下颌骨骨折愈合中 CD8+ TEMRA 与 CD4+Treg 失衡的预后影响:免疫特征的前瞻性分析。

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Frontiers in Immunology Pub Date : 2024-10-23 eCollection Date: 2024-01-01 DOI:10.3389/fimmu.2024.1476009
Jan Oliver Voss, Fabio Pivetta, Aboelyazid Elkilany, Katharina Schmidt-Bleek, Georg N Duda, Kento Odaka, Ioanna Maria Dimitriou, Melanie Jasmin Ort, Mathias Streitz, Max Heiland, Steffen Koerdt, Simon Reinke, Sven Geissler
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引用次数: 0

摘要

介绍:切开复位和固定是治疗下颌骨骨折的标准方法,通常能使骨折成功愈合。然而,延迟愈合、不愈合和感染等并发症会影响患者的治疗效果并增加医疗费用。最初的炎症反应,尤其是涉及特定 CD8+ T 细胞亚群的反应,被认为在长骨骨折愈合中起着关键作用。在这项研究中,我们调查了这些免疫细胞在下颌骨骨折愈合受损患者中的作用:在这项前瞻性研究中,我们纳入了2020年9月至2022年12月期间在德国柏林夏里特大学接受手术治疗的下颌骨骨折患者。我们使用随访成像和临床评估来评估骨愈合情况。此外,我们还使用流式细胞术分析了免疫细胞概况,并使用基于电化学发光的多重免疫测定法对术前血液样本中的细胞因子水平进行了量化:在 55 例入选患者中,38 例符合纳入标准(男性 30 例,女性 8 例;平均年龄 32.18 岁)。影像学评估显示,31 例愈合正常,7 例不完全愈合,包括 1 例未愈合。与愈合正常的患者相比,愈合受损的患者表现出终末分化效应记忆CD8+ T细胞(TEMRA)水平升高,TEMRA与调节性T细胞(Treg)的比率升高:我们对下颌骨骨折病例的分析证实了我们最初从长骨骨折愈合中得出的假设:监测术前血液中 TEMRA 与 Treg 的比值可作为早期指标,用于判断患者是否存在骨愈合受损的风险。放射学随访使我们能够发现仅靠临床评估可能无法发现的愈合并发症。这项研究强调了个体免疫特征在预测成功愈合方面的潜力,并可能为未来管理愈合并发症的策略奠定基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic implications of a CD8+ TEMRA to CD4+Treg imbalance in mandibular fracture healing: a prospective analysis of immune profiles.

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.

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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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