dc.contributor.author
Voss, Jan Oliver
dc.contributor.author
Pivetta, Fabio
dc.contributor.author
Elkilany, Aboelyazid
dc.contributor.author
Schmidt-Bleek, Katharina
dc.contributor.author
Duda, Georg N.
dc.contributor.author
Odaka, Kento
dc.contributor.author
Dimitriou, Ioanna Maria
dc.contributor.author
Ort, Melanie Jasmin
dc.contributor.author
Streitz, Mathias
dc.contributor.author
Heiland, Max
dc.contributor.author
Koerdt, Steffen
dc.contributor.author
Reinke, Simon
dc.contributor.author
Geissler, Sven
dc.date.accessioned
2024-11-06T06:25:15Z
dc.date.available
2024-11-06T06:25:15Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/45529
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-45241
dc.description.abstract
Introduction: Open reduction and fixation are the standard of care for treating mandibular fractures and usually lead to successful healing. However, complications such as delayed healing, non-union, and infection can compromise patient outcomes and increase healthcare costs. The initial inflammatory response, particularly the response involving specific CD8+ T cell subpopulations, is thought to play a critical role in healing long bone fractures. In this study, we investigated the role of these immune cell profiles in patients with impaired healing of mandibular fractures.
Materials and methods: In this prospective study, we included patients with mandibular fractures surgically treated at Charité – Universitätsmedizin Berlin, Germany, between September 2020 and December 2022. We used follow-up imaging and clinical assessment to evaluate bone healing. In addition, we analyzed immune cell profiles using flow cytometry and quantified cytokine levels using electrochemiluminescence-based multiplex immunoassays in preoperative blood samples.
Results: Out of the 55 patients enrolled, 38 met the inclusion criteria (30 men and 8 women; mean age 32.18 years). Radiographic evaluation revealed 31 cases of normal healing and 7 cases of incomplete consolidation, including 1 case of non-union. Patients with impaired healing exhibited increased levels of terminally differentiated effector memory CD8+ T cells (TEMRA) and a higher TEMRA to regulatory T cell (Treg) ratio, compared with those with normal healing.
Conclusions: Our analysis of mandibular fracture cases confirms our initial hypothesis derived from long bone fracture healing: monitoring the TEMRA to Treg ratio in preoperative blood can be an early indicator of patients at risk of impaired bone healing. Radiologic follow-up enabled us to detect healing complications that might not be detected by clinical assessment only. This study highlights the potential of individual immune profiles to predict successful healing and may form the basis for future strategies to manage healing complications.
en
dc.format.extent
13 Seiten
dc.rights
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
ossification
en
dc.subject
mandibular fractures
en
dc.subject
bone healing
en
dc.subject
pseudarthrosis
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::570 Biowissenschaften; Biologie
dc.title
Prognostic implications of a CD8+ TEMRA to CD4+Treg imbalance in mandibular fracture healing: a prospective analysis of immune profiles
dc.type
Wissenschaftlicher Artikel
dc.date.updated
2024-11-06T05:57:51Z
dcterms.bibliographicCitation.articlenumber
1476009
dcterms.bibliographicCitation.doi
10.3389/fimmu.2024.1476009
dcterms.bibliographicCitation.journaltitle
Frontiers in Immunology
dcterms.bibliographicCitation.volume
15
dcterms.bibliographicCitation.url
https://doi.org/10.3389/fimmu.2024.1476009
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1664-3224
refubium.resourceType.provider
DeepGreen