Abstract
Interleukin-1 (IL-1) is a proinflammatory cytokine produced by a wide variety of cell types with an equally pleiotropic range of activities including the induction of fever, hypotension, adhesion molecule expression, neutrophilia, cartilage destruction, prostanoid production, and induction of the expression of a number of other cytokines. Two forms of IL-1 (IL-1α and IL-1β) have been cloned and, although sharing only approximately 25% amino acid homology, these two molecules have essentially identical biological activities. The biological role for IL-1 in normal physiology and in the development of disease has been extensively reviewed elsewhere [1]. Support for a role of IL-1 as an important mediator of pathological events observed in a number of acute and chronic inflammatory diseases has been demonstrated in a large number of animal models. A common characteristic of many of these acute and chronic inflammatory diseases is that the production even of small amounts of IL-1 can have severe consequences in terms of tissue destruction and systemic homeostasis. The discovery of a naturally occurring IL-1 receptor antagonist (IL-1Ra) has suggested a means through which the pathological effects of IL-1 can be modulated.
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Smith, M.F. (2000). Interleukin-1 receptor antagonist. In: Higgs, G.A., Henderson, B. (eds) Novel Cytokine Inhibitors. Progress in Inflammation Research. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-8450-1_9
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