ADAM33: a novel therapeutic target for asthma

Expert Opin Ther Targets. 2003 Aug;7(4):485-94. doi: 10.1517/14728222.7.4.485.

Abstract

The incidence of asthma worldwide is increasing, and the disease has a large unmet clinical need. Despite the availability of anti-inflammatory and bronchodilator medication, there is persisting morbidity and mortality. New approaches are needed to understand the role that structural changes in the airways (remodelling) play in this process. Studies of the genetic basis of asthma have identified the ADAM33 (a disintegrase and metalloproteinase 33) gene, a novel member of the ADAM family of zinc-dependent metalloproteases, as a risk factor for the development of asthma and bronchial hyperresponsiveness (BHR). The identification of ADAM33 as a major risk factor involved in the pathogenesis of BHR and airway wall remodelling provides insight into the pathogenesis of asthma and represents a novel therapeutic target.

Publication types

  • Review

MeSH terms

  • ADAM Proteins / antagonists & inhibitors*
  • ADAM Proteins / physiology
  • Animals
  • Anti-Asthmatic Agents / pharmacology*
  • Anti-Asthmatic Agents / therapeutic use
  • Asthma / drug therapy*
  • Asthma / enzymology
  • Asthma / etiology
  • Asthma / immunology
  • Bronchial Hyperreactivity / drug therapy
  • Bronchial Hyperreactivity / enzymology
  • Bronchial Hyperreactivity / genetics
  • Bronchial Hyperreactivity / pathology
  • Case-Control Studies
  • Cell Differentiation
  • Cell Division
  • Chromosomes, Human, Pair 20 / genetics
  • Drug Design*
  • Genetic Predisposition to Disease
  • Humans
  • Lod Score
  • Mice
  • Multigene Family
  • Muscle, Smooth / enzymology
  • Protease Inhibitors / pharmacology*
  • Protease Inhibitors / therapeutic use
  • Protein Structure, Tertiary
  • Substrate Specificity

Substances

  • Anti-Asthmatic Agents
  • Protease Inhibitors
  • ADAM Proteins
  • ADAM33 protein, human