Literature DB >> 11045424

Lentiviral vectors: excellent tools for experimental gene transfer and promising candidates for gene therapy.

E Vigna1, L Naldini.   

Abstract

Lentiviral vectors are tools for gene transfer derived from lentiviruses. From their first application to now they have been strongly developed in design, in biosafety and in their ability of transgene expression into target cells. Primate and non-primate derived lentiviral vectors are now available and with both types of systems a lot of studies tuned to improve their performances in a large number of tissues are ongoing. Here we review the state of the art of lentiviral vector systems discussing their potential for gene therapy.

Mesh:

Year:  2000        PMID: 11045424     DOI: 10.1002/1521-2254(200009/10)2:5<308::AID-JGM131>3.0.CO;2-3

Source DB:  PubMed          Journal:  J Gene Med        ISSN: 1099-498X            Impact factor:   4.565


  78 in total

1.  A new hybrid system capable of efficient lentiviral vector production and stable gene transfer mediated by a single helper-dependent adenoviral vector.

Authors:  Shuji Kubo; Kohnosuke Mitani
Journal:  J Virol       Date:  2003-03       Impact factor: 5.103

2.  Optimization of the transductional efficiency of lentiviral vectors: effect of sera and polycations.

Authors:  Warren Denning; Suvendu Das; Siqi Guo; Jun Xu; John C Kappes; Zdenek Hel
Journal:  Mol Biotechnol       Date:  2013-03       Impact factor: 2.695

3.  Transduction efficiency of MLV but not of HIV-1 vectors is pseudotype dependent on human primary T lymphocytes.

Authors:  Michael D Mühlebach; Isabel Schmitt; Stefanie Steidl; Jörn Stitz; Matthias Schweizer; Thomas Blankenstein; Klaus Cichutek; Wolfgang Uckert
Journal:  J Mol Med (Berl)       Date:  2003-10-24       Impact factor: 4.599

Review 4.  Imaging intracellular protein dynamics by spinning disk confocal microscopy.

Authors:  Samantha Stehbens; Hayley Pemble; Lyndsay Murrow; Torsten Wittmann
Journal:  Methods Enzymol       Date:  2012       Impact factor: 1.600

Review 5.  Advances in the field of lentivector-based transduction of T and B lymphocytes for gene therapy.

Authors:  Cecilia Frecha; Camille Lévy; François-Loïc Cosset; Els Verhoeyen
Journal:  Mol Ther       Date:  2010-08-24       Impact factor: 11.454

6.  Expression and immunological analysis of capsid protein precursor of swine vesicular disease virus HK/70.

Authors:  Hong Tian; Jing-yan Wu; You-jun Shang; Shuang-hui Ying; Hai-xue Zheng; Xiang-tao Liu
Journal:  Virol Sin       Date:  2010-06-06       Impact factor: 4.327

Review 7.  Gene therapy for the neurological manifestations in lysosomal storage disorders.

Authors:  Seng H Cheng
Journal:  J Lipid Res       Date:  2014-03-29       Impact factor: 5.922

8.  A microRNA-regulated and GP64-pseudotyped lentiviral vector mediates stable expression of FVIII in a murine model of Hemophilia A.

Authors:  Hideto Matsui; Carol Hegadorn; Margareth Ozelo; Erin Burnett; Angie Tuttle; Andrea Labelle; Paul B McCray; Luigi Naldini; Brian Brown; Christine Hough; David Lillicrap
Journal:  Mol Ther       Date:  2011-02-01       Impact factor: 11.454

Review 9.  Integration-deficient lentiviral vectors: a slow coming of age.

Authors:  Klaus Wanisch; Rafael J Yáñez-Muñoz
Journal:  Mol Ther       Date:  2009-06-02       Impact factor: 11.454

10.  Feline immunodeficiency virus as a gene transfer vector in the rat nucleus tractus solitarii.

Authors:  L H Lin; J E Langasek; L S Talman; O M Taktakishvili; W T Talman
Journal:  Cell Mol Neurobiol       Date:  2009-09-24       Impact factor: 5.046

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