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A Bivariate Mixture Model for Natural Antibody Levels to Human Papillomavirus Types 16 and 18: Baseline Estimates for Monitoring the Herd Effects of Immunization

机译:人乳头瘤病毒16型和18型天然抗体水平的双变量混合物模型:用于监测免疫群效应的基线估计

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摘要

Post-vaccine monitoring programs for human papillomavirus (HPV) have been introduced in many countries, but HPV serology is still an underutilized tool, partly owing to the weak antibody response to HPV infection. Changes in antibody levels among non-vaccinated individuals could be employed to monitor herd effects of immunization against HPV vaccine types 16 and 18, but inference requires an appropriate statistical model. The authors developed a four-component bivariate mixture model for jointly estimating vaccine-type seroprevalence from correlated antibody responses against HPV16 and -18 infections. This model takes account of the correlation between HPV16 and -18 antibody concentrations within subjects, caused e.g. by heterogeneity in exposure level and immune response. The model was fitted to HPV16 and -18 antibody concentrations as measured by a multiplex immunoassay in a large serological survey (3,875 females) carried out in the Netherlands in 2006/2007, before the introduction of mass immunization. Parameters were estimated by Bayesian analysis. We used the deviance information criterion for model selection; performance of the preferred model was assessed through simulation. Our analysis uncovered elevated antibody concentrations in doubly as compared to singly seropositive individuals, and a strong clustering of HPV16 and -18 seropositivity, particularly around the age of sexual debut. The bivariate model resulted in a more reliable classification of singly and doubly seropositive individuals than achieved by a combination of two univariate models, and suggested a higher pre-vaccine HPV16 seroprevalence than previously estimated. The bivariate mixture model provides valuable baseline estimates of vaccine-type seroprevalence and may prove useful in seroepidemiologic assessment of the herd effects of HPV vaccination.
机译:在许多国家已经引入了针对人乳头瘤病毒(HPV)的疫苗接种后监测计划,但是HPV血清学仍未得到充分利用,部分原因是对HPV感染的抗体反应较弱。未接种疫苗的个体中抗体水平的变化可用于监测针对16和18型HPV疫苗的免疫群效应,但推断需要适当的统计模型。作者开发了一种四组分双变量混合模型,用于根据针对HPV16和-18感染的相关抗体反应共同估算疫苗类型的血清阳性率。该模型考虑了受试者中HPV16和-18抗体浓度之间的相关性,例如通过暴露水平和免疫反应的异质性。该模型适合于HPV16和-18抗体浓度,该浓度是在2006/2007年在荷兰进行的大规模血清学调查(通过大规模免疫学调查)中通过多重免疫测定法测量的(3,875名女性),然后开始大规模免疫。通过贝叶斯分析估计参数。我们使用偏差信息准则进行模型选择;通过仿真评估了首选模型的性能。我们的分析发现与单独血清反应阳性的个体相比,抗体浓度增加了两倍,并且HPV16和-18血清反应阳性的聚集性很强,尤其是在性初次出现时。与通过两个单变量模型的组合所实现的相比,双变量模型对单个和双重血清反应阳性的个体进行了更可靠的分类,并且表明疫苗接种前的HPV16血清阳性率高于先前估计的水平。双变量混合模型提供了有价值的疫苗类型血清阳性基线估计值,并且可能被证明可用于HPV疫苗接种群的血清流行病学评估。

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