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澳大利亚女性 HPV 疫苗接种计划后异性恋男性中四价疫苗针对的人乳头瘤病毒基因型:一项回顾性观察研究。

Quadrivalent vaccine-targeted human papillomavirus genotypes in heterosexual men after the Australian female human papillomavirus vaccination programme: a retrospective observational study.

机构信息

Melbourne Sexual Health Centre, Alfred Health, Melbourne, VIC, Australia; Central Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, VIC, Australia.

Murdoch Childrens Research Institute, Parkville, VIC, Australia; Department of Microbiology and Infectious Diseases, The Royal Women's Hospital, Parkville, VIC, Australia.

出版信息

Lancet Infect Dis. 2017 Jan;17(1):68-77. doi: 10.1016/S1473-3099(16)30116-5. Epub 2016 Jun 6.

Abstract

BACKGROUND

Australia introduced a national quadrivalent human papillomavirus (4vHPV) vaccination programme for girls and young women in April, 2007. The HPV genotypes targeted by the female vaccine could also affect the protection afforded to heterosexual men. We examined the prevalence of 4vHPV targeted vaccine genotypes and the nine-valent HPV (9vHPV)-targeted vaccines genotypes among sexually active, predominantly unvaccinated heterosexual men from 2004 to 2015.

METHODS

We did a retrospective, observational study of urine and urethral swab specimens from heterosexual men aged 25 years or younger attending the Melbourne Sexual Health Centre between July 1, 2004, and June 30, 2015, who tested positive for Chlamydia trachomatis. We extracted HPV DNA and used the PapType HPV assay to detect 14 high-risk HPV genotypes (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68) and two low-risk genotypes (6 and 11). We calculated the prevalence of any HPV genotype, genotypes 6 or 11, genotypes 16 or 18, genotypes in the 4vHPV group (6, 11, 16, or 18), five additional genotypes in the 9vHPV group (31, 33, 45, 52, or 58), and non-vaccine-targeted genotypes (31, 33, 35, 39, 45, 51, 56, 58, 59, 66, or 68).

FINDINGS

We obtained data between July 1, 2004, and June 30, 2015, and did the data analysis in December, 2015. Of 1764 specimens obtained, we included 1466 in our final analysis (the others were excluded because they had indeterminate results or were duplicates). The prevalence of any HPV genotype and genotypes 31, 33, 45, 52, and 58 did not change from 2004-05 to 2014-15, but we noted reductions in genotypes 6 and 11 (from 12% [95% CI 6-21%], to 3% [1-7%], p=0·008), 16 and 18 (from 13% [95% CI 7-22%] to 3% [1-6%], p<0·0001), and 4vHPV-targeted genotypes (from 22% [95% CI 14-33%] to 6% [3-10%], p<0·0001). Prevalence of non-vaccine-targeted genotypes increased from 16% [95% CI 9-26%] to 22% [17-29%], p<0·0001). In Australian-born men, 4vHPV-targeted genotype prevalence decreased from 11 of 55 [20%, 95% CI 10-33%] to two of 74 [3%, 0-11%], p<0·0001); an even greater decline occurred in Australian-born men aged 21 years or younger (from four of 13 [31%, 95% CI 9-61%] to none of 25; p<0·0001). Genotypes 16 and 18 decreased (adjusted prevalence ratio [PR] 0·32, 95% CI 0·14-0·74; p=0·008) but not genotypes 6 and 11 (adjusted PR 0·50, 0·16-1·56; p=0·234) in the postvaccination period among men who had arrived in Australia within 2 years from countries with a bivalent vaccine (2vHPV) programme (England, Scotland, Wales, Cook Islands, Northern Ireland, or the Netherlands), compared with the prevaccination period. No change was noted in 4vHPV genotypes in men born overseas in other countries.

INTERPRETATION

The marked reduction in prevalence of 4vHPV genotypes among mainly unvaccinated Australian-born men suggests herd protection has occurred from the female vaccination programme. Additionally, the decline in genotypes 16 and 18, but not genotypes 6 and 11, among overseas-born men predominantly from countries with a 2vHPV vaccine programme suggests that these men received benefits from herd protection for genotypes 16 and 18 from their vaccinated female partners in their own countries. These reductions could translate to reductions in HPV-related malignant conditions in men, even in countries with female-only vaccination programmes.

FUNDING

The Australian National Health and Medical Research Council Program.

摘要

背景

澳大利亚于 2007 年 4 月为女孩和年轻女性推出了一种四价人乳头瘤病毒(4vHPV)疫苗接种计划。女性疫苗针对的 HPV 基因型也可能影响对异性恋男性的保护。我们检测了在性活跃、主要未接种的异性恋男性中,2004 年至 2015 年期间,4vHPV 疫苗针对的疫苗基因型和九价 HPV(9vHPV)疫苗针对的疫苗基因型的流行率。

方法

我们对 2004 年 7 月 1 日至 2015 年 6 月 30 日期间在墨尔本性健康中心就诊的 25 岁或以下、沙眼衣原体检测阳性的异性恋男性的尿液和尿道拭子标本进行了回顾性、观察性研究。我们提取了 HPV DNA,并使用 PapType HPV 检测方法检测了 14 种高危 HPV 基因型(16、18、31、33、35、39、45、51、52、56、58、59、66 和 68)和两种低危基因型(6 和 11)。我们计算了任何 HPV 基因型、6 或 11 基因型、16 或 18 基因型、4vHPV 组(6、11、16 或 18)中的五种额外基因型、9vHPV 组(31、33、45、52 或 58)中的五种额外基因型以及非疫苗针对的基因型(31、33、35、39、45、51、56、58、59、66 或 68)的流行率。

结果

我们于 2004 年 7 月 1 日获得数据,并于 2015 年 12 月进行数据分析。在 1764 个标本中,我们最终分析了 1466 个标本(其余标本由于结果不确定或为重复标本而被排除)。任何 HPV 基因型以及 31、33、45、52 和 58 型的流行率从 2004-05 年到 2014-15 年没有变化,但我们注意到 6 和 11 型(从 12%[95%CI 6-21%]降至 3%[1-7%],p=0.008)、16 和 18 型(从 13%[95%CI 7-22%]降至 3%[1-6%],p<0.0001)和 4vHPV 靶向基因型(从 22%[95%CI 14-33%]降至 6%[3-10%],p<0.0001)的流行率有所降低。非疫苗针对的基因型的流行率从 16%[95%CI 9-26%]增加到 22%[17-29%],p<0.0001)。在澳大利亚出生的男性中,4vHPV 靶向基因型的流行率从 55 例中的 11 例[20%,95%CI 10-33%]降至 74 例中的 2 例[3%,0-11%],p<0.0001);在 21 岁或以下的澳大利亚出生男性中,这一降幅更大(从 13 例中的 4 例[31%,95%CI 9-61%]降至 25 例中无 1 例;p<0.0001)。在最近接种疫苗的人群中,16 型和 18 型的流行率下降(调整后患病率比[PR]0.32,95%CI 0.14-0.74;p=0.008),但 6 型和 11 型的流行率没有下降(调整后 PR 0.50,0.16-1.56;p=0.234),而在最近接种疫苗的人群中,澳大利亚境内在最近两年内来自有双价疫苗(2vHPV)计划的国家(英格兰、苏格兰、威尔士、库克群岛、北爱尔兰或荷兰)的男性。在其他国家出生的海外出生男性中,4vHPV 基因型没有变化。

结论

主要未接种的澳大利亚出生男性中 4vHPV 基因型的流行率显著降低,表明女性疫苗接种计划已产生群体保护作用。此外,海外出生的男性中,16 型和 18 型的流行率下降,但 6 型和 11 型的流行率没有下降,这表明这些男性从其在本国接种疫苗的女性伴侣那里获得了针对 16 型和 18 型的群体保护作用。这些减少可能转化为男性 HPV 相关恶性疾病的减少,即使在只有女性接种疫苗的国家也是如此。

资金来源

澳大利亚国家卫生和医学研究理事会计划。

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