Clinics in Dermatology
Volume 26, Issue 5 , Pages 486-502, September 2008

Tumor necrosis factor antagonists in the therapy of psoriasis

  • Rotraut Mössner, MD

      Affiliations

    • Department of Dermatology, Georg-August University, von-Siebold-Str. 3, 37075 Göttingen, Germany
  • ,
  • Michael P. Schön, MD

      Affiliations

    • Rudolf Virchow Center, Deutsche Forschungsgemeinschaft Research Center for Experimental Biomedicine, Versbacher Str 9, 97078 Würzburg, Germany
    • Department of Dermatology, University of Würzburg, Josef-Schneider-Straße 2, 97080 Würzburg, Germany
    • Department of Dermatology and Venerology, University Medical Center Göttingen, von-Siebold Str 3, 37075 Göttingen, Germany
  • ,
  • Kristian Reich, MD

      Affiliations

    • Department of Dermatology, Georg-August University, von-Siebold-Str. 3, 37075 Göttingen, Germany
    • Dermatologikum, Stephansplatz 5, 20354 Hamburg, Germany
    • Corresponding Author InformationCorresponding author. Dermatologikum Hamburg, Stephansplatz 5, 20354 Hamburg, Germany. Tel.: +49 0 551 396427; fax: +49 0 551 396418.

Abstract 

The identification of new pathophysiological mechanisms in chronic inflammatory diseases and the development of techniques that allow production of antibodies and fusion proteins that antagonize target molecules with high specificity has not only revolutionized the treatment of rheumatoid arthritis and chronic inflammatory bowel disease, but it also has revolutionized the treatment of psoriasis in recent years. Two different classes of so-called biological therapies (biologics) have become available to treat psoriasis: tumor necrosis factor (TNF) antagonists and T-cell modulators. TNF antagonists that have been studied with psoriasis include the antibodies infliximab and adalimumab and the fusion protein etanercept. These treatments differ in their capacity to reduce the skin symptoms of psoriasis and other important characteristics of the drug profile. This article summarizes the important aspects of efficacy, safety, and practicability of TNF antagonists in the treatment of psoriasis. This article may be helpful for the daily routine when selecting the right therapy for a patient and managing the TNF antagonist during maintenance therapy.

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 R. M. has received travel grants from Essex (Munich, Germany) and Wyeth (Münster, Germany). M. P. S. has received lecture fees from Serono (Munich, Germany), Wyeth, Essex, and Abbott (Wiesbaden, Germany), and research grants from Schering/Berlex (Richmond, Calif). K. R. has served as a consultant and paid speaker for Abbott, Biogen Idec (Tsamaning, Germany), Centocor (Horsham, PA), Essex, Schering-Plough (Kenilworth, NJ), Serono, and Wyeth. He has also received grant funding from Biogen Idec.

PII: S0738-081X(07)00254-4

doi:10.1016/j.clindermatol.2007.10.030

Clinics in Dermatology
Volume 26, Issue 5 , Pages 486-502, September 2008