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人乳头瘤病毒疫苗有效性与接种剂量:国家免疫规划数据系统评价。

Human papillomavirus vaccine effectiveness by number of doses: Systematic review of data from national immunization programs.

机构信息

National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Centre de recherche du CHU de Québec - Université Laval, Axe santé des populations et pratiques optimales en santé, Québec, Canada.

出版信息

Vaccine. 2018 Aug 6;36(32 Pt A):4806-4815. doi: 10.1016/j.vaccine.2018.01.057. Epub 2018 May 22.

Abstract

BACKGROUND

Human papillomavirus (HPV) vaccines were first licensed as a three-dose series; a two-dose series is now recommended in some age groups and there is interest in possible one-dose vaccination.

METHODS

We conducted a systematic literature review of HPV vaccine effectiveness by number of doses, including assessment of biases and impact of varying buffer periods (time between vaccination and outcome counting).

RESULTS

Of 3787 articles identified, 26 full articles were assessed and 14 included in our review. All studies were conducted within the context of recommended three-dose schedules of bivalent (3) or quadrivalent HPV vaccine (11). Two evaluated effectiveness for prevention of HPV prevalence, six anogenital warts, and six abnormal cervical cytology or histology. Many studies found differences between three-, two- and one-dose vaccine recipients, indicating possible differences in HPV exposure prior to vaccination or in risk behavior. Adjusted or stratified analyses were conducted to control for potential confounding. All studies found significant vaccine effectiveness with three doses, 11 with two doses at various intervals, and six with one dose. Most studies showed a relationship (not always statistically significant) between effectiveness and number of doses, with greater decreases in HPV-related outcomes with three, followed by two and one dose(s). Few studies conducted formal comparisons of three vs fewer doses. Three of four studies that examined buffer periods found higher effectiveness and a smaller difference by number of doses with longer periods.

CONCLUSION

Most post-licensure studies report highest effectiveness with three doses; some found no statistically significant difference between two and three doses. Additionally, almost half found some effectiveness with one dose. Several biases impact estimates, with most biasing two- and one-dose results away from showing effectiveness. Future effectiveness studies, examining persons vaccinated prior to sexual activity and using methods to reduce potential sources of bias, can help inform vaccination policy.

摘要

背景

人乳头瘤病毒(HPV)疫苗最初以三剂系列获得许可;现在建议在某些年龄组中使用两剂系列,并且对可能的一剂接种也有兴趣。

方法

我们对 HPV 疫苗剂量的有效性进行了系统的文献综述,包括对偏倚的评估以及不同缓冲期(疫苗接种和结果计数之间的时间)的影响。

结果

在确定的 3787 篇文章中,评估了 26 篇全文,其中 14 篇包含在我们的综述中。所有研究均在推荐的二价(3)或四价 HPV 疫苗(11)三剂方案的背景下进行。两项研究评估了预防 HPV 流行的有效性,六项评估了肛门生殖器疣的有效性,六项评估了异常宫颈细胞学或组织学的有效性。许多研究发现了三剂、两剂和一剂疫苗接种者之间的差异,这表明在疫苗接种前 HPV 暴露或风险行为方面可能存在差异。进行了调整或分层分析以控制潜在的混杂因素。所有研究均发现三剂疫苗具有显著的有效性,11 项研究在不同的间隔时间内发现了两剂疫苗的有效性,6 项研究发现了一剂疫苗的有效性。大多数研究表明,有效性与剂量之间存在关系(并不总是具有统计学意义),三剂疫苗可使 HPV 相关结果的下降幅度最大,其次是两剂和一剂。很少有研究对三剂与较少剂量进行正式比较。四项研究中有三项研究检查了缓冲期,发现随着时间的延长,有效性更高,剂量之间的差异更小。

结论

大多数上市后研究报告了三剂疫苗的最高有效性;有些研究发现两剂和三剂之间没有统计学上的显著差异。此外,几乎有一半的研究发现一剂疫苗具有一定的有效性。有几个偏倚会影响估计值,其中大多数偏倚会使两剂和一剂的结果偏向于无效。未来的有效性研究,检查在性行为前接种疫苗的人群,并使用方法减少潜在的偏倚来源,可以为疫苗接种政策提供信息。

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