| pubmed-article:9560258 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C0025914 | lld:lifeskim |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C0567416 | lld:lifeskim |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C0011306 | lld:lifeskim |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C0205148 | lld:lifeskim |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C0456387 | lld:lifeskim |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
| pubmed-article:9560258 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
| pubmed-article:9560258 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:9560258 | pubmed:dateCreated | 1998-6-4 | lld:pubmed |
| pubmed-article:9560258 | pubmed:abstractText | Here, we show that bacteria induce de novo synthesis of both major histocompatability complex (MHC) class I and II molecules in a mouse dendritic cell culture system. The neo-biosynthesis of MHC class I molecules is delayed as compared with that of MHC class II. Furthermore, bacteria stabilize MHC class I molecules by a 3-fold increase of their half-life. This has important consequences for the capacity of dendritic cells to present bacterial antigens in the draining lymph nodes. In addition, a model antigen, ovalbumin, expressed on the surface of recombinant Streptococcus gordonii is processed and presented on MHC class I molecules. This presentation is 10(6) times more efficient than that of soluble OVA protein. This exogenous pathway of MHC class I presentation is transporter associated with antigen processing (TAP)-dependent, indicating that there is a transport from phagolysosome to cytosol in dendritic cells. Thus, bacteria are shown to be a potentially useful mean for the correct delivery of exogenous antigens to be presented efficiently on MHC class I molecules. | lld:pubmed |
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| pubmed-article:9560258 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:9560258 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9560258 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9560258 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:9560258 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:9560258 | pubmed:author | pubmed-author:Ricciardi-Cas... | lld:pubmed |
| pubmed-article:9560258 | pubmed:author | pubmed-author:PozziGG | lld:pubmed |
| pubmed-article:9560258 | pubmed:author | pubmed-author:AmigorenaSS | lld:pubmed |
| pubmed-article:9560258 | pubmed:author | pubmed-author:RittigMM | lld:pubmed |
| pubmed-article:9560258 | pubmed:author | pubmed-author:RescignoMM | lld:pubmed |
| pubmed-article:9560258 | pubmed:author | pubmed-author:MedagliniDD | lld:pubmed |
| pubmed-article:9560258 | pubmed:author | pubmed-author:CitterioSS | lld:pubmed |
| pubmed-article:9560258 | pubmed:author | pubmed-author:ThèryCC | lld:pubmed |
| pubmed-article:9560258 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9560258 | pubmed:day | 28 | lld:pubmed |
| pubmed-article:9560258 | pubmed:volume | 95 | lld:pubmed |
| pubmed-article:9560258 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9560258 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9560258 | pubmed:pagination | 5229-34 | lld:pubmed |
| pubmed-article:9560258 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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