Evidence map›Paper›PMID 31617568›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2020

Immunogenicity of 2 and 3 Doses of the Quadrivalent Human Papillomavirus Vaccine up to 120 Months Postvaccination: Follow-up of a Randomized Clinical Trial.

Robine Donken, Simon R M Dobson, Kim D Marty, Darrel Cook, Chantal Sauvageau, Vladimir Gilca, Marc Dionne, Shelly McNeil, Mel Krajden, Deborah Money and 9 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 12% of its field
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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 43 citations in OpenAlex.

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  17. Efficacy, effectiveness and immunogenicity of reduced HPV vaccination schedules: A review of available evidence.Canada communicable disease report = Releve des maladies transmissibles au Canada · 2024
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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

19 authors at 8 institutions in 1 country.

Robine DonkenVaccine Evaluation Center, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Simon R M DobsonVaccine Evaluation Center, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Kim D MartyVaccine Evaluation Center, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Darrel CookPublic Health Laboratory, BC Centre for Disease Control, Vancouver, British Columbia, Canada.
Chantal SauvageauInstitut National de Sante Publique du Quebec, Quebec, Canada.
Vladimir GilcaInstitut National de Sante Publique du Quebec, Quebec, Canada.
Marc DionneDepartment of Social and Preventive Medicine, Laval University, Quebec, Canada.
Shelly McNeilCanadian Center for Vaccinology, IWK Health Centre and Nova Scotia Health Authority, Dalhousie University, Nova Scotia, Canada.
Mel KrajdenFaculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Deborah MoneyWomen's Health Research Institute, BC Women's Hospital and Health Service, Vancouver, British Columbia, Canada.
James KellnerAlberta Children's Hospital Infectious Diseases Epidemiology & Vaccine Evaluation Team, Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.
David W ScheifeleVaccine Evaluation Center, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Tobias KollmannVaccine Evaluation Center, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Julie A BettingerVaccine Evaluation Center, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Shuzhen LiuVaccine Evaluation Center, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Joel SingerFaculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Monika NausFaculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Manish SadaranganiVaccine Evaluation Center, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Gina S OgilvieWomen's Health Research Institute, BC Women's Hospital and Health Service, Vancouver, British Columbia, Canada.
University of British Columbia · CABC Children's Hospital · CABC Centre for Disease Control · CAUniversité Laval · CAAlberta Children's Hospital · CAInstitut National de Santé Publique du Québec · CANova Scotia Health Authority · CAWomen's Health Research Institute · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral countries have implemented a 2-dose (2D) human papillomavirus (HPV) vaccination schedule for adolescents based on immunobridging studies. We compared immunogenicity of 2D vs 3-dose (3D) schedules of the quadrivalent vaccine (4vHPV) up to 10 years after the first dose.

methodsGirls aged 9-13 years were randomized to receive 2D or 3D and were compared with women aged 16-26 receiving 3D at day 1 and months 7, 24, and 120 after the first dose. Antibody levels for HPV6/11/16/18 were evaluated using the competitive Luminex immunoassay (cLIA) and total immunoglobulin G assay. Geometric mean titers (GMTs) and seropositivity rates were compared between the different groups at different time points. Noninferiority of GMT ratios was defined as the lower bound of the 2-sided 95% confidence interval (CI) being greater than 0.5. Kinetics of antibody titers over time among study groups were examined.

resultsAt 120 months, data from 35 2D girls, 38 3D girls, and 30 3D women were used for analyses. cLIA seropositivity rates were above 95% for all HPV vaccine types and all schedules, except HPV18, with the lowest seropositivity observed among 3D women (60.0%; 95% CI, 40.6%-77.3%). GMT ratios (cLIA) for both 2D and 3D girls were noninferior to 3 doses in women for HPV6/11/16/18. Trends were comparable between assays.

conclusionsGMTs for HPV6/11/16/18 after 2D or 3D of 4vHPV in girls were noninferior to 3D in adult women up to 120 months postvaccination. This study demonstrates long-term immunogenicity of the 2D HPV vaccine schedule.

Indexed as

Papillomavirus InfectionsPapillomavirus VaccinesAdolescentAdultAntibodies, ViralChildFemaleFollow-Up StudiesHuman Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18HumansImmunization ScheduleImmunogenicity, VaccineYoung AdultAntibodies, ViralHuman Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18Papillomavirus Vaccineshuman papillomavirus vaccineimmunization scheduleimmunogenicitypapillomavirus infections

Identifiers

PMID31617568
PMCPMC7428395
OpenAlexW2980648130

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.