Evidence map›Paper›PMID 28537062›Full record

Trial reportJournal of the International AIDS Society2017

Evaluation of the immunogenicity and impact on the latent HIV-1 reservoir of a conserved region vaccine, MVA.HIVconsv, in antiretroviral therapy-treated subjects.

Gemma Hancock, Sara Morón-López, Jakub Kopycinski, Maria C Puertas, Eleni Giannoulatou, Annie Rose, Maria Salgado, Emma-Jo Hayton, Alison Crook, Catharine Morgan and 6 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the International AIDS Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01024842 (HIV-CORE 001 - A Randomised Placebo-controlled Study to Evaluate the Safety and Immunogenicity of a Candidate HIV-1 Vaccine, MVA.HIVconsv, Delivered by Intramuscular Needle Injection to HIV-1 Seropositive Adult Subjects Receiving Antiretroviral Therapy), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 8% 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.

NCT01024842 phase1terminatednot on this map

HIV-CORE 001 - A Randomised Placebo-controlled Study to Evaluate the Safety and Immunogenicity of a Candidate HIV-1 Vaccine, MVA.HIVconsv, Delivered by Intramuscular Needle Injection to HIV-1 Seropositive Adult Subjects Receiving Antiretroviral Therapy (ART).

TypeinterventionalSponsorUniversity of OxfordRan2009 to 2013Enrolled19ConditionsHIV-1ArmsMVA.HIVconsv low dose, Placebo low dose, MVA.HIVconsv high dose, Placebo high dose
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Frontiers in immunology · 2020
    Article
  10. Article
  11. Article
  12. Nucleic acid testing and molecular characterization of HIV infections.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2019
    Review
  13. Article
  14. The Safety and Immunogenicity of GTUFrontiers in immunology · 2019
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Conserved multiepitope vaccine constructs: A potent HIV-1 therapeutic vaccine in clinical trials.The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases
    Review
  20. 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

16 authors at 7 institutions in 3 countries.

Gemma HancockOxford NIHR Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Sara Morón-LópezAIDS Research Institute IrsiCaixa, Institut d'Investigació en Cièncias de la Salut Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.
Jakub KopycinskiOxford NIHR Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Maria C PuertasAIDS Research Institute IrsiCaixa, Institut d'Investigació en Cièncias de la Salut Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.
Eleni GiannoulatouComputational Genomics Laboratory, Victor Chang Cardiac Research Institute, Darlinghurst, Australia.
Annie RoseOxford NIHR Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Maria SalgadoAIDS Research Institute IrsiCaixa, Institut d'Investigació en Cièncias de la Salut Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.
Emma-Jo HaytonOxford NIHR Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Alison CrookOxford NIHR Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Catharine MorganOxfordshire Sexual Health Service, Oxford University Hospitals NHS Trust, Oxford, UK.
Brian AngusOxford NIHR Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Fabian ChenThe Florey: Sexual Health, Royal Berkshire NHS Foundation Trust, Reading, UK.
Hongbing YangOxford NIHR Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Javier Martinez-PicadoAIDS Research Institute IrsiCaixa, Institut d'Investigació en Cièncias de la Salut Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.
Tomas HankeOxford NIHR Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Lucy DorrellOxford NIHR Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Oxford BioMedica (United Kingdom) · GBUniversitat Autònoma de Barcelona · ESUniversity of Oxford · GBIrsiCaixa · ESOxford University Hospitals NHS Trust · GBRoyal Berkshire NHS Foundation Trust · GBUNSW Sydney · AU

Funding

Medical Research Council G0502048Medical Research Council G0701669Medical Research Council G1001757Medical Research Council MC_U137884179Medical Research Council MR/N023668/1UK Medical Research Council G0502048
6 · The paper itself

Abstract

introductionVaccines may be key components of a curative strategy for HIV-1. We investigated whether a novel immunogen, HIVconsv, designed to re-direct T cell responses to conserved viral epitopes, could impact the HIV-1 reservoir in chronic antiretroviral therapy (ART)-treated subjects when delivered by modified vaccinia virus Ankara (MVA).

methodsNineteen virologically suppressed individuals were randomized to receive vaccinations with MVA.HIVconsv (5.5 × 10

results90% of subjects completed the vaccine regimen; there were no serious vaccine-related adverse events. The magnitude of HIVconsv-specific IFN-

conclusionsHomologous prime-boost vaccination with MVA.HIVconsv was safe in HIV-positive ART-treated subjects but showed modest immunogenicity and did not significantly change the size of the viral reservoir. MVA.HIVconsv may be more effective when used in a heterologous prime-boost vaccination regimen and when combined with a latency-reversing agent. CLINICAL TRIALS REGISTRATION: NCT01024842.

Indexed as

Immunogenicity, VaccineAIDS VaccinesAnti-HIV AgentsConserved SequenceDouble-Blind MethodFemaleHIV-1HIV InfectionsHumansMaleT-LymphocytesVaccines, SyntheticVaccinia virusViral LoadAIDS VaccinesAnti-HIV AgentsVaccines, Syntheticconservationhuman immunodeficiency virusimmunogen designMVAphase I trialT cellstherapeutic vaccineviral inhibition assay

Identifiers

PMID28537062
PMCPMC5515041
OpenAlexW2620340782

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.