Evidence map›Paper›PMID 15731258›Full record

ArticleJournal of virology2005

Ligand-directed gene targeting to mammalian cells by pseudotype baculoviruses.

Yoshinori Kitagawa, Hideki Tani, Chang Kwang Limn, Tomoko M Matsunaga, Kohji Moriishi, Yoshiharu Matsuura

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
  2. Article
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  4. Baculovirus Production and Infection in Axolotls.Methods in molecular biology (Clifton, N.J.) · 2023
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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

6 authors at 1 institution in 1 country.

Yoshinori KitagawaResearch Center for Emerging Infectious Diseases, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan.
Hideki Tani
Chang Kwang Limn
Tomoko M Matsunaga
Kohji Moriishi
Yoshiharu Matsuura
Osaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV) can infect a variety of mammalian cells, as well as insect cells, facilitating its use as a viral vector for gene delivery into mammalian cells. Glycoprotein gp64, a major component of the budded AcMNPV envelope, is involved in viral entry into cells by receptor-mediated endocytosis and subsequent membrane fusion. We examined the potential production of pseudotype baculovirus particles transiently carrying ligands of interest in place of gp64 as a method of ligand-directed gene delivery into target cells. During amplification of a gp64-null pseudotype baculovirus carrying a green fluorescent protein gene in gp64-expressing insect cells, however, we observed the high-frequency appearance of a replication-competent virus incorporating the gp64 gene into the viral genome. To avoid generation of replication-competent revertants, we prepared pseudotype baculoviruses by transfection with recombinant bacmids without further amplification in the gp64-expressing cells. We constructed gp64-null recombinant bacmids carrying cDNAs encoding either vesicular stomatitis virus G protein (VSVG) or measles virus receptors (CD46 or SLAM). The VSVG pseudotype baculovirus efficiently transduced a reporter gene into a variety of mammalian cell lines, while CD46 and SLAM pseudotype baculoviruses allowed ligand-receptor-directed reporter gene transduction into target cells expressing measles virus envelope glycoproteins. Gene transduction mediated by the pseudotype baculoviruses could be inhibited by pretreatment with specific antibodies. These results indicate the possible application of pseudotype baculoviruses in ligand-directed gene delivery into target cells.

Indexed as

Genetic VectorsTransduction, GeneticAntigens, CDGene DeletionGenes, ReporterGene TargetingGenetic TherapyGlycoproteinsGreen Fluorescent ProteinsImmunoglobulinsMembrane Cofactor ProteinMembrane GlycoproteinsNucleopolyhedrovirusesOcclusion Body Matrix ProteinsPromoter Regions, GeneticReceptors, Cell SurfaceAntigens, CDGlycoproteinsG protein, vesicular stomatitis virusGreen Fluorescent ProteinsImmunoglobulinsMembrane Cofactor ProteinMembrane GlycoproteinsOcclusion Body Matrix Proteinspolyhedrin protein, NucleopolyhedrovirusReceptors, Cell SurfaceSignaling Lymphocytic Activation Molecule Family Member 1Viral Envelope ProteinsViral Fusion ProteinsViral ProteinsViral Structural Proteins

Identifiers

PMID15731258
PMCPMC1075727
OpenAlexW2101263068

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.