Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Communicable Disease Control and Prevention for Stockholm County, Stockholm, Sweden3Department of Medicine, Infectious Disease Unit, Karolinska Institutet, Stockholm, Sweden.
JAMA. 2014 Feb 12;311(6):597-603. doi: 10.1001/jama.2014.95.
Determining vaccine dose-level protection is essential to minimize program costs and increase mass vaccination program feasibility. Currently, a 3-dose vaccination schedule is recommended for both the quadrivalent and bivalent human papillomavirus (HPV) vaccines. Although the primary goal of HPV vaccination programs is to prevent cervical cancer, condyloma related to HPV types 6 and 11 is also prevented with the quadrivalent vaccine and represents the earliest measurable preventable disease outcome for the HPV vaccine.
To examine the association between quadrivalent HPV vaccination and first occurrence of condyloma in relation to vaccine dose in a population-based setting.
DESIGN, SETTING, AND PARTICIPANTS: An open cohort of all females aged 10 to 24 years living in Sweden (n = 1,045,165) was followed up between 2006 and 2010 for HPV vaccination and first occurrence of condyloma using the Swedish nationwide population-based health data registers.
Incidence rate ratios (IRRs) and incidence rate differences (IRDs) of condyloma were estimated using Poisson regression with vaccine dose as a time-dependent exposure, adjusting for attained age and parental education, and stratified on age at first vaccination. To account for prevalent infections, models included a buffer period of delayed case counting.
A total of 20,383 incident cases of condyloma were identified during follow-up, including 322 cases after receipt of at least 1 dose of the vaccine. For individuals aged 10 to 16 years at first vaccination, receipt of 3 doses was associated with an IRR of 0.18 (95% CI, 0.15-0.22) for condyloma, whereas receipt of 2 doses was associated with an IRR of 0.29 (95% CI, 0.21-0.40). One dose was associated with an IRR of 0.31 (95% CI, 0.20-0.49), which corresponds to an IRD of 384 cases (95% CI, 305-464) per 100,000 person-years, compared with no vaccination. The corresponding IRDs for 2 doses were 400 cases (95% CI, 346-454) and for 3 doses, 459 cases (95% CI, 437-482). The number of prevented cases between 3 and 2 doses was 59 (95% CI, 2-117) per 100,000 person-years.
Although maximum reduction in condyloma risk was seen after receipt of 3 doses of quadrivalent HPV vaccine, receipt of 2 vaccine doses was also associated with a considerable reduction in condyloma risk. The implications of these findings for the relationship between number of vaccine doses and cervical cancer risk require further investigation.
确定疫苗剂量水平的保护作用对于降低项目成本和提高大规模疫苗接种项目的可行性至关重要。目前,建议对四价和二价人乳头瘤病毒(HPV)疫苗均采用 3 剂疫苗接种方案。尽管 HPV 疫苗接种项目的主要目标是预防宫颈癌,但四价 HPV 疫苗还可预防与 HPV 型 6 和 11 相关的湿疣,这也是 HPV 疫苗可预防的最早可衡量的疾病结果。
在人群中研究四价 HPV 疫苗接种与剂量相关的湿疣首次发病的关联。
设计、地点和参与者:在瑞典,对年龄在 10 至 24 岁之间的所有女性(n=1045165 人)进行了一项开放性队列研究,在 2006 年至 2010 年期间,通过瑞典全国人群健康数据登记系统,对 HPV 疫苗接种和湿疣首次发病情况进行随访。
使用泊松回归估计湿疣的发病率比(IRR)和发病率差异(IRD),疫苗剂量作为时间依赖性暴露因素进行调整,并按首次接种年龄分层。为了考虑到已有的感染,模型包括了一个延迟病例计数的缓冲期。
在随访期间共发现 20383 例湿疣病例,其中 322 例在至少接种 1 剂疫苗后发病。对于首次接种年龄为 10 至 16 岁的个体,接种 3 剂疫苗与湿疣的 IRR 为 0.18(95%CI,0.15-0.22),而接种 2 剂疫苗与 IRR 为 0.29(95%CI,0.21-0.40)。接种 1 剂疫苗与 IRR 为 0.31(95%CI,0.20-0.49),这相当于每 100000 人年发生 384 例湿疣(95%CI,305-464),与未接种疫苗相比。接种 2 剂疫苗对应的 IRD 为 400 例(95%CI,346-454),接种 3 剂疫苗对应的 IRD 为 459 例(95%CI,437-482)。每 100000 人年可预防的病例数在 3 剂和 2 剂疫苗之间为 59 例(95%CI,2-117)。
虽然四价 HPV 疫苗接种 3 剂可最大程度地降低湿疣发病风险,但接种 2 剂疫苗也与湿疣发病风险的显著降低相关。这些发现对疫苗剂量与宫颈癌风险之间的关系的意义需要进一步研究。