New therapeutic targets in systemic lupus

Reumatol Clin. 2012 Jul-Aug;8(4):201-7. doi: 10.1016/j.reuma.2012.01.012. Epub 2012 Apr 6.
[Article in English, Spanish]

Abstract

Glucocorticoids, aspirin, antimalarials and conventional immunosuppressants are the mainstay of treatment of Systemic Lupus Erythematosus (SLE). Until recently, the first three were the only agents approved for treatment. A better understanding of the pathophysiology of the immune system has identified new therapeutic targets. In fact, belimumab, a human monoclonal antibody to BLyS inhibitor has become, in recent months, the first drug approved for the treatment of SLE since 1957, underscoring difficulties of all kinds, including economic and organizational ones inherent to clinical trials on this disease. Many other molecules are in various stages of development and soon will have concrete results. In this review, we examined the mechanism of action and most relevant clinical data for these molecules.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antibodies, Monoclonal / therapeutic use
  • Apoptosis / immunology
  • Autoimmunity
  • Clinical Trials as Topic
  • Complement Inactivating Agents / therapeutic use
  • Drugs, Investigational / therapeutic use
  • Humans
  • Immune Tolerance / drug effects
  • Inflammation
  • Interferons / antagonists & inhibitors
  • Lupus Erythematosus, Systemic / drug therapy*
  • Lupus Erythematosus, Systemic / immunology
  • Lupus Erythematosus, Systemic / physiopathology
  • Lymphocyte Depletion
  • Molecular Targeted Therapy*
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use
  • Recombinant Fusion Proteins / pharmacology
  • Recombinant Fusion Proteins / therapeutic use
  • Signal Transduction / drug effects
  • Therapies, Investigational
  • Toll-Like Receptors / antagonists & inhibitors

Substances

  • Antibodies, Monoclonal
  • Complement Inactivating Agents
  • Drugs, Investigational
  • Protein Kinase Inhibitors
  • Recombinant Fusion Proteins
  • Toll-Like Receptors
  • Interferons