Evidence map›Paper›PMID 32404527›Full record

ArticleJournal of virology2020

Orf Virus-Based Therapeutic Vaccine for Treatment of Papillomavirus-Induced Tumors.

M Schneider, M Müller, A Yigitliler, J Xi, C Simon, T Feger, H-J Rziha, F Stubenrauch, H-G Rammensee, T Iftner and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. The cooperation between orf virus andFrontiers in cellular and infection microbiology · 2023
    Review
  9. Article
  10. Article
  11. Vaccines · 2020
    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

11 authors at 2 institutions in 1 country.

M SchneiderUniversity Hospital Tuebingen, Institute for Medical Virology and Epidemiology of Viral Diseases, Tuebingen, Germany.
M MüllerUniversity of Tuebingen, Interfaculty Institute for Cell Biology, Department of Immunology, Tuebingen, Germany.
A YigitlilerUniversity Hospital Tuebingen, Institute for Medical Virology and Epidemiology of Viral Diseases, Tuebingen, Germany.
J XiUniversity Hospital Tuebingen, Institute for Medical Virology and Epidemiology of Viral Diseases, Tuebingen, Germany.
C SimonUniversity Hospital Tuebingen, Institute for Medical Virology and Epidemiology of Viral Diseases, Tuebingen, Germany.
T FegerUniversity of Tuebingen, Interfaculty Institute for Cell Biology, Department of Immunology, Tuebingen, Germany.
H-J RzihaUniversity of Tuebingen, Interfaculty Institute for Cell Biology, Department of Immunology, Tuebingen, Germany.
F StubenrauchUniversity Hospital Tuebingen, Institute for Medical Virology and Epidemiology of Viral Diseases, Tuebingen, Germany.
H-G RammenseeUniversity of Tuebingen, Interfaculty Institute for Cell Biology, Department of Immunology, Tuebingen, Germany.
T IftnerUniversity Hospital Tuebingen, Institute for Medical Virology and Epidemiology of Viral Diseases, Tuebingen, Germany thomas.iftner@med.uni-tuebingen.de ralf.amann@ifiz.uni-tuebingen.de.
R AmannUniversity of Tuebingen, Interfaculty Institute for Cell Biology, Department of Immunology, Tuebingen, Germany thomas.iftner@med.uni-tuebingen.de ralf.amann@ifiz.uni-tuebingen.de.
University of Tübingen · DEGerman Cancer Research Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Orf virus (ORFV) represents a suitable vector for the generation of efficient, prophylactic antiviral vaccines against different pathogens. The present study investigated for the first time the therapeutic application of ORFV vector-based vaccines against tumors induced by cottontail rabbit papillomavirus (CRPV). ORFV-CRPV recombinants were constructed expressing the early CRPV gene E1, E2, E7, or LE6. In two independent experiments we used in total 23 rabbits which were immunized with a mixture of the four ORFV-CRPV recombinants or empty ORFV vector as a control 5 weeks after the appearance of skin tumors. For the determination of the therapeutic efficacy, the subsequent growth of the tumors was recorded. In the first experiment, we could demonstrate that three immunizations of rabbits with high tumor burden with the combined four ORFV-CRPV recombinants resulted in significant growth retardation of the tumors compared to the control. A second experiment was performed to test the therapeutic effect of 5 doses of the combined vaccine in rabbits with a lower tumor burden than in nonimmunized rabbits. Tumor growth was significantly reduced after immunization, and one vaccinated rabbit even displayed complete tumor regression until the end of the observation period at 26 weeks. Results of delayed-type hypersensitivity (DTH) skin tests suggest the induction of a cellular immune response mediated by the ORFV-CRPV vaccine. The data presented show for the first time a therapeutic potential of the ORFV vector platform and encourage further studies for the development of a therapeutic vaccine against virus-induced tumors.

Indexed as

AnimalsCancer VaccinesChlorocebus aethiopsCottontail rabbit papillomavirusNeoplasmsOrf virusPapillomavirus InfectionsRabbitsVero CellsViral ProteinsViral VaccinesCancer VaccinesViral ProteinsViral Vaccinescottontail rabbit papillomavirusCRPVORFVOrf viruspapillomavirustherapeutic vector vaccine

Identifiers

PMID32404527
PMCPMC7375371
OpenAlexW3024529149

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.