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摘要
An expanding spectrum of acute and chronic non-infectious inflammatory diseases is uniquely responsive to IL-1 beta neutralization. IL-1 beta-mediated diseases are often called "auto-inflammatory'' and the dominant finding is the release of the active form of IL-1 beta driven by endogenous molecules acting on the monocyte/macrophage. IL-1 beta activity is tightly controlled and requires the conversion of the primary transcript, the inactive IL-1 beta precursor, to the active cytokine by limited proteolysis. Limited proteolysis can take place extracellularly by serine proteases, released in particular by infiltrating neutrophils or intracellularly by the cysteine protease caspase-1. Therefore, blocking IL-1 beta resolves inflammation regardless of how the cytokine is released from the cell or how the precursor is cleaved. Endogenous stimulants such as oxidized fatty acids and lipoproteins, high glucose concentrations, uric acid crystals, activated complement, contents of necrotic cells, and cytokines, particularly IL-1 itself, induce the synthesis of the inactive IL-1 beta precursor, which awaits processing to the active form. Although bursts of IL-1 beta precipitate acute attacks of systemic or local inflammation, IL-1 beta also contributes to several chronic diseases. For example, ischemic injury, such as myocardial infarction or stroke, causes acute and extensive damage, and slowly progressive inflammatory processes take place in atherosclerosis, type 2 diabetes, osteoarthritis and smoldering myeloma. Evidence for the involvement of IL-1 beta and the clinical results of reducing IL-1 beta activity in this broad spectrum of inflammatory diseases are the focus of this review.
- 出版日期2011-5
