Unveiling immunity gaps and determining a suitable age for a third dose of the measles-containing vaccine: a strategic approach to accelerating measles elimination.

IF 5 Q1 HEALTH CARE SCIENCES & SERVICES The Lancet regional health. Southeast Asia Pub Date : 2024-12-21 eCollection Date: 2025-01-01 DOI:10.1016/j.lansea.2024.100523
Somya Mehra, Sajikapon Kludkleeb, Chutikarn Chaimayo, Pornsawan Leaungwutiwong, Saranath Lawpoolsri, Wirichada Pan-Ngum, Kulkanya Chokephaibulkit, Thundon Ngamprasertchai
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Abstract

Background: In highly measles immunized countries, immunity gaps in adolescents and young adults are a key issue posing an obstacle to measles elimination. This study aims to identify the gaps by estimating the age-stratified probability of seropositivity, and to ascertain a suitable age for the administration of a third dose of a measles-containing vaccine (MCV3) to effectively fill these gaps.

Methods: We retrospectively obtained measles serological results from hospital setting among among individuals aged 13-39 years and developed a serocatalytic dynamic probability model, stratifying seropositivity due to vaccination or natural infection. We calibrated the model to age-stratified seropositivity data within a Bayesian setting using the Metropolis-Hastings algorithm. A scenario analysis to determine a suitable age for MCV3 administration was also performed.

Findings: The overall prevalence of measles seropositivity was 65.6% (95% confidence interval [CI]: 61.5-69.6). Posterior predictive curves for the age-stratified seroprevalence exhibited a decreasing trend from ages 13-20 years but an upward trend from 26 to 30 years. The age at which a given individual's serostatus reached a 50% probability of seronegativity was found to be approximately 18-20 years depending on the annual measles force of infection.

Interpretation: Our findings highlight a significant measles immunity gap in young adults aged 20-26 years, posing an increased risk of transmission. A MCV3 at the age of 18-20 years potentially closes the gap and aids measles elimination programmes.

Funding: This work was supported by Faculty of Tropical Medicine (MCTM, ICTM grant), Mahidol University (to T.N.) and APC fee was supported by Mahidol University (to T.N.). S.M. and W.P. were funded in whole, or in part, by the Wellcome Trust [Grant number 220211]. For the purpose of open access, the authors have applied a CC BY public copyright licence to any Author Accepted Manuscript version arising from this submission.

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背景:在麻疹免疫接种率较高的国家,青少年和年轻人的免疫空白是阻碍消除麻疹的一个关键问题。本研究旨在通过估算血清阳性的年龄分层概率来确定差距,并确定接种第三剂含麻疹成分疫苗(MCV3)的合适年龄,以有效填补这些差距:我们回顾性地从医院环境中获取了 13-39 岁人群的麻疹血清学结果,并建立了一个血清催化动态概率模型,对疫苗接种或自然感染导致的血清阳性率进行了分层。我们使用 Metropolis-Hastings 算法在贝叶斯环境下对该模型进行了校准,以校准年龄分层的血清阳性率数据。我们还进行了情景分析,以确定接种 MCV3 的合适年龄:结果:麻疹血清阳性的总体流行率为 65.6%(95% 置信区间 [CI]:61.5-69.6)。年龄分层血清阳性率的后验预测曲线显示,13-20 岁呈下降趋势,26-30 岁呈上升趋势。根据每年的麻疹感染力,特定个体的血清状态达到50%血清阴性概率的年龄约为18-20岁:我们的研究结果表明,20-26 岁的青壮年存在明显的麻疹免疫差距,这增加了传播的风险。在 18-20 岁时接种 MCV3 有可能缩小这一差距,并有助于消除麻疹计划:这项工作得到了玛希隆大学热带医学系(MCTM,ICTM资助)的支持(T.N.),APC费用由玛希隆大学提供(T.N.)。S.M.和W.P.的全部或部分研究经费由威康信托基金会(Wellcome Trust)提供[拨款号:220211]。出于开放存取的目的,作者已对本论文的任何作者接受稿件版本申请了 CC BY 公共版权许可。
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