Evidence map›Paper›PMID 29306506›Full record

ArticleVaccine2018

Antibody responses among adolescent females receiving two or three quadrivalent human papillomavirus vaccine doses at standard and prolonged intervals.

Lea E Widdice, Elizabeth R Unger, Gitika Panicker, Rebecca Hoagland, S Todd Callahan, Lisa A Jackson, Andrea A Berry, Karen Kotloff, Sharon E Frey, Christopher J Harrison and 5 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Vaccine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00524745 (Comparison of the Immunogenicity and Reactogenicity of Alternative Schedules of Gardasil Vaccine to Prevent HPV Infection), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 22% 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.

NCT00524745 nacompletednot on this map

Comparison of the Immunogenicity and Reactogenicity of Alternative Schedules of Gardasil Vaccine to Prevent HPV Infection

TypeinterventionalSponsorPATHRan2007 to 2010Enrolled903ConditionsDose Schedule StudyArmsBiological: quadrivalent human papillomavirus (types 6, 11, 16, 18) recombinant vaccine
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Immunogenicity of anHuman vaccines & immunotherapeutics · 2020
    Trial
  2. Trial
  3. Historical Advances in Clinical Trial Design and Expanding Representation as the New Frontier for Innovation.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Article
  4. Vaccine and Treatment Evaluation Units: A Historical Perspective.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Article
  5. 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

15 authors at 10 institutions in 1 country.

Lea E WiddiceDivision of Adolescent and Transition Medicine, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 4000, Cincinnati, OH 45229, United States. Electronic address: lea.widdice@cchmc.org.
Elizabeth R UngerDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30329, United States. Electronic address: eru0@cdc.gov.
Gitika PanickerDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30329, United States. Electronic address: dhv1@cdc.gov.
Rebecca HoaglandCota Enterprises, Inc., 16570 46th Street, McLouth, KS 66054, United States. Electronic address: rhoagland@cotaenterprises.com.
S Todd CallahanDivision of Adolescent and Young Adult Health, Vanderbilt University, 719 Thompson Lane, Suite 36300, Nashville, TN 37204, United States. Electronic address: todd.callahan@vanderbilt.edu.
Lisa A JacksonGroup Health Research Institute, 1730 Minor Avenue, Suite 1600, Seattle, WA 98101, United States. Electronic address: jackson.l@ghc.org.
Andrea A BerryDivision of Infectious Disease and Tropical Pediatrics, Center for Vaccine Development, Institute for Global Health, University of Maryland School of Medicine, 685 W. Baltimore Street, HSF 480, Baltimore, MD 21201, United States. Electronic address: aberry@medicine.umaryland.edu.
Karen KotloffDivision of Infectious Disease and Tropical Pediatrics, Center for Vaccine Development, Institute for Global Health, University of Maryland School of Medicine, 685 W. Baltimore Street, HSF 480, Baltimore, MD 21201, United States. Electronic address: kkotloff@medicine.umaryland.edu.
Sharon E FreyDivision of Infectious Diseases, Allergy and Immunology, Saint Louis University, 1100 S. Grand Boulevard, St. Louis, MO 63104, United States. Electronic address: freyse@slu.edu.
Christopher J HarrisonDivision of Pediatric Infectious Diseases, Children's Mercy - Kansas City, 2401 Gillham Road, MO 64108, United States. Electronic address: cjharrison@cmh.edu.
Barbara A PahudDivision of Pediatric Infectious Diseases, Children's Mercy - Kansas City, 2401 Gillham Road, MO 64108, United States. Electronic address: bapahud@cmh.edu.
Kathryn M EdwardsDivision of Pediatric Infectious Diseases, Vanderbilt Vaccine Research Program, D7227 Medical Center North, Vanderbilt University School of Medicine, Nashville, TN 37232, United States. Electronic address: kathryn.edwards@vanderbilt.edu.
Mark J MulliganThe Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, 500 Irvin Court, Suite 200, Decatur, GA 30030, United States. Electronic address: mark.mulligan@emory.edu.
Jon SudmanKaiser Permanente Georgia, 200 Crescent Centre Parkway, Lower Level, Tucker, GA 30084, United States. Electronic address: jon.sudman@kp.org.
David I BernsteinDivision of Infectious Diseases, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 6014, Cincinnati, OH 45229, United States. Electronic address: david.bernstein@cchmc.org.
Centers for Disease Control and Prevention · USCincinnati Children's Hospital Medical Center · USMercy Hospital · USUniversity of Maryland, Baltimore · USHOPE Clinic · USKaiser Permanente · USKaiser Permanente Washington Health Research Institute · USSaint Louis University · USVanderbilt University · USVanderbilt University Medical Center · US

Funding

Protein microarray antibody responses to P. falciparum in a human challenge modelK23AI125720 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI BERRY, ANDREA · 2017 to 2021
$915k
NIAID NIH HHS HHSN272200800003CNIAID NIH HHS HHSN272200800004CNIAID NIH HHS HHSN272200800005CNIAID NIH HHS HHSN272200800006CNIAID NIH HHS HHSN272200800007CNIAID NIH HHS HHSN272200800013CNIAID NIH HHS HHSN272201300018INIAID NIH HHS HHSN272201300022INIAID NIH HHS N01 AI080006
6 · The paper itself

Abstract

backgroundThe originally recommended dosing schedule, 0, 2, 6 months, for the 3-dose quadrivalent human papillomavirus vaccine (4vHPV) was often not followed, resulting in longer than recommended intervals between doses and interest in the effect of prolonged intervals. Recent two-dose recommendations require investigations into the effect of delaying dose 2.

methodsThis multi-site, prospective study enrolled healthy 9-17 year old girls (n = 1321) on the day of or within 28 days following a third dose of 4vHPV vaccination. Antibody titers to 4vHPV types were measured at one and six months post-dose 3 from all participants and post-dose 2 from participants who were on time for dose 3. To compare antibody responses, participants were categorized into groups: second and third doses on time (control group); on-time dose 2, substantially late dose 3 (group 2); substantially late dose 2, on-time dose 3 (group 3); both doses substantially late (group 4). Analyses compared age-adjusted geometric mean titers (GMTs) at one-month and six-months post-dose 3, effect of delaying the second dose, and two versus three doses as well as post-dose 2 GMTs, stratified by age.

resultsCompared to on-time dosing, one-month post-dose 3 GMTs were non-inferior in groups 2, 3, and 4 and were superior in group 2. Six month post-dose 3 GMTs were superior in groups 2, 3, and 4 for each genotype, except HPV 18 in group 3. Age-adjusted post does 2 titers were significantly lower than post-dose 3 titers when dose 2 was on time but were significantly higher when dose 2 was substantially late. Participants ≥15 years old had no difference in post-dose 2 titers compared to <15 year olds when dose 2 was substantially delayed.

conclusionsProlonged intervals between doses do not appear to diminish and may enhance antibody response to 4vHPV. ClinicalTrials.gov (NCT00524745).

Indexed as

Antibody FormationAdolescentAlphapapillomavirusAntibodies, ViralChildFemaleHumansImmunization ScheduleImmunization, SecondaryPapillomavirus InfectionsPapillomavirus VaccinesProspective StudiesSex FactorsTime FactorsVaccinationAntibodies, ViralPapillomavirus VaccinesDosingGeometric mean titersHuman papillomavirusImmunityIntervalVaccine

Identifiers

PMID29306506
PMCPMC6055998
OpenAlexW2781943803

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.