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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1986-10-7
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pubmed:abstractText |
It has been previously shown that endothelial cells (EC) can modulate T-cell responsiveness by mimicking monocyte (AC) function in several different in vitro systems. We now report that EC and AC differ quantitatively in their ability to provide help for IL-2 generation and T-cell induced B-cell differentiation into immunoglobulin secreting cells (ISC). Equal numbers of EC were deficient when compared to AC for promoting ISC generation, but exceeded AC for IL-2 production. Adding optimal numbers of EC drive non-adherent cell cultures to produce more than twice as much IL-2 as adding any number of AC. Furthermore, small numbers of EC were capable of modulating ongoing immune responses when added to cultures containing AC. IL-2 production by PBM was doubled by the addition of enough EC to comprise only 3% of the total culture. EC do not just mimic monocytes in immune responses, but modulate these responses in unique ways.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0008-8749
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
100
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
210-23
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3488818-Antibody-Producing Cells,
pubmed-meshheading:3488818-Antigen-Presenting Cells,
pubmed-meshheading:3488818-B-Lymphocytes,
pubmed-meshheading:3488818-Cell Differentiation,
pubmed-meshheading:3488818-Endothelium,
pubmed-meshheading:3488818-Interleukin-2,
pubmed-meshheading:3488818-Mitogens,
pubmed-meshheading:3488818-Monocytes,
pubmed-meshheading:3488818-Staphylococcal Protein A,
pubmed-meshheading:3488818-T-Lymphocytes
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pubmed:year |
1986
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pubmed:articleTitle |
Comparison of accessory cell functions of endothelial cells and monocytes: IL-2 production by T cells and PFC generation.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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