Bradley J R
NIHR Cambridge Biomedical Research Centre, Addenbrooke's Hospital, Cambridge, UK.
J Pathol. 2008 Jan;214(2):149-60. doi: 10.1002/path.2287.
TNF was originally described as a circulating factor that can cause necrosis of tumours, but has since been identified as a key regulator of the inflammatory response. This review describes the known signalling pathways and cell biological effects of TNF, and our understanding of the role of TNF in human disease. TNF interacts with two different receptors, designated TNFR1 and TNFR2, which are differentially expressed on cells and tissues and initiate both distinct and overlapping signal transduction pathways. These diverse signalling cascades lead to a range of cellular responses, which include cell death, survival, differentiation, proliferation and migration. Vascular endothelial cells respond to TNF by undergoing a number of pro-inflammatory changes, which increase leukocyte adhesion, transendothelial migration and vascular leak and promote thrombosis. The central role of TNF in inflammation has been demonstrated by the ability of agents that block the action of TNF to treat a range of inflammatory conditions, including rheumatoid arthritis, ankylosing spondylitis, inflammatory bowel disease and psoriasis. The increased incidence of infection in patients receiving anti-TNF treatment has highlighted the physiological role of TNF in infectious diseases.
肿瘤坏死因子最初被描述为一种可导致肿瘤坏死的循环因子,但后来被确定为炎症反应的关键调节因子。本综述描述了肿瘤坏死因子已知的信号通路和细胞生物学效应,以及我们对其在人类疾病中作用的理解。肿瘤坏死因子与两种不同的受体相互作用,分别称为肿瘤坏死因子受体1(TNFR1)和肿瘤坏死因子受体2(TNFR2),它们在细胞和组织上的表达存在差异,并启动不同但又重叠的信号转导通路。这些多样的信号级联反应导致一系列细胞反应,包括细胞死亡、存活、分化、增殖和迁移。血管内皮细胞对肿瘤坏死因子的反应是发生一系列促炎变化,这些变化会增加白细胞黏附、跨内皮迁移和血管渗漏,并促进血栓形成。阻断肿瘤坏死因子作用的药物能够治疗一系列炎症性疾病,包括类风湿性关节炎、强直性脊柱炎、炎症性肠病和牛皮癣,这证明了肿瘤坏死因子在炎症中的核心作用。接受抗肿瘤坏死因子治疗的患者感染发生率增加,这突出了肿瘤坏死因子在传染病中的生理作用。