Evidence map›Paper›PMID 16541121›Full record

ArticleGene therapy2006

Adenovirus serotype 35 vector-mediated transduction into human CD46-transgenic mice.

F Sakurai, K Kawabata, N Koizumi, N Inoue, M Okabe, T Yamaguchi, T Hayakawa, H Mizuguchi

Abstract read
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In one paragraph

Article in Gene therapy, 2006. 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
4.5field-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

20 citing papers in PubMed, 43 citations in OpenAlex.

  1. Frontiers in cellular and infection microbiology · 2025
    Review
  2. Review
  3. Construction and application of adenoviral vectors.Molecular therapy. Nucleic acids · 2023
    Review
  4. Article
  5. Review
  6. Article
  7. In Vivo Hematopoietic Stem Cell Transduction.Hematology/oncology clinics of North America · 2017
    Review
  8. Article
  9. Article
  10. Article
  11. Adenovirus vectors targeting distinct cell types in the retina.Investigative ophthalmology & visual science · 2010
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 4 institutions in 1 country.

F SakuraiLaboratory of Gene Transfer and Regulation, National Institute of Biomedical Innovation, Osaka, Japan.
K Kawabata
N Koizumi
N Inoue
M Okabe
T Yamaguchi
T Hayakawa
H Mizuguchi
National Institute of Biomedical Innovation, Health and Nutrition · JPOsaka University · JPNational Institute of Health Sciences · JPPharmaceuticals and Medical Devices Agency · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously demonstrated that systemic administration of adenovirus serotype 35 (Ad35) vectors to mice does not mediate efficient transduction in organs, probably because expression of the mouse analog of the subgroup B Ad receptor, human CD46 (membrane cofactor protein), is limited to the testis. Here, we describe the in vitro and in vivo transduction characteristics of Ad35 vectors by using homozygous and hemizygous human CD46-transgenic (CD46TG) mice, which ubiquitously express human CD46. An Ad35 vector more efficiently transduced the primary dendritic cells and macrophages prepared from CD46TG mice than those from wild-type mice. In vivo transduction experiments demonstrated that CD46TG mice are more susceptible to Ad35 vector-mediated in vivo transduction than are wild-type mice. In particular, homozygous CD46TG mice, which express higher levels of CD46 in the organs than hemizygous CD46TG mice, tend to exhibit higher transduction efficiencies after intraperitoneal administration than hemizygous CD46TG mice. Intraperitoneal administration of Ad35 vectors resulted in efficient transduction into the mesothelial cells of the peritoneal organs in homozygous CD46TG mice. These results indicate that an Ad35 vector recognizes human CD46 as a cellular receptor in CD46TG mice. However, the in vivo transduction efficiencies of Ad35 vectors in CD46TG mice are much lower than those of conventional Ad5 vectors in wild-type mice.

Indexed as

AdenoviridaeAnimalsBlotting, WesternDendritic CellsFlow CytometryGene ExpressionGenetic TherapyGenetic VectorsHumansInjections, IntraperitonealMacrophagesMaleMembrane Cofactor ProteinMiceMice, TransgenicSpermatozoaMembrane Cofactor Protein

Identifiers

PMID16541121
OpenAlexW2068095734

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.