Bhatia Ramya, Kavanagh Kimberley, Cubie Heather Ann, Serrano Itziar, Wennington Holli, Hopkins Mark, Pan Jiafeng, Pollock Kevin G, Palmer Tim J, Cuschieri Kate
HPV Research Group, University of Edinburgh, Edinburgh, United Kingdom.
Department of Mathematics and Statistics, Strathclyde University, Glasgow, United Kingdom.
Int J Cancer. 2016 Jun 15;138(12):2922-31. doi: 10.1002/ijc.30030. Epub 2016 Feb 26.
The management of cervical disease is changing worldwide as a result of HPV vaccination and the increasing use of HPV testing for cervical screening. However, the impact of vaccination on the performance of HPV based screening strategies is unknown. The SHEVa (Scottish HPV Prevalence in Vaccinated women) projects are designed to gain insight into the impact of vaccination on the performance of clinically validated HPV assays. Samples collated from women attending for first cervical smear who had been vaccinated as part of a national "catch-up" programme were tested with three clinically validated HPV assays (2 DNA and 1 RNA). Overall HR-HPV and type specific positivity was assessed in total population and according to underlying cytology and compared to a demographically equivalent group of unvaccinated women. HPV prevalence was significantly lower in vaccinated women and was influenced by assay-type, reducing by 23-25% for the DNA based assays and 32% for the RNA assay (p = 0.0008). All assays showed over 75% reduction of HPV16 and/or 18 (p < 0.0001) whereas the prevalence of non 16/18 HR-HPV was not significantly different in vaccinated vs unvaccinated women. In women with low grade abnormalities, the proportion associated with non 16/18 HR-HPV was significantly higher in vaccinated women (p < 0.0001). Clinically validated HPV assays are affected differentially when applied to vaccinated women, dependent on assay chemistry. The increased proportion of non HPV16/18 infections may have implications for clinical performance, consequently, longitudinal studies linking HPV status to disease outcomes in vaccinated women are warranted.
由于人乳头瘤病毒(HPV)疫苗接种以及HPV检测在宫颈癌筛查中的使用增加,全球范围内宫颈癌的管理正在发生变化。然而,疫苗接种对基于HPV的筛查策略性能的影响尚不清楚。SHEVa(接种疫苗女性中的苏格兰HPV流行率)项目旨在深入了解疫苗接种对经临床验证的HPV检测性能的影响。对参加首次宫颈涂片检查、作为国家“补种”计划一部分接种过疫苗的女性收集的样本,使用三种经临床验证的HPV检测方法(2种DNA检测和1种RNA检测)进行检测。在总人群中,并根据潜在的细胞学情况,评估总体高危型HPV(HR-HPV)和型特异性阳性率,并与人口统计学特征相当的未接种疫苗女性组进行比较。接种疫苗的女性中HPV流行率显著较低,且受检测方法类型的影响,基于DNA的检测方法降低了23%-25%,RNA检测方法降低了32%(p = 0.0008)。所有检测方法均显示HPV16和/或18的流行率降低了75%以上(p < 0.0001),而接种疫苗和未接种疫苗的女性中,非16/18型HR-HPV的流行率没有显著差异。在低度异常的女性中,接种疫苗的女性中与非16/18型HR-HPV相关的比例显著更高(p < 0.0001)。当应用于接种疫苗的女性时,经临床验证的HPV检测方法受到的影响不同,这取决于检测化学方法。非HPV16/18感染比例的增加可能对临床性能有影响,因此,有必要进行纵向研究,将接种疫苗女性的HPV状态与疾病结局联系起来。