pubmed-article:6196405 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C0020204 | lld:lifeskim |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C1522642 | lld:lifeskim |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C0026377 | lld:lifeskim |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C1521721 | lld:lifeskim |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C0037791 | lld:lifeskim |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C0205232 | lld:lifeskim |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C0205372 | lld:lifeskim |
pubmed-article:6196405 | lifeskim:mentions | umls-concept:C0332120 | lld:lifeskim |
pubmed-article:6196405 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:6196405 | pubmed:dateCreated | 1984-1-7 | lld:pubmed |
pubmed-article:6196405 | pubmed:abstractText | Two groups of cloned insulin-specific T cell hybridomas were derived from the fusion of (BALB/c X A/J)F1 T cells with the BW5147 tumor line. Group I responded only to the immunogen pork insulin and failed to respond to rat insulin, which differs only at amino acids A4 and B3. The second group of T cell hybridomas exhibited a broader pattern of reactivity to heterologous insulins because they could be stimulated with the B chain-identical pork, beef, sheep, and human insulins, as well as by isolated oxidized B chain. These hybridomas, however, displayed a much greater reactivity to pork insulin than to beef insulin or to the oxidized B chain. Comparison of the reactivity profiles of these two groups of hybridomas with the three-dimensional structure of the insulin molecule strongly suggested that group I cells were recognizing an immunogenic moiety composed of residues A4 and/or B3 in association with A chain loop determinants and that group II hybrids recognized a moiety composed of the amino acid sequence of the B chain and the A chain loop. Both groups of hybrids were restricted to the high-responder I-Ad allele but could be distinguished by their pattern of alloreactivity. We were unable to show any effect of a panel of monoclonal anti-insulin antibodies on the induction of interleukin 2 secretion by these hybridomas or to demonstrate the presence of idiotypic determinants on these T hybrids by using a panel of anti-idiotypic reagents raised against the monoclonal anti-insulin antibodies. | lld:pubmed |
pubmed-article:6196405 | pubmed:language | eng | lld:pubmed |
pubmed-article:6196405 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6196405 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:6196405 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:6196405 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:6196405 | pubmed:month | Dec | lld:pubmed |
pubmed-article:6196405 | pubmed:issn | 0022-1767 | lld:pubmed |
pubmed-article:6196405 | pubmed:author | pubmed-author:ShevachE MEM | lld:pubmed |
pubmed-article:6196405 | pubmed:author | pubmed-author:SchroerJ AJA | lld:pubmed |
pubmed-article:6196405 | pubmed:author | pubmed-author:ChanCC | lld:pubmed |
pubmed-article:6196405 | pubmed:author | pubmed-author:GlimcherL HLH | lld:pubmed |
pubmed-article:6196405 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:6196405 | pubmed:volume | 131 | lld:pubmed |
pubmed-article:6196405 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:6196405 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:6196405 | pubmed:pagination | 2868-74 | lld:pubmed |
pubmed-article:6196405 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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pubmed-article:6196405 | pubmed:year | 1983 | lld:pubmed |
pubmed-article:6196405 | pubmed:articleTitle | Fine specificity of cloned insulin-specific T cell hybridomas: evidence supporting a role for tertiary conformation. | lld:pubmed |
pubmed-article:6196405 | pubmed:publicationType | Journal Article | lld:pubmed |
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