Source:http://linkedlifedata.com/resource/pubmed/id/11908951
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2002-3-22
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pubmed:abstractText |
ICA512/IA-2, a tyrosine phosphatase-like protein, is one of the major autoantigens in type 1 diabetes. Following phage display characterization of ICA512 autoantigenic epitopes, we developed fluid phase autoantibody radioimmunoassays for a series of ICA512 fragments (F1 [amino acids (aa): 761-964], F2A [aa 256-760], F2B [aa 761-928], and F2C [aa 929-979]). With the hypothesis that 'non-diabetes associated' ICA512 autoantibodies would differ from diabetes associated ICA512 autoantibodies in terms of epitopes recognized, we analyzed ten such serum samples (two from normal control individuals, one from a general population subject with transient ICA512 autoantibodies and seven from relatives of patients with type 1 diabetes who had single transient ICA512 positivity). All but one of the 'non-diabetes associated' ICA512 positive samples (9/10) did not react with Fragment 1 which contains the major antigenic epitopes of the molecule that were recognized by almost all (51/52) ICA512 positive new onset patient samples and pre-diabetic relatives (P< 10(-6)). The great majority of samples (44/52) from the new onset patients and pre-diabetic relatives reacted with at least two fragments and 60% (31/52) with three or more fragments. In contrast, only one sample of the ICA512 'non-diabetes associated' sera reacted with multiple fragments (P< 10(-4)). Our findings suggest that diabetes associated anti-ICA512 autoantibodies react with multiple ICA512 epitopes while non-diabetes associated ICA512 autoantibodies may usually represent reactivity of antibodies with determinants of ICA512 unrelated to type 1 diabetes. The ability to distinguish diabetes associated from non-diabetes associated anti-ICA512 autoantibodies should provide prognostic information and more importantly suggests that even with highly specific radioassays positivity may occur unrelated to type 1 diabetes.
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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/Autoantibodies,
http://linkedlifedata.com/resource/pubmed/chemical/Autoantigens,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/ICA512 autoantibody,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/PTPRN protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatase...,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor-Like Protein Tyrosine...
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0896-8411
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2002 Elsevier Science Ltd.
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pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
191-6
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:11908951-Autoantibodies,
pubmed-meshheading:11908951-Autoantigens,
pubmed-meshheading:11908951-Diabetes Mellitus, Type 1,
pubmed-meshheading:11908951-Epitopes,
pubmed-meshheading:11908951-Humans,
pubmed-meshheading:11908951-Islets of Langerhans,
pubmed-meshheading:11908951-Membrane Proteins,
pubmed-meshheading:11908951-Models, Immunological,
pubmed-meshheading:11908951-Peptide Fragments,
pubmed-meshheading:11908951-Protein Tyrosine Phosphatase, Non-Receptor Type 1,
pubmed-meshheading:11908951-Protein Tyrosine Phosphatases,
pubmed-meshheading:11908951-Receptor-Like Protein Tyrosine Phosphatases, Class 8
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pubmed:year |
2002
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pubmed:articleTitle |
ICA512(IA-2) epitope specific assays distinguish transient from diabetes associated autoantibodies.
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pubmed:affiliation |
Barbara Davis Center for Childhood Diabetes, University of Colorado, Denver 80262, USA.
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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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