Tumor necrosis factor (TNF), originally discovered and namedon the basis of its tumor regression activity, is an importantcytokine that regulates the pathogenetic mechanisms of chronicinflammatory diseases.1,2 The translation of research findingsto patient care resulted in the first successful cytokine-specifictargeted therapies, the TNF inhibitors. Currently availableinhibitors include the monoclonal antibodies against TNF-, infliximaband adalimumab, and the soluble TNF receptor fused to humanIgG, etanercept.1,2 Agents that block TNF- suppress inflammation,slow disease progression, and in some cases, induce remissionin patients with rheumatoid arthritis, ankylosing spondylitis,psoriasis, and Crohn's disease.2 In this issue . . . [Full Text of this Article]
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From the Departments of Pathobiology and Pulmonary, Allergy, and Critical Care Medicine, Cleveland Clinic, Cleveland.
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