National Institute for Health and Welfare, Oulu, Finland.
Int J Cancer. 2011 Mar 1;128(5):1114-9. doi: 10.1002/ijc.25675. Epub 2010 Nov 28.
To understand likelihood of type replacement after vaccination against the high-risk human papillomavirus (HPV) types, we evaluated competition of the seven most common genital HPV types in a population sample of unvaccinated, fertile-aged Finnish women. First trimester sera from two consecutive pregnancies were retrieved from 3,183 Finnish women (mean age, 23.1 years) of whom 42.3% had antibodies to at least one HPV type (6/11/16/18/31/33/45) at the baseline. Antibody positivity to more than one HPV types by the second pregnancy was common among the baseline HPV seropositives. However, compared to baseline HPV-seronegative women, significantly increased incidence rate ratios (IRRs), indicating an increased risk to seroconvert for another HPV type, were consistently noted only for HPV33 among baseline HPV16 or HPV18 antibody (ab)-positive women: HPV(16ab only) (→) (16&33ab) IRR 2.9 [95% confidence interval (CI) 1.6-5.4] and HPV(18ab only) (→) (18&33ab) IRR 2.5 (95% CI 1.1-6.0), irrespectively of the presence of antibodies to other HPV types at baseline: HPV(16ab) (→) (16&33ab) IRR 3.2 (95% CI 2.0-5.2) and HPV(18ab) (→) (18&33ab) IRR 3.6 (95% CI 2.1-5.9). Our findings suggest a possible competitive advantage for HPV33 over other genital HPV types in the unvaccinated population. HPV33 should be monitored for type replacement after HPV mass vaccination.
为了了解接种高危型人乳头瘤病毒(HPV)疫苗后 HPV 型别替代的可能性,我们评估了在未接种、育龄芬兰女性的人群样本中,7 种最常见的生殖器 HPV 型别的竞争情况。从 3183 名芬兰女性(平均年龄 23.1 岁)的连续两次妊娠的孕早期血清中,我们发现 42.3%的女性(6/11/16/18/31/33/45)在基线时对至少一种 HPV 型别有抗体。在基线时 HPV 血清学阳性的女性中,第二次妊娠时同时存在多种 HPV 型别的抗体阳性是很常见的。然而,与基线时 HPV 血清学阴性的女性相比,HPV16 或 HPV18 抗体阳性的女性中,HPV33 型的 HPV 血清学转化率(seroconversion)显著增加,表明感染另一种 HPV 型别的风险增加:HPV(16ab 仅)(→)(16&33ab)风险比(IRR)为 2.9(95%置信区间 [CI],1.6-5.4),HPV(18ab 仅)(→)(18&33ab)IRR 为 2.5(95%CI,1.1-6.0),而与基线时是否存在其他 HPV 型别的抗体无关:HPV(16ab)(→)(16&33ab)IRR 为 3.2(95%CI,2.0-5.2),HPV(18ab)(→)(18&33ab)IRR 为 3.6(95%CI,2.1-5.9)。我们的研究结果表明,在未接种疫苗的人群中,HPV33 可能比其他生殖器 HPV 型别具有竞争优势。HPV 大规模接种后,应监测 HPV33 型别的替代情况。