pubmed-article:7519170 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C0025919 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C0026845 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C0034792 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C0003316 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C0017963 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C0443146 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C1332714 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C1519249 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C1709915 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C0205431 | lld:lifeskim |
pubmed-article:7519170 | lifeskim:mentions | umls-concept:C1321758 | lld:lifeskim |
pubmed-article:7519170 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:7519170 | pubmed:dateCreated | 1994-8-31 | lld:pubmed |
pubmed-article:7519170 | pubmed:abstractText | BALB/c mice develop myasthenic symptoms after immunization with rodent acetylcholine receptor (AChR). After immunization with Torpedo AChR (TAChR), their CD4+ cells become strongly sensitized against a conserved region of the TAChR alpha subunit sequence (residues alpha 304-322), and cross-react vigorously with the homologous sequences of mouse and human AChR, which are almost identical. Therefore AChR-specific potentially autoreactive CD4+ cells exist in this strain. We immunized BALB/c mice with the synthetic TAChR sequence alpha 304-322. The CD4+ cells thus sensitized responded to TAChR, indicating that they recognize an epitope(s) produced upon TAChR processing. They recognized peptide alpha 304-322 in association with the I-Ad molecule. Anti-alpha 304-322 CD4+ cells cross-reacted well with the corresponding murine and human synthetic sequences. To identify residues involved in formation of an autoimmune epitope(s), CD4+ cells from mice immunized with peptide alpha 304-322 were challenged in vitro with single residue glycine-substituted analogues of this sequence. Substitution of residue W311, and of any residue within the sequence alpha 313-319 (RKVFIDT), consistently and, in some cases, strongly affected the CD4+ cells response. Substitution of residues in the region alpha 311-319 had variable effects in different experiments, and in general affected moderately the CD4+ response. These results suggest that anti-alpha 304-322 CD4+ cells comprise several clones, recognizing overlapping epitopes which share residues alpha 311-319. The importance of the sequence region alpha 311-319 for formation of CD4+ cell epitope(s) was verified by testing CD4+ cells sensitized to T alpha 304-322 with analogues of this sequence, carrying non-conservative substitutions at positions Q310, K314 and D318. Substitution of Q310 had minimal or no effects, while those of K314 or D318 strongly affected the CD4+ cell response. | lld:pubmed |
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pubmed-article:7519170 | pubmed:language | eng | lld:pubmed |
pubmed-article:7519170 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7519170 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:7519170 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7519170 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7519170 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7519170 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7519170 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7519170 | pubmed:month | May | lld:pubmed |
pubmed-article:7519170 | pubmed:issn | 0019-2805 | lld:pubmed |
pubmed-article:7519170 | pubmed:author | pubmed-author:Conti-Troncon... | lld:pubmed |
pubmed-article:7519170 | pubmed:author | pubmed-author:BelloneMM | lld:pubmed |
pubmed-article:7519170 | pubmed:author | pubmed-author:OstlieNN | lld:pubmed |
pubmed-article:7519170 | pubmed:author | pubmed-author:KarachunskiP... | lld:pubmed |
pubmed-article:7519170 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7519170 | pubmed:volume | 82 | lld:pubmed |
pubmed-article:7519170 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7519170 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7519170 | pubmed:pagination | 22-7 | lld:pubmed |
pubmed-article:7519170 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:7519170 | pubmed:year | 1994 | lld:pubmed |
pubmed-article:7519170 | pubmed:articleTitle | Residues within the alpha subunit sequence 304-322 of muscle acetylcholine receptor forming autoimmune CD4+ epitopes in BALB/c mice. | lld:pubmed |
pubmed-article:7519170 | pubmed:affiliation | Department of Biochemistry, College of Biological Sciences, University of Minnesota, Minneapolis, St. Paul 55108. | lld:pubmed |
pubmed-article:7519170 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7519170 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:7519170 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |