Evidence map›Paper›PMID 27256157›Full record

ArticleThe Journal of infectious diseases2016

Cervical Infection With Vaccine-Associated Human Papillomavirus (HPV) Genotypes as a Predictor of Acquisition and Clearance of Other HPV Infections.

Joseph E Tota, Agnihotram V Ramanakumar, Luisa L Villa, Harriet Richardson, Ann N Burchell, François Coutlée, Eduardo L Franco

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. HPV Type Replacement After HPV Vaccination.Current topics in microbiology and immunology · 2026
    Review
  4. Article
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  6. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Joseph E TotaDivision of Cancer Epidemiology, Department of Oncology Department of Epidemiology, Biostatistics, and Occupational Health, McGill University Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
Agnihotram V RamanakumarDivision of Cancer Epidemiology, Department of Oncology.
Luisa L VillaDepartment of Radiology and Oncology, School of Medicine, Universidade de São Paulo, Brazil.
Harriet RichardsonDepartment of Community Health and Epidemiology, Queens University, Kingston.
Ann N BurchellDivision of Cancer Epidemiology, Department of Oncology Department of Family and Community Medicine, St. Michael's Hospital Centre for Research on Inner City Health, Li Ka Shing Knowledge Institute, Toronto, Canada.
François CoutléeDépartement de Microbiologie et Infectiologie, Université de Montréal.
Eduardo L FrancoDivision of Cancer Epidemiology, Department of Oncology Department of Epidemiology, Biostatistics, and Occupational Health, McGill University.

Funding

MOLECULAR EPIDEMIOLOGY OF PERSISTENT HPV INFECTIONR01CA070269 · NCI · MCGILL UNIVERSITY · PI FRANCO, EDUARDO L. · 1996 to 2003
$793k
HITCH: A Study of HPV Transmission in Young CouplesR01AI073889 · NIAID · MCGILL UNIVERSITY · PI FRANCO, EDUARDO L. · 2010 to 2013
$419k
CIHR CRN83320CIHR MA13647CIHR MOP49396CIHR MOP53111CIHR MOP68893NCI NIH HHS R01 CA070269NIAID NIH HHS R01 AI073889
6 · The paper itself

Abstract

backgroundRecent birth cohorts vaccinated against human papillomavirus (HPV) may be protected against up to 4 genotypes (HPV-6, -11, -16, and -18). If natural competition exists between these and other HPV types, then the prevalence of other types may increase after vaccination.

methodsCohort information from 3 studies was used to compare acquisition and clearance of 30 different HPV types (individually and grouped by species), according to infection status with vaccine-targeted types at baseline and the time of the index infection, respectively. Hazard ratios (HRs) were adjusted for predictors of multiple-type infection.

resultsAmong 3200 females across all studies, 857 were infected with HPV at baseline, and 994 acquired new infections during follow-up. Females infected with HPV-16 were at higher risk of acquiring other α-9 HPV types (HR, 1.9; 95% confidence interval [CI], 1.2-3.0) but at similar risk of clearing existing α-9 HPV infections (HR, 0.9; 95% CI, .7-1.3). Females infected with vaccine-targeted types were generally at higher risk of acquiring additional types (HRs, > 1.0) and at equal risk of clearing existing infections. Accounting for multiple comparisons, none of the HRs of < 1.0 or >1.0 were statistically significant in our analyses of acquisition or clearance.

conclusionsVaccine-targeted HPV types do not appear to compete with other types, suggesting that HPV type replacement is unlikely to occur.

Indexed as

GenotypeAdolescentAdultCohort StudiesFemaleFollow-Up StudiesHumansMiddle AgedPapillomaviridaePapillomavirus InfectionsPapillomavirus VaccinesPrevalenceYoung AdultPapillomavirus Vaccinesfemaleshuman papillomavirustype competitiontype replacementvaccination

Identifiers

PMID27256157
PMCPMC4978368

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.