Evidence map›Paper›PMID 32589686›Full record

Trial reportPLoS pathogens2020

Optimal priming of poxvirus vector (NYVAC)-based HIV vaccine regimens for T cell responses requires three DNA injections. Results of the randomized multicentre EV03/ANRS VAC20 Phase I/II Trial.

Yves Lévy, Christine Lacabaratz, Kim Ellefsen-Lavoie, Wolfgang Stöhr, Jean-Daniel Lelièvre, Pierre-Alexandre Bart, Odile Launay, Jonathan Weber, Bernd Salzberger, Aurélie Wiedemann and 15 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in PLoS pathogens, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00490074 (A Phase I/II Trial to Compare the Immunogenicity and Safety of 3 DNA C Prime Followed by 1 NYVAC C Boost to 2 DNA C Prime Followed by 2 NYVAC C Boost), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-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.

NCT00490074 phase1 / phase2completednot on this map

A Phase I/II Trial to Compare the Immunogenicity and Safety of 3 DNA C Prime Followed by 1 NYVAC C Boost to 2 DNA C Prime Followed by 2 NYVAC C Boost

TypeinterventionalSponsorANRS, Emerging Infectious DiseasesRan2007 to 2009Enrolled147ConditionsHIV InfectionsArmsDNA-C, NYVAC-C
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Advancements in protein nanoparticle vaccine platforms to combat infectious disease.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2021
    Review
  8. Review
  9. Article
  10. Article
  11. Poxvirus vectors as HIV/AIDS vaccines in humans.Human vaccines & immunotherapeutics · 2012
    Review
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

25 authors at 12 institutions in 5 countries.

Yves LévyVaccine Research Institute, Université Paris-Est Créteil, Faculté de Médecine, INSERM U955, équipe 16, Créteil, France.ORCID 0000-0002-5549-6256
Christine LacabaratzVaccine Research Institute, Université Paris-Est Créteil, Faculté de Médecine, INSERM U955, équipe 16, Créteil, France.ORCID 0000-0001-6925-0225
Kim Ellefsen-LavoieCentre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.
Wolfgang StöhrMRC Clinical Trials Unit at UCL, London, United Kingdom.
Jean-Daniel LelièvreVaccine Research Institute, Université Paris-Est Créteil, Faculté de Médecine, INSERM U955, équipe 16, Créteil, France.
Pierre-Alexandre BartCentre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.
Odile LaunayUniversité de Paris, Faculté de médecine Paris Descartes; Inserm, CIC 1417, F-CRIN I-REIVAC; Assistance Publique-Hôpitaux de Paris, CIC Cochin Pasteur, Paris, France.
Jonathan WeberImperial College London, London, United Kingdom.
Bernd SalzbergerUniversity Hospital, Institute of Clinical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Aurélie WiedemannVaccine Research Institute, Université Paris-Est Créteil, Faculté de Médecine, INSERM U955, équipe 16, Créteil, France.ORCID 0000-0002-4224-3137
Mathieu SurenaudVaccine Research Institute, Université Paris-Est Créteil, Faculté de Médecine, INSERM U955, équipe 16, Créteil, France.ORCID 0000-0002-3312-7871
David M KoelleDepartment of Medicine & Department of Global Health, University of Washington, Fred Hutchinson Cancer Research Center Seattle, Washington, United States of America.
Hans WolfUniversity Hospital, Institute of Clinical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Ralf WagnerUniversity Hospital, Institute of Clinical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany.
Véronique RieuxVaccine Research Institute, Université Paris-Est Créteil, Faculté de Médecine, INSERM U955, équipe 16, Créteil, France.
David C MontefioriDepartment of Surgery, Duke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, United States of America.ORCID 0000-0003-0856-6319
Nicole L YatesDepartment of Surgery, Duke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, United States of America.ORCID 0000-0003-2678-1311
Georgia D TomarasDepartment of Surgery, Duke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, United States of America.
Raphael GottardoVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Bryan MayerVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.ORCID 0000-0003-2258-5276
Song DingEuroVacc Foundation, Lausanne, Switzerland.
Rodolphe ThiébautInserm, Bordeaux Population Health Research Center, UMR 1219, University Bordeaux, ISPED, CIC 1401-EC, Univ Bordeaux, Bordeaux, France.
Sheena McCormackMRC Clinical Trials Unit at UCL, London, United Kingdom.
Geneviève ChêneInserm, Bordeaux Population Health Research Center, UMR 1219, University Bordeaux, ISPED, CIC 1401-EC, Univ Bordeaux, Bordeaux, France.
Giuseppe PantaleoCentre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.
Inserm · FRDuke Medical Center · USUniversity Hospital of Lausanne · CHUniversity Hospital Regensburg · DEFred Hutch Cancer Center · USMRC Clinical Trials Unit at UCL · GBDélégation Paris 5 · FREurovacc Foundation · CHImperial College London · GBInstitut national de recherche en sciences et technologies du numérique · FRUniversité de Bordeaux · FRUniversity of Washington · US

Funding

Medical Research Council MC_UU_12023/23NIAID NIH HHS HHSN272201400049C
6 · The paper itself

Abstract

DNA vectors have been widely used as a priming of poxvirus vaccine in prime/boost regimens. Whether the number of DNA impacts qualitatively or quantitatively the immune response is not fully explored. With the aim to reinforce T-cell responses by optimizing the prime-boost regimen, the multicentric EV03/ANRS VAC20 phase I/II trial, randomized 147 HIV-negative volunteers to either 3xDNA plus 1xNYVAC (weeks 0, 4, 8 plus 24; n = 74) or to 2xDNA plus 2xNYVAC (weeks 0, 4 plus 20, 24; n = 73) groups. T-cell responses (IFN-γ ELISPOT) to at least one peptide pool were higher in the 3xDNA than the 2xDNA groups (91% and 80% of vaccinees) (P = 0.049). In the 3xDNA arm, 26 (37%) recipients developed a broader T-cell response (Env plus at least to one of the Gag, Pol, Nef pools) than in the 2xDNA (15; 22%) arms (primary endpoint; P = 0.047) with a higher magnitude against Env (at week 26) (P<0.001). In both groups, vaccine regimens induced HIV-specific polyfunctional CD4 and CD8 T cells and the production of Th1, Th2 and Th17/IL-21 cytokines. Antibody responses were also elicited in up to 81% of vaccines. A higher percentage of IgG responders was noted in the 2xDNA arm compared to the 3xDNA arm, while the 3xDNA group tended to elicit a higher magnitude of IgG3 response against specific Env antigens. We show here that the modulation of the prime strategy, without modifying the route or the dose of administration, or the combination of vectors, may influence the quality of the responses.

Indexed as

AdolescentAdultAIDS VaccinesCD8-Positive T-Lymphocytesenv Gene Products, Human Immunodeficiency VirusFemaleGenetic VectorsHIV AntigensHumansInterferon-gammaMaleMiddle AgedPoxviridaeT-Lymphocytes, Helper-InducerVaccines, DNAAIDS Vaccinesenv Gene Products, Human Immunodeficiency VirusHIV AntigensIFNG protein, humanInterferon-gammaVaccines, DNA

Identifiers

PMID32589686
PMCPMC7319597
OpenAlexW3038088767

What OpenQuestion holds

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LicenceCC BY
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.