Therapeutic development in psoriasis

Semin Cutan Med Surg. 2014 Jun;33(4 Suppl):S69-72. doi: 10.12788/j.sder.0098.

Abstract

Advances in molecular biology have provided the basis for development of new therapeutic approaches to psoriasis. New, more effective therapies target specific molecules in the inflammatory cascade involved in the pathogenesis of psoriasis.The biologic era of psoriasis therapy began with inhibitors of T-cell activation, tumor necrosis factor-α, and interleukin (IL)-12/23. Continued investigation has led to therapies and therapeutic candidates that target IL-17, IL-23, phosphodiesterase-4, and isomers of Janus kinase.

Keywords: JAK interlukin-17 inhibitors; Janus kinase inhibitors; apremilast; brodalumab; inflammation; interleukin-12/23; ixekizumab; monoclonal antibody; phosphodiesterase-4; psoriasis; secukinumab; tofacitinib; tumor necrosis factors.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal / therapeutic use*
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Clinical Trials as Topic
  • Humans
  • Immunologic Factors / therapeutic use*
  • Interleukin-23 / antagonists & inhibitors
  • Phosphodiesterase Inhibitors / therapeutic use
  • Piperidines / therapeutic use
  • Protein Kinase Inhibitors / therapeutic use
  • Psoriasis / drug therapy*
  • Psoriasis / physiopathology
  • Pyrimidines / therapeutic use
  • Pyrroles / therapeutic use
  • Thalidomide / analogs & derivatives
  • Thalidomide / therapeutic use
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Immunologic Factors
  • Interleukin-23
  • Phosphodiesterase Inhibitors
  • Piperidines
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Pyrroles
  • Thalidomide
  • brodalumab
  • tofacitinib
  • ixekizumab
  • secukinumab
  • apremilast