Evidence map›Paper›PMID 25196484›Full record

ArticleViruses2014

Fiber-modified adenovirus for central nervous system Parkinson's disease gene therapy.

Travis B Lewis, Joel N Glasgow, Ashley S Harms, David G Standaert, David T Curiel

Abstract read
In one paragraph

Article in Viruses, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. High-Capacity Adenoviral Vectors: Expanding the Scope of Gene Therapy.International journal of molecular sciences · 2020
    Review
  4. Review
  5. Therapies for Parkinson's diseases: alternatives to current pharmacological interventions.Journal of neural transmission (Vienna, Austria : 1996) · 2016
    Review
  6. 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

5 authors.

Travis B LewisDepartment of Cell Biology, The University of Alabama at Birmingham, Birmingham, AL 35294, USA. travis.lewis@uphs.upenn.edu.
Joel N GlasgowDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. jng@uab.edu.
Ashley S HarmsCenter for Neurodegeneration and Experimental Therapeutics, Department of Neurology, The University of Alabama at Birmingham, Birmingham, AL 35294, USA. anharms@uab.edu.
David G StandaertCenter for Neurodegeneration and Experimental Therapeutics, Department of Neurology, The University of Alabama at Birmingham, Birmingham, AL 35294, USA. dstandaert@uab.edu.
David T CurielDepartment of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63108, USA. dcuriel@radonc.wustl.edu.

Funding

Regulatory T Cells and Oncolytic Virotherapy of GliomaR01CA122930 · NCI · UNIVERSITY OF CHICAGO · PI LESNIAK, MACIEJ S · 2008 to 2015
$2.5M
Developing an Adenoviral Vector Platform for Selective Gene Delivery to NeuronsF30NS065661 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LEWIS, TRAVIS B. · 2009 to 2012
$143k
NCI NIH HHS R01 CA122930NCI NIH HHS R01CA122930NINDS NIH HHS F30 NS065661NINDS NIH HHS F30NS065661
6 · The paper itself

Abstract

Gene-based therapies for neurological diseases continue to develop briskly. As disease mechanisms are elucidated, flexible gene delivery platforms incorporating transcriptional regulatory elements, therapeutic genes and targeted delivery are required for the safety and efficacy of these approaches. Adenovirus serotype 5 (Ad5)-based vectors can carry large genetic payloads to provide this flexibility, but do not transduce neuronal cells efficiently. To address this, we have developed a tropism-modified Ad5 vector with neuron-selective targeting properties for evaluation in models of Parkinson disease therapy. A panel of tropism-modified Ad5 vectors was screened for enhanced gene delivery in a neuroblastoma cell line model system. We used these observations to design and construct an unbiased Ad vector platform, consisting of an unmodified Ad5 and a tropism-modified Ad5 vector containing the fiber knob domain from canine Ad serotype 2 (Ad5-CGW-CK2). Delivery to the substantia nigra or striatum showed that this vector produced a neuronally-restricted pattern of gene expression. Many of the transduced neurons were from regions with afferent projections to the injection site, implicating that the vector binds the presynaptic terminal resulting in presynaptic transduction. We show that Ad5-CGW-CK2 can selectively transduce neurons in the brain and hypothesize that this modular platform is potentially adaptable to clinical use.

Indexed as

Transduction, GeneticViral TropismAdenoviridaeAnimalsBrainCapsid ProteinsCell LineGenetic TherapyMiceNeuronsOrganisms, Genetically ModifiedParkinson DiseaseCapsid Proteinshexon capsid protein, Adenovirus

Identifiers

PMID25196484
PMCPMC4147696

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.