Evidence map›Paper›PMID 30715452›Full record

Trial reportThe Journal of infectious diseases2019

Long-term Cross-reactivity Against Nonvaccine Human Papillomavirus Types 31 and 45 After 2- or 3-Dose Schedules of the AS04-Adjuvanted Human HPV-16/18 Vaccine.

Nicolas Folschweiller, Ulrich Behre, Marc Dionne, Paolo Durando, Susanna Esposito, Linda Ferguson, Murdo Ferguson, Peter Hillemanns, Shelly A McNeil, Klaus Peters and 9 more

2 registry-linked trialsOpen access · hybridAbstract readClinical Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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.

NCT00541970 phase1completednot on this map

Evaluation of the Safety and Immunogenicity of GSK Biologicals' HPV Vaccine 580299 When Administered in Healthy Females Aged 9 - 25 Years Using an Alternative Schedule and an Alternative Dosing as Compared to the Standard Schedule and Dosing

TypeinterventionalSponsorGlaxoSmithKlineRan2007 to 2013Enrolled961ConditionsInfections, PapillomavirusArmsCervarix, Placebo
NCT01381575 phase3completednot on this map

Immunogenicity and Safety Study of GlaxoSmithKline Biologicals' HPV-16/18 L1 AS04 Vaccine When Administered According to Alternative 2-dose Schedules in 9 - 14 Year Old Females

TypeinterventionalSponsorGlaxoSmithKlineRan2011 to 2014Enrolled1,447ConditionsInfections, PapillomavirusArmsGSK Biologicals' HPV vaccine 580299
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Immune Responses to Human Papillomavirus After Infection and Vaccination.Current topics in microbiology and immunology · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
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 11 institutions in 7 countries.

Nicolas FolschweillerGSK, Wavre, Belgium.
Ulrich Behre
Marc DionneCentre Hospitalier Universitaire, Québec.
Paolo DurandoDepartment of Health Sciences, University of Genoa.
Susanna EspositoPediatric Clinic, Department of Surgical and Biomedical Sciences, Università degli Studi di Perugia, Perugia, Italy.
Linda FergusonColchester Research Group, Truro.
Murdo FergusonColchester Research Group, Truro.
Peter HillemannsMedizinischeHochschule Hannover; Hannover.
Shelly A McNeilCanadian Center for Vaccinology, IWK Health Centre and Nova Scotia Health Authority, Dalhousie University, Halifax.
Klaus Peters
Brian RamjattanFirst Line Medical Services, St. John's, Canada.
Tino F SchwarzInstitute of Laboratory Medicine and Vaccination Centre, Klinikum Würzburg Mitte, Standort Juliusspital, Würzburg, Germany.
Khuanchai SupparatpinyoChiang Mai University, Thailand.
Pemmaraju V SuryakirianGSK, Bangalore, India.
Michel JanssensGSK, Wavre, Belgium.
Philippe MorisGSK, Wavre, Belgium.
Annabelle DecreuxGSK, Wavre, Belgium.
Sylviane PonceletGSK, Wavre, Belgium.
Frank StruyfGSK, Wavre, Belgium.
GlaxoSmithKline (Belgium) · BECentre hospitalier universitaire de Québec · CAChiang Mai University · THDalhousie University · CAGlaxoSmithKline (India) · INHealth First · USKlinikum Würzburg Mitte · DEMedizinische Hochschule Hannover · DEOspedale Policlinico San Martino · ITUniversity of Applied Sciences Kehl · DEUniversity of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This analysis focused on long-term cross-reactive immunogenicity against nonvaccine human papillomavirus (HPV) types 31 and 45 following 2 doses of AS04-adjuvanted HPV-16/18 vaccine in girls aged 9-14 years or following 3 doses in women aged 15-25 years, for up to 3 years (HPV-070 study) and up to 5 years (HPV-048 study) after the first vaccination. Both schedules elicited antibodies against HPV-31 and HPV-45 up to 5 years after first dose. The antibody concentration was similar in young girls as compared to women. Specific CD4+ T-cell and B-cell responses to HPV-31 and HPV-45 at month 36 were similar across groups. Clinical trials registration: NCT01381575 and NCT00541970.

Indexed as

Adjuvants, ImmunologicAdolescentAdultAntibodies, ViralB-LymphocytesCD4-Positive T-LymphocytesChildCross ReactionsFemaleHumansImmunization SchedulePapillomaviridaePapillomavirus InfectionsPapillomavirus VaccinesVaccinationYoung AdultAdjuvants, ImmunologicAntibodies, ViralPapillomavirus VaccinesAS04-HPV-16/18 vaccinecross-reactivityHPV-31HPV-45immunogenicitynonvaccine types

Identifiers

PMID30715452
PMCPMC6500548
OpenAlexW2914712469

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.