Anti-beta-crystallin antibodies (mouse) or sera from humans with age-related cataract are cytotoxic for lens epithelial cells in culture

Exp Eye Res. 1997 Feb;64(2):229-38. doi: 10.1006/exer.1996.0203.

Abstract

Circulating autoantibodies against lens antigens are prevalent in patients with age-related cataract (ARC), but their pathogenic significance is unknown. We hypothesized that these autoantibodies are cytotoxic for lens epithelial cells (LECs). To test this hypothesis. We incubated LECs with mouse polyclonal or monoclonal antibodies against beta-crystallin (anti-beta) in the presence or absence of guinea pig complement. We found that anti-beta in the presence of the complement bound to and killed mouse LECs (MLECs) and human LECs (HLECs). Sera obtained from patients with ARC also were cytotoxic to both HLECs and MLECs in culture. Heat-inactivated human sera were not cytotoxic to LECs in the absence of the complement, but were cytotoxic to both HLECs and MLECs in the presence of additional complement. These results support the hypothesis that autoantibodies against lens antigens are cytotoxic to LECs, and that cell death may involve complement-mediated pathways.

Publication types

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

MeSH terms

  • Animals
  • Antibodies / immunology
  • Autoantibodies / blood
  • Autoantibodies / immunology
  • Binding Sites, Antibody
  • Cataract / blood
  • Cataract / immunology*
  • Cell Differentiation
  • Cell Survival
  • Cells, Cultured
  • Complement System Proteins / physiology
  • Crystallins / immunology*
  • Cytotoxicity, Immunologic*
  • Epithelium / immunology
  • Epithelium / pathology
  • Humans
  • Infant
  • Lens, Crystalline / immunology*
  • Lens, Crystalline / pathology
  • Mice

Substances

  • Antibodies
  • Autoantibodies
  • Crystallins
  • Complement System Proteins