Rapid and efficient gene transfer in human hepatocytes by herpes viral vectors
Yuman Fong, Howard J. Federoff, Michael Brownlee, David Blumberg, Leslie H. Blumgart, Murray F. Brennan – 1 September 1995 – Retroviral vectors have been widely studied as vehicles for hepatocyte gene therapy, but they are limited by an inability to infect nondividing cells and the need for prolonged cell culture. Two replication deficient herpes simplex viral vectors (HSV) were constructed with the marker genes lac‐Z/β‐galactosidase (HSVlac) or human‐growth hormone (HSVhGH) to determine the efficiency of HSV gene transfer into adult human hepatocytes.