A simple, versatile and efficient method to genetically modify human monocyte-derived dendritic cells with HIV-1-derived lentiviral vectors (Q84261542)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21637200%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

A simple, versatile and efficient method to genetically modify human monocyte-derived dendritic cells with HIV-1-derived lentiviral vectors (English)

1 reference

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2 February 2020

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21637200%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Grégory Berger

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21637200%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Stéphanie Durand

1 reference

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2 February 2020

Caroline Goujon

1 reference

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2 February 2020

Xuan-Nhi Nguyen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21637200%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Stéphanie Cordeil

1 reference

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2 February 2020

Jean-Luc Darlix

1 reference

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2 February 2020

publication date

19 May 2011

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2 February 2020

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2 February 2020

volume

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2 February 2020

issue

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2 February 2020

page(s)

806-816

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Immunobiology of dendritic cells

2 February 2020

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High levels of transduction of human dendritic cells with optimized SIV vectors

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SIVMAC Vpx improves the transduction of dendritic cells with nonintegrative HIV-1-derived vectors.

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With a little help from a friend: increasing HIV transduction of monocyte-derived dendritic cells with virion-like particles of SIV(MAC).

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SIVSM/HIV-2 Vpx proteins promote retroviral escape from a proteasome-dependent restriction pathway present in human dendritic cells

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The human immunodeficiency virus type 2 Vpx protein usurps the CUL4A-DDB1 DCAF1 ubiquitin ligase to overcome a postentry block in macrophage infection

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Primate lentiviral Vpx commandeers DDB1 to counteract a macrophage restriction

31 March 2020

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Lentiviral Vpx accessory factor targets VprBP/DCAF1 substrate adaptor for cullin 4 E3 ubiquitin ligase to enable macrophage infection

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The cytoplasmic body component TRIM5alpha restricts HIV-1 infection in Old World monkeys

31 March 2020

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Removal of arginine 332 allows human TRIM5alpha to bind human immunodeficiency virus capsids and to restrict infection

31 March 2020

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Isolation of a human gene that inhibits HIV-1 infection and is suppressed by the viral Vif protein

31 March 2020

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Tetherin inhibits retrovirus release and is antagonized by HIV-1 Vpu

31 March 2020

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The interferon-induced protein BST-2 restricts HIV-1 release and is downregulated from the cell surface by the viral Vpu protein

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APOBEC3G/3F mediates intrinsic resistance of monocyte-derived dendritic cells to HIV-1 infection

31 March 2020

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31 March 2020

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Nuclear import and cell cycle arrest functions of the HIV-1 Vpr protein are encoded by two separate genes in HIV-2/SIV(SM).

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Production and purification of lentiviral vectors

31 March 2020

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Design and cloning of lentiviral vectors expressing small interfering RNAs

31 March 2020

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Production, concentration and titration of pseudotyped HIV-1-based lentiviral vectors

31 March 2020

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Use of a lentivirus/VSV pseudotype virus for highly efficient genetic redirection of human peripheral blood lymphocytes

31 March 2020

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GM-CSF and TNF-α cooperate in the generation of dendritic Langerhans cells

31 March 2020

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Efficient presentation of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and downregulated by tumor necrosis factor alpha

31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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PubMed

https://pubmed.ncbi.nlm.nih.gov/21637200

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A conserved dileucine-containing motif in p6(gag) governs the particle association of Vpx and Vpr of simian immunodeficiency viruses SIV(mac) and SIV(agm)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21637200