Evidence map›Paper›PMID 25462341›Full record

ArticleVirology2015

Attenuation of vesicular stomatitis virus infection of brain using antiviral drugs and an adeno-associated virus-interferon vector.

Guido Wollmann, Justin C Paglino, Patrick R Maloney, Sebastian A Ahmadi, Anthony N van den Pol

Abstract read
In one paragraph

Article in Virology, 2015. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Review
  4. Oncolytic Virotherapy: A New Paradigm in Cancer Immunotherapy.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Article
  7. Oncolytic Virotherapy in Glioma Tumors.International journal of molecular sciences · 2020
    Review
  8. Optimizing oncolytic virotherapy in cancer treatment.Nature reviews. Drug discovery · 2019
    Review
  9. Article
  10. 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

5 authors.

Guido WollmannDepartment of Neurosurgery, Yale University School of Medicine, New Haven, CT 06520, United States.
Justin C PaglinoDepartment of Neurosurgery, Yale University School of Medicine, New Haven, CT 06520, United States.
Patrick R MaloneyDepartment of Neurosurgery, Yale University School of Medicine, New Haven, CT 06520, United States.
Sebastian A AhmadiDepartment of Neurosurgery, Yale University School of Medicine, New Haven, CT 06520, United States.
Anthony N van den PolDepartment of Neurosurgery, Yale University School of Medicine, New Haven, CT 06520, United States. Electronic address: anthony.vandenpol@yale.edu.

Funding

Vesicular stomatitis VSVrp30 selectively destroys human metastatic melanomaR01CA161048 · NCI · YALE UNIVERSITY · PI VAN DEN POL, ANTHONY N · 2012 to 2016
$1.7M
Oncolytic Virus Targets Brain TumorsR01CA124737 · NCI · YALE UNIVERSITY · PI VAN DEN POL, ANTHONY N · 2007 to 2011
$1.6M
LuIII parvovirus targets gliomaR01CA175577 · NCI · YALE UNIVERSITY · PI VAN DEN POL, ANTHONY N · 2013 to 2015
$1.0M
Glioma immunotherapy with strategies based on autonomous parvovirus MVMpK08CA169005 · NCI · YALE UNIVERSITY · PI PAGLINO, JUSTIN COBB · 2013 to 2017
$587k
NCI NIH HHS CA124737NCI NIH HHS CA161048NCI NIH HHS CA175577NCI NIH HHS K08 CA169005NCI NIH HHS K08CA169005NCI NIH HHS R01 CA124737NCI NIH HHS R01 CA161048NCI NIH HHS R01 CA175577
6 · The paper itself

Abstract

Vesicular stomatitis virus (VSV) shows promise as a vaccine-vector and oncolytic virus. However, reports of neurotoxicity of VSV remain a concern. We compared 12 antiviral compounds to control infection of VSV-CT9-M51 and VSV-rp30 using murine and human brain cultures, and in vivo mouse models. Inhibition of replication, cytotoxicity and infectivity was strongest with ribavirin and IFN-α and to some extent with mycophenolic acid, chloroquine, and adenine 9-β-d-arabinofuranoside. To generate continuous IFN exposure, we made an adeno-associated virus vector expressing murine IFN; AAV-mIFN-β protected mouse brain cells from VSV, as did a combination of IFN, ribavirin and chloroquine. Intracranial AAV-mIFN-β protected the brain against VSV-CT9-M51. In SCID mice bearing human glioblastoma, AAV-mIFN-β moderately enhanced survival. VSV-CT9-M51 doubled median survival when administered after AAV-mIFN-β; some surviving mice showed complete tumor destruction. Together, these data suggest that AAV-IFN or IFN with ribavirin and chloroquine provide an optimal anti-virus combination against VSV in the brain.

Indexed as

AnimalsAntiviral AgentsBrainCells, CulturedDependovirusGenetic VectorsHumansInterferonsMiceMice, SCIDNeurogliaNeuronsOncolytic VirotherapyOncolytic VirusesVesicular StomatitisVesiculovirusAntiviral AgentsInterferonsAAVAntiviralBrainInterferonOncolytic virusRibavirinVSV

Identifiers

PMID25462341
PMCPMC4326005

What OpenQuestion holds

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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.