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评价人乳头瘤病毒疫苗接种后潜在的病毒类型替代的流行病学方法。

Epidemiologic approaches to evaluating the potential for human papillomavirus type replacement postvaccination.

机构信息

Division of Cancer Epidemiology, Department of Oncology, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.

出版信息

Am J Epidemiol. 2013 Aug 15;178(4):625-34. doi: 10.1093/aje/kwt018. Epub 2013 May 9.

Abstract

Currently, 2 vaccines exist that prevent infection by the genotypes of human papillomavirus (HPV) responsible for approximately 70% of cervical cancer cases worldwide. Although vaccination is expected to reduce the prevalence of these HPV types, there is concern about the effect this could have on the distribution of other oncogenic types. According to basic ecological principles, if competition exists between ≥2 different HPV types for niche occupation during natural infection, elimination of 1 type may lead to an increase in other type(s). Here, we discuss this issue of "type replacement" and present different epidemiologic approaches for evaluation of HPV type competition. Briefly, these approaches involve: 1) calculation of the expected frequency of coinfection under independence between HPV types for comparison with observed frequency; 2) construction of hierarchical logistic regression models for each vaccine-targeted type; and 3) construction of Kaplan-Meier curves and Cox models to evaluate sequential acquisition and clearance of HPV types according to baseline HPV status. We also discuss a related issue concerning diagnostic artifacts arising when multiple HPV types are present in specific samples (due to the inability of broad-spectrum assays to detect certain types present in lower concentrations). This may result in an apparent increase in previously undetected types postvaccination.

摘要

目前,有 2 种疫苗可以预防导致全球约 70%宫颈癌病例的 HPV 基因型感染。尽管疫苗接种有望降低这些 HPV 类型的流行率,但人们担心这可能会对其他致癌类型的分布产生影响。根据基本生态学原理,如果在自然感染过程中,≥2 种不同的 HPV 类型存在对生态位的竞争,那么消灭 1 种类型可能会导致其他类型的增加。在这里,我们讨论了“类型替代”的问题,并提出了不同的流行病学方法来评估 HPV 类型竞争。简而言之,这些方法包括:1)计算 HPV 类型之间独立性下的合并感染预期频率,与观察到的频率进行比较;2)为每个疫苗靶向类型构建分层逻辑回归模型;3)构建 Kaplan-Meier 曲线和 Cox 模型,根据基线 HPV 状态评估 HPV 类型的顺序获得和清除。我们还讨论了一个与特定样本中存在多种 HPV 类型(由于广谱检测无法检测到浓度较低的某些类型)时出现的诊断伪影相关的问题。这可能会导致接种疫苗后以前未检测到的类型明显增加。

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