USE OF LENTIVIRAL VECTOR COMPRISING GENE THAT INHIBITS INTRAOCULAR CELLULAR PROLIFERATION OR INTRAOCULAR NEOVASCULARIZATION IN PREPARING MEDICAMENT FOR INHIBITING SAME

摘要

The present invention provides a means of human gene therapy for inherited or acquired proliferative ocular disease. It furnishes methods to exploit the ability of lentiviral vectors to transduce both mitotically active and inactive cells so that eye diseases may be treated.