Source:http://linkedlifedata.com/resource/pubmed/id/10445813
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rdf:type | |
lifeskim:mentions |
umls-concept:C0011209,
umls-concept:C0011306,
umls-concept:C0019682,
umls-concept:C0019699,
umls-concept:C0025260,
umls-concept:C0033684,
umls-concept:C0039195,
umls-concept:C0086418,
umls-concept:C0332307,
umls-concept:C0871261,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1948023,
umls-concept:C2911692
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pubmed:issue |
11
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pubmed:dateCreated |
1999-9-14
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pubmed:abstractText |
An important aspect of vaccine development involves delivery of antigens to antigen-presenting cells for the induction of potent antigen-specific T lymphocyte responses. We investigated the effect of a cationic liposome, lipofectin, on delivery of whole proteins to human dendritic cells (DCs) derived from blood mononuclear cells by culture in interleukin 4 and granulocyte-monocyte colony-stimulating factor for stimulation of human immunodeficiency virus type 1 (HIV-1)-specific memory cytotoxic T lymphocyte (CTL) responses. Delivery of HIV-1 Gag, Pol, and Env proteins to DCs by lipofectin stimulated greater anti-HIV-1 memory CTL responses in cells from HIV-1-infected subjects than those induced by DCs loaded with protein alone. The CTLs were CD8+ and HLA class I restricted. Antigen presentation was enhanced by chloroquine, but blocked by brefeldin A and peptide aldehyde inhibitors of proteasomes, indicating that the classic MHC class I cytosolic pathway was used for processing and presentation of HIV-1 protein by the DCs. Stimulation of anti-HIV-1 CTLs by this safe, inexpensive, and broadly applicable approach may be used in DC-based therapies for HIV-1 infection.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antiviral Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Brefeldin A,
http://linkedlifedata.com/resource/pubmed/chemical/Chloroquine,
http://linkedlifedata.com/resource/pubmed/chemical/Liposomes,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0889-2229
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1011-20
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:10445813-Adult,
pubmed-meshheading:10445813-Antigen Presentation,
pubmed-meshheading:10445813-Antiviral Agents,
pubmed-meshheading:10445813-Brefeldin A,
pubmed-meshheading:10445813-Cells, Cultured,
pubmed-meshheading:10445813-Chloroquine,
pubmed-meshheading:10445813-Cohort Studies,
pubmed-meshheading:10445813-Dendritic Cells,
pubmed-meshheading:10445813-HIV-1,
pubmed-meshheading:10445813-Homosexuality, Male,
pubmed-meshheading:10445813-Humans,
pubmed-meshheading:10445813-Immunologic Memory,
pubmed-meshheading:10445813-Liposomes,
pubmed-meshheading:10445813-Male,
pubmed-meshheading:10445813-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:10445813-Viral Proteins
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pubmed:year |
1999
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pubmed:articleTitle |
Delivery of liposome-encapsulated HIV type 1 proteins to human dendritic cells for stimulation of HIV type 1-specific memory cytotoxic T lymphocyte responses.
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pubmed:affiliation |
Graduate School of Public Health, University of Pittsburgh, Pennsylvania 15261, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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