Hepatic lentiviral gene transfer is associated with clonal selection, but not with tumor formation in serially transplanted rodents
Ina Rittelmeyer, Michael Rothe, Martijn H. Brugman, Marcus Iken, Axel Schambach, Michael P. Manns, Christopher Baum, Ute Modlich, Michael Ott – 19 December 2012 – Lentiviral (LV) vectors are promising tools for long‐term genetic correction of hereditary diseases. In hematopoietic stem cell gene therapies adverse events in patients due to vector integration‐associated genotoxicity have been observed. Only a few studies have explored the potential risks of LV gene therapy targeting the liver.