Source:http://linkedlifedata.com/resource/pubmed/id/12359442
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2002-10-2
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pubmed:abstractText |
Monocyte-derived dendritic cells (DCs) from adult T cell leukemia are impaired in taking up exogenous antigens. To overcome this impairment, we fused unpulsed DCs to human T-lymphotropic virus type I (HTLV-I)-infected CD4(+) T cells (fusion DC-T cells). The efficiency of fusion was 50% and the fusion cells expressed higher HLA-ABC and CD86 Ags than HTLV-I-infected DCs. The fusion DC-T cells stimulated autologous CD4(+) and CD8(+) T cells, but DCs fused to itself or PHA-blasts did not stimulate any subsets. The functionally highest fusion DC-T cells was obtained when a DC and HTLV-I-infected T cells were fused at a ratio of 3:1. Expression of HTLV-Igag Ag on CD4(+) T cells was up-regulated when infected in the presence of 8-azaguanine, and these fusion DC-T cells were quite efficient in induction of higher CD8(+) T cell response. The results suggest that fusion DC-T cells produce functionally competent Ag-presenting cells and may be a likely candidate for immunotherapeutic use.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0042-6822
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
301
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
13-20
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:12359442-Antigen Presentation,
pubmed-meshheading:12359442-Antigen-Presenting Cells,
pubmed-meshheading:12359442-Cell Fusion,
pubmed-meshheading:12359442-Dendritic Cells,
pubmed-meshheading:12359442-Human T-lymphotropic virus 1,
pubmed-meshheading:12359442-Humans,
pubmed-meshheading:12359442-Immunophenotyping,
pubmed-meshheading:12359442-Immunotherapy,
pubmed-meshheading:12359442-Leukemia-Lymphoma, Adult T-Cell,
pubmed-meshheading:12359442-T-Lymphocytes
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pubmed:year |
2002
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pubmed:articleTitle |
Fusion of mature dendritic cells and human T-lymphotropic virus type I infected T cells: its efficiency as an antigen-presenting cell.
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pubmed:affiliation |
Department of Microbiology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo, 189-0002, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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