Evidence map›Paper›PMID 23568262›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2013

The epitope integration site for vaccine antigens determines virus control while maintaining efficacy in an engineered cancer vaccine.

Kevin D Pavelko, Michael P Bell, Lavakumar Karyampudi, Michael J Hansen, Kathleen S Allen, Keith L Knutson, Larry R Pease

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Breaking tolerance with engineered class I antigen-presenting molecules.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Improved Treatment Efficacy of Antiangiogenic Therapy when Combined with Picornavirus Vaccination in the GL261 Glioma Model.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2016
    Article
  11. Article
  12. Article
  13. 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

7 authors at 2 institutions in 1 country.

Kevin D PavelkoDepartment of Immunology, Mayo Clinic, Rochester, Minnesota 55905, USA. pavelko.kevin@mayo.edu
Michael P Bell
Lavakumar Karyampudi
Michael J Hansen
Kathleen S Allen
Keith L Knutson
Larry R Pease
Mayo Clinic · USMayo Clinic in Florida · US

Funding

Promoting Tumor Immunity by Cross-Linking B7-DCR01CA104996 · NCI · MAYO CLINIC ROCHESTER · PI PEASE, LARRY R · 2004 to 2013
$2.1M
NCI NIH HHS 5R01CA104996-08NCI NIH HHS R01 CA104996
6 · The paper itself

Abstract

Picornaviruses have been developed as potential therapies for gene delivery and vaccination. One drawback to their use is the potential for recombination and viral persistence. Therefore, the engineering strategies used must take into account the possibility for virus escape. We have developed Theiler's murine encephalomyelitis virus (TMEV) as a potential vaccine vector for use in immunotherapy. This study shows that insertion of a vaccine epitope at a unique site within the TMEV leader protein can dramatically increase the type I interferon (IFN) response to infection and promote rapid viral clearance. This live virus vaccine maintains its ability to drive antigen-specific CD8(+) T-cell responses to a model antigen as well as to the weakly immunogenic tumor antigen Her2/neu. Furthermore, the epitope integration site does not affect the efficacy of this vaccine as cancer immunotherapy for treating models of melanoma and breast cancer as demonstrated by delayed tumor outgrowth and increased survival in animals implanted with these tumors. These findings show that an attenuated virus retaining limited ability to replicate nonetheless can effectively mobilize CD8(+) cellular immunity and will be important for the design of picornavirus vectors used as immunotherapy in clinical settings.

Indexed as

Amino Acid SequenceAnimalsAntigensBase SequenceBreast NeoplasmsCancer VaccinesCardiovirus InfectionsCD8-Positive T-LymphocytesCell Line, TumorEpitopesErb-b2 Receptor Tyrosine KinasesFemaleGenetic VectorsHumansImmunotherapyInterferon Type IAntigensCancer VaccinesEpitopesErb-b2 Receptor Tyrosine KinasesInterferon Type IVaccines, AttenuatedViral Proteins

Identifiers

PMID23568262
PMCPMC3666639
OpenAlexW1998717583

What OpenQuestion holds

Textmetadata
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.