Evidence map›Paper›PMID 38698956›Full record

ArticleActa naturae

A Method for the Production of Recombinant VSVs with Confirmation of Biological Activity.

V D Moroz, N B Gasanov, A D Egorov, A S Malogolovkin, M O Nagornykh, E N Subcheva, E S Kolosova, A Yu Fizikova, R A Ivanov, A V Karabelsky

Abstract read
In one paragraph

Article in Acta naturae. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Interferon-Based Therapeutics in Cancer Therapy: Past, Present, and Future.International journal of molecular sciences · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. 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

10 authors.

V D MorozSirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.
N B GasanovSirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.
A D EgorovSirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.
A S MalogolovkinSirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.
M O NagornykhSirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.
E N SubchevaSirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.
E S KolosovaSirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.
A Yu FizikovaSirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.
R A IvanovSirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.
A V KarabelskySirius University of Science and Technology, Krasnodar Region, Sirius, 354340 Russian Federation.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The design of new effective cancer treatment methods is a promising and important research field in translational medicine. Oncolytic viruses can induce immunogenic cell death by activating the body's immune system to recognize tumor cells. This work presents the results for optimizing the production of recombinant vesicular stomatitis viruses (rVSVs). To ensure the assembly of viral particles, we developed the HEK293TN-T7 cell line, which stably expresses DNA-dependent RNA polymerase 7 for viral genome transcription, and obtained helper plasmids encoding viral genes under the control of the CAG promoter. The oncolytic activity of the purified virus preparation was assessed in a murine model of B16F10Red melanoma cells expressing a red fluorescent protein. The presented method makes it possible to obtain purified viral preparations with a high titer and oncolytic activity. The amplification of viral particles in a HEK293 suspension culture allows for rapid scalability. Therefore, the developed approach can be used to obtain other recombinant VSV-based oncolytic viruses for tumor immunotherapy.

Indexed as

cancercytopathic effectmelanomaoncolytic virusesrecombinant vesicular stomatitis virusvesicular stomatitis virus

Identifiers

PMID38698956
PMCPMC11062106

What OpenQuestion holds

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Registered trials

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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.