pubmed-article:11867564 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11867564 | lifeskim:mentions | umls-concept:C0011306 | lld:lifeskim |
pubmed-article:11867564 | lifeskim:mentions | umls-concept:C0259309 | lld:lifeskim |
pubmed-article:11867564 | lifeskim:mentions | umls-concept:C0542341 | lld:lifeskim |
pubmed-article:11867564 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:11867564 | lifeskim:mentions | umls-concept:C1420813 | lld:lifeskim |
pubmed-article:11867564 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:11867564 | lifeskim:mentions | umls-concept:C0591833 | lld:lifeskim |
pubmed-article:11867564 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:11867564 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:11867564 | pubmed:dateCreated | 2002-2-27 | lld:pubmed |
pubmed-article:11867564 | pubmed:abstractText | 4-1BB (CDw137) and its ligand (4-1BBL) have been implicated in cellular immune responses. To further characterize the expression and function of 4-1BBL, we newly generated an anti-mouse 4-1BBL mAb (TKS-1), which can inhibit the interaction of 4-1BBL with 4-1BB. Flow cytometric analyses using TKS-1 and an anti-mouse 4-1BB mAb indicated that 4-1BB was inducible on both CD4(+) and CD8(+) splenic T cells by stimulation with immobilized anti-CD3 mAb, but 4-1BBL was not expressed on resting or activated T cells. 4-1BBL expression was inducible on splenic B cells by stimulation with anti-IgM antibody plus anti-CD40 mAb, on peritoneal macrophages by stimulation with lipopolysaccharide (LPS) and on splenic dendritic cells (DC) by stimulation with anti-CD40 mAb or LPS. Interestingly, splenic DC expressed 4-1BB constitutively, which was down-regulated by anti-CD40 stimulation. Co-culture of splenic DC with 4-1BBL-transfected cells or 4-1BBL-expressing tumor cell lines led to cytokine (IL-6 and IL-12) production and co-stimulatory molecule up-regulation by splenic DC, indicating that 4-1BBL can directly activate DC. Moreover, IL-12 production by anti-CD40-stimulated DC was partially inhibited by TKS-1. These results suggest that 4-1BB expressed on DC may be involved in DC activation through DC--tumor interaction and DC--DC interaction. | lld:pubmed |
pubmed-article:11867564 | pubmed:language | eng | lld:pubmed |
pubmed-article:11867564 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11867564 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:11867564 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11867564 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11867564 | pubmed:month | Mar | lld:pubmed |
pubmed-article:11867564 | pubmed:issn | 0953-8178 | lld:pubmed |
pubmed-article:11867564 | pubmed:author | pubmed-author:TakedaKazuyos... | lld:pubmed |
pubmed-article:11867564 | pubmed:author | pubmed-author:YagitaHideoH | lld:pubmed |
pubmed-article:11867564 | pubmed:author | pubmed-author:OkumuraKoK | lld:pubmed |
pubmed-article:11867564 | pubmed:author | pubmed-author:FutagawaToshi... | lld:pubmed |
pubmed-article:11867564 | pubmed:author | pubmed-author:AkibaHisayaH | lld:pubmed |
pubmed-article:11867564 | pubmed:author | pubmed-author:KodamaTomohir... | lld:pubmed |
pubmed-article:11867564 | pubmed:author | pubmed-author:HosodaYasuyuk... | lld:pubmed |
pubmed-article:11867564 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11867564 | pubmed:volume | 14 | lld:pubmed |
pubmed-article:11867564 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11867564 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11867564 | pubmed:pagination | 275-86 | lld:pubmed |
pubmed-article:11867564 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:11867564 | pubmed:year | 2002 | lld:pubmed |
pubmed-article:11867564 | pubmed:articleTitle | Expression and function of 4-1BB and 4-1BB ligand on murine dendritic cells. | lld:pubmed |
pubmed-article:11867564 | pubmed:affiliation | Department of Immunology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan. | lld:pubmed |
pubmed-article:11867564 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11867564 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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