Evidence map›Paper›PMID 33568510›Full record

Trial reportJournal of virology2021

A Randomized Placebo-Controlled Efficacy Study of a Prime Boost Therapeutic Vaccination Strategy in HIV-1-Infected Individuals: VRI02 ANRS 149 LIGHT Phase II Trial.

Y Lévy, C Lacabaratz, E Lhomme, A Wiedemann, C Bauduin, C Fenwick, E Foucat, M Surenaud, L Guillaumat, V Boilet and 10 more

Open access · hybridAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. A novel and safe SmartCapFrontiers in immunology · 2025
    Article
  4. Review
  5. Article
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

20 authors at 6 institutions in 2 countries.

Y Lévy *Vaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France yves.levy@aphp.fr.ORCID 0000-0002-5549-6256
C Lacabaratz *Vaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.
E LhommeVaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.
A WiedemannVaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.
C BauduinUniversity of Bordeaux, ISPED, Inserm, Population Health Research Center, Team MORPH3EUS, UMR 1219, CIC-EC 1401, Bordeaux, France.
C FenwickVaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.ORCID 0000-0002-9435-0110
E FoucatVaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.
M SurenaudVaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.
L GuillaumatVaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.
V BoiletUniversity of Bordeaux, ISPED, Inserm, Population Health Research Center, Team MORPH3EUS, UMR 1219, CIC-EC 1401, Bordeaux, France.
V RieuxInserm-ANRS, Vaccine Research Office, Paris, France.
O BouchaudHôpital Avicenne, AP-HP, Université Paris 13, Bobigny, France.
P-M GirardHôpital Saint Antoine, AP-HP, INSERM UMR S_1136, Paris, France.
J-M MolinaHôpital Saint-Louis, AP-HP, Université Paris Diderot INSERM U941, Paris, France.
P MorlatCHU de Bordeaux, Bordeaux, France.
L HocquelouxCHR d'Orléans, La Source, France.
L RichertVaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.
G PantaleoVaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.ORCID 0000-0003-3651-2721
J D Lelièvre *Vaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.
R Thiébaut *Vaccine Research Institute-VRI, Hôpital Henri Mondor, Créteil, France.
Inserm · FRUniversité de Bordeaux · FRUniversity Hospital of Lausanne · CHCentre Hospitalier Universitaire de Bordeaux · FRCentre hospitalier universitaire d'Orléans · FRUniversité Sorbonne Paris Nord · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this placebo-controlled phase II randomized clinical trial, 103 human immunodeficiency virus type 1 (HIV-1)-infected patients under cART (combined antiretroviral treatment) were randomized 2:1 to receive either 3 doses of DNA GTU-MultiHIV B (coding for Rev, Nef, Tat, Gag, and gp160) at week 0 (W0), W4, and W12, followed by 2 doses of LIPO-5 vaccine containing long peptides from Gag, Pol, and Nef at W20 and W24, or placebo. Analytical treatment interruption (ATI) was performed between W36 to W48. At W28, vaccinees experienced an increase in functional CD4

Indexed as

AIDS VaccinesVaccines, DNAAdultAnti-Retroviral AgentsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesFemaleHIV-1HIV InfectionsHumansImmunization, SecondaryMaleMiddle AgedAIDS VaccinesAnti-Retroviral AgentsVaccines, DNAantiretroviral therapy interruptionclinical trialsHIVhuman immunodeficiency virustherapeutic vaccine

Identifiers

PMID33568510
PMCPMC8104102
OpenAlexW3127729601

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.