Evidence map›Paper›PMID 17106277›Full record

Trial reportJournal of acquired immune deficiency syndromes (1999)2007

Phase 2 study of an HIV-1 canarypox vaccine (vCP1452) alone and in combination with rgp120: negative results fail to trigger a phase 3 correlates trial.

Nina D Russell, Barney S Graham, Michael C Keefer, M Juliana McElrath, Steve G Self, Kent J Weinhold, David C Montefiori, Guido Ferrari, Helen Horton, Georgia D Tomaras and 11 more

Abstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal of acquired immune deficiency syndromes (1999), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

63 citing papers in PubMed, 104 citations in OpenAlex.

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3 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

21 authors at 7 institutions in 1 country.

Nina D RussellProgram in Infectious Diseases, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. nina.russell@gatesfoundation.org
Barney S Graham
Michael C Keefer
M Juliana McElrath
Steve G Self
Kent J Weinhold
David C Montefiori
Guido Ferrari
Helen Horton
Georgia D Tomaras
Sanjay Gurunathan
Lynn Baglyos
Sharon E Frey
Mark J Mulligan
Clayton D Harro
Susan P Buchbinder
Lindsey R Baden
William A Blattner
Beryl A Koblin
Lawrence Corey
National Institute of Allergy and Infectious Diseases HIV Vaccine Trials Network
New York Blood Center · USUniversity of Maryland, Baltimore · USBrigham and Women's Hospital · USJohns Hopkins University · USNational Institutes of Health · USFred Hutch Cancer Center · USUniversity of Washington · US

Funding

HIV VACCINE TRIALS NETWORK LEADERSHIP GROUPU01AI046747 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI COREY, LAWRENCE · 1999 to 2005
$124.7M
San Francisco Vaccine and Prevention UnitUM1AI069496 · NIAID · PUBLIC HEALTH FOUNDATION ENTERPRISES · PI Susan Buchbinder, Diane V Havlir · 2012 to 2026
$30.5M
San Francisco Vaccine and Prevention UnitU01AI069496 · NIAID · PUBLIC HEALTH FOUNDATION ENTERPRISES · PI BUCHBINDER, SUSAN · 2007 to 2011
$7.3M
Intramural NIH HHS Z99 AI999999NIAID NIH HHS U01 AI046747NIAID NIH HHS U01 AI069496NIAID NIH HHS UM1 AI069496NIAID NIH HHS UO1 AI 46747
6 · The paper itself

Abstract

backgroundA goal of T-cell HIV vaccines is to define the correlation between a vaccine-induced immune response and protection from HIV infection. We conducted a phase 2 trial to determine if a canarypox vaccine candidate (vCP1452) administered with rgp120 subunit protein would "qualify" for a trial to define a correlate of efficacy.

methodsA total of 330 healthy volunteers were enrolled into 4 groups: 120 received vCP1452 alone (0, 1, 3, and 6 months), 120 received vCP1452 with 2 different regimens of rgp120 coadministration, and 90 received placebo. HIV-specific antibody responses were measured by enzyme-linked immunoassay (ELISA) and neutralizing activity. T-cell responses were measured by chromium release and interferon-gamma (IFNgamma) enzyme-linked immunospot (ELISpot) assay.

resultsSignificant neutralizing antibody responses to the HIV MN strain were detected in all vaccine groups, with net responses ranging from 57% (95% confidence interval [CI]: 40% to 71%) to 94% (95% CI: 85% to 99%). Net cumulative HIV-specific CD8 IFNgamma ELISpot assay responses were 13% (95% CI: -1% to 26%) for recipients of vCP1452 alone and 16% (95% CI: 2% to 29%) for recipients of vCP1452 plus rgp120.

conclusionsOverall, the HIV-specific CD8 cytotoxic T lymphocyte (CTL) response was not sufficient to qualify the regimen for a subsequent trial designed to detect an immune correlate of protection requiring a minimum CD8 CTL frequency of 30%.

Indexed as

AdolescentAdultAIDS VaccinesCanarypox virusCD4-Positive T-LymphocytesChromiumEnzyme-Linked Immunosorbent AssayFemaleGenetic VectorsHIV-1HIV AntibodiesHIV Envelope Protein gp120HumansInterferon-gammaMaleMiddle AgedAIDS VaccinesAIDSVAXChromiumHIV AntibodiesHIV Envelope Protein gp120Interferon-gammaVaccines, SubunitVaccines, Synthetic

Identifiers

PMID17106277
PMCPMC2362395
OpenAlexW2084808899

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.