Evidence map›Paper›PMID 28266565›Full record

ArticleScientific reports2017

Preclinical evaluation of multi antigenic HCV DNA vaccine for the prevention of Hepatitis C virus infection.

Hyojin Lee, Moonsup Jeong, Jooyeon Oh, Youngran Cho, Xuefei Shen, John Stone, Jian Yan, Zachary Rothkopf, Amir S Khan, Byung Mun Cho and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
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  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
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  11. Article
  12. Article
  13. A Review of DNA Vaccines Against Influenza.Frontiers in immunology · 2018
    Review
  14. 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

14 authors at 4 institutions in 2 countries.

Hyojin LeeGeneOne Life Science, Seoul, Korea.
Moonsup JeongGeneOne Life Science, Seoul, Korea.
Jooyeon OhGeneOne Life Science, Seoul, Korea.
Youngran ChoGeneOne Life Science, Seoul, Korea.
Xuefei ShenInovio Pharmaceuticals, Plymouth Meeting, PA, USA.
John StoneInovio Pharmaceuticals, Plymouth Meeting, PA, USA.
Jian YanInovio Pharmaceuticals, Plymouth Meeting, PA, USA.
Zachary RothkopfDepartment of Medicine, Morristown Medical Center, Morristown, NJ, USA.
Amir S KhanInovio Pharmaceuticals, Plymouth Meeting, PA, USA.
Byung Mun ChoGeneOne Life Science, Seoul, Korea.
Young K ParkGeneOne Life Science, Seoul, Korea.
David B WeinerWistar Institute, Philadelphia, PA, USA.
Woo-Chan SonDepartment of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
Joel N MaslowGeneOne Life Science, Seoul, Korea.
Inovio Pharmaceuticals (United States) · USAsan Medical Center · KRMorristown Medical Center · USThe Wistar Institute · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
NCI NIH HHS P30 CA010815
6 · The paper itself

Abstract

Direct-acting antiviral treatment for hepatitis C virus (HCV) infection is costly and does not protect from re-infection. For human and chimpanzees, recovery from acute HCV infection correlates with host CD4+ and CD8+ T cell responses. DNA plasmids targeting the HCV non-structural antigens NS3, NS4, and NS5, were previously reported to induce robust and sustained T cell responses in mice and primates. These plasmids were combined with a plasmid encoding cytokine IL-28B, together named as VGX-6150. The dose-dependent T cell response and safety of VGX-6150 administered intramuscularly and followed by electroporation was assessed in mice. Immune responses plateaued at 20 μg/dose with IL-28B demonstrating significant immunoadjuvant activity. Mice administered VGX-6150 at 40, 400, and 800 μg given either as a single injection or as 14 injections given bi-weekly over 26 weeks showed no vaccine related changes in any clinical parameter compared to placebo recipients. There was no evidence of VGX-6150 accumulation at the injection site or in any organ 1 month following the 14

Indexed as

AnimalsCytokinesDisease Models, AnimalDose-Response Relationship, ImmunologicFemaleHepacivirusHepatitis CHepatitis C AntigensHumansImmunity, CellularImmunizationImmunization ScheduleInterferon LambdaInterleukinsMaleMiceCytokinesHepatitis C AntigensInterferon Lambdainterferon-lambda protein, mouseInterleukinsVaccines, DNAViral Hepatitis Vaccines

Identifiers

PMID28266565
PMCPMC5339862
OpenAlexW2593489625

What OpenQuestion 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 OpenQuestion graph.