DEVELOPING ADENOVIRAL-MEDIATED IN-VIVO GENE-THERAPY FOR ORNITHINE TRANSCARBAMYLASE DEFICIENCY

There are a number of reasons for choosing ornithine transcarbamylase (OTC) deficiency as a candidate for gene therapy: the gene has been cl oned; the disorder is relatively common; the current clinical outcome is poor; and there are authentic animal models. In considering the dev elopment of gene therapy for OTC deficiency, we focused on the use of in vivo gene therapy with an adenoviral vector. Using the partially OT C-deficient sparse fur mouse we found transduction and expression coul d be achieved using an intravenous infusion of a recombinant adenoviru s containing the OTC cDNA. The results were transient as a result of i mmune activation in response to the vector and vector-transduced cells . By modifying the adenoviral construct, creating an E1 deletion-E2 te mperature-sensitive mutation, we blunted the cytotoxic T lymphocyte im mune response and achieved correction of biochemical abnormalities for 2-3 months. We also found that transduction and expression following gene transfer occurred sufficiently rapidly to protect against acute h yperammonaemia within 24 h. Subsequent preclinical studies in mice and nonhuman primates demonstrated that E1-E4-deleted vectors had a subst antially improved safety profile and similar efficacy. With this evide nce of efficacy and safety of adenoviral vectors, we are embarking on a phase I trial of intravascular gene transfer using an E1-E4-deleted vector in adults with partial OTC deficiency.