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Emerging role of anti-tumor necrosis factor therapy in rheumatic diseases
Arthritis Research Vol 4 Suppl 2
Kalden
Emerging role of anti-tumor necrosis factor therapy in rheumatic
diseases
Joachim R Kalden
Department of Internal Medicine III and Institute for Clinical Immunology, University of Erlangen-Nurnberg, Erlangen, Germany
Correspondence: Professor Dr Joachim R Kalden, MD, Department of Internal Medicine III and Institute for Clinical Immunology, University of
Erlangen-Nurnberg, Krandenhausstrasse 12, Erlangen 91054, Germany. Tel: +49 9131 853 418; fax: +49 9131 8534 770;
e-mail: martina.Seidel@med3.imed.uni-erlangen.de
Received: 3 December 2001
Revisions requested: 10 December 2001
Revisions received: 24 January 2002
Accepted: 28 March 2002
Arthritis Res 2002, 4 (suppl 2):S34-S40
This article may contain supplementary data which can only be found
online at /content/4/S2/S34
? 2002 BioMed Central Ltd
Published: 24 May 2002
(Print ISSN 1465-9905; Online ISSN 1465-9913)
Abstract
Tumor necrosis factor alpha (TNF-α) is an inflammatory cytokine that has been implicated in a variety of
rheumatic and inflammatory diseases. New understanding of the importance of TNF-α in the
pathophysiology of rheumatoid arthritis and Crohn’s disease led to the development of a new class of
targeted anti-TNF therapies. Anti-TNF-α agents including etanercept (a fusion protein of the p75 TNF
receptor and IgG1) and infliximab (a chimeric monoclonal antibody specific for TNF-α) have been
approved for the treatment of rheumatoid arthritis. In addition, infliximab has been approved in the
treatment of patients with active or fistulating Crohn’s disease. A new appreciation of the importance
of TNF-α in other rheumatic and inflammatory diseases has led to a broadening of the application of
anti-TNF agents. Both etanercept and infliximab have been used in open-label and randomized studies
in patients with psoriatic arthritis. Although larger randomized trials are needed to confirm early results,
both these anti-TNF-α a
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