Adhesion molecules in experimental phacoanaphylactic endophthalmitis

Invest Ophthalmol Vis Sci. 1992 Nov;33(12):3417-23.

Abstract

Intraocular accumulation of inflammatory neutrophils is an important feature of experimental phacoanaphylactic endophthalmitis (EPE). Increasing evidence suggests that localization of neutrophils to the site of inflammation requires the participation of neutrophil and endothelial adhesion molecules. These studies were undertaken to determine if blocking of adhesion molecules on neutrophils (CD18) or endothelium (ELAM-1) could attenuate EPE in Lewis rats. Treatment of experimental animals with anti-CD18 or anti-ELAM-1 significantly suppressed intraocular neutrophil accumulation, retinal hemorrhage, and vasculitis, and attenuated retinal edema formation by 48% and 70%, respectively. These observations demonstrate that antibodies directed against adhesion molecules on the neutrophil (CD18) or the vascular endothelial cell (ELAM-1) exhibit potent anti-inflammatory effects, resulting in a striking amelioration of injury in EPE in rats.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / therapeutic use
  • Antigens, CD / immunology
  • CD18 Antigens
  • Cell Adhesion Molecules / immunology
  • Cell Adhesion Molecules / metabolism*
  • Crystallins / immunology*
  • E-Selectin
  • Endophthalmitis / etiology*
  • Endophthalmitis / metabolism
  • Endophthalmitis / therapy
  • Eye / pathology
  • Hypersensitivity / complications*
  • Hypersensitivity / immunology
  • IgA Vasculitis / etiology
  • IgA Vasculitis / metabolism
  • IgA Vasculitis / therapy
  • Male
  • Rats
  • Rats, Inbred Lew

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • CD18 Antigens
  • Cell Adhesion Molecules
  • Crystallins
  • E-Selectin