The use of integrating vectors for gene therapy — required for stable correction of gene expression — carries the risk of insertional mutagenesis, which can lead to activation of a tumorigenic program. In this issue of the JCI, Moiani et al. and Cesana et al. investigate how viral vectors can induce aberrant splicing, resulting in chimeric cellular-viral transcripts. The finding that this is a general phenomenon is concerning, but some of their results do suggest approaches for the development of safeguards in gene therapy vector design.
Didier Trono
Title and authors | Publication | Year |
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In situ bone tissue engineering via ultrasound-mediated gene delivery to endogenous progenitor cells in mini-pigs.
Bez M, Sheyn D, Tawackoli W, Avalos P, Shapiro G, Giaconi JC, Da X, David SB, Gavrity J, Awad HA, Bae HW, Ley EJ, Kremen TJ, Gazit Z, Ferrara KW, Pelled G, Gazit D |
Science Translational Medicine | 2017 |
Towards a Safer, More Randomized Lentiviral Vector Integration Profile Exploring Artificial LEDGF Chimeras
LS Vranckx, J Demeulemeester, Z Debyser, R Gijsbers, Y Ikeda |
PloS one | 2016 |
A single epidermal stem cell strategy for safe ex vivo gene therapy
SD Lathion, A Rochat, G Knott, A Recchia, D Martinet, S Benmohammed, N Grasset, A Zaffalon, NB Schmutz, E Savioz-Dayer, JS Beckmann, J Rougemont, F Mavilio, Y Barrandon |
EMBO Molecular Medicine | 2015 |