Evidence map›Paper›PMID 24554655›Full record

ArticleJournal of virology2014

VSV-GP: a potent viral vaccine vector that boosts the immune response upon repeated applications.

Reinhard Tober, Zoltan Banki, Lisa Egerer, Alexander Muik, Sandra Behmüller, Florian Kreppel, Ute Greczmiel, Annette Oxenius, Dorothee von Laer, Janine Kimpel

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
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  9. Review
  10. Characterization of VSV-GP morphology by cryo-EM imaging and SEC-MALS.Molecular therapy. Methods & clinical development · 2025
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Repeated harvest enables efficient production of VSV-GP.Frontiers in bioengineering and biotechnology · 2024
    Article
  17. Lassa fever vaccine candidates: A scoping review of vaccine clinical trials.Tropical medicine & international health : TM & IH · 2023
    Article
  18. Article
  19. Review
  20. Review
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 4 institutions in 3 countries.

Reinhard ToberDivision of Virology, Innsbruck Medical University, Innsbruck, Austria.
Zoltan Banki
Lisa Egerer
Alexander Muik
Sandra Behmüller
Florian Kreppel
Ute Greczmiel
Annette Oxenius
Dorothee von Laer
Janine Kimpel
Innsbruck Medical University · ATETH Zurich · CHUniversität Ulm · DEGeorg Speyer Haus · DE

Funding

Austrian Science Fund FWF P 25499
6 · The paper itself

Abstract

unlabelledAntivector immunity limits the response to homologous boosting for viral vector vaccines. Here, we describe a new, potent vaccine vector based on replication-competent vesicular stomatitis virus pseudotyped with the glycoprotein of the lymphocytic choriomeningitis virus (VSV-GP), which we previously showed to be safe in mice. In mice, VSV and VSV-GP encoding ovalbumin (OVA) as a model antigen (VSV-OVA and VSV-GP-OVA) induced equal levels of OVA-specific humoral and cellular immune responses upon a single immunization. However, boosting with the same vector was possible only for VSV-GP-OVA as neutralizing antibodies to VSV limited the immunogenicity of the VSV-OVA boost. OVA-specific cytotoxic T-lymphocyte (CTL) responses induced by VSV-GP-OVA were at least as potent as those induced by an adenoviral state-of-the-art vaccine vector and completely protected mice in a Listeria monocytogenes challenge model. VSV-GP is so far the only replication-competent vaccine vector that does not lose efficacy upon repeated application. IMPORTANCE: Although there has been great progress in treatment and prevention of infectious diseases in the past several years, effective vaccines against some of the most serious infections, e.g., AIDS, malaria, hepatitis C, or tuberculosis, are urgently needed. Here, several approaches based on viral vector vaccines are under development. However, for all viral vaccine vectors currently in clinical testing, repeated application is limited by neutralizing antibodies to the vector itself. Here, we have exploited the potential of vesicular stomatitis virus pseudotyped with the glycoprotein of the lymphocytic choriomeningitis virus (VSV-GP) as a vaccine platform. VSV-GP is the first replication-competent viral vector vaccine that does not induce vector-specific humoral immunity, i.e., neutralizing antibodies, and therefore can boost immune responses against a foreign antigen by repeated applications. The vector allows introduction of various antigens and therefore can serve as a platform technology for the development of novel vaccines against a broad spectrum of diseases.

Indexed as

Drug CarriersAnimalsAntibodies, NeutralizingAntibodies, ViralAntigens, ViralGenetic VectorsLymphocytic choriomeningitis virusMiceMice, Inbred C57BLOvalbuminT-Lymphocytes, CytotoxicVaccinationVesiculovirusViral VaccinesAntibodies, NeutralizingAntibodies, ViralAntigens, ViralDrug CarriersOvalbuminViral Vaccines

Identifiers

PMID24554655
PMCPMC3993835
OpenAlexW2023607235

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.