COINJECTION OF ADENOVIRUS EXPRESSING CTLA4-IG PROLONGS ADENOVIRALLY MEDIATED LACZ REPORTER GENE-EXPRESSION IN THE MOUSE RETINA

There is growing interest in gene delivery to the eye in order to deve lop gene therapy for the many ocular disorders which may be amenable t o this approach. To date, recombinant adenoviruses (AV) have been the main vector used for gene delivery to anterior and posterior segments in animal models. As with delivery to other organs, immune responses t o vector and transgene limit the duration of expression in the eye. Us ing an El-deleted adenoviral vector carrying a lacZ reporter gene, we have previously demonstrated that a T cell-mediated immune response re duces the level of infra-ocular transgene expression over time and lim its if to around 3 weeks in mice. This report describes a strategy for prolonging gene expression by blocking the B7-CD28 interactions betwe en antigen presenting cells (APC) and T cells in order to prevent the costimulatory signals required for T cell survival and proliferation. This was achieved by the co-injection of AV encoding a secreted immuno modulatory molecule (CTLA4-Ig) which consists of the extra-cellular do main of mouse CTLA4: fused to the Fc region of human IgG. Subretinal c oinjection of AV encoding beta galactosidase with AV encoding CTLA4-Ig results in prolonged expression in retinal cells compared with subret inal injection of only adenovirus encoding beta galactosidase.