Evidence map›Paper›PMID 26174978›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2016

Local delivery of mutant CCL2 protein-reduced orthopaedic implant wear particle-induced osteolysis and inflammation in vivo.

Xinyi Jiang, Taishi Sato, Zhenyu Yao, Michael Keeney, Jukka Pajarinen, Tzu-Hua Lin, Florence Loi, Kensuke Egashira, Stuart Goodman, Fan Yang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

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  11. Distinct release strategies are required to modulate macrophage phenotype in young versus aged animals.Journal of controlled release : official journal of the Controlled Release Society · 2019
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  15. Tissue engineering. Part C, Methods · 2017
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  18. Potential Role of Chemokines in Fracture Repair.Frontiers in endocrinology · 2017
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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 2 institutions in 2 countries.

Xinyi JiangDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
Taishi SatoDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
Zhenyu YaoDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
Michael KeeneyDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
Jukka PajarinenDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
Tzu-Hua LinDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
Florence LoiDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
Kensuke EgashiraDepartment of Cardiovascular Research, Development, and Translational Medicine, Kyushu University, Fukuoka, Japan.
Stuart GoodmanDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
Fan YangDepartment of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
Stanford University · USKyushu University · JP

Funding

Microribbon scaffold-mediated Immunomodulation for Cranial Bone RepairR01DE024772 · NIDCR · STANFORD UNIVERSITY · PI YANG, FAN · 2015 to 2025
$4.6M
Wear Particle Disease and NF-kappa B SignalingR01AR063717 · NIAMS · STANFORD UNIVERSITY · PI GOODMAN, STUART B · 2012 to 2021
$3.5M
Chemokine Directed Cell Trafficking during Continuous Infusion of Wear ParticlesR01AR055650 · NIAMS · STANFORD UNIVERSITY · PI GOODMAN, STUART B · 2007 to 2016
$3.3M
NIAMS NIH HHS 1R01AR063717NIAMS NIH HHS 2R01AR055650NIAMS NIH HHS R01 AR055650NIAMS NIH HHS R01 AR063717NIDCR NIH HHS R01 DE024772
6 · The paper itself

Abstract

Total joint replacement (TJR) has been widely used as a standard treatment for late-stage arthritis. One challenge for long-term efficacy of TJR is the generation of ultra-high molecular weight polyethylene wear particles from the implant surface that activates an inflammatory cascade which may lead to bone loss, prosthetic loosening and eventual failure of the procedure. Here, we investigate the efficacy of local administration of mutant CCL2 proteins, such as 7ND, on reducing wear particle-induced inflammation and osteolysis in vivo using a mouse calvarial model. Mice were treated with local injection of 7ND or phosphate buffered saline (PBS) every other day for up to 14 days. Wear particle-induced osteolysis and the effects of 7ND treatment were evaluated using micro-CT, histology, and immunofluorescence staining. Compared with the PBS control, 7ND treatment significantly decreased wear particle-induced osteolysis, which led to a higher bone volume fraction and bone mineral density. Furthermore, immunofluorescence staining showed 7ND treatment decreased the number of recruited inflammatory cells and osteoclasts. Together, our results support the feasibility of local delivery of 7ND for mitigating wear particle-induced inflammation and osteolysis, which may offer a promising strategy for extending the life time of TJRs.

Indexed as

AnimalsChemokine CCL2Drug Evaluation, PreclinicalForeign-Body ReactionJoint ProsthesisMaleMice, Inbred C57BLOsteolysisPolyethylenesX-Ray MicrotomographyCcl2 protein, mouseChemokine CCL2Polyethylenesultra-high molecular weight polyethylenemacrophagemutant CCL2 protein (7ND)osteolysistotal joint replacementwear particles

Identifiers

PMID26174978
PMCPMC4817847
OpenAlexW2160446030

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.