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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0011306,
umls-concept:C0020204,
umls-concept:C0023509,
umls-concept:C0025914,
umls-concept:C0026809,
umls-concept:C0035820,
umls-concept:C0039194,
umls-concept:C0175727,
umls-concept:C0205165,
umls-concept:C0205225,
umls-concept:C0443199,
umls-concept:C0871261,
umls-concept:C1516240,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1708726,
umls-concept:C2911692
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pubmed:issue |
4
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pubmed:dateCreated |
1989-3-13
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pubmed:abstractText |
The response of T cells to minor lymphocyte-stimulating locus (Mls) determinants remains poorly understood with respect to the antigenic determinants responsible for T cell stimulation and the types of APC capable of stimulating the response. In this report, we demonstrate that highly purified dendritic cells (DC) as well as B cells have the capacity to stimulate Mls-specific responses. Unseparated spleen cells, purified DC, resting B cells, and activated B cells were compared for their capacity to stimulate several Mls-reactive T cell hybridomas. Whereas the entire panel of Mls-reactive T cell hybridomas was stimulated strongly by unseparated spleen cells and activated B cells, the hybridomas responded only weakly to purified DC or resting B cells. Activation of resting B cells with either B cell stimulatory factor-1 (1 day pre-treatment) or LPS/dextran (2 or 3 day pre-treatment) greatly augmented their Mls-stimulatory capacity. In contrast, the Mls-stimulatory capacity of DC was not augmented by a 1-day pre-treatment with either B cell stimulatory factor-1 or supernatant from the DC-induced primary anti-Mls-MLR. In the primary anti-Mls-MLR, both purified DC and LPS/dextran-stimulated B blasts were found to elicit vigorous T cell proliferative responses. Much weaker responses were elicited by unseparated spleen cells. The stimulation of the primary anti-Mls-MLR by purified DC was further confirmed by producing Mls-specific T cell clones which were preferentially stimulated by DC. Autologous (Mlsb) DC were found to markedly enhance the primary anti-Mls-MLR response to small numbers of Mlsa B blasts. Thus, DC possess other "accessory cell" properties that augment the primary anti-Mls-MLR despite the predicted low level of Mls determinant expression on DC based on the results obtained with Mls-reactive hybridomas. Possible accessory cell properties of DC relevant to this phenomenon are discussed.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
142
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1069-78
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2464636-Animals,
pubmed-meshheading:2464636-Antigens, Surface,
pubmed-meshheading:2464636-B-Lymphocytes,
pubmed-meshheading:2464636-Cell Separation,
pubmed-meshheading:2464636-Dendritic Cells,
pubmed-meshheading:2464636-Dextrans,
pubmed-meshheading:2464636-Hybridomas,
pubmed-meshheading:2464636-Interphase,
pubmed-meshheading:2464636-Lipopolysaccharides,
pubmed-meshheading:2464636-Lymphocyte Activation,
pubmed-meshheading:2464636-Lymphocyte Culture Test, Mixed,
pubmed-meshheading:2464636-Mice,
pubmed-meshheading:2464636-Mice, Inbred AKR,
pubmed-meshheading:2464636-Mice, Inbred BALB C,
pubmed-meshheading:2464636-Mice, Inbred C3H,
pubmed-meshheading:2464636-Mice, Inbred CBA,
pubmed-meshheading:2464636-Mice, Inbred DBA,
pubmed-meshheading:2464636-Minor Lymphocyte Stimulatory Antigens,
pubmed-meshheading:2464636-Phenotype,
pubmed-meshheading:2464636-T-Lymphocytes
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pubmed:year |
1989
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pubmed:articleTitle |
The role of dendritic cells as stimulators of minor lymphocyte-stimulating locus-specific T cell responses in the mouse. I. Differential capacity of dendritic cells to stimulate minor lymphocyte-stimulating locus-reactive T cell hybridomas and the primary anti-minor lymphocyte-stimulating locus mixed lymphocyte reaction.
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pubmed:affiliation |
Anna Perahia Addato Clinical Research Facilities, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.
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