Heard Isabelle, Tondeur Laura, Arowas Laurence, Demazoin Marie, Falguières Michaël, Parent Du Chatelet Isabelle
Centre National de Référence des papillomavirus humains, Institut Pasteur, Paris, France.
Groupe Hospitalier Pitié-Salpêtrière, AP-HP, Paris, France.
J Infect Dis. 2017 Mar 1;215(5):757-763. doi: 10.1093/infdis/jiw639.
Effectiveness of human papillomavirus (HPV) vaccines in the context of both guidelines, which recommend vaccination at 14 years and modest vaccine coverage, is poorly documented.
Residual specimens from females aged <25 years undergoing chlamydia testing were collected, together with demographic, sexual behavior, and vaccine status data. Human pappilomavirus genotypes were determined using the PapilloCheck test system. We compared vaccine type (VT; types 6, 11, 16, 18) prevalence according to vaccination status and identified factors associated with VT prevalence.
Of 3736 eligible samples, 822 were from vaccinated women according to immunization record, 1021 from women self-reporting vaccination, and 1893 from unvaccinated women. Adjusted vaccine effectiveness for confirmed vaccinated compared with unvaccinated women was 95.93% (95% confidence interval [CI] = 90.22-98.32) against VT HPV and 38.37% (95% CI = 12.68-56.51) against cross-reactive genotypes (HPV 31, 33, 45), respectively. Vaccine type HPV prevalence was significantly lower (0.61%) among confirmed-vaccinated women than among those who self-reported vaccination or unvaccinated women (1.76% and 15.0%, respectively). Factors associated with prevalent VT in multivariable analysis were vaccine status, positive Chlamydia trachomatis and ≥4 partners in the preceding year.
Our study demonstrates evidence of high effectiveness of HPV prophylactic vaccines at an individual level, supporting that wider implementation will help to reduce cervical cancer and precursors incidence.
人乳头瘤病毒(HPV)疫苗在两种指南背景下的有效性记录不足,这两种指南都建议在14岁时接种疫苗且疫苗覆盖率适中。
收集了年龄小于25岁接受衣原体检测的女性的剩余样本,以及人口统计学、性行为和疫苗接种状况数据。使用PapilloCheck检测系统确定人乳头瘤病毒基因型。我们根据疫苗接种状况比较了疫苗类型(VT;6、11、16、18型)的流行率,并确定了与VT流行率相关的因素。
在3736份合格样本中,根据免疫记录,822份来自接种疫苗的女性,1021份来自自我报告接种疫苗的女性,1893份来自未接种疫苗的女性。与未接种疫苗的女性相比,确诊接种疫苗的女性针对VT型HPV的调整后疫苗效力为95.93%(95%置信区间[CI]=90.22-98.32),针对交叉反应基因型(HPV 31、33、45)的调整后疫苗效力为38.37%(95%CI=12.68-56.51)。确诊接种疫苗的女性中疫苗类型HPV的流行率(0.61%)显著低于自我报告接种疫苗的女性或未接种疫苗的女性(分别为1.76%和15.0%)。多变量分析中与流行的VT相关的因素是疫苗接种状况、沙眼衣原体阳性以及前一年有≥4个性伴侣。
我们的研究证明了HPV预防性疫苗在个体水平上具有高效力的证据,支持更广泛的实施将有助于降低宫颈癌及其癌前病变的发病率。