Evidence map›Paper›PMID 33348052›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2021

Fusogenic oncolytic vaccinia virus enhances systemic antitumor immune response by modulating the tumor microenvironment.

Motomu Nakatake, Nozomi Kuwano, Emi Kaitsurumaru, Hajime Kurosaki, Takafumi Nakamura

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  9. Article
  10. Current status and research progress of oncolytic virus.Pharmaceutical science advances · 2024
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. The microbiome, gastrointestinal cancer, and immunotherapy.Journal of gastroenterology and hepatology · 2022
    Review
  18. Review
  19. Article
  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

5 authors at 1 institution in 1 country.

Motomu NakatakeDivision of Molecular Medicine, Department of Genomic Medicine and Regenerative Therapeutics, School of Medicine, Tottori University Faculty of Medicine, 86 Nishi-cho, Yonago 683-8503, Japan.
Nozomi KuwanoDivision of Molecular Medicine, Department of Genomic Medicine and Regenerative Therapeutics, School of Medicine, Tottori University Faculty of Medicine, 86 Nishi-cho, Yonago 683-8503, Japan.
Emi KaitsurumaruDivision of Molecular Medicine, Department of Genomic Medicine and Regenerative Therapeutics, School of Medicine, Tottori University Faculty of Medicine, 86 Nishi-cho, Yonago 683-8503, Japan.
Hajime KurosakiDivision of Molecular Medicine, Department of Genomic Medicine and Regenerative Therapeutics, School of Medicine, Tottori University Faculty of Medicine, 86 Nishi-cho, Yonago 683-8503, Japan.
Takafumi NakamuraDivision of Molecular Medicine, Department of Genomic Medicine and Regenerative Therapeutics, School of Medicine, Tottori University Faculty of Medicine, 86 Nishi-cho, Yonago 683-8503, Japan. Electronic address: taka@tottori-u.ac.jp.
Tottori University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncolytic viruses induce antitumor immunity following direct viral oncolysis. However, their therapeutic effects are limited in distant untreated tumors because their antitumor function depends on indirect antitumor immunity. Here, we generated a novel fusogenic oncolytic vaccinia virus (FUVAC) and compared its antitumor activity with that of its parental non-fusogenic virus. Compared with the parent, FUVAC exerted the cytopathic effect and induced immunogenic cell death in human and murine cancer cells more efficiently. In a bilateral tumor-bearing syngeneic mouse model, FUVAC administration significantly inhibited tumor growth in both treated and untreated tumors. However, its antitumor effects were completely suppressed by CD8

Indexed as

A549 CellsAnimalsCell Line, TumorColonic NeoplasmsCombined Modality TherapyFemaleHumansImmune Checkpoint InhibitorsMiceMutationOncolytic VirotherapyOncolytic VirusesTumor MicroenvironmentVaccinia virusVirus InternalizationXenograft Model Antitumor AssaysImmune Checkpoint Inhibitorsantitumor immunitycell membrane fusionimmune checkpoint blockadeoncolytic functionvaccinia virus

Identifiers

PMID33348052
PMCPMC8116573
OpenAlexW3117393565

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.