Cited by 667Orthopaedic implants and arthroplastyOrthopedic Infections and TreatmentsBone Metabolism and Diseases

The role of macrophages in osteolysis of total joint replacement

Ingham, Eileen, Fisher, John·2005·Biomaterials

Abstract

The osteolysis associated with conventional polyethylene on metal total joint replacements is associated with the formation of an inflamed periprosthetic membrane rich in macrophages, cytokines and implant-derived wear particles. There is a wealth of evidence to indicate that the presence and activation of macrophages in the periprosthetic tissues around joint replacements is stimulated by UHMWPE particles. Particles within the size range 0.1-1.0 microm have been shown to be the most reactive. Animal studies have provided increasing evidence that, of the milieu of cytokines produced by particle-stimulated macrophages, TNF-alpha is a key cytokine involved in osteolysis. Recent advances in the understanding of the mechanisms of osteoclastogenesis and osteoclast activation at the cellular and molecular level have indicated that bone marrow-derived macrophages may play a dual role in osteolysis associated with total joint replacement. Firstly, as the major cell in host defence responding to UHMWPE particles via the production of cytokines and secondly as precursors for the osteoclasts responsible for the ensuing bone resorption.

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Registry

Crossref · 10.1016/j.biomaterials.2004.04.035

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6 of 6 references verified0 citation errors · 0 not checkable

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  • Wear byproducts from total joint replacements include particulate polymeric, ceramic, and metallic debris and metallic ions, which cause pro-inflammatory responses that can persist for the life of the implant.

    “The byproducts of wear include particulate polymeric, ceramic and metallic debris (mostly in the nano, submicron, and micron size range) and in the case of metal-on-metal implants, metallic ions [143]. These byproducts are well known to cause pro-inflammatory responses which can persist for the life of the implant [144,145].”

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Authors
Ingham, E., & Fisher, J.
Affiliations
University of Leeds (GB)
Corresponding author
Ingham, Eileen
Venue
Biomaterials
Publisher
Elsevier BV
Published
2005-04
Volume
26
Issue
11
Pages
1271-1286
ISSN
0142-9612 (ISSN-L)
OpenAlex
W2158193380
Cited by
667
References
6
Citations by year
2026: 9 · 2025: 17 · 2024: 19 · 2023: 18 · 2022: 27 · 2021: 34 · 2020: 28 · 2019: 28 · 2018: 35 · 2017: 39 · 2016: 32 · 2015: 43 · 2014: 45 · 2013: 48 · 2012: 50
FWCI
3.94
Type
journal article
Language
en
Open access
closed
Locations
  • Biomaterials (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Orthopaedic implants and arthroplasty
  • Health Sciences › Medicine › Surgery › Orthopedic Infections and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
Keywords
macrophages, periprosthetic osteolysis, total joint arthroplasty, polyethylene wear particles, periprosthetic membrane, TNF-α, osteoclastogenesis, osteoclast activation, bone resorption, bone marrow-derived macrophages, cytokines
MeSH terms
Animals, Foreign-Body Reaction, Hip Prosthesis, Humans, Macrophages, Osteolysis, Prosthesis Failure, Cytokines, Prosthesis-Related Infections, Arthroplasty, Replacement, Hip

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