Istituto per lo Studio e la Prevenzione Oncologica (ISPO), Florence, Italy.
Ospedale Madonna delle Grazie di Matera, Matera, Italy.
BMC Infect Dis. 2018 Jan 15;18(1):38. doi: 10.1186/s12879-018-2945-8.
A large free-of-charge quadrivalent HPV (qHPV) vaccination program, covering four cohorts annually (women 11, 14, 17 and 24 years), has been implemented in Basilicata since 2007. This study evaluated vaccine and non-vaccine HPV prevalence 5-7 years post-vaccination program implementation in vaccinated and unvaccinated women.
This population-based, cross-sectional study was conducted in the public screening centers of the Local Health Unit in Matera between 2012 and 2014. Cervical samples were obtained for Pap and HPV testing (HC2, LiPA Extra® assay) and participants completed a sociodemographic and behavioral questionnaire. Detailed HPV vaccination status was retrieved from the official HPV vaccine registry. HPV prevalence was described overall, by type and vaccination status. The association between HPV type-detection and risk/protective factors was studied. Direct vaccine protection (qHPV vaccine effectiveness [VE]), cross-protection, and type-replacement were evaluated in cohorts eligible for vaccination, by analyzing HPV prevalence of vaccine and non-vaccine types according to vaccination status.
Overall, 2793 women (18-50 years) were included, 1314 of them having been in birth cohorts eligible for the HPV vaccination program (18- to 30-year-old women at enrolment). Among the latter, qHPV vaccine uptake was 59% (at least one dose), with 94% completing the schedule; standardized qHPV type prevalence was 0.6% in vaccinated versus 5.5% in unvaccinated women (P <0.001); adjusted VE against vaccine type infections was 90% (95% CI: 73%-96%) for all fully vaccinated women and 100% (95% CI not calculable) in women vaccinated before sexual debut. No statistically significant difference in overall high-risk HPV, high-risk non-vaccine HPV, or any single non-vaccine type prevalence was observed between vaccinated and unvaccinated women.
These results, conducted in a post-vaccine era, suggest a high qHPV VE and that a well-implemented catch-up vaccination program may be efficient in reducing vaccine-type infections in a real-world setting. No cross-protective effect or evidence of type-replacement was observed a few years after HPV vaccine introduction.
自 2007 年以来,巴西利卡塔一直在实施一项大型免费四价人乳头瘤病毒(qHPV)疫苗接种计划,每年覆盖四个队列(11、14、17 和 24 岁的女性)。本研究评估了接种和未接种疫苗的女性接种疫苗后 5-7 年疫苗和非疫苗 HPV 的流行率。
这项基于人群的横断面研究于 2012 年至 2014 年在马泰拉地方卫生局的公共筛查中心进行。采集宫颈样本进行巴氏涂片和 HPV 检测(HC2、LiPA Extra®检测),参与者完成了社会人口统计学和行为问卷。详细的 HPV 疫苗接种状况从官方 HPV 疫苗登记处检索。总体上按类型和疫苗接种状况描述 HPV 流行率。研究了 HPV 类型检测与风险/保护因素之间的关系。在符合接种条件的队列中,通过分析根据疫苗接种状况的疫苗和非疫苗类型的 HPV 流行率,评估了直接疫苗保护(qHPV 疫苗效力[VE])、交叉保护和类型替代。
总体而言,共纳入 2793 名女性(18-50 岁),其中 1314 名女性处于 HPV 疫苗接种计划的出生队列(登记时为 18-30 岁的女性)。在这些女性中,qHPV 疫苗接种率为 59%(至少一剂),94%完成了全程接种;标准化 qHPV 类型流行率在接种组为 0.6%,未接种组为 5.5%(P<0.001);所有完全接种疫苗的女性的调整后针对疫苗型感染的 VE 为 90%(95%CI:73%-96%),在初次性行为前接种疫苗的女性为 100%(95%CI 不可计算)。在接种和未接种疫苗的女性之间,总体高危 HPV、高危非疫苗 HPV 或任何单一非疫苗类型的流行率均无统计学差异。
这些在疫苗接种后时代进行的结果表明,qHPV 具有较高的 VE,并且在现实环境中,实施良好的补种疫苗接种计划可能有效减少疫苗型感染。HPV 疫苗引入几年后,未观察到交叉保护作用或类型替代的证据。