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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1995-6-7
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pubmed:abstractText |
Staphylococcus enterotoxins bind class II MHC molecules on antigen presenting cells (APC) and stimulate T cells expressing appropriate V beta gene products. Although the role of non-TCR associated co-stimulatory receptors during antigen-specific T cell stimulation has been clearly established, the involvement of co-stimulatory activity in T cell activation by superantigens has been the matter of controversy. In this report, we examine the role of co-stimulation provided by selected APC populations in the response to bacterial exotoxins (staphylococcal enterotoxin A, staphylococcal enterotoxin B and toxic shock syndrome type 1). We demonstrate that the APC population able to activate naive T cells to IL-2 production is heterogeneous, comprising both adherent (presumably dendritic) and non-adherent (mostly B lymphocytes) cells. By stimulating naive T cells in the presence of graded doses of superantigens, we have observed that half-maximal IL-2 production was achieved at lower doses of superantigens in the presence of dendritic cells. Similarly, addition of antibodies to CD28 or B7.1-transfected cell lines increased the sensitivity of naive T cells to lower doses of superantigens. These observations indicate therefore that superantigens can be presented to naive T cells by APC displaying distinct levels of co-stimulatory activity, although with different efficacy. Thus, naive T cells are sensitive to CD28-mediated co-stimulation during superantigen-mediated responses but IL-2 production can be induced by high doses of superantigens in the presence of APC expressing weak co-stimulatory activity. These observations are compatible with the hypothesis that CD28-mediated signals participate in T cell activation by lowering T cell sensitivity to TCR ligands.
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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/Enterotoxins,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Superantigens,
http://linkedlifedata.com/resource/pubmed/chemical/enterotoxin A, Staphylococcal,
http://linkedlifedata.com/resource/pubmed/chemical/enterotoxin B, staphylococcal
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0953-8178
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
295-304
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7734424-Animals,
pubmed-meshheading:7734424-Antigen-Presenting Cells,
pubmed-meshheading:7734424-Base Sequence,
pubmed-meshheading:7734424-Cell Line,
pubmed-meshheading:7734424-Enterotoxins,
pubmed-meshheading:7734424-Female,
pubmed-meshheading:7734424-Flow Cytometry,
pubmed-meshheading:7734424-Interleukin-2,
pubmed-meshheading:7734424-Lymphocyte Activation,
pubmed-meshheading:7734424-Mice,
pubmed-meshheading:7734424-Mice, Inbred BALB C,
pubmed-meshheading:7734424-Molecular Sequence Data,
pubmed-meshheading:7734424-Signal Transduction,
pubmed-meshheading:7734424-Spleen,
pubmed-meshheading:7734424-Superantigens,
pubmed-meshheading:7734424-T-Lymphocytes
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pubmed:year |
1995
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pubmed:articleTitle |
Co-stimulation lowers the threshold for activation of naive T cells by bacterial superantigens.
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pubmed:affiliation |
Département de Biologie Moléculaire, Université Libre de Bruxelles, Rhode-St-Genèse, Belgium.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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