Evidence map›Paper›PMID 29577591›Full record

ArticleJournal of biomedical materials research. Part A2018

Effects of antigen removal on a porcine osteochondral xenograft for articular cartilage repair.

Steve Elder, Hudson Chenault, Paul Gloth, Katie Webb, Ruth Recinos, Emily Wright, Dalton Moran, James Butler, Abdolsamad Borazjani, Avery Cooley

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Steve ElderDepartment of Agricultural and Biological Engineering, James Worth Bagley College of Engineering, Mississippi State University, Starkville, Mississippi.
Hudson ChenaultDepartment of Agricultural and Biological Engineering, James Worth Bagley College of Engineering, Mississippi State University, Starkville, Mississippi.
Paul GlothDepartment of Agricultural and Biological Engineering, James Worth Bagley College of Engineering, Mississippi State University, Starkville, Mississippi.
Katie WebbDepartment of Agricultural and Biological Engineering, James Worth Bagley College of Engineering, Mississippi State University, Starkville, Mississippi.
Ruth RecinosDepartment of Agricultural and Biological Engineering, James Worth Bagley College of Engineering, Mississippi State University, Starkville, Mississippi.
Emily WrightDepartment of Agricultural and Biological Engineering, James Worth Bagley College of Engineering, Mississippi State University, Starkville, Mississippi.
Dalton MoranDepartment of Agricultural and Biological Engineering, James Worth Bagley College of Engineering, Mississippi State University, Starkville, Mississippi.
James ButlerDepartment of Clinical Sciences, College of Veterinary Medicine, Mississippi State University, Starkville, Mississippi.
Abdolsamad BorazjaniDepartment of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Starkville, Mississippi.
Avery CooleyDepartment of Pathobiology and Population Medicine, College of Veterinary Medicine, Mississippi State University, Starkville, Mississippi.
Mississippi State University · US

Funding

Development of an Ostoechondral Xenograft for Articular Cartilage RepairR15AR066926 · NIAMS · MISSISSIPPI STATE UNIVERSITY · PI ELDER, STEVEN HOWARD · 2015 to 2015
$367k
NIAMS NIH HHS R15 AR066926
6 · The paper itself

Abstract

Given the limited availability of fresh osteochondral allografts and uncertainty regarding performance of decellularized allografts, this study was undertaken as part of an effort to develop an osteochondral xenograft for articular cartilage repair. The purpose was to evaluate a simple antigen removal procedure based mainly on treatment with SDS and nucleases. Histology demonstrated a preservation of collagenous structure and removal of most nuclei. Immunohistochemistry revealed the apparent retention of α-Gal within osteocyte lacunae unless the tissue underwent an additional α-galactosidase processing step. Cytoplasmic protein was completely removed as shown by Western blot. Quantitatively, the antigen removal protocol was found to extract approximately 90% of DNA from cartilage and bone, and it extracted over 80% of glycosaminoglycan from cartilage. Collagen content was not affected. Mechanical testing of cartilage and bone were performed separately, in addition to testing the cartilage-bone interface, and the main effect of antigen removal was an increase in cartilage hydraulic permeability. In vivo immunogenicity was assessed by subcutaneous implantation into DBA/1 J mice, and the response was typical of a foreign body rather than immune reaction. Thus, an osteochondral xenograft produced as described has the potential for further development into a treatment for osteochondral lesions in the human knee. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 2251-2260, 2018.

Indexed as

ChondrogenesisOsteogenesisRegenerationAnimalsAntigensBone and BonesCartilage, ArticularCollagenDNAExtracellular MatrixHeterograftsMaleMice, Inbred DBASwineVimentinAntigensCollagenDNAVimentinantigen removalbiomechanicsimmunogenicityosteochondral xenograftα-Gal

Identifiers

PMID29577591
PMCPMC6779129
OpenAlexW2790443020

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.