Source:http://linkedlifedata.com/resource/pubmed/id/18202769
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007082,
umls-concept:C0011306,
umls-concept:C0017262,
umls-concept:C0033414,
umls-concept:C0039195,
umls-concept:C0205263,
umls-concept:C0205349,
umls-concept:C0205369,
umls-concept:C0871261,
umls-concept:C0918027,
umls-concept:C1171362,
umls-concept:C1515670,
umls-concept:C1516240,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911692
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pubmed:issue |
2
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pubmed:dateCreated |
2008-1-18
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pubmed:abstractText |
Cancer immunotherapy using dendritic cells (DCs) adenovirally transduced with the whole tumor-associated antigen (TAA) gene is an effective approach. Streptococcal preparation OK-432 is useful for stimulating DCs in terms of maturation. In this study, we established carcinoembryonic antigen (CEA)-specific cytotoxic T lymphocytes (CTLs) using in vitro stimulation with adenovirally modified human DCs that express CEA. We investigated whether OK-432 stimulation could be more effective in inducing CEA-specific CTLs compared with other typical stimuli. DCs adenovirally transduced with the CEA gene were cultured under various conditions with tumor necrosis factor (TNF)-alpha, lipopolysaccharide (LPS), or OK-432. A cytotoxicity assay using peripheral blood mononuclear cell (PBMC)-derived CTLs was performed in a 4 h-51Cr release assay. OK-432 stimulated immature DCs to acquire a mature phenotype and to produce significant amounts of T-helper 1 cytokines. In all groups (immature DCs, TNF-alpha/DCs, LPS/DCs, OK-432/DCs), CEA-specific CTLs were generated. OK-432-stimulated DCs (HLA-A24) induced the most potent cytotoxic activity against CEA-expressing targets (A24) but not against controls. OK-432/DCs were able to induce markedly potent CTLs specific to target cells pulsed with CEA652 peptide (HLA-A24-restricted peptide), although others failed to induce potent CTLs. In conclusion, the CTL induction protocol using adenovirally modified DCs that express CEA after maturation with OK-432 showed a potent antitumor activity against CEA-expressing target cells, and is therefore promising for clinical applications as a cancer vaccine therapy.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carcinoembryonic Antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-12,
http://linkedlifedata.com/resource/pubmed/chemical/Picibanil,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1019-6439
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pubmed:author |
pubmed-author:IidaTakeshiT,
pubmed-author:IwahashiMakotoM,
pubmed-author:KatsudaMasahiroM,
pubmed-author:MatsudaKenjiK,
pubmed-author:MiyazawaMotokiM,
pubmed-author:NakaTeijiT,
pubmed-author:NakamoriMikihitoM,
pubmed-author:NakamuraMasakiM,
pubmed-author:OjimaToshiyasuT,
pubmed-author:UedaKentaroK,
pubmed-author:YamaueHirokiH
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pubmed:issnType |
Print
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
459-66
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:18202769-Carcinoembryonic Antigen,
pubmed-meshheading:18202769-Cell Line, Tumor,
pubmed-meshheading:18202769-Cell Membrane,
pubmed-meshheading:18202769-Dendritic Cells,
pubmed-meshheading:18202769-Flow Cytometry,
pubmed-meshheading:18202769-Genetic Techniques,
pubmed-meshheading:18202769-Humans,
pubmed-meshheading:18202769-Immunotherapy,
pubmed-meshheading:18202769-Interferon-gamma,
pubmed-meshheading:18202769-Interleukin-12,
pubmed-meshheading:18202769-Leukocytes, Mononuclear,
pubmed-meshheading:18202769-Picibanil,
pubmed-meshheading:18202769-Recombinant Proteins,
pubmed-meshheading:18202769-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:18202769-Tumor Necrosis Factor-alpha
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pubmed:year |
2008
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pubmed:articleTitle |
Streptococcal preparation OK-432 promotes the capacity of dendritic cells (DCs) to prime carcinoembryonic antigen (CEA)-specific cytotoxic T lymphocyte responses induced with genetically modified DCs that express CEA.
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pubmed:affiliation |
Second Department of Surgery, Wakayama Medical University, School of Medicine, 811-1 Kimidera, Wakayama 641-8510, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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