Lentiviral vector-mediated gene transfer and uses thereof

Drug – bio-affecting and body treating compositions – Whole live micro-organism – cell – or virus containing – Genetically modified micro-organism – cell – or virus

Reexamination Certificate

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C424S093100, C424S093600, C435S069100, C435S320100, C435S325000, C435S455000, C514S04400A

Reexamination Certificate

active

07122181

ABSTRACT:
The present invention provides lentiviral vectors that are useful in 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.

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