Adeno-associated viral vector-mediated gene transfer of
coagulation factor IX to the skeletal muscle or to liver has resulted in sustained correction of
hemophilia B in mice and dogs. The two initial phase I/II AAV clinical trials for
hemophilia B, delivering
a factor IX
cDNA to skeletal muscle or liver, showed no serious adverse events. Although the muscle trial failed to achieve a therapeutic level of
factor IX in the circulation, long-term expression of
clotting factor was demonstrated on muscle biopsies taken up to 3 years after vector injection. Administration of vector to liver via the hepatic artery identified a therapeutic dose, which agreed closely with the doses predicted by studies in hemophilic dogs. However, expression in human subjects lasted for only a period of weeks, followed by a gradual decline in
factor IX levels accompanied by a self-limited, asymptomatic rise and fall in liver
enzymes. Immune responses to vector capsid may account for this difference in outcome between humans and other species. Here we review the results from both preclinical and clinical studies of adeno-associated viral vector gene transfer for
hemophilia B, and the problems that have been identified and that must be overcome to achieve successful transduction and sustained expression.