Velentzis Louiza S, Sitas Freddy, O'Connell Dianne L, Darlington-Brown Jessica, Egger Sam, Sinha Rohit, Banks Emily, Frazer Ian H, Canfell Karen
Cancer Research Division, Cancer Council NSW, King's Cross, NSW, 1340, Australia.
Present address: Lowy Cancer Research Centre, Prince of Wales Clinical School, University of New South Wales, NSW Sydney, 2052, NSW, Australia.
BMC Infect Dis. 2014 Dec 21;14:3861. doi: 10.1186/s12879-014-0676-z.
Australia commenced human papillomavirus (HPV) vaccination in 2007, with a two-year catch-up to the age of 26; catch-up cohorts are thus now entering their thirties. Plans for monitoring vaccine impact involve pre- and post-vaccination assessment of cervical HPV DNA in the general population and in high grade abnormalities. Although HPV serology is less sensitive than DNA genotyping, it assesses lifetime exposure and may be easier to measure in the general population. However, benchmark pre-vaccination seroprevalence of vaccine-included types in unvaccinated women with high grade abnormalities has not previously been reported.
We assessed seroprevalence for HPV16/18 from a population-based sample of 3,729 women with normal cytology and 971 women with confirmed high grade abnormalities (CIN2/3), aged 30-64 years, unvaccinated, and recruited in New South Wales in 2006-2010. We examined the variation in HPV16/18 seropositivity by age and in relation to a range of reproductive and behavioural characteristics in the subgroup of normal cytology women with no recent history of high grade cervical disease.
The HPV 16, 18 and combined seroprevalence was 19%, 7% and 24% among women with normal cytology, and 39%, 13% and 44% among women with CIN2/3, respectively. For both groups, HPV16/18 seroprevalence was highest at age 30-39 years and decreased with age. In multivariable analysis for women with normal cytology, HPV16 and HPV18 seropositivity were each associated with the number of lifetime sexual partners (p-trend <0.001 and 0.052, respectively) and for HPV16 this was also associated with age (p-trend <0.001) and prior diagnosis of Chlamydia (adjusted OR 1.89, 95% CI 1.27-2.80).
The findings of this study inform pre-vaccination estimates of HPV seropositivity in women with normal cytology and women with high grade abnormalities. Almost a quarter of unvaccinated women aged over 30 years with normal cytology, and more than 40% of those with CIN2/3, had seroconverted to HPV 16 or 18. These findings provide a potential additional benchmark for assessing the effects of HPV vaccination.
澳大利亚于2007年开始接种人乳头瘤病毒(HPV)疫苗,对26岁及以下人群进行了为期两年的补种;因此,补种队列现在已步入三十多岁。监测疫苗影响的计划包括对普通人群和高级别异常人群进行接种前和接种后宫颈HPV DNA评估。虽然HPV血清学检测的敏感性低于DNA基因分型,但它可以评估终生暴露情况,并且在普通人群中可能更容易检测。然而,此前尚未报道未接种疫苗的高级别异常女性中疫苗所含型别的接种前血清阳性率基准。
我们评估了2006年至2010年在新南威尔士州招募的3729名细胞学正常、971名确诊为高级别异常(CIN2/3)、年龄在30至64岁之间且未接种疫苗的女性基于人群样本中的HPV16/18血清阳性率。我们研究了HPV16/18血清阳性率在年龄方面的差异,以及在近期无高级别宫颈疾病史的细胞学正常女性亚组中与一系列生殖和行为特征的关系。
细胞学正常的女性中,HPV 16、18及联合血清阳性率分别为19%、7%和24%;CIN2/3的女性中分别为39%、13%和44%。两组中,HPV16/18血清阳性率在30至39岁时最高,并随年龄增长而下降。在对细胞学正常女性的多变量分析中,HPV16和HPV18血清阳性率分别与终生性伴侣数量相关(p趋势分别<0.001和0.052),对于HPV16,这也与年龄相关(p趋势<0.001)以及既往衣原体诊断相关(校正OR 1.89,95%CI 1.27至2.80)。
本研究结果为细胞学正常女性和高级别异常女性的HPV血清阳性率接种前估计提供了参考。近四分之一的30岁以上未接种疫苗且细胞学正常的女性,以及超过40%的CIN2/3女性,已血清转化为HPV 16或18。这些发现为评估HPV疫苗接种效果提供了一个潜在的额外基准。