Intercellular adhesion molecule-1 as a drug target in asthma and rhinitis

Respirology. 2014 May;19(4):508-13. doi: 10.1111/resp.12285. Epub 2014 Apr 1.

Abstract

Intercellular adhesion molecule-1 (ICAM-1) is a transmembrane glycoprotein receptor of the immunoglobulin superfamily. Endothelial cells, epithelial cells, leukocytes and neutrophils are the major cells expressing ICAM-1. Ligands of ICAM-1 are macrophage adhesion ligand-1, leukocyte function-associated antigen-1 and fibrinogen (extracellular matrix protein). In normal physiological conditions, engagement of ICAM-1 receptor with immunological cells surface ligands assists in homing and trafficking of inflammatory cells to distant tissues. ICAM-1 has also long been known to mediate cell-to-cell interaction during antigen presentation and outside-in cell signalling pathways. ICAM-1-mediated elevated inflammation is implicated in asthma. On respiratory epithelial cells surface, ICAM-1 acts as natural binding site for human rhinovirus (HRV), a common cold virus that ultimately causes exacerbation of asthma. This review presents the findings on the role of ICAM-1 in the complication of asthma and in particular asthma exacerbation by HRV.

Keywords: ICAM-1; asthma; human rhinovirus; inflammation; rhinitis..

Publication types

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

MeSH terms

  • Asthma* / drug therapy
  • Asthma* / etiology
  • Asthma* / immunology
  • Cell Adhesion Molecules / antagonists & inhibitors*
  • Cell Communication* / drug effects
  • Cell Communication* / immunology
  • Common Cold / complications*
  • Common Cold / immunology
  • Common Cold / virology
  • Humans
  • Immunologic Factors / pharmacology*
  • Intercellular Adhesion Molecule-1 / immunology*
  • Molecular Targeted Therapy
  • Respiratory Mucosa / metabolism
  • Rhinitis* / drug therapy
  • Rhinitis* / etiology
  • Rhinitis* / immunology
  • Rhinovirus / pathogenicity

Substances

  • Cell Adhesion Molecules
  • Immunologic Factors
  • Intercellular Adhesion Molecule-1