Assessing the impact of revising MenACWY vaccination schedule for adolescents in the United States: a modelling study

IF 7 Q1 HEALTH CARE SCIENCES & SERVICES Lancet Regional Health-Americas Pub Date : 2025-04-01 Epub Date: 2025-02-19 DOI:10.1016/j.lana.2025.101033
Affan Shoukat , Chad R. Wells , Thomas Shin , Lilia Potter-Schwartz , Alison P. Galvani , Seyed M. Moghadas
{"title":"Assessing the impact of revising MenACWY vaccination schedule for adolescents in the United States: a modelling study","authors":"Affan Shoukat ,&nbsp;Chad R. Wells ,&nbsp;Thomas Shin ,&nbsp;Lilia Potter-Schwartz ,&nbsp;Alison P. Galvani ,&nbsp;Seyed M. Moghadas","doi":"10.1016/j.lana.2025.101033","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>The current recommendation for MenACWY vaccination against invasive meningococcal disease (IMD) in the United States (US) includes two doses: the first dose at ages 11–12 and a booster dose at age 16. The Advisory Committee on Immunization Practices has proposed options for revising this schedule by either eliminating the first dose or adjusting the timing of the first dose to age 15 and the booster to ages 17–18. The impact of these alternative schedules on IMD incidence remains undetermined.</div></div><div><h3>Methods</h3><div>We developed an age-stratified, agent-based Monte-Carlo simulation model of meningococcal transmission dynamics, parameterised with US age demographics, to assess the impact of the proposed changes to the MenACWY vaccination schedules. Excluding serogroup A, absent in the US for decades, the model included serogroups C, W, and Y for asymptomatic infection (carriage) and vaccine effectiveness against IMD. We calibrated serogroup-specific transmission and IMD development probabilities by fitting the model to reported IMD cases from 1997 to 2004, before vaccine introduction. The calibrated model then simulated the current vaccination schedule (CVS) starting in 2005 and alternative schedules from January 1, 2025 to December 31, 2035, comparing outcomes over the same period.</div></div><div><h3>Findings</h3><div>Switching from the CVS to a single-dose program at age 16 with 61% vaccine uptake (as reported for the booster in 2022) would result in 1062 (95% Uncertainty Range [UR]: 724–1419) additional IMD cases during the 11-year study period. With a case fatality rate of 14.5%, this change could cause an estimated 154 (95% UR: 105–206) additional deaths. Even if vaccine uptake increased to 90% at age 16, the program would still result in 934 (95% UR: 640–1242) additional cases and 135 (95% UR: 93–180) more deaths compared to the CVS. The second alternative schedule (i.e. first dose at age 15, booster at ages 17–18) also increased IMD cases, notably shifting a substantial burden to adolescents aged 11–15 years.</div></div><div><h3>Interpretation</h3><div>Our findings indicate that the current MenACWY vaccination program remains more effective than the proposed alternatives, even with increased vaccine uptake during late adolescence. Improving the uptake rate of the booster at age 16 while maintaining the 11–12-year dose within the existing program would reduce the IMD burden among high-risk adolescents and young adults.</div></div><div><h3>Funding</h3><div>This study was in part supported by Sanofi. Seyed M. Moghadas acknowledges support from the <span>Natural Sciences and Engineering Research Council</span> of Canada Discovery Grant and Alliance Grant (ALLRP 576914-22). Alison P. Galvani acknowledges support from The <span>Notsew Orm Sands Foundation</span>.</div></div>","PeriodicalId":29783,"journal":{"name":"Lancet Regional Health-Americas","volume":"44 ","pages":"Article 101033"},"PeriodicalIF":7.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lancet Regional Health-Americas","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667193X25000432","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
引用次数: 0

Abstract

Background

The current recommendation for MenACWY vaccination against invasive meningococcal disease (IMD) in the United States (US) includes two doses: the first dose at ages 11–12 and a booster dose at age 16. The Advisory Committee on Immunization Practices has proposed options for revising this schedule by either eliminating the first dose or adjusting the timing of the first dose to age 15 and the booster to ages 17–18. The impact of these alternative schedules on IMD incidence remains undetermined.

Methods

We developed an age-stratified, agent-based Monte-Carlo simulation model of meningococcal transmission dynamics, parameterised with US age demographics, to assess the impact of the proposed changes to the MenACWY vaccination schedules. Excluding serogroup A, absent in the US for decades, the model included serogroups C, W, and Y for asymptomatic infection (carriage) and vaccine effectiveness against IMD. We calibrated serogroup-specific transmission and IMD development probabilities by fitting the model to reported IMD cases from 1997 to 2004, before vaccine introduction. The calibrated model then simulated the current vaccination schedule (CVS) starting in 2005 and alternative schedules from January 1, 2025 to December 31, 2035, comparing outcomes over the same period.

Findings

Switching from the CVS to a single-dose program at age 16 with 61% vaccine uptake (as reported for the booster in 2022) would result in 1062 (95% Uncertainty Range [UR]: 724–1419) additional IMD cases during the 11-year study period. With a case fatality rate of 14.5%, this change could cause an estimated 154 (95% UR: 105–206) additional deaths. Even if vaccine uptake increased to 90% at age 16, the program would still result in 934 (95% UR: 640–1242) additional cases and 135 (95% UR: 93–180) more deaths compared to the CVS. The second alternative schedule (i.e. first dose at age 15, booster at ages 17–18) also increased IMD cases, notably shifting a substantial burden to adolescents aged 11–15 years.

Interpretation

Our findings indicate that the current MenACWY vaccination program remains more effective than the proposed alternatives, even with increased vaccine uptake during late adolescence. Improving the uptake rate of the booster at age 16 while maintaining the 11–12-year dose within the existing program would reduce the IMD burden among high-risk adolescents and young adults.

Funding

This study was in part supported by Sanofi. Seyed M. Moghadas acknowledges support from the Natural Sciences and Engineering Research Council of Canada Discovery Grant and Alliance Grant (ALLRP 576914-22). Alison P. Galvani acknowledges support from The Notsew Orm Sands Foundation.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
评估修订MenACWY疫苗接种计划对美国青少年的影响:一项模型研究
背景:美国目前推荐的针对侵袭性脑膜炎球菌病(IMD)的MenACWY疫苗接种包括两剂:11-12岁的第一剂和16岁的加强剂。免疫实践咨询委员会提出了修订该计划的备选方案,要么取消第一剂,要么调整至15岁的第一剂和17-18岁的加强剂的接种时间。这些替代时间表对IMD发病率的影响仍未确定。方法我们建立了一个年龄分层的、基于个体的脑膜炎球菌传播动力学蒙特卡洛模拟模型,以美国年龄人口统计数据为参数,以评估脑膜炎球菌疫苗接种计划拟议变化的影响。排除美国几十年来缺少的血清A组,该模型包括无症状感染(携带)和抗IMD疫苗有效性的血清C、W和Y组。我们通过将模型拟合到1997年至2004年疫苗引入之前报告的IMD病例,校准了血清组特异性传播和IMD发展概率。然后,校准的模型模拟了2005年开始的现行疫苗接种计划(CVS)和2025年1月1日至2035年12月31日的替代计划,比较了同一时期的结果。研究结果:在11年的研究期间,从CVS转向单剂量计划,在16岁时接种61%的疫苗(如2022年加强剂的报道),将导致1062例(95%不确定性范围[UR]: 724-1419)额外的IMD病例。在病死率为14.5%的情况下,这一变化可能导致估计154例(95% UR: 105-206)额外死亡。即使疫苗接种率在16岁时提高到90%,与CVS相比,该计划仍将导致934例(95% UR: 640-1242)额外病例和135例(95% UR: 93-180)额外死亡。第二种替代方案(即在15岁时接种第一剂,在17-18岁接种加强剂)也增加了IMD病例,显著地将一个重大负担转移给了11-15岁的青少年。解释:我们的研究结果表明,目前的MenACWY疫苗接种计划仍然比建议的替代方案更有效,即使在青春期后期疫苗接种率增加。提高16岁儿童加强剂的接种率,同时在现有计划中保持11 - 12年的剂量,将减少高风险青少年和年轻人的IMD负担。这项研究得到了赛诺菲的部分支持。Seyed M. Moghadas感谢加拿大自然科学与工程研究委员会发现基金和联盟基金(ALLRP 576914-22)的支持。Alison P. Galvani感谢Notsew Orm Sands基金会的支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
8.00
自引率
0.00%
发文量
0
期刊介绍: The Lancet Regional Health – Americas, an open-access journal, contributes to The Lancet's global initiative by focusing on health-care quality and access in the Americas. It aims to advance clinical practice and health policy in the region, promoting better health outcomes. The journal publishes high-quality original research advocating change or shedding light on clinical practice and health policy. It welcomes submissions on various regional health topics, including infectious diseases, non-communicable diseases, child and adolescent health, maternal and reproductive health, emergency care, health policy, and health equity.
期刊最新文献
Reframing computed tomography-associated cancer concerns in lifesaving screening: keeping the focus on lives saved Tree cover loss in the Americas: a critical indicator linking climate mitigation and planetary health Language matters: advancing linguistic equity in health research in the Americas Public health research and health equity threatened by new US policies: impact and opportunities for Latin America Making US public health a good idea again
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1