Evidence map›Paper›PMID 30232179›Full record

ArticleJournal of virology2018

A Novel Chimeric Oncolytic Virus Vector for Improved Safety and Efficacy as a Platform for the Treatment of Hepatocellular Carcinoma.

Sarah Abdullahi, Melanie Jäkel, Sabine J Behrend, Katja Steiger, Geoffrey Topping, Teresa Krabbe, Alessio Colombo, Volker Sandig, Tobias S Schiergens, Wolfgang E Thasler and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 65 citations in OpenAlex.

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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

15 authors at 4 institutions in 1 country.

Sarah AbdullahiDepartment of Internal Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Melanie JäkelDepartment of Internal Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Sabine J BehrendDepartment of Internal Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Katja SteigerDepartment of Pathology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Geoffrey ToppingDepartment of Nuclear Medicine, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Teresa KrabbeDepartment of Internal Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Alessio ColomboGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Volker SandigProBioGen AG, Berlin, Germany.
Tobias S SchiergensDepartment of General, Visceral, Vascular and Transplant Surgery, Hospital of the University of Munich, Munich, Germany.
Wolfgang E ThaslerDepartment of General and Visceral Surgery, Red Cross Hospital, Munich, Germany.
Jens WernerDepartment of General, Visceral, Vascular and Transplant Surgery, Hospital of the University of Munich, Munich, Germany.
Stefan F LichtenthalerGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Roland M SchmidDepartment of Internal Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Oliver EbertDepartment of Internal Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Jennifer AltomonteDepartment of Internal Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany jennifer.altomonte@tum.de.ORCID 0000-0003-1079-3633
TUM Klinikum · DEGerman Center for Neurodegenerative Diseases · DELMU Klinikum · DEGerman Red Cross · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncolytic viruses represent an exciting new aspect of the evolving field of cancer immunotherapy. We have engineered a novel hybrid vector comprising vesicular stomatitis virus (VSV) and Newcastle disease virus (NDV), named recombinant VSV-NDV (rVSV-NDV), wherein the VSV backbone is conserved but its glycoprotein has been replaced by the hemagglutinin-neuraminidase (HN) and the modified, hyperfusogenic fusion (F) envelope proteins of recombinant NDV. In comparison to wild-type VSV, which kills cells through a classical cytopathic effect, the recombinant virus is able to induce tumor-specific syncytium formation, allowing efficient cell-to-cell spread of the virus and a rapid onset of immunogenic cell death. Furthermore, the glycoprotein exchange substantially abrogates the off-target effects in brain and liver tissue associated with wild-type VSV, resulting in a markedly enhanced safety profile, even in immune-deficient NOD.CB17-prkdc

Indexed as

Oncolytic VirotherapyAnimalsCarcinoma, HepatocellularCell SurvivalGenetic VectorsHumansLiver NeoplasmsMaleMiceMice, Inbred NODMice, SCIDNewcastle disease virusOncolytic VirusesTumor Cells, CulturedVesicular stomatitis Indiana virusVirus Replicationchimeric virusfusion proteinhepatocellular carcinomaimmunotherapyoncolytic virussyncytia

Identifiers

PMID30232179
PMCPMC6232488
OpenAlexW2892314541

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.