Evidence map›Paper›PMID 28832561›Full record

ArticleGene therapy2017

Stent-based delivery of adeno-associated viral vectors with sustained vascular transduction and iNOS-mediated inhibition of in-stent restenosis.

I Fishbein, D T Guerrero, I S Alferiev, J B Foster, N G Minutolo, M Chorny, A M Monteys, K H Driesbaugh, C Nagaswami, R J Levy

Open access · greenAbstract read
In one paragraph

Article in Gene therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Progress towards permanent respiratory support.Current opinion in organ transplantation · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Stent-Based Gene Delivery for Coronary Disease.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  9. Applying Principles of Regenerative Medicine to Vascular Stent Development.Frontiers in bioengineering and biotechnology · 2022
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
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

10 authors at 2 institutions in 1 country.

I FishbeinThe Children's Hospital of Philadelphia, Philadelphia, PA, USA.
D T GuerreroThe Children's Hospital of Philadelphia, Philadelphia, PA, USA.
I S AlferievThe Children's Hospital of Philadelphia, Philadelphia, PA, USA.
J B FosterThe Children's Hospital of Philadelphia, Philadelphia, PA, USA.
N G MinutoloThe Children's Hospital of Philadelphia, Philadelphia, PA, USA.
M ChornyThe Children's Hospital of Philadelphia, Philadelphia, PA, USA.
A M MonteysThe Children's Hospital of Philadelphia, Philadelphia, PA, USA.
K H DriesbaughThe Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, USA.
C NagaswamiThe Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, USA.
R J LevyThe Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · US

Funding

Oxidation Resistant ApoA1 Gene Delivery StentsR01HL137762 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI FISHBEIN, ILIA, LEVY, ROBERT J · 2017 to 2020
$3.3M
Uniform field controlled magnetic cell targeting to stentsR01HL111118 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI CHORNY, MICHAEL · 2012 to 2016
$2.1M
Integrated drug-in-cell therapy of in-stent restenosisR21HL131016 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI CHORNY, MICHAEL · 2016 to 2017
$462k
Gene Delivery Stents AAV FormulationsR56HL072108 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI FISHBEIN, ILIA, LEVY, ROBERT J · 2015 to 2015
$420k
NHLBI NIH HHS R01 HL111118NHLBI NIH HHS R01 HL137762NHLBI NIH HHS R21 HL131016NHLBI NIH HHS R56 HL072108
6 · The paper itself

Abstract

In-stent restenosis remains an important clinical problem in the era of drug eluting stents. Development of clinical gene therapy protocols for the prevention and treatment of in-stent restenosis is hampered by the lack of adequate local delivery systems. Herein we describe a novel stent-based gene delivery platform capable of providing local arterial gene transfer with adeno-associated viral (AAV) vectors. This system exploits the natural affinity of protein G (PrG) to bind to the Fc region of mammalian IgG, making PrG a universal adaptor for surface immobilization of vector-capturing antibodies (Ab). Our results: 1) demonstrate the feasibility of reversible immobilization of AAV2 vectors using vector tethering by AAV2-specific Ab appended to the stent surface through covalently attached PrG, 2) show sustained release kinetics of PrG/Ab-immobilized AAV2 vector particles into simulated physiological medium in vitro and site-specific transduction of cultured cells, 3) provide evidence of long-term (12 weeks) arterial expression of luciferase with PrG/Ab-tethered AAV2

Indexed as

AnimalsCarotid ArteriesCell LineCoronary RestenosisDependovirusDrug Delivery SystemsDrug-Eluting StentsGenetic TherapyGenetic VectorsGene Transfer TechniquesHEK293 CellsHumansMaleNitric Oxide Synthase Type IIRatsRats, Sprague-DawleyNitric Oxide Synthase Type II

Identifiers

PMID28832561
PMCPMC5709213
OpenAlexW2748578419

What OpenQuestion holds

Textmetadata
LicenceTDM
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.