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Reduction in Human Papillomavirus (HPV) Prevalence Among Young Women Following HPV Vaccine Introduction in the United States, National Health and Nutrition Examination Surveys, 2003–2010

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TLDR
Within 4 years of vaccine introduction, the vaccine-type HPV prevalence decreased among females aged 14-19 years despite low vaccine uptake, and the estimated vaccine effectiveness was high.
Abstract
Background. Human papillomavirus (HPV) vaccination was introduced into the routine immunization schedule in the United States in late 2006 for females aged 11 or 12 years with catch-up vaccination recommended for those aged 13-26 years. In 2010 3-dose vaccine coverage was only 32% among 13-17 year-olds. Reduction in the prevalence of HPV types targeted by the quadrivalent vaccine (HPV-6 -11 -16 and -18) will be one of the first measures of vaccine impact. Methods. We analyzed HPV prevalence data from the vaccine era (2007-2010) and the prevaccine era (2003-2006) that were collected during National Health and Nutrition Examination Surveys. HPV prevalence was determined by the Linear Array HPV Assay in cervicovaginal swab samples from females aged 14-59 years; 4150 provided samples in 2003-2006 and 4253 provided samples in 2007-2010. Results. Among females aged 14-19 years the vaccine-type HPV prevalence (HPV-6 -11 -16 or -18) decreased from 11.5% (95% confidence interval [CI] 9.2-14.4) in 2003-2006 to 5.1% (95% CI 3.8-6.6) in 2007-2010 a decline of 56% (95% CI 38-69). Among other age groups the prevalence did not differ significantly between the 2 time periods (P > .05). The vaccine effectiveness of at least 1 dose was 82% (95% CI 53-93). Conclusions. Within 4 years of vaccine introduction the vaccine-type HPV prevalence decreased among females aged 14-19 years despite low vaccine uptake. The estimated vaccine effectiveness was high.

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Systematic literature review of cross-protective effect of HPV vaccines based on data from randomized clinical trials and real-world evidence.

TL;DR: In this paper, a systematic literature review was conducted to establish the duration and magnitude of cross-protection in interventional and observational studies of the bivalent and quadrivalent vaccines against 6-and 12-month persistent infection or genital lesions.
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Vaccins contre les papillomavirus humains (HPV) - Dernières recommandations du Haut conseil de la santé publique, et premiers résultats cliniques et virologiques

TL;DR: Au plan virologique, une diminution de the prevalence of l’infection par les virus dont les genotypes sont compris dans les vaccins a ete rapportee dans plusieurs etudes.
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Differences between vaccinated and unvaccinated women explain increase in non-vaccine-type human papillomavirus in unvaccinated women after vaccine introduction.

TL;DR: The observed increase in non-vaccine-type HPV prevalence in unvaccinated women may be explained by differences between un vaccinated and vaccinated women.
Journal ArticleDOI

Skin and mucosal human papillomavirus seroprevalence in persons with Fanconi Anemia.

TL;DR: It is demonstrated that the unvaccinated participants had serologic evidence of prior skin and mucosal HPV infections and that seroprevalence increased among adults; in self-reported vaccinees, serop revalence of HPV vaccine types was 75 to 96%.
Journal ArticleDOI

A University Health Initiative to Increase Human Papillomavirus Vaccination Rates

TL;DR: A 16-week QI initiative used evidence-based interventions including preventing missed opportunities for vaccination, provision of strong vaccine recommendations, use of patient reminders, and campus-based marketing strategies to increase human papillomavirus vaccination rates.
References
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Journal ArticleDOI

A review of human carcinogens--Part B: biological agents

TL;DR: In this paper, the carcinogenicity of the biological agents classifi ed as "carcinogenic to humans" (Group 1) and to identify additional tumour sites and mechanisms of carcinogenesis (tables 1 and 2).
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Human papillomavirus genotype attribution in invasive cervical cancer: a retrospective cross-sectional worldwide study

Silvia de Sanjosé, +62 more
- 01 Nov 2010 - 
TL;DR: HPV types 16, 18, 31, 33, 35, 45, 52, and 58 should be given priority when the cross-protective effects of current vaccines are assessed, and for formulation of recommendations for the use of second-generation polyvalent HPV vaccines, according to this largest assessment of HPV genotypes to date.
Journal ArticleDOI

Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions

TL;DR: In young women who had not been previously infected with HPV-16 or HPV-18, those in the vaccine group had a significantly lower occurrence of high-grade cervical intraepithelial neoplasia related to HPV- 16 or HPV -18 than did those inThe placebo group.
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