G.E.R.N. Center for Tissue Replacement, Regeneration & Neogenesis, Department of Orthopedics and Trauma Surgery, Faculty of Medicine, Medical Center-Albert-Ludwigs-University of Freiburg, 79085 Freiburg im Breisgau, Germany.
Int J Mol Sci. 2021 Feb 17;22(4):1996. doi: 10.3390/ijms22041996.
Understanding the causality of the post-traumatic osteoarthritis (PTOA) disease process of the knee joint is important for diagnosing early disease and developing new and effective preventions or treatments. The aim of this review was to provide detailed clinical data on inflammatory and other biomarkers obtained from patients after acute knee trauma in order to (i) present a timeline of events that occur in the acute, subacute, and chronic post-traumatic phases and in PTOA, and (ii) to identify key factors present in the synovial fluid, serum/plasma and urine, leading to PTOA of the knee in 23-50% of individuals who had acute knee trauma. In this context, we additionally discuss methods of simulating knee trauma and inflammation in in vivo, ex vivo articular cartilage explant and in vitro chondrocyte models, and answer whether these models are representative of the clinical inflammatory stages following knee trauma. Moreover, we compare the pro-inflammatory cytokine concentrations used in such models and demonstrate that, compared to concentrations in the synovial fluid after knee trauma, they are exceedingly high. We then used the Bradford Hill Framework to present evidence that TNF-α and IL-6 cytokines are causal factors, while IL-1β and IL-17 are credible factors in inducing knee PTOA disease progresssion. Lastly, we discuss beneficial infrastructure for future studies to dissect the role of local vs. systemic inflammation in PTOA progression with an emphasis on early disease.
了解膝关节创伤后骨关节炎(PTOA)疾病过程的因果关系对于早期诊断疾病以及开发新的有效预防或治疗方法非常重要。本综述的目的是提供有关急性膝关节创伤后患者获得的炎症和其他生物标志物的详细临床数据,以便:(i) 呈现发生在急性、亚急性和慢性创伤后阶段以及 PTOA 中的事件时间线;(ii) 确定在滑膜液、血清/血浆和尿液中存在的关键因素,这些因素导致 23-50%发生急性膝关节创伤的个体出现膝关节 PTOA。在这方面,我们还讨论了在体内、关节软骨离体和体外软骨细胞模型中模拟膝关节创伤和炎症的方法,并回答这些模型是否代表膝关节创伤后的临床炎症阶段。此外,我们比较了这些模型中使用的促炎细胞因子浓度,并证明与膝关节创伤后滑膜液中的浓度相比,这些浓度非常高。然后,我们使用布拉德福德·希尔框架来提供证据表明 TNF-α 和 IL-6 细胞因子是因果因素,而 IL-1β 和 IL-17 是诱导膝关节 PTOA 疾病进展的可信因素。最后,我们讨论了有益的基础设施,用于未来的研究,以剖析局部炎症与系统性炎症在 PTOA 进展中的作用,重点关注早期疾病。