Adhesion molecules in inflammatory bowel disease: therapeutic implications for gut inflammation

Dig Liver Dis. 2005 Nov;37(11):811-8. doi: 10.1016/j.dld.2005.03.013. Epub 2005 Sep 13.

Abstract

Mucosal endothelium has become one of the major areas of investigation in gut inflammation. It is now well recognised that it plays an active role in the pathogenesis of both forms of inflammatory bowel disease, Crohn's disease and ulcerative colitis, since endothelial cells regulate mucosal immune homeostasis, acting as "gatekeepers", controlling leukocyte accumulation in the interstitial compartment. This process is mediated by leukocyte-endothelial adhesion molecules. This paper reviews the major molecules that mediate leukocyte-endothelial interactions, and summarises the results of the most recent clinical trials targeting adhesion molecules in inflammatory bowel disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antibodies, Monoclonal / therapeutic use
  • Antibodies, Monoclonal, Humanized
  • Endothelium, Vascular / physiopathology*
  • Humans
  • Immunoglobulins / physiology*
  • Inflammatory Bowel Diseases / drug therapy*
  • Inflammatory Bowel Diseases / physiopathology*
  • Integrin alpha4 / therapeutic use
  • Integrins / physiology*
  • Intercellular Adhesion Molecule-1 / physiology
  • Intestinal Mucosa / cytology
  • Intestines / cytology
  • Leukocytes
  • Ligands
  • Natalizumab
  • Rats
  • Selectins / physiology*
  • Up-Regulation / physiology
  • Vascular Cell Adhesion Molecule-1 / physiology

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Immunoglobulins
  • Integrins
  • Ligands
  • Natalizumab
  • Selectins
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1
  • Integrin alpha4