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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1990-9-18
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pubmed:abstractText |
We have examined the T cell specificity of a Lewis rat T cell line (R208) specific for a pathogenic, 123 residue cyanogen bromide produced peptide of bovine S-antigen by using two independent sets of overlapping synthetic peptides representing the entire length of the 123 residue fragment. S-antigen, a 48 kDa immunopathogenic photoreceptor cell autoantigen induces T cell mediated experimental autoimmune uveoretinitis (EAU) in experimental animals. Extensive analyses revealed a heterogenous response by the R208 line to the panel of synthetic peptides, proliferating weakly to 4 distinct sites. Unexpectedly, peptides representing sequences (residues 286-297 and 303-320 of bovine S-antigen) known to actively induce the autoimmune pathology were unable to significantly stimulate the R208 line as assessed by proliferation assays. Similarly, attempts to isolate T cells specific for these sequences from the R208 line have proven unsuccessful. However, two sequences, residues 253-269 and 273-289, sufficiently stimulated R208 cells to allow isolation of sub-lines, R208:26 and R208:28, respectively. Neither of these peptides actively induce an autoimmune response. R208:26 does not transfer EAU and R208:28 transfers moderate EAU. As a control, we are able to isolate a pathogenic T cell line (R502) specific for the actively pathogenic sequence, residues 303-320, when this peptide is used as the immunogen. However, the R502 line proliferates to peptides (e.g. 305-322) which do not contain residues 303 and 304 which are critical for the active induction of disease. These results show a multiplicity of distinct T cell epitopes within a relatively small region of S-antigen.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Arrestin,
http://linkedlifedata.com/resource/pubmed/chemical/Cyanogen Bromide,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/Eye Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments
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pubmed:status |
MEDLINE
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pubmed:issn |
0271-3683
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
9 Suppl
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
111-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1696530-Amino Acid Sequence,
pubmed-meshheading:1696530-Animals,
pubmed-meshheading:1696530-Antigens,
pubmed-meshheading:1696530-Arrestin,
pubmed-meshheading:1696530-Cattle,
pubmed-meshheading:1696530-Cell Line,
pubmed-meshheading:1696530-Cyanogen Bromide,
pubmed-meshheading:1696530-Epitopes,
pubmed-meshheading:1696530-Eye Proteins,
pubmed-meshheading:1696530-Female,
pubmed-meshheading:1696530-Gene Library,
pubmed-meshheading:1696530-Immunization, Passive,
pubmed-meshheading:1696530-Lymphocyte Activation,
pubmed-meshheading:1696530-Molecular Sequence Data,
pubmed-meshheading:1696530-Peptide Fragments,
pubmed-meshheading:1696530-Rats,
pubmed-meshheading:1696530-Rats, Inbred Lew,
pubmed-meshheading:1696530-T-Lymphocytes
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pubmed:year |
1990
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pubmed:articleTitle |
Multiple, spatially distinct T cell epitopes within a pathogenic 123 residue cyanogen bromide peptide of bovine retinal s-antigen.
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pubmed:affiliation |
Department of Microbiology, University of Minnesota, Minneapolis.
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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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