Evidence map›Paper›PMID 19211122›Full record

ArticleVirology2009

Comparative analysis of vector biodistribution, persistence and gene expression following intravenous delivery of bovine, porcine and human adenoviral vectors in a mouse model.

Anurag Sharma, Dinesh S Bangari, Manish Tandon, Aseem Pandey, Harm HogenEsch, Suresh K Mittal

Abstract read
In one paragraph

Article in Virology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

31 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Controlling timing and location in vaccines.Advanced drug delivery reviews · 2020
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. A potential approach for assessing the quality of human and nonhuman adenoviral vector preparations.Canadian journal of veterinary research = Revue canadienne de recherche veterinaire · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Oncolytic viruses: From bench to bedside with a focus on safety.Human vaccines & immunotherapeutics · 2015
    Review
  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

6 authors.

Anurag SharmaDepartment of Comparative Pathobiology, School of Veterinary Medicine, Purdue University, West Lafayette, IN 47907, USA.
Dinesh S Bangari
Manish Tandon
Aseem Pandey
Harm HogenEsch
Suresh K Mittal

Funding

Nonhuman adenoviral vectors for gene therapyR01CA110176 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI MITTAL, SURESH K · 2005 to 2008
$915k
NONHUMAN ADENOVIRUS VECTORS FOR GENE THERAPYR29GM055168 · NIGMS · PURDUE UNIVERSITY WEST LAFAYETTE · PI MITTAL, SURESH K · 1997 to 2001
$220k
NCI NIH HHS CA110176NCI NIH HHS R01 CA110176NIGMS NIH HHS R29 GM055168
6 · The paper itself

Abstract

Nonhuman adenoviruses including bovine adenovirus serotype 3 (BAd3) and porcine adenovirus serotype 3 (PAd3) can circumvent pre-existing immunity against human adenovirus serotype 5 (HAd5) and are being developed as alternative vectors for gene delivery. To assess the usefulness of these vectors for in vivo gene delivery, we compared biodistribution, persistence, state of vector genome, and transgene and vector gene expression by replication-defective BAd3 and PAd3 vectors with those of HAd5 vector in a FVB/n mouse model following intravenous inoculation. BAd3 vector efficiently transduced the heart, kidney and lung in addition to the liver and spleen and persisted for a longer duration compared to PAd3 or HAd5 vectors. Biodistribution of PAd3 vector was comparable to that of HAd5 vector but showed more rapid vector clearance. Only linear episomal forms of BAd3, PAd3, and HAd5 vector genomes were detected. All three vectors efficiently expressed the green fluorescent protein (GFP) transgene proportionate to the vector genome copy number in various tissues. Furthermore, leaky expression of vector genes, both the early (E4) and the late (hexon) was observed in all three vectors and gradually declined with time. These results suggest that BAd3 and PAd3 vectors could serve as an alternative or supplement to HAd5 for gene delivery applications.

Indexed as

Gene ExpressionTransduction, GeneticAdenoviridaeAnimalsDNA, ViralFemaleGenes, ReporterGenetic TherapyGenetic VectorsGreen Fluorescent ProteinsInjections, IntravenousMiceModels, AnimalTime FactorsDNA, ViralGreen Fluorescent Proteins

Identifiers

PMID19211122
PMCPMC2728445

What OpenQuestion holds

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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.