Evidence map›Paper›PMID 24504509›Full record

Trial reportPloS one2014

Vaccine-induced IgG antibodies to V1V2 regions of multiple HIV-1 subtypes correlate with decreased risk of HIV-1 infection.

Susan Zolla-Pazner, Allan deCamp, Peter B Gilbert, Constance Williams, Nicole L Yates, William T Williams, Robert Howington, Youyi Fong, Daryl E Morris, Kelly A Soderberg and 18 more

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00223080 (A Phase III Trial of Aventis Pasteur Live Recombinant ALVAC-HIV), which is not on this map. Cited by 222 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
222citing papers in PubMed, 1 pooled it
19.1field-weighted citation impact, top 1% 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.

NCT00223080 phase3completednot on this map

A Phase III Trial of Aventis Pasteur Live Recombinant ALVAC-HIV (vCP1521) Priming With VaxGen gp120 B/E (AIDSVAX B/E) Boosting in HIV-uninfected Thai Adults

TypeinterventionalSponsorU.S. Army Medical Research and Development CommandRan2003 to 2009Enrolled16,402ConditionsHIV InfectionArmsALVAC-HIV vCP1521 + AIDSVAX, ALVAC Placebo + AIDSVAX Placebo
3 · Its place in the literature

Who cites it

222 citing papers in PubMed, 1 synthesis or guideline pooled it, 270 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Trial
  13. Trial
  14. Trial
  15. Trial
  16. Trial
  17. Trial
  18. Trial
  19. Trial
  20. Trial

162 more citing papers are in PubMed but not listed here.

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

28 authors at 9 institutions in 2 countries.

Susan Zolla-PaznerDepartment of Veterans Affairs New York Harbor Healthcare System, New York, New York, United States of America ; New York University School of Medicine, New York, New York, United States of America.
Allan deCampVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Peter B GilbertVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Constance WilliamsNew York University School of Medicine, New York, New York, United States of America.
Nicole L YatesDuke University, Durham, North Carolina, United States of America.
William T WilliamsDuke University, Durham, North Carolina, United States of America.
Robert HowingtonDuke University, Durham, North Carolina, United States of America.
Youyi FongVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Daryl E MorrisVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Kelly A SoderbergDuke University, Durham, North Carolina, United States of America.
Carmela IrenePublic Health Research Institute, University of Medicine and Dentistry, Newark, New Jersey, United States of America.
Charles ReichmanPublic Health Research Institute, University of Medicine and Dentistry, Newark, New Jersey, United States of America.
Abraham PinterPublic Health Research Institute, University of Medicine and Dentistry, Newark, New Jersey, United States of America.
Robert ParksDuke University, Durham, North Carolina, United States of America.
Punnee PitisuttithumFaculty of Tropical Medicine, Mahidol, Thailand.
Jaranit KaewkungwalFaculty of Tropical Medicine, Mahidol, Thailand.
Supachai Rerks-NgarmMinistry of Public Health, Bangkok, Thailand.
Sorachai NitayaphanArmed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
Charla AndrewsMilitary HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.
Robert J O'ConnellMilitary HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.
Zhi-yong YangVirology Laboratory, Vaccine Research Center, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
Gary J NabelVirology Laboratory, Vaccine Research Center, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
Jerome H KimMilitary HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.
Nelson L MichaelMilitary HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, United States of America.
David C MontefioriDuke University, Durham, North Carolina, United States of America.
Hua-Xin LiaoDuke University, Durham, North Carolina, United States of America.
Barton F HaynesDuke University, Durham, North Carolina, United States of America.
Georgia D TomarasDuke University, Durham, North Carolina, United States of America.
Duke University · USFred Hutch Cancer Center · USWalter Reed Army Institute of Research · USMahidol Oxford Tropical Medicine Research Unit · THNational Institute of Allergy and Infectious Diseases · USArmed Forces Research Institute of Medical Science · THMinistry of Public Health · THNew York University · USVA NY Harbor Healthcare System · US

Funding

SDMC: HIV Vaccine Trials NetworkUM1AI068635 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Peter B. Gilbert, Yunda Huang · 2011 to 2026
$385.9M
Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI Nwora Lance Okeke · 2005 to 2026
$50.5M
Vaccines to Induce Functional Antibodies Targeting the V2 Loop P01AI100151 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KONG, XIANGPENG, ZOLLA-PAZNER, SUSAN B · 2012 to 2017
$15.4M
PROTECTIVE HUMAN MONOCLONAL ANTIBODIES TO HIV1R01HL059725 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ZOLLA-PAZNER, SUSAN B · 1997 to 2014
$8.8M
Optimizing protective vaccine targets in the V1/V2 domain of HIV-1 gp120R01AI102718 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI PINTER, ABRAHAM · 2012 to 2015
$2.7M
FILARIASIS REPOSITORY RESEARCH SERVICEN01AI002642 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI MC CALL, JOHN W · 1985 to 1987
–
NHLBI NIH HHS R01 HL059725NHLBI NIH HHS R01 HL59725NIAID NIH HHS P01 AI100151NIAID NIH HHS P01 AI64518NIAID NIH HHS P30 AI064518NIAID NIH HHS R01 AI102718NIAID NIH HHS UM1 AI068635NIAID NIH HHS Y1-AI-2642-12
6 · The paper itself

Abstract

unlabelledIn the RV144 HIV-1 vaccine efficacy trial, IgG antibody (Ab) binding levels to variable regions 1 and 2 (V1V2) of the HIV-1 envelope glycoprotein gp120 were an inverse correlate of risk of HIV-1 infection. To determine if V1V2-specific Abs cross-react with V1V2 from different HIV-1 subtypes, if the nature of the V1V2 antigen used to asses cross-reactivity influenced infection risk, and to identify immune assays for upcoming HIV-1 vaccine efficacy trials, new V1V2-scaffold antigens were designed and tested. Protein scaffold antigens carrying the V1V2 regions from HIV-1 subtypes A, B, C, D or CRF01_AE were assayed in pilot studies, and six were selected to assess cross-reactive Abs in the plasma from the original RV144 case-control cohort (41 infected vaccinees, 205 frequency-matched uninfected vaccinees, and 40 placebo recipients) using ELISA and a binding Ab multiplex assay. IgG levels to these antigens were assessed as correlates of risk in vaccine recipients using weighted logistic regression models. Levels of Abs reactive with subtype A, B, C and CRF01_AE V1V2-scaffold antigens were all significant inverse correlates of risk (p-values of 0.0008-0.05; estimated odds ratios of 0.53-0.68 per 1 standard deviation increase). Thus, levels of vaccine-induced IgG Abs recognizing V1V2 regions from multiple HIV-1 subtypes, and presented on different scaffolds, constitute inverse correlates of risk for HIV-1 infection in the RV144 vaccine trial. The V1V2 antigens provide a link between RV144 and upcoming HIV-1 vaccine trials, and identify reagents and methods for evaluating V1V2 Abs as possible correlates of protection against HIV-1 infection.

trial registrationClinicalTrials.gov NCT00223080.

Indexed as

AdolescentAdultAIDS VaccinesAmino Acid SequenceCase-Control StudiesCluster AnalysisEnzyme-Linked Immunosorbent AssayFemaleHIV-1HIV AntibodiesHIV AntigensHIV Envelope Protein gp120HIV InfectionsHumansImmunoglobulin GMaleAIDS Vaccinesgp120 protein, Human immunodeficiency virus 1HIV AntibodiesHIV AntigensHIV Envelope Protein gp120Immunoglobulin GPlacebos

Identifiers

PMID24504509
PMCPMC3913641
OpenAlexW2036297695

What OpenQuestion holds

Textmetadata
LicenceCC0
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.