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      TNF-mediated inflammatory disease.

      The Journal of Pathology

      Anti-Inflammatory Agents, Non-Steroidal, therapeutic use, Arthritis, drug therapy, immunology, Communicable Diseases, Humans, Inflammation, Receptors, Tumor Necrosis Factor, metabolism, Signal Transduction, Tumor Necrosis Factor-alpha, antagonists & inhibitors, biosynthesis

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          Abstract

          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. 2007 Pathological Society of Great Britain and Ireland

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          Journal
          18161752
          10.1002/path.2287

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