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Notable reduction in illegitimate integration mediated by a PPT-deleted, nonintegrating lentiviral vector.
Kantor, Boris; Bayer, Matthew; Ma, Hong; Samulski, Jude; Li, Chengwen; McCown, Thomas; Kafri, Tal.
Affiliation
  • Kantor B; Gene Therapy Center, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599, USA.
Mol Ther ; 19(3): 547-56, 2011 Mar.
Article in En | MEDLINE | ID: mdl-21157436
ABSTRACT
Nonintegrating lentiviral vectors present a means of reducing the risk of insertional mutagenesis in nondividing cells and enabling short-term expression of potentially hazardous gene products. However, residual, integrase-independent integration raises a concern that may limit the usefulness of this system. Here we present a novel 3' polypurine tract (PPT)-deleted lentiviral vector that demonstrates impaired integration efficiency and, when packaged into integrase-deficient particles, significantly reduced illegitimate integration. Cells transduced with PPT-deleted vectors exhibited predominantly 1-long terminal repeat (LTR) circles and a low level of linear genomes after reverse transcription (RT). Importantly, the PPT-deleted vector exhibited titers and in vitro and in vivo expression levels matching those of conventional nonintegrating lentiviral vectors. This safer nonintegrating lentiviral vector system will support emerging technologies, such as those based on transient expression of zinc-finger nucleases (ZFNs) for gene editing, as well as reprogramming factors for inducing pluripotency.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Integration / Gene Deletion / Lentivirus / Genetic Vectors Type of study: Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: Mol Ther Journal subject: BIOLOGIA MOLECULAR / TERAPEUTICA Year: 2011 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Integration / Gene Deletion / Lentivirus / Genetic Vectors Type of study: Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: Mol Ther Journal subject: BIOLOGIA MOLECULAR / TERAPEUTICA Year: 2011 Document type: Article Affiliation country: