Evidence map›Paper›PMID 22634875›Full record

Trial reportThe Journal of infectious diseases2012

Magnitude and breadth of the neutralizing antibody response in the RV144 and Vax003 HIV-1 vaccine efficacy trials.

David C Montefiori, Chitraporn Karnasuta, Ying Huang, Hasan Ahmed, Peter Gilbert, Mark S de Souza, Robert McLinden, Sodsai Tovanabutra, Agnes Laurence-Chenine, Eric Sanders-Buell and 24 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 215 papers.

0numbers the graph read from it
0cells of the map it votes in
215citing papers in PubMed
17.6field-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.

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

215 citing papers in PubMed, 283 citations in OpenAlex.

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155 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 3 countries.

David C MontefioriDepartment of Surgery, Duke University Medical Center, Durham, North Carolina 27710, USA. monte@duke.edu
Chitraporn Karnasuta
Ying Huang
Hasan Ahmed
Peter Gilbert
Mark S de Souza
Robert McLinden
Sodsai Tovanabutra
Agnes Laurence-Chenine
Eric Sanders-Buell
M Anthony Moody
Mattia Bonsignori
Christina Ochsenbauer
John Kappes
Haili Tang
Kelli Greene
Hongmei Gao
Celia C LaBranche
Charla Andrews
Victoria R Polonis
Supachai Rerks-Ngarm
Punnee Pitisuttithum
Sorachai Nitayaphan
Jaranit Kaewkungwal
Steve G Self
Phillip W Berman
Donald Francis
Faruk Sinangil
Carter Lee
Jim Tartaglia
Merlin L Robb
Barton F Haynes
Nelson L Michael
Jerome H Kim
Walter Reed Army Institute of Research · USDuke University · USFred Hutch Cancer Center · USArmed Forces Research Institute of Medical Science · THGlobal Solutions for Infectious Diseases · USUniversity of Alabama at Birmingham · USDuke Medical Center · USMahidol Oxford Tropical Medicine Research Unit · THMahidol University · THSanofi (Canada) · CAUniversity of California, Santa Cruz · US

Funding

Viral Sequencing CoreU19AI067854 · NIAID · DUKE UNIVERSITY · PI CRUMP, JOHN ANDREW · 2006 to 2011
$290.5M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OLAF KUTSCH · 1988 to 2026
$84.1M
FILARIASIS REPOSITORY RESEARCH SERVICEN01AI002642 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI MC CALL, JOHN W · 1985 to 1987
–
NIAID NIH HHS AI678501NIAID NIH HHS P30 AI027767NIAID NIH HHS U19 AI067854NIAID NIH HHS Y1-AI-2642-12
6 · The paper itself

Abstract

backgroundA recombinant canarypox vector expressing human immunodeficiency virus type 1 (HIV-1) Gag, Pro, and membrane-linked gp120 (vCP1521), combined with a bivalent gp120 protein boost (AIDSVAX B/E), provided modest protection against HIV-1 infection in a community-based population in Thailand (RV144 trial). No protection was observed in Thai injection drug users who received AIDSVAX B/E alone (Vax003 trial). We compared the neutralizing antibody response in these 2 trials.

methodsNeutralization was assessed with tier 1 and tier 2 strains of virus in TZM-bl and A3R5 cells.

resultsNeutralization of several tier 1 viruses was detected in both RV144 and Vax003. Peak titers were higher in Vax003 and waned rapidly in both trials. The response in RV144 was targeted in part to V3 of gp120.vCP1521 priming plus 2 boosts with gp120 protein was superior to 2 gp120 protein inoculations alone, confirming a priming effect for vCP1521. Sporadic weak neutralization of tier 2 viruses was detected only in Vax003 and A3R5 cells.

conclusionThe results suggest either that weak neutralizing antibody responses can be partially protective against HIV-1 in low-risk heterosexual populations or that the modest efficacy seen in RV144 was mediated by other immune responses, either alone or in combination with neutralizing antibodies.

Indexed as

AIDS VaccinesAntibodies, MonoclonalAntibodies, NeutralizingCanarypox virusEpitope MappingHIV-1HIV AntibodiesHIV InfectionsHuman Immunodeficiency Virus ProteinsHumansImmunization ScheduleSubstance Abuse, IntravenousThailandAIDS VaccinesAntibodies, MonoclonalAntibodies, NeutralizingHIV AntibodiesHuman Immunodeficiency Virus Proteins

Identifiers

PMID22634875
PMCPMC3392187
OpenAlexW2108823547

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.