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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5010
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pubmed:dateCreated |
1991-11-20
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pubmed:abstractText |
In the presence of antigen presenting cells, a murine T helper (Th) cell specific for murine hemoglobin (Hb) responded to its immunogenic peptide by both cytokine (interleukin-4) secretion and proliferation. An altered Hb peptide with a single amino acid substitution induced only cytokine secretion and did not induce proliferation. Interleukin-1 costimulated and restored the Th proliferative response to normal levels. The altered peptide also supported cognate T cell-B cell interactions indicative of T cell helper function. Thus, this result suggests that the T cell receptor has the capacity of differential signaling.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0036-8075
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
31
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pubmed:volume |
252
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
1308-10
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1833816-Amino Acid Sequence,
pubmed-meshheading:1833816-Animals,
pubmed-meshheading:1833816-Cell Division,
pubmed-meshheading:1833816-Clone Cells,
pubmed-meshheading:1833816-Hemoglobins,
pubmed-meshheading:1833816-Interleukin-4,
pubmed-meshheading:1833816-Lymphocyte Activation,
pubmed-meshheading:1833816-Mice,
pubmed-meshheading:1833816-Molecular Sequence Data,
pubmed-meshheading:1833816-Peptide Fragments,
pubmed-meshheading:1833816-Receptors, Antigen, T-Cell,
pubmed-meshheading:1833816-Signal Transduction,
pubmed-meshheading:1833816-T-Lymphocytes, Helper-Inducer
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pubmed:year |
1991
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pubmed:articleTitle |
Separation of IL-4 production from Th cell proliferation by an altered T cell receptor ligand.
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pubmed:affiliation |
Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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