Lund Minna Christiansen, Clausen Bettina Hjelm, Brambilla Roberta, Lambertsen Kate Lykke
Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
BRIGDE-Brain Research-Inter-Disciplinary Guided Excellence, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Cell Mol Neurobiol. 2023 Apr;43(3):925-950. doi: 10.1007/s10571-022-01229-0. Epub 2022 May 23.
Pre-clinical studies place tumor necrosis factor (TNF) as a central player in the inflammatory response after spinal cord injury (SCI), and blocking its production and/or activity has been proposed as a possible treatment option after SCI. This systematic review provides an overview of the literature on the temporal and cellular expression of TNF after SCI and clarifies the potential for its therapeutic manipulation in SCI. A systematic search was performed in EMBASE (Ovid), MEDLINE (Ovid), and Web of Science (Core Collection). The search terms were the MeSH forms of tumor necrosis factor and spinal cord injury in the different databases, and the last search was performed on February 3, 2021. We found twenty-four articles examining the expression of TNF, with most using a thoracic contusive SCI model in rodents. Two articles described the expression of TNF receptors in the acute phase after SCI. Twenty-one articles described the manipulation of TNF signaling using genetic knock-out, pharmaceutical inhibition, or gain-of-function approaches. Overall, TNF expression increased rapidly after SCI, within the first hours, in resident cells (neurons, astrocytes, oligodendrocytes, and microglia) and again in macrophages in the chronic phase after injury. The review underscores the complexity of TNF's role after SCI and indicates that TNF inhibition is a promising therapeutic option. This review concludes that TNF plays a significant role in the inflammatory response after SCI and suggests that targeting TNF signaling is a feasible therapeutic approach.
临床前研究表明肿瘤坏死因子(TNF)是脊髓损伤(SCI)后炎症反应的核心参与者,并且有人提出阻断其产生和/或活性可能是SCI后的一种治疗选择。本系统综述概述了SCI后TNF的时间和细胞表达相关文献,并阐明了其在SCI中进行治疗性调控的潜力。在EMBASE(Ovid)、MEDLINE(Ovid)和Web of Science(核心合集)中进行了系统检索。检索词为不同数据库中肿瘤坏死因子和脊髓损伤的医学主题词(MeSH)形式,最后一次检索于2021年2月3日进行。我们发现24篇文章研究了TNF的表达,其中大多数使用啮齿动物胸段挫伤性SCI模型。两篇文章描述了SCI急性期TNF受体的表达。21篇文章描述了使用基因敲除、药物抑制或功能获得方法对TNF信号传导的调控。总体而言,SCI后TNF表达在最初数小时内迅速增加,在驻留细胞(神经元、星形胶质细胞、少突胶质细胞和小胶质细胞)中如此,在损伤后的慢性期巨噬细胞中也再次出现这种情况。该综述强调了SCI后TNF作用的复杂性,并表明抑制TNF是一种有前景的治疗选择。本综述得出结论,TNF在SCI后的炎症反应中起重要作用,并表明靶向TNF信号传导是一种可行的治疗方法。