根据血清学数据得出的血清型特异性感染力,巴西登革热疫苗接种的最佳年龄。

IF 0.8 4区 数学 Q4 BIOLOGY Mathematical Medicine and Biology-A Journal of the Ima Pub Date : 2021-03-15 DOI:10.1093/imammb/dqaa007
Sandra B Maier, Eduardo Massad, Marcos Amaku, Marcelo N Burattini, David Greenhalgh
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引用次数: 0

摘要

在本文中,我们研究了登革热的单一血清型传播模型,以确定登革热的最佳接种年龄。传染动力学以年龄依赖性感染力为模型。每种血清型的感染力来自巴西无血清型区分的登革热血清学概况和血清型特异性报告病例。根据巴西卫生部的数据,通过需要住院的概率来衡量感染风险。针对四种不同登革热病毒血清型DENv1-4的任意数量和组合确定最佳接种年龄。终生预期风险包括抗体依赖性增强(ADE)和两次异种感染后的永久性交叉免疫。这种风险被认为与血清状态有关。最佳接种年龄是根据恒定的血清状态特异性疫苗效力计算的。此外,将疫苗接种年龄限制在符合巴西登卡夏许可证的范围内,并比较了可实现的和最小的终生预期风险。住院风险的最佳接种年龄随着ADE和交叉免疫的假设而显著不同。无风险的原发性感染导致较高的最佳疫苗接种年龄,无症状的第三和第四次感染也是如此。有时根本不建议接种疫苗,例如在任何单一血清型的流行地区,如果原发感染无风险。将疫苗接种年龄限制在登卡夏许可年龄通常只会导致终生预期风险略高,疫苗接种应尽可能接近最佳疫苗接种年龄。
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The optimal age of vaccination against dengue in Brazil based on serotype-specific forces of infection derived from serological data.

In this paper, we study a single serotype transmission model of dengue to determine the optimal vaccination age for Dengvaxia. The transmission dynamics are modelled with an age-dependent force of infection. The force of infection for each serotype is derived from the serological profile of dengue in Brazil without serotype distinction and from serotype-specific reported cases. The risk due to an infection is measured by the probability of requiring hospitalization based on Brazilian Ministry of Health data. The optimal vaccination age is determined for any number and combination of the four distinct dengue virus serotypes DENv1-4. The lifetime expected risk is adapted to include antibody dependent enhancement (ADE) and permanent cross-immunity after two heterologous infections. The risk is assumed to be serostatus-dependent. The optimal vaccination age is computed for constant, serostatus-specific vaccine efficacies. Additionally, the vaccination age is restricted to conform to the licence of Dengvaxia in Brazil and the achievable and minimal lifetime expected risks are compared. The optimal vaccination age obtained for the risk of hospitalization varies significantly with the assumptions relating to ADE and cross-immunity. Risk-free primary infections lead to higher optimal vaccination ages, as do asymptomatic third and fourth infections. Sometimes vaccination is not recommended at all, e.g. for any endemic area with a single serotype if primary infections are risk-free. Restricting the vaccination age to Dengvaxia licensed ages mostly leads to only a slightly higher lifetime expected risk and the vaccine should be administered as close as possible to the optimal vaccination age.

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来源期刊
CiteScore
2.20
自引率
0.00%
发文量
15
审稿时长
>12 weeks
期刊介绍: Formerly the IMA Journal of Mathematics Applied in Medicine and Biology. Mathematical Medicine and Biology publishes original articles with a significant mathematical content addressing topics in medicine and biology. Papers exploiting modern developments in applied mathematics are particularly welcome. The biomedical relevance of mathematical models should be demonstrated clearly and validation by comparison against experiment is strongly encouraged. The journal welcomes contributions relevant to any area of the life sciences including: -biomechanics- biophysics- cell biology- developmental biology- ecology and the environment- epidemiology- immunology- infectious diseases- neuroscience- pharmacology- physiology- population biology
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