Abstract

Psoriasis is a prevalent chronic inflammatory skin disease of unknown etiology. Recent advances in understanding the pathogenesis of psoriasis suggest that IL-17 is a key proinflammatory mediator present in the skin. Several agents targeting IL-17 or its receptor are in clinical trials for the treatment of psoriasis. This review focuses on the biological rationale and the results of clinical trials with ixekizumab, a humanized IgG4 monoclonal antibody. Ixekizumab binds the IL-17A homodimer, thereby blocking the binding of IL-17A to the IL-17 receptor. The currently available Phase I-III data indicate that ixekizumab is a promising drug, although long-term data of efficacy and safety are needed before ixekizumab and other IL-17 targeting therapeutics can find their place in clinical practice.

Original languageEnglish
JournalExpert Review of Clinical Immunology
Volume11
Issue number4
Pages (from-to)435-42
Number of pages8
ISSN1744-666X
DOIs
Publication statusPublished - 1 Apr 2015

Keywords

  • Animals
  • Antibodies, Monoclonal, Humanized
  • Clinical Trials as Topic
  • Humans
  • Interleukin-17
  • Molecular Targeted Therapy
  • Protein Binding
  • Psoriasis
  • Receptors, Interleukin-17
  • Skin

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