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在马拉维引入肺炎球菌结合疫苗后,疫苗血清型肺炎链球菌的高残留携带率。

High residual carriage of vaccine-serotype Streptococcus pneumoniae after introduction of pneumococcal conjugate vaccine in Malawi.

机构信息

Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.

NIHR Global Health Research Unit on Mucosal Pathogens, Division of Infection and Immunity, University College London, London, UK.

出版信息

Nat Commun. 2020 May 6;11(1):2222. doi: 10.1038/s41467-020-15786-9.

DOI:10.1038/s41467-020-15786-9
PMID:32376860
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7203201/
Abstract

There are concerns that pneumococcal conjugate vaccines (PCVs) in sub-Saharan Africa sub-optimally interrupt Streptococcus pneumoniae vaccine-serotype (VT) carriage and transmission. Here we assess PCV carriage using rolling, prospective nasopharyngeal carriage surveys between 2015 and 2018, 3.6-7.1 years after Malawi's 2011 PCV13 introduction. Carriage decay rate is analysed using non-linear regression. Despite evidence of reduction in VT carriage over the study period, there is high persistent residual carriage. This includes among PCV-vaccinated children 3-5-year-old (16.1% relative reduction from 19.9% to 16.7%); PCV-unvaccinated children 6-8-year-old (40.5% reduction from 26.4% to 15.7%); HIV-infected adults 18-40-years-old on antiretroviral therapy (41.4% reduction from 15.2% to 8.9%). VT carriage prevalence half-life is similar among PCV-vaccinated and PCV-unvaccinated children (3.26 and 3.34 years, respectively). Compared with high-income settings, there is high residual VT carriage 3.6-7.1 years after PCV introduction. Rigorous evaluation of strategies to augment vaccine-induced control of carriage, including alternative schedules and catch-up campaigns, is required.

摘要

人们担心在撒哈拉以南非洲地区,肺炎球菌结合疫苗(PCV)不能最佳地中断肺炎球菌疫苗血清型(VT)的携带和传播。在这里,我们评估了 2015 年至 2018 年期间使用滚动式前瞻性鼻咽携带调查的 PCV 携带情况,这是在马拉维 2011 年引入 PCV13 后的 3.6-7.1 年。使用非线性回归分析携带衰减率。尽管有证据表明在研究期间 VT 携带有所减少,但仍存在高残留携带。这包括 PCV 疫苗接种儿童 3-5 岁(从 19.9%降至 16.7%,相对减少 16.1%);PCV 未接种儿童 6-8 岁(从 26.4%降至 15.7%,减少 40.5%);接受抗逆转录病毒治疗的 18-40 岁 HIV 感染成年人(从 15.2%降至 8.9%,减少 41.4%)。PCV 疫苗接种和未接种儿童的 VT 携带流行半衰期相似(分别为 3.26 年和 3.34 年)。与高收入国家相比,在 PCV 引入后 3.6-7.1 年,仍存在高残留的 VT 携带。需要严格评估增强疫苗诱导的携带控制的策略,包括替代方案和补种运动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/7203201/835c069b6548/41467_2020_15786_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/7203201/8f7f0bf9028d/41467_2020_15786_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/7203201/660e4deed083/41467_2020_15786_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/7203201/9019b6f8eb7a/41467_2020_15786_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/7203201/835c069b6548/41467_2020_15786_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/7203201/8f7f0bf9028d/41467_2020_15786_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/7203201/660e4deed083/41467_2020_15786_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/7203201/9019b6f8eb7a/41467_2020_15786_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/7203201/835c069b6548/41467_2020_15786_Fig4_HTML.jpg

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