Evidence map›Paper›PMID 24999962›Full record

ArticlePloS one2014

Measurement of neutralizing serum antibodies of patients vaccinated with human papillomavirus L1 or L2-based immunogens using furin-cleaved HPV Pseudovirions.

Joshua W Wang, Subhashini Jagu, Chenguang Wang, Henry C Kitchener, Sai Daayana, Peter L Stern, Susana Pang, Patricia M Day, Warner K Huh, Richard B S Roden

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Pseudotyped Virus for Papillomavirus.Advances in experimental medicine and biology · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
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

10 authors at 6 institutions in 2 countries.

Joshua W WangDepartments of Pathology, The Johns Hopkins University, Baltimore, Maryland, United States of America.
Subhashini JaguDepartments of Pathology, The Johns Hopkins University, Baltimore, Maryland, United States of America.
Chenguang WangDepartment of Biostatistics, The Johns Hopkins University, Baltimore, Maryland, United States of America.
Henry C KitchenerWoman's Cancer Centre, St Mary's Hospital, Institute of Cancer Sciences, University of Manchester, Manchester, United Kingdom.
Sai DaayanaWoman's Cancer Centre, St Mary's Hospital, Institute of Cancer Sciences, University of Manchester, Manchester, United Kingdom.
Peter L SternPaterson Building, Institute of Cancer Sciences, University of Manchester, Manchester, United Kingdom.
Susana PangLaboratory of Cellular Oncology, National Cancer Institute, Bethesda, Maryland, United States of America.
Patricia M DayLaboratory of Cellular Oncology, National Cancer Institute, Bethesda, Maryland, United States of America.
Warner K HuhDivision of Gynecologic Oncology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Richard B S RodenDepartments of Pathology, The Johns Hopkins University, Baltimore, Maryland, United States of America; Department of Oncology, The Johns Hopkins University, Baltimore, Maryland, United States of America; Department of Gynecology and Obstetrics, The Johns Hopkins University, Baltimore, Maryland, United States of America.
Johns Hopkins University · USNational Cancer Institute · USCancer Research UK Manchester Institute · GBSt Mary's Hospital · GBUniversity of Alabama at Birmingham · USUniversity of Manchester · GB

Funding

Treatment of HIV- and HIV+ Patients with HPV16+ CIN2/3 Using pNGLV4a-hCRTE6E7L2 DNA vaccine administered intramuscularly via electroporationP50CA098252 · NCI · JOHNS HOPKINS UNIVERSITY · PI Richard Bruce Roden · 2003 to 2026
$53.5M
Mechanisms of Papillomavirus NeutralizationR01CA118790 · NCI · JOHNS HOPKINS UNIVERSITY · PI RODEN, RICHARD BRUCE · 2007 to 2018
$2.9M
A Phase I Study to Evaluate the Safety and Immunogenicity of HPV 16 L2 11-200R01CA133749 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HUH, WARNER KING · 2008 to 2012
$1.4M
Cancer Research UKIntramural NIH HHSNCI NIH HHS CA118790NCI NIH HHS P50 CA098252NCI NIH HHS R01 CA118790NCI NIH HHS R01 CA133749
6 · The paper itself

Abstract

Antibodies specific for neutralizing epitopes in either Human papillomavirus (HPV) capsid protein L1 or L2 can mediate protection from viral challenge and thus their accurate and sensitive measurement at high throughput is likely informative for monitoring response to prophylactic vaccination. Here we compare measurement of L1 and L2-specific neutralizing antibodies in human sera using the standard Pseudovirion-Based Neutralization Assay (L1-PBNA) with the newer Furin-Cleaved Pseudovirion-Based Neutralization Assay (FC-PBNA), a modification of the L1-PBNA intended to improve sensitivity towards L2-specific neutralizing antibodies without compromising assay of L1-specific responses. For detection of L1-specific neutralizing antibodies in human sera, the FC- PBNA and L1-PBNA assays showed similar sensitivity and a high level of correlation using WHO standard sera (n = 2), and sera from patients vaccinated with Gardasil (n = 30) or an experimental human papillomavirus type 16 (HPV16) L1 VLP vaccine (n = 70). The detection of L1-specific cross-neutralizing antibodies in these sera using pseudovirions of types phylogenetically-related to those targeted by the L1 virus-like particle (VLP) vaccines was also consistent between the two assays. However, for sera from patients (n = 17) vaccinated with an L2-based immunogen (TA-CIN), the FC-PBNA was more sensitive than the L1-PBNA in detecting L2-specific neutralizing antibodies. Further, the neutralizing antibody titers measured with the FC-PBNA correlated with those determined with the L2-PBNA, another modification of the L1-PBNA that spacio-temporally separates primary and secondary receptor engagement, as well as the protective titers measured using passive transfer studies in the murine genital-challenge model. In sum, the FC-PBNA provided sensitive measurement for both L1 VLP and L2-specific neutralizing antibody in human sera. Vaccination with TA-CIN elicits weak cross-protective antibody in a subset of patients, suggesting the need for an adjuvant.

Indexed as

VaccinationAntibodies, NeutralizingAntibodies, ViralAntibody SpecificityCapsid ProteinsFurinHuman Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18HumansNeutralization TestsOncogene Proteins, ViralPapillomaviridaePapillomavirus VaccinesProteolysisReference StandardsVirionAntibodies, NeutralizingAntibodies, ViralCapsid ProteinsFurinHPV L1 protein, Human papillomavirusHuman Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18Oncogene Proteins, ViralPapillomavirus Vaccines

Identifiers

PMID24999962
PMCPMC4084990
OpenAlexW2055747158

What OpenQuestion holds

Textmetadata
LicenceCC0
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.