Efficient gene transfer to human peripheral blood monocyte-derived dendritic cells using human immunodeficiency virus type 1-based lentiviral vectors.
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Development of an avian leukosis-sarcoma virus subgroup A pseudotyped lentiviral vectorThe CD8 and CD4 T-cell response against Kaposi's sarcoma-associated herpesvirus is skewed towards early and late lytic antigens.Nonintegrating Lentiviral Vector-Based Vaccine Efficiently Induces Functional and Persistent CD8+ T Cell Responses in Mice.Genetically modified dendritic cells--a new, promising cancer treatment strategy?An effective cancer vaccine modality: lentiviral modification of dendritic cells expressing multiple cancer-specific antigensInduction of primary anti-HIV CD4 and CD8 T cell responses by dendritic cells transduced with self-inactivating lentiviral vectors.Activation of antigen-presenting cells by DNA delivery vectors.Lentivirus as a potent and mechanistically distinct vector for genetic immunizationRecombinant lentivector as a genetic immunization vehicle for antitumor immunity.Targeted transduction of CD34+ hematopoietic progenitor cells in nonpurified human mobilized peripheral blood mononuclear cellsDendritic cell-based vaccines for the therapy of experimental tumors.Lentiviral vectors in cancer immunotherapy.Postentry restriction to human immunodeficiency virus-based vector transduction in human monocytesHighly efficient transduction of human plasmacytoid dendritic cells without phenotypic and functional maturation.Tubulovesicular structures within vesicular stomatitis virus G protein-pseudotyped lentiviral vector preparations carry DNA and stimulate antiviral responses via Toll-like receptor 9.Induction of effective therapeutic antitumor immunity by direct in vivo administration of lentiviral vectors.Dual-reporter Imaging and its Potential Application in Tracking Studies.Lentiviral vectors pseudotyped with baculovirus gp64 efficiently transduce mouse cells in vivo and show tropism restriction against hematopoietic cell types in vitro.Inhibition of HIV-1 replication by novel lentiviral vectors expressing transdominant Rev and HIV-1 env antisense.Multicistronic lentiviral vectors containing the FMDV 2A cleavage factor demonstrate robust expression of encoded genes at limiting MOIDifferential effects of HIV-1 protease inhibitors on dendritic cell immunophenotype and function.Lentiviral-mediated gene delivery in human monocyte-derived dendritic cells: optimized design and procedures for highly efficient transduction compatible with clinical constraints.Lentivectors are efficient tools to manipulate the dendritic cell cytoskeleton.Ex vivo generation of genetically modified dendritic cells for immunotherapy: implications of lymphocyte contamination.
P2860
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P2860
Efficient gene transfer to human peripheral blood monocyte-derived dendritic cells using human immunodeficiency virus type 1-based lentiviral vectors.
description
2000 nî lūn-bûn
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2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh-hant
name
Efficient gene transfer to hum ...... pe 1-based lentiviral vectors.
@en
Efficient gene transfer to hum ...... pe 1-based lentiviral vectors.
@nl
type
label
Efficient gene transfer to hum ...... pe 1-based lentiviral vectors.
@en
Efficient gene transfer to hum ...... pe 1-based lentiviral vectors.
@nl
prefLabel
Efficient gene transfer to hum ...... pe 1-based lentiviral vectors.
@en
Efficient gene transfer to hum ...... pe 1-based lentiviral vectors.
@nl
P2093
P1433
P1476
Efficient gene transfer to hum ...... pe 1-based lentiviral vectors.
@en
P2093
Candotti F
Chinnasamy D
Chinnasamy N
Lapointe R
P304
P356
10.1089/10430340050129512
P577
2000-09-01T00:00:00Z