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二价人乳头瘤病毒疫苗在日本人群中的效果:高疫苗型特异性效果和交叉保护证据。

Bivalent Human Papillomavirus Vaccine Effectiveness in a Japanese Population: High Vaccine-Type-Specific Effectiveness and Evidence of Cross-Protection.

机构信息

Department of Obstetrics and Gynecology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Departments of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Suita, Japan.

出版信息

J Infect Dis. 2019 Jan 9;219(3):382-390. doi: 10.1093/infdis/jiy516.

Abstract

BACKGROUND

Proactive recommendations for human papillomavirus (HPV) vaccines in Japan have been suspended for 5 years because of safety concerns. While no scientific evidence exists to substantiate these concerns, one reason given for not reinstating recommendations is the lack of reliable vaccine effectiveness (VE) data in a Japanese population. This study reports the VE of the bivalent HPV vaccine in Japanese women aged 20-22 years.

METHODS

During cervical screening between 2014 and 2016, women had Papanicolaou smears and HPV tests performed and provided data about their sexual history. Estimates of VE for vaccine-targeted HPV type 16 (HPV16) and 18 and cross-protection against other types were calculated.

RESULTS

Overall, 2197 women were tested, and 1814 were included in the analysis. Of these, 1355 (74.6%) were vaccinated, and 1295 (95.5%) completed the 3-dose schedule. In women sexually naive at vaccination, the pooled VEs against HPV16 and 18 and for HPV31, 45, and 52 were 95.5% (P < .01) and 71.9% (P < .01), respectively. When adjusted for number of sex partners and birth year, pooled VEs were 93.9% (P = .01) and 67.7% (P = .01) for HPV16 and 18 and HPV31, 45, and 52, respectively.

CONCLUSIONS

The bivalent HPV vaccine is highly effective against HPV16 and 18. Furthermore, significant cross-protection against HPV31, 45, and 52 was demonstrated and sustained up to 6 years after vaccination. These findings should reassure politicians about the VE of bivalent HPV vaccine in a Japanese population.

摘要

背景

由于安全性问题,日本已暂停对人乳头瘤病毒(HPV)疫苗的主动推荐 5 年。虽然没有科学证据证实这些担忧,但不恢复推荐的原因之一是缺乏日本人群中可靠的疫苗有效性(VE)数据。本研究报告了二价 HPV 疫苗在 20-22 岁日本女性中的 VE。

方法

在 2014 年至 2016 年期间的宫颈筛查期间,对女性进行巴氏涂片和 HPV 检测,并提供有关其性行为史的数据。计算了针对疫苗靶向 HPV 型 16(HPV16)和 18 以及针对其他类型的交叉保护的 VE 估计值。

结果

共有 2197 名女性接受了检测,其中 1814 名女性纳入了分析。其中,1355 名(74.6%)接种了疫苗,1295 名(95.5%)完成了 3 剂接种。在接种疫苗时性经历为零的女性中,针对 HPV16 和 18 以及 HPV31、45 和 52 的总体 VE 分别为 95.5%(P <.01)和 71.9%(P <.01)。调整性伴侣数量和出生年份后,针对 HPV16 和 18 以及 HPV31、45 和 52 的总体 VE 分别为 93.9%(P =.01)和 67.7%(P =.01)。

结论

二价 HPV 疫苗对 HPV16 和 18 具有高度有效性。此外,还证明了针对 HPV31、45 和 52 的显著交叉保护作用,并在接种疫苗后 6 年内持续存在。这些发现应该让政治家们对二价 HPV 疫苗在日本人群中的 VE 感到放心。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fea2/6325350/02a3702327c8/jiy51601.jpg

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