Viruses 2011, 3(2), 132-159; doi:10.3390/v3020132
Review

The Inside Out of Lentiviral Vectors

1,2,3,4email and 1,2,3,4,* email
Received: 26 November 2010; in revised form: 25 January 2011 / Accepted: 8 February 2011 / Published: 14 February 2011
(This article belongs to the Special Issue Retroviral Vectors)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Lentiviruses induce a wide variety of pathologies in different animal species. A common feature of the replicative cycle of these viruses is their ability to target non-dividing cells, a property that constitutes an extremely attractive asset in gene therapy. In this review, we shall describe the main basic aspects of the virology of lentiviruses that were exploited to obtain efficient gene transfer vectors. In addition, we shall discuss some of the hurdles that oppose the efficient genetic modification mediated by lentiviral vectors and the strategies that are being developed to circumvent them.
Keywords: lentivirus; lentiviral vector; gene therapy; HIV; SIV; EIAV; FIV
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MDPI and ACS Style

Durand, S.; Cimarelli, A. The Inside Out of Lentiviral Vectors. Viruses 2011, 3, 132-159.

AMA Style

Durand S, Cimarelli A. The Inside Out of Lentiviral Vectors. Viruses. 2011; 3(2):132-159.

Chicago/Turabian Style

Durand, Stéphanie; Cimarelli, Andrea. 2011. "The Inside Out of Lentiviral Vectors." Viruses 3, no. 2: 132-159.


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