Therefore, we now know that under certain situations recombinant viruses can be oncogenic if they insert into the genome in the proximity of a gene that regulates cellular growth. As a consequence of this

serious issue, clinical studies are now using gene-transfer systems based on lentiviral vectors. Lentiviral vectors, such as those derived from HIV-1, have Dasatinib cell line multiple advantages compared to γ-retroviruses. Recent evidence shows that the use of advanced generation, self-inactivating recombinant lentiviral vectors for HSC gene transfer is safer than γ-retroviruses. It now is well documented that lentiviral vectors, unlike γ-retroviruses, do not integrate with high frequency near the promoters of proto-oncogenes and genes that control cell proliferation, and recent studies showed that

they have a much BGB324 ic50 lower oncogenic potential than other retroviruses. In addition, lentiviral vectors transduce HSCs as efficiently or, under some conditions, more efficiently than γ-retrovirus vectors. The use of haematopoietic stem cells (HSCs) as the target cell population for lentiviral-mediated gene therapy applications is the most advanced application of this technology, and the use of lentiviral vectors for the treatment of haemophilia A has benefited from clinical trials that targeted HSCs for other genetic diseases. Because lentiviral-based gene transfer results in the genetic modification of the transduced nearly cell’s genome, the transduction process permanently

modifies the DNA of the targeted cell. Bone marrow transplant studies in children have shown that transplanted HSCs survive for the lifetime of the recipient and that genetically engineered HSCs can both self replicate and/or differentiate into all cells of the haematopoietic system. In theory, transduction and transplantation of a single genetically modified HSC can result in the complete repopulation of the haematopoietic compartment, whereby all cells would be genetically modified. In the clinical setting, many diseases have already been treated using lentiviral-modified HSCs, including adrenoleukodystrophy, metachromatic leukodystrophy, Wiskott-Aldrich syndrome, chronic granulomatous disease, SCID-X1, HIV and thalassemia [65-71]. Based on encouraging clinical results using lentiviral vectors, preclinical studies using genetically engineered HSCs to treat haemophilia A are advancing towards clinical trials. Platelet-specific promoters have been used to treat both murine and canine models of haemophilia A. It is thought that this technology can be most useful in the setting of patients with pre-existing FVIII inhibitors. Lentiviral designs using promoters with more ubiquitous expression patterns have advanced to the stage of US FDA review.