Evidence map›Paper›PMID 12587064›Full record

ArticleJournal of neurovirology2003

A novel neurotropic expression vector based on the avirulent A7(74) strain of Semliki Forest virus.

Markus J V Vähä-Koskela, Minna T Tuittila, Petra T Nygårdas, Jonas K-E Nyman, Markus U Ehrengruber, Martin Renggli, Ari E Hinkkanen

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Article in Journal of neurovirology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.4field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 65 citations in OpenAlex.

  1. Viral Vector-Based Cancer Vaccines.Methods in molecular biology (Clifton, N.J.) · 2025
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  7. Generation and FunctionalFrontiers in immunology · 2017
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  10. Review
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  13. Interferon-β sensitivity of tumor cells correlates with poor response to VA7 virotherapy in mouse glioma models.Molecular therapy : the journal of the American Society of Gene Therapy · 2012
    Article
  14. Article
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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

7 authors at 3 institutions in 2 countries.

Markus J V Vähä-KoskelaDepartment of Biochemistry and Pharmacy, Abo Akademi University, Turku, Finland. makoskel@abo.fi
Minna T Tuittila
Petra T Nygårdas
Jonas K-E Nyman
Markus U Ehrengruber
Martin Renggli
Ari E Hinkkanen
Turku Centre for Biotechnology · FIÅbo Akademi University · FIUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Semliki Forest virus (SFV), an enveloped alphavirus of the family Togaviridae, infects a wide range of mammalian host cells. Most strains are neurotropic but differ in virulence. The authors took advantage of the nonpathogenic properties of SFV strain A7(74), cloned recently in their laboratory, and constructed a replication-proficient expression vector to target the central nervous system (CNS) for heterologous gene expression. The vector, termed VA7, was engineered to drive expression of foreign inserts through a second subgenomic promoter inserted in the viral 3' nontranslated region (NTR). Infectious virus was obtained by in vitro transcription and transfection into BHK cells, and was shown to direct synthesis of heterologous proteins in several mammalian cell lines. Although novel expression vehicle is not applicable for targeting specific cell populations within the CNS in its present form, in cultured rat hippocampal slices, VA7 encoding enhanced green fluorescent protein (EGFP) efficiently transduced pyramidal cells, interneurons, and glial cells. With prolonged time post infection, the number of EGFP-expressing neurons in hippocampal slices increased. Mice infected intraperitoneally with the recombinant virus remained completely asymptomatic but showed CNS expression of EGFP as evidenced by immunohistochemistry. SFV A7(74) is a nonintegrating virus, which gives rise to a randomly distributed, patchy infection of the adult CNS that is cleared within 10 days. With the advantage of noninvasive administration, the expression vector described in this work is thus applicable for short-term gene expression in the CNS.

Indexed as

Genetic VectorsAnimalsCHO CellsCricetinaeEpithelial CellsFemaleGene Expression Regulation, ViralGliomaGliosarcomaGreen Fluorescent ProteinsHippocampusIndicators and ReagentsKidneyLuminescent ProteinsMelanomaMiceGreen Fluorescent ProteinsIndicators and ReagentsLuminescent Proteins

Identifiers

PMID12587064
OpenAlexW2006602823

What OpenQuestion holds

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Read underepoch 390

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.