Lentivirus-mediated gene transfer to the respiratory epithelium: a promising approach to gene therapy of cystic fibrosis. (Q35904439)

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3 January 2020

review article

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title

Lentivirus-mediated gene transfer to the respiratory epithelium: a promising approach to gene therapy of cystic fibrosis (English)

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3 January 2020

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4

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3 January 2020

author name string

Copreni E

series ordinal

1

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3 January 2020

Penzo M

series ordinal

2

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3 January 2020

Carrabino S

series ordinal

3

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3 January 2020

publication date

1 October 2004

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3 January 2020

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3 January 2020

volume

11 Suppl 1

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3 January 2020

page(s)

S67-75

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3 January 2020

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Gene therapy progress and prospects: cystic fibrosis

21 January 2018

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Airway epithelial CFTR mRNA expression in cystic fibrosis patients after repetitive administration of a recombinant adenovirus

21 January 2018

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Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector

21 January 2018

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Adeno-associated virus vector gene expression occurs in nondividing cells in the absence of vector DNA integration

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In vivo retroviral gene transfer into human bronchial epithelia of xenografts

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A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells

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Lentiviral vectors: turning a deadly foe into a therapeutic agent

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Lentiviral vectors: optimization of packaging, transduction and gene expression

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FIV: from lentivirus to lentivector

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In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector

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Surface-engineering of lentiviral vectors.

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Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences

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Non-viral approach toward gene therapy of cystic fibrosis lung disease.

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Immunological hurdles to lung gene therapy.

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Gene therapy for airway diseases: continued progress toward identifying and overcoming barriers to efficiency

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Direct gene transfer of human CFTR into human bronchial epithelia of xenografts with E1-deleted adenoviruses.

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Gene therapy in a xenograft model of cystic fibrosis lung corrects chloride transport more effectively than the sodium defect.

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Human beta-defensin-1 is a salt-sensitive antibiotic in lung that is inactivated in cystic fibrosis

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Lentiviral vectors for gene therapy of cystic fibrosis.

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Vesicular stomatitis virus G-pseudotyped lentivirus vectors mediate efficient apical transduction of polarized quiescent primary alveolar epithelial cells

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Pseudotyped human lentiviral vector-mediated gene transfer to airway epithelia in vivo.

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Recovery of airway cystic fibrosis transmembrane conductance regulator function in mice with cystic fibrosis after single-dose lentivirus-mediated gene transfer

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Evidence for stem-cell niches in the tracheal epithelium

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Feline immunodeficiency virus vectors persistently transduce nondividing airway epithelia and correct the cystic fibrosis defect

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Efficient adenovirus-mediated gene transfer to basal but not columnar cells of cartilaginous airway epithelia

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Polarity influences the efficiency of recombinant adenoassociated virus infection in differentiated airway epithelia.

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Endosomal processing limits gene transfer to polarized airway epithelia by adeno-associated virus.

21 January 2018

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Filovirus-pseudotyped lentiviral vector can efficiently and stably transduce airway epithelia in vivo

21 January 2018

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Cell surface heparan sulfate is a receptor for attachment of envelope protein-free retrovirus-like particles and VSV-G pseudotyped MLV-derived retrovirus vectors to target cells

21 January 2018

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Human immunodeficiency virus type 1 enters primary human brain microvascular endothelial cells by a mechanism involving cell surface proteoglycans independent of lipid rafts

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Syndecan captures, protects, and transmits HIV to T lymphocytes

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Syndecans serve as attachment receptors for human immunodeficiency virus type 1 on macrophages

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Distinct mechanisms of entry by envelope glycoproteins of Marburg and Ebola (Zaire) viruses

21 January 2018

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Lentiviral vectors pseudotyped with minimal filovirus envelopes increased gene transfer in murine lung

21 January 2018

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In vivo gene transfer using a nonprimate lentiviral vector pseudotyped with Ross River Virus glycoproteins

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Update on pathogenesis of cystic fibrosis lung disease

21 January 2018

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Status of gene therapy for cystic fibrosis lung disease

21 January 2018

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Localization of cystic fibrosis transmembrane conductance regulator mRNA in human fetal lung tissue by in situ hybridization

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Lung epithelial stem cells

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Stem cells in lung development, disease, and therapy

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Human airway xenograft models of epithelial cell regeneration

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Human fetal trachea-SCID mouse xenografts: efficacy of vesicular stomatitis virus-G pseudotyped lentiviral-mediated gene transfer.

21 January 2018

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Increased Chimerism of Bronchial and Alveolar Epithelium in Human Lung Allografts Undergoing Chronic Injury

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Bone marrow stem cells do not repopulate the healthy upper respiratory tract

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