Evidence map›Paper›PMID 25692288›Full record

ArticlePloS one2015

Plant virus particles carrying tumour antigen activate TLR7 and Induce high levels of protective antibody.

Jantipa Jobsri, Alex Allen, Deepa Rajagopal, Michael Shipton, Kostya Kanyuka, George P Lomonossoff, Christian Ottensmeier, Sandra S Diebold, Freda K Stevenson, Natalia Savelyeva

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
9.8field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
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  3. Article
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  7. Article
  8. Review
  9. Virus-like Particles for TEM Regulation and Antitumor Therapy.Journal of functional biomaterials · 2022
    Review
  10. Review
  11. Review
  12. Plant Virus Nanoparticles for Anti-cancer Therapy.Frontiers in bioengineering and biotechnology · 2021
    Review
  13. Article
  14. Review
  15. Biomimetic Nanotechnology toward Personalized Vaccines.Advanced materials (Deerfield Beach, Fla.) · 2020
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  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

10 authors at 3 institutions in 1 country.

Jantipa JobsriCancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Alex AllenCancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Deepa RajagopalKing's College London, Peter Gorer Department of Immunobiology, Guy's Hospital, London, United Kingdom.
Michael ShiptonCancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Kostya KanyukaPlant Biology and Crop Science Department, Rothamsted Research, Harpenden, United Kingdom.
George P LomonossoffDepartment of Biological Chemistry, John Innes Centre, Norwich, United Kingdom.
Christian OttensmeierCancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Sandra S DieboldKing's College London, Peter Gorer Department of Immunobiology, Guy's Hospital, London, United Kingdom.
Freda K StevensonCancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Natalia SavelyevaCancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
University of Southampton · GBJohn Innes Centre · GBRothamsted Research · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J004561/1Biotechnology and Biological Sciences Research Council BBS/E/J/00000166Cancer Research UK 15951Cancer Research UK 20613
6 · The paper itself

Abstract

Induction of potent antibody is the goal of many vaccines targeted against infections or cancer. Modern vaccine designs that use virus-like particles (VLP) have shown efficacy for prophylactic vaccination against virus-associated cancer in the clinic. Here we used plant viral particles (PVP), which are structurally analogous to VLP, coupled to a weak idiotypic (Id) tumour antigen, as a conjugate vaccine to induce antibody against a murine B-cell malignancy. The Id-PVP vaccine incorporates a natural adjuvant, the viral ssRNA, which acts via TLR7. It induced potent protective anti-Id antibody responses in an in vivo mouse model, superior to the "gold standard" Id vaccine, with prevalence of the IgG2a isotype. Combination with alum further increased antibody levels and maintained the IgG2a bias. Engagement of TLR7 in vivo was followed by secretion of IFN-α by plasmacytoid dendritic cells and by activation of splenic CD11chi conventional dendritic cells. The latter was apparent from up-regulation of co-stimulatory molecules and from secretion of a wide range of inflammatory cytokines and chemokines including the Th1-governing cytokine IL-12, in keeping with the IgG2a antibody isotype distribution. PVP conjugates are a novel cancer vaccine design, offering an attractive molecular form, similar to VLP, and providing T-cell help. In contrast to VLP, they also incorporate a safe "in-built" ssRNA adjuvant.

Indexed as

AnimalsAntibodies, ViralDendritic CellsFemaleImmunoglobulin GInterleukin-12LymphomaMaleMiceMice, Inbred C57BLNicotianaPlant VirusesToll-Like Receptor 7VirionAntibodies, ViralImmunoglobulin GInterleukin-12Toll-Like Receptor 7

Identifiers

PMID25692288
PMCPMC4332868
OpenAlexW2003697352

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.