Evidence map›Paper›PMID 24942630›Full record

ArticleGene therapy2014

Vero/BC-F: an efficient packaging cell line stably expressing F protein to generate single round-infectious human parainfluenza virus type 2 vector.

J Ohtsuka, M Fukumura, M Tsurudome, K Hara, M Nishio, M Kawano, T Nosaka

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 93% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 2 institutions in 1 country.

J Ohtsuka1] Department of Microbiology and Molecular Genetics, Mie University Graduate School of Medicine, Tsu, Japan [2] Biocomo Inc., Komono, Komono-cho, Mie, Japan.
M Fukumura1] Department of Microbiology and Molecular Genetics, Mie University Graduate School of Medicine, Tsu, Japan [2] Biocomo Inc., Komono, Komono-cho, Mie, Japan.
M TsurudomeDepartment of Microbiology and Molecular Genetics, Mie University Graduate School of Medicine, Tsu, Japan.
K HaraDepartment of Microbiology and Molecular Genetics, Mie University Graduate School of Medicine, Tsu, Japan.
M NishioDepartment of Microbiology and Molecular Genetics, Mie University Graduate School of Medicine, Tsu, Japan.
M KawanoDepartment of Microbiology and Molecular Genetics, Mie University Graduate School of Medicine, Tsu, Japan.
T NosakaDepartment of Microbiology and Molecular Genetics, Mie University Graduate School of Medicine, Tsu, Japan.
Mie University · JPWakayama Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A stable packaging cell line (Vero/BC-F) constitutively expressing fusion (F) protein of the human parainfluenza virus type 2 (hPIV2) was established for production of the F-defective and single round-infectious hPIV2 vector in a strategy for recombinant vaccine development. The F gene expression has not evoked cytostatic or cytotoxic effects on the Vero/BC-F cells and the F protein was physiologically active to induce syncytial formation with giant polykaryocytes when transfected with a plasmid expressing hPIV2 hemagglutinin-neuraminidase (HN). Transduction of the F-defective replicon RNA into the Vero/BC-F cells led to the release of the infectious particles that packaged the replicon RNA (named as hPIV2ΔF) without detectable mutations, limiting the infectivity to a single round. The maximal titer of the hPIV2ΔF was 6.0 × 10(8) median tissue culture infections dose per ml. The influenza A virus M2 gene was inserted into hPIV2ΔF, and the M2 protein was found to be highly expressed in a human lung cancer cell line after transduction. Furthermore, in vivo airway infection experiments revealed that the hPIV2ΔF was capable of delivering transgenes to hamster tracheal cells. Thus, non-transmissible or single round-infectious hPIV2 vector will be potentially applicable to human gene therapy or recombinant vaccine development.

Indexed as

Genetic VectorsGene Transfer TechniquesAnimalsCell LineCells, CulturedChlorocebus aethiopsCricetinaeHumansInfluenza A virusParainfluenza Virus 2, HumanRecombinant ProteinsVaccines, SyntheticVero CellsViral Fusion ProteinsViral Matrix ProteinsViroporin ProteinsM2 protein, Influenza A virusRecombinant ProteinsVaccines, SyntheticViral Fusion ProteinsViral Matrix ProteinsViroporin Proteins

Identifiers

PMID24942630
OpenAlexW1974008700

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.