Evidence map›Paper›PMID 19539680›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2009

Sustained viral gene delivery through core-shell fibers.

I-Chien Liao, Sulin Chen, Jason B Liu, Kam W Leong

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

37 citing papers in PubMed, 151 citations in OpenAlex.

  1. Article
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  9. Article
  10. Article
  11. Review
  12. Electrospinning Nanofibers for Therapeutics Delivery.Nanomaterials (Basel, Switzerland) · 2019
    Review
  13. Article
  14. Review
  15. Poly(lactic-co-glycolic acid) devices: Production and applications for sustained protein delivery.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2018
    Review
  16. Article
  17. Review
  18. Review
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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

4 authors at 1 institution in 1 country.

I-Chien LiaoDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Sulin Chen
Jason B Liu
Kam W Leong
Duke University · US

Funding

Oral Nonviral Gene Delivery for Hemophilla AR01HL089764 · NHLBI · DUKE UNIVERSITY · PI LEONG, KAM W · 2008 to 2011
$1.7M
Mechanistic Studies on Polymeric Controlled Oral GeneR01EB002849 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI LEONG, KAM W · 2003 to 2007
$1.3M
Biofunctional fibers by polyelectrolyte complexationR01EB003447 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI LEONG, KAM W · 2005 to 2008
$1.1M
NHLBI NIH HHS R01 HL089764NIBIB NIH HHS R01 EB002849NIBIB NIH HHS R01 EB003447
6 · The paper itself

Abstract

Although viral gene transfer is efficient in achieving transgene expression for tissue engineering, drawbacks of virus dissemination, toxicity and transient gene expression due to immune response have hindered its widespread application. Many tissue engineering studies thus opt to genetically engineer cells in vitro prior to their introduction in vivo. However, it would be attractive to obviate the need for in vitro manipulation by transducing the infiltrating progenitor cells in situ. This study introduces the fabrication of a virus-encapsulated electrospun fibrous scaffold to achieve sustained and localized transduction. Adenovirus encoding the gene for green fluorescent protein was efficiently encapsulated into the core of poly(epsilon-caprolactone) fibers through co-axial electrospinning and was subsequently released via a porogen-mediated process. HEK 293 cells seeded on the scaffolds expressed high level of transgene expression over a month, while cells inoculated by scaffold supernatant showed only transient expression for a week. RAW 264.7 cells cultured on the virus-encapsulated fibers produced a lower level of IL-1 beta, TNF-alpha and IFN-alpha, suggesting that the activation of macrophage cells by the viral vector was reduced when encapsulated in the core-shell PCL fibers. In demonstrating sustained and localized cell transduction, this study presents an attractive alternative mode of applying viral gene transfer for regenerative medicine.

Indexed as

NanotubesAdenoviridaeCytomegalovirusDelayed-Action PreparationsEnzyme-Linked Immunosorbent AssayGene ExpressionGene Transfer TechniquesHumansKineticsMacrophagesMicroscopy, Electron, ScanningMicroscopy, Electron, TransmissionPolyestersPromoter Regions, GeneticTransgenesVirus ReplicationDelayed-Action PreparationspolycaprolactonePolyesters

Identifiers

PMID19539680
PMCPMC2747809
OpenAlexW2017964313

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.