The local and systemic effects of immune function on fracture healing.

fracture healing immune modulation precision medicine

Journal

OTA international : the open access journal of orthopaedic trauma
ISSN: 2574-2167
Titre abrégé: OTA Int
Pays: United States
ID NLM: 101770383

Informations de publication

Date de publication:
Mar 2024
Historique:
received: 13 12 2023
revised: 28 12 2023
accepted: 04 01 2024
medline: 15 3 2024
pubmed: 15 3 2024
entrez: 15 3 2024
Statut: epublish

Résumé

The immune system plays an integral role in the regulation of cellular processes responsible for fracture healing. Local and systemic influences on fracture healing correlate in many ways with fracture-related outcomes, including soft tissue healing quality and fracture union rates. Impaired soft tissue healing, restricted perfusion of a fracture site, and infection also in turn affect the immune response to fracture injury. Modern techniques used to investigate the relationship between immune system function and fracture healing include precision medicine, using vast quantities of data to interpret broad patterns of inflammatory response. Early data from the PRECISE trial have demonstrated distinct patterns of inflammatory response in polytrauma patients, which thereby directly and indirectly regulate the fracture healing response. The clearly demonstrated linkage between immune function and fracture healing suggests that modulation of immune function has significant potential as a therapeutic target that can be used to enhance fracture healing.

Identifiants

pubmed: 38487403
doi: 10.1097/OI9.0000000000000328
pii: OTAI-D-23-00083
pmc: PMC10936162
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

e328

Informations de copyright

Copyright © 2024 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Orthopaedic Trauma Association.

Déclaration de conflit d'intérêts

No conflict of interest for all authors and no funding received. Authors of this study wish to acknowledge the Major Extremity Trauma Research Consortium (METRC) for its contribution to the PRECISE Trial results reported in this manuscript.

Auteurs

Andrew R Evans (AR)

Warren Alpert School of Medicine at Brown University, University Orthopedics, Inc, Providence, RI.

Peter V Giannoudis (PV)

Academic Department of Trauma and Orthopaedics, School of Medicine, University of Leeds, Leeds General Infirmary, Clarendon Wing, Level D, Leeds, West Yorkshire, United Kingdom.

Philip Leucht (P)

NYU Langone Orthopedic Hospital, New York, NY.

Todd O McKinley (TO)

University of Indiana, Indianapolis, IN.

Greg E Gaski (GE)

University of Virginia School of Medicine, Inova Fairfax Medical Campus, Falls Church, VA.

Katherine P Frey (KP)

Department of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.

Joseph C Wenke (JC)

UTMB Department of Orthopaedic Surgery and Rehabilitation, Shriners Children's Texas, Galveston, TX.

Christopher Lee (C)

UCLA, Los Angeles, CA.

Classifications MeSH