Evidence map›Paper›PMID 25069854›Full record

ArticleScientific reports2014

Adeno-associated viral vectors show serotype specific transduction of equine joint tissue explants and cultured monolayers.

Daniel D Hemphill, C Wayne McIlwraith, R Jude Samulski, Laurie R Goodrich

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Gene therapy approaches for equine osteoarthritis.Frontiers in veterinary science · 2022
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. The challenges of promoting osteogenesis in segmental bone defects and osteoporosis.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2018
    Review
  11. Review
  12. 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

4 authors at 2 institutions in 1 country.

Daniel D HemphillOrthopaedic Research Center, College of Veterinary Medicine, Colorado State University, Fort Collins, CO 80523.
C Wayne McIlwraithOrthopaedic Research Center, College of Veterinary Medicine, Colorado State University, Fort Collins, CO 80523.
R Jude SamulskiUniversity of North Carolina Gene Therapy Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Laurie R GoodrichOrthopaedic Research Center, College of Veterinary Medicine, Colorado State University, Fort Collins, CO 80523.
Colorado State University · USUniversity of North Carolina at Chapel Hill · US

Funding

VECTOR AND MOLECULAR BIOLOGY COREP01HL112761 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SAMULSKI, RICHARD J · 2013 to 2017
$11.3M
Rational and Combinatorial Engineering of AAV VectorsR01AI072176 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HIRSCH, MATTHEW LOUIS, SAMULSKI, RICHARD J · 2008 to 2017
$3.7M
AAV Gene Therapy for AAT DeficiencyR01DK084033 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, CHENGWEN · 2009 to 2016
$2.2M
Overcoming our clinical complications: AAV vector design for the treatment of DMDR01AR064369 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HIRSCH, MATTHEW LOUIS, SAMULSKI, RICHARD J · 2013 to 2017
$1.6M
Gene Therapeutic Approaches to Cartilage RepairK08AR054903 · NIAMS · COLORADO STATE UNIVERSITY · PI GOODRICH, LAURIE · 2008 to 2012
$720k
NHLBI NIH HHS P01 HL112761NHLBI NIH HHS P01 HL112761-01A1NIAID NIH HHS 2-R01-AI072176-06A1NIAID NIH HHS R01 AI072176NIAMS NIH HHS K08 AR054903NIAMS NIH HHS K08AR054903NIAMS NIH HHS R01 AR064369NIDDK NIH HHS 1R01DK084033NIDDK NIH HHS R01 DK084033
6 · The paper itself

Abstract

Adeno-associated virus (AAV) receptors range from heparan sulfate proteoglycan to sialic acid moieties present on cell surfaces. Abundance of the glycan profiles is greatly influenced by animal species, cell type, and culture conditions. The objective of this study was to determine whether AAV serotypes' transduction efficiencies specifically in the equine monolayer culture model are an accurate representation of transduction efficiencies in tissue explants, a model more closely related to in vivo transduction. It was found that AAV 2 and 2.5 transduced cells more efficiently in explants than in monolayers. Through experiments involving assessing enzyme degradation of cell surface proteoglycans, this change could not be attributed to differences in the extra cellular matrix (ECM), but a similar change in AAV 5 transduction efficiency could be readily explained by differences in cell surface sialylated glycan. Unexpectedly it was found that in a small but diverse sample of horses evidence for serum neutralizing antibodies was only found to AAV 5. This suggests a unique relationship between this capsid and the equine host or an unresolved relationship between similar bovine AAV and the AAV 5 capsid immune response.

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralCapsidCattleCell Culture TechniquesDependovirusFoot JointsGenetic VectorsHorsesNeutralization TestsProteoglycansSerotypingSynovial MembraneTissue Culture TechniquesTransduction, GeneticAntibodies, NeutralizingAntibodies, ViralProteoglycans

Identifiers

PMID25069854
PMCPMC4894424
OpenAlexW2087372826

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.