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      Cryopyrin-associated periodic syndromes: background and therapeutics.

      Modern Rheumatology
      Antibodies, Monoclonal, therapeutic use, Carrier Proteins, genetics, immunology, Cryopyrin-Associated Periodic Syndromes, therapy, Humans, Interleukin-1, antagonists & inhibitors, Monocytes, Recombinant Fusion Proteins

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          Abstract

          Cryopyrin-associated periodic syndromes (CAPS) are caused by mutations of the gene encoding the NLR family protein NLRP3, which together with caspase-1 and adaptor proteins constitutes a protein complex termed the inflammasome. In innate immune reactions, a variety of stimuli activate the NLRP3 inflammasome, triggering caspase-1 to process proIL-1 and thus to produce mature IL-1. Excessive production of IL-1 by monocytes/macrophages is the central pathophysiology of CAPS, and daily injection of the IL-1 receptor antagonist anakinra rapidly ameliorates the inflammatory symptoms in most cases. Furthermore, double-blind, placebo-controlled clinical trials have recently confirmed the efficacy and safety of rilonacept, a fusion protein of the IL-1 receptor and IgG Fc, and canakinumab, a human anti-IL-1 monoclonal antibody, as novel long-lasting agents for treating CAPS.

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