Evidence map›Paper›PMID 25105367›Full record

Trial reportThe Journal of clinical investigation2014

FCGR2C polymorphisms associate with HIV-1 vaccine protection in RV144 trial.

Shuying S Li, Peter B Gilbert, Georgia D Tomaras, Gustavo Kijak, Guido Ferrari, Rasmi Thomas, Chul-Woo Pyo, Susan Zolla-Pazner, David Montefiori, Hua-Xin Liao and 24 more

Abstract readClinical Trial, Phase III
In one paragraph

Trial report in The Journal of clinical investigation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% 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

85 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.

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25 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

34 authors at 11 institutions in 2 countries.

Shuying S Li
Peter B Gilbert
Georgia D Tomaras
Gustavo Kijak
Guido Ferrari
Rasmi Thomas
Chul-Woo Pyo
Susan Zolla-Pazner
David Montefiori
Hua-Xin Liao
Gary Nabel
Abraham Pinter
David T Evans
Raphael Gottardo
James Y Dai
Holly Janes
Daryl Morris
Youyi Fong
Paul T Edlefsen
Fusheng Li
Nicole Frahm
Michael D Alpert
Heather Prentice
Supachai Rerks-Ngarm
Punnee Pitisuttithum
Jaranit Kaewkungwal
Sorachai Nitayaphan
Merlin L Robb
Robert J O'Connell
Barton F Haynes
Nelson L Michael
Jerome H Kim
M Juliana McElrath
Daniel E Geraghty
Fred Hutch Cancer Center · USWalter Reed Army Institute of Research · USDuke University · USMahidol University · THHarvard University Press · USMinistry of Public Health · THNew York University · USRAND Corporation · USRoyal Thai ArmyRutgers, The State University of New Jersey · USUniversity of Wisconsin–Madison · US

Funding

LC: HIV Vaccine Trials NetworkUM1AI068618 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Margaret Juliana McElrath · 2011 to 2026
$483.6M
SDMC: HIV Vaccine Trials NetworkUM1AI068635 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Peter B. Gilbert, Yunda Huang · 2011 to 2026
$385.9M
Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Viral Sequencing CoreU19AI067854 · NIAID · DUKE UNIVERSITY · PI HAYNES, BARTON F. · 2006 to 2011
$290.5M
Vaccines to Induce Functional Antibodies Targeting the V2 Loop P01AI100151 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WANG, SHIXIA · 2012 to 2017
$15.4M
Viral and Host Determinants of HIV-1 TransmissionU01AI067854 · NIAID · DUKE UNIVERSITY · PI HAYNES, BARTON F · 2005 to 2005
$14.9M
Statistical Methods in HIV Vaccine Efficacy TrialsR37AI054165 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Peter B. Gilbert · 2010 to 2026
$6.7M
KIR and MHC Class I Immunogenetics in SIV InfectionR01AI095098 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI EVANS, DAVID T · 2012 to 2016
$2.7M
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
Lentiviral Resistance to TetherinR01AI098485 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI EVANS, DAVID T · 2012 to 2016
$2.2M
Statistical inference in genome-wide association and sequencing studiesR01HL114901 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DAI, JAMES · 2012 to 2015
$1.7M
FILARIASIS REPOSITORY RESEARCH SERVICEN01AI002642 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI MC CALL, JOHN W · 1985 to 1987
–
NCI NIH HHS P30 CA015704NHLBI NIH HHS R01 HL114901NIAID NIH HHS AI067854NIAID NIH HHS P01 AI100151NIAID NIH HHS R01 AI098485NIAID NIH HHS R01 AI102718NIAID NIH HHS R37 AI054165NIAID NIH HHS R37AI054165NIAID NIH HHS U01 AI067854NIAID NIH HHS U19 AI067854NIAID NIH HHS UM1 AI068618NIAID NIH HHS UM1AI-068618NIAID NIH HHS UM1 AI068635NIAID NIH HHS Y1-AI-2642-12
6 · The paper itself

Abstract

The phase III RV144 HIV-1 vaccine trial estimated vaccine efficacy (VE) to be 31.2%. This trial demonstrated that the presence of HIV-1-specific IgG-binding Abs to envelope (Env) V1V2 inversely correlated with infection risk, while the presence of Env-specific plasma IgA Abs directly correlated with risk of HIV-1 infection. Moreover, Ab-dependent cellular cytotoxicity responses inversely correlated with risk of infection in vaccine recipients with low IgA; therefore, we hypothesized that vaccine-induced Fc receptor-mediated (FcR-mediated) Ab function is indicative of vaccine protection. We sequenced exons and surrounding areas of FcR-encoding genes and found one FCGR2C tag SNP (rs114945036) that associated with VE against HIV-1 subtype CRF01_AE, with lysine at position 169 (169K) in the V2 loop (CRF01_AE 169K). Individuals carrying CC in this SNP had an estimated VE of 15%, while individuals carrying CT or TT exhibited a VE of 91%. Furthermore, the rs114945036 SNP was highly associated with 3 other FCGR2C SNPs (rs138747765, rs78603008, and rs373013207). Env-specific IgG and IgG3 Abs, IgG avidity, and neutralizing Abs inversely correlated with CRF01_AE 169K HIV-1 infection risk in the CT- or TT-carrying vaccine recipients only. These data suggest a potent role of Fc-γ receptors and Fc-mediated Ab function in conferring protection from transmission risk in the RV144 VE trial.

Indexed as

Polymorphism, Single NucleotideAcquired Immunodeficiency SyndromeAIDS VaccinesGenotypeHIV-1HIV AntibodiesHIV Envelope Protein gp120HumansReceptors, IgGVaccinationAIDS VaccinesFc gamma receptor IICgp120 protein, Human immunodeficiency virus 1HIV AntibodiesHIV Envelope Protein gp120Receptors, IgG

Identifiers

PMID25105367
PMCPMC4151214
OpenAlexW2146343022

What OpenQuestion holds

Textmetadata
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.