Macrophage Polarization and the Osteoimmunology of Periprosthetic Osteolysis.

Inflammation Innate immune system Joint replacement Macrophage Osteoimmunology Periprosthetic osteolysis Prosthesis

Journal

Current osteoporosis reports
ISSN: 1544-2241
Titre abrégé: Curr Osteoporos Rep
Pays: United States
ID NLM: 101176492

Informations de publication

Date de publication:
02 2022
Historique:
accepted: 16 11 2021
pubmed: 9 2 2022
medline: 10 5 2022
entrez: 8 2 2022
Statut: ppublish

Résumé

Joint replacement has revolutionized the treatment of end-stage arthritis. We highlight the key role of macrophages in the innate immune system in helping to ensure that the prosthesis-host interface remains biologically robust. Osteoimmunology is of great interest to researchers investigating the fundamental biological and material aspects of joint replacement. Constant communication between cells of the monocyte/macrophage/osteoclast lineage and the mesenchymal stem cell-osteoblast lineage determines whether a durable prosthesis-implant interface is obtained, or whether implant loosening occurs. Tissue and circulating monocytes/macrophages provide local surveillance of stimuli such as the presence of byproducts of wear and can quickly polarize to pro- and anti-inflammatory phenotypes to re-establish tissue homeostasis. When these mechanisms fail, periprosthetic osteolysis results in progressive bone loss and painful failure of mechanical fixation. Immune modulation of the periprosthetic microenvironment is a potential intervention to facilitate long-term durability of prosthetic interfaces.

Identifiants

pubmed: 35133558
doi: 10.1007/s11914-022-00720-3
pii: 10.1007/s11914-022-00720-3
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

43-52

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR063713
Pays : United States
Organisme : Ministerstvo Zdravotnictví Ceské Republiky
ID : AZV NU21-06-00370.
Organisme : NIAMS NIH HHS
ID : R01 AR073145
Pays : United States

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Auteurs

Stuart B Goodman (SB)

Departments of Orthopaedic Surgery and Bioengineering, Stanford University, Stanford, CA, USA. goodbone@stanford.edu.

Emmanuel Gibon (E)

Department of Orthopaedic Surgery, Mayo Clinic, Rochester, MN, USA.

Jiri Gallo (J)

Department of Orthopaedics, Faculty of Medicine and Dentistry, Palacky University, University Hospital, Olomouc, Czech Republic.

Michiaki Takagi (M)

Department of Orthopaedic Surgery, Yamagata University Faculty of Medicine, Yamagata, Japan.

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Classifications MeSH