响很小或没有,导致持续传播和疾病。

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