Complement depletion with humanized cobra venom factor in a mouse model of age-related macular degeneration

Adv Exp Med Biol. 2010:703:151-62. doi: 10.1007/978-1-4419-5635-4_11.

Abstract

The effect of complement depletion with humanized cobra venom factor (CVF) on retinal lesion development/neovascularization was determined in a mouse model of wet age-related macular degeneration (AMD). Mice were treated with the humanized CVF protein HC3-1496 prior to, and once daily for 28 days after laser coagulation surgery of the retina. CVF transgenic mice exhibiting permanently low levels of serum complement activity and PBS-treated mice served as positive and negative controls, respectively. Fluorescein isothiocyanate (FITC)-dextran funduscopy after laser surgery indicated the presence of lesions in all mice that underwent laser surgery. In HC3-1496-treated mice as well as CVF transgenic mice smaller lesions were seen after 8 days. Measurement of lesion sizes by histopathological examination of eyes after 28 days revealed a significant reduction of lesion area and volume in both HC3-1496-treated animals and CVF transgenic animals compared to PBS-treated control animals. Systemic complement depletion with a complement depletor, such as the humanized CVF protein HC3-1496, represents a promising therapeutic concept for patients with wet AMD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Complement C3 / genetics
  • Complement Inactivating Agents / pharmacology*
  • Disease Models, Animal
  • Elapid Venoms / genetics
  • Elapid Venoms / pharmacology*
  • Humans
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Recombinant Fusion Proteins / genetics
  • Wet Macular Degeneration / drug therapy*
  • Wet Macular Degeneration / immunology
  • Wet Macular Degeneration / pathology
  • Wet Macular Degeneration / surgery

Substances

  • Complement C3
  • Complement Inactivating Agents
  • Elapid Venoms
  • Recombinant Fusion Proteins
  • cobra venom factor