Evidence map›Paper›PMID 20428210›Full record

ArticleGene therapy2010

Cell-based osteoprotegerin therapy for debris-induced aseptic prosthetic loosening on a murine model.

L Zhang, T-H Jia, A C M Chong, L Bai, H Yu, W Gong, P H Wooley, S-Y Yang

Open access · greenAbstract read
In one paragraph

Article in Gene therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Arthrotomy-based preclinical models of particle-induced osteolysis: A systematic review.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2017
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  14. Macromolecular prodrug of dexamethasone prevents particle-induced peri-implant osteolysis with reduced systemic side effects.Journal of controlled release : official journal of the Controlled Release Society · 2014
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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

8 authors at 3 institutions in 2 countries.

L ZhangOrthopaedic Research Institute, Via Christi Regional Medical Center, 929 N St Francis Street, Wichita, KS 67214, USA.
T-H Jia
A C M Chong
L Bai
H Yu
W Gong
P H Wooley
S-Y Yang
Via Christi Regional Medical Center · USJinan Central Hospital · CNShandong University · CN

Funding

The study of gene therapy for aseptic loosening using a mouse implant modelR03AR054929 · NIAMS · WAYNE STATE UNIVERSITY · PI YANG, SHANG-YOU · 2007 to 2009
$202k
NIAMS NIH HHS 5R03 AR 054929NIAMS NIH HHS R03 AR054929
6 · The paper itself

Abstract

Exogenous osteoprotegerin (OPG) gene modification appears a therapeutic strategy for osteolytic aseptic loosening. The feasibility and efficacy of a cell-based OPG gene delivery approach were investigated using a murine model of knee prosthesis failure. A titanium pin was implanted into mouse proximal tibia to mimic a weight-bearing knee arthroplasty, followed by titanium particles challenge to induce periprosthetic osteolysis. Mouse fibroblast-like synoviocytes were transduced in vitro with either AAV-OPG or AAV-LacZ before transfused into the osteolytic prosthetic joint 3 weeks post surgery. Successful transgene expression at the local site was confirmed 4 weeks later after killing. Biomechanical pullout test indicated a significant restoration of implant stability after the cell-based OPG gene therapy. Histology revealed that inflammatory pseudo-membranes existed ubiquitously at bone-implant interface in control groups, whereas only observed sporadically in OPG gene-modified groups. Tartrate-resistant acid phosphatase+osteoclasts and tumor necrosis factor α, interleukin-1β, CD68+ expressing cells were significantly reduced in periprosthetic tissues of OPG gene-modified mice. No transgene dissemination or tumorigenesis was detected in remote organs and tissues. Data suggest that cell-based ex vivo OPG gene therapy was comparable in efficacy with in vivo local gene transfer technique to deliver functional therapeutic OPG activities, effectively halted the debris-induced osteolysis and regained the implant stability in this model.

Indexed as

Prosthesis FailureAcid PhosphataseAnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 MoleculeGenetic TherapyGenetic VectorsIsoenzymesKnee ProsthesisMiceMice, Inbred BALB COsteolysisOsteoprotegerinTartrate-Resistant Acid PhosphataseWeight-BearingAcid PhosphataseAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 antigen, humanCD68 MoleculeIsoenzymesOsteoprotegerinTartrate-Resistant Acid Phosphatase

Identifiers

PMID20428210
PMCPMC2914841
OpenAlexW2008754581

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.