| Literature DB >> 23110943 |
Stephanie Krause1, Ruth Chmiel, Ezio Bonifacio, Marlon Scholz, Michael Powell, Jadwiga Furmaniak, Bernard Rees Smith, Anette-G Ziegler, Peter Achenbach.
Abstract
Autoantibodies to insulinoma-associated protein 2 (IA-2A) are associated with increased risk for type 1 diabetes. Here we examined IA-2A affinity and epitope specificity to assess heterogeneity in response intensity in relation to pathogenesis and diabetes risk in 50 children who were prospectively followed from birth. At first IA-2A appearance, affinity ranged from 10(7) to 10(11)L/mol and was high (>1.0×10(9)L/mol) in 41 (82%) children. IA-2A affinity was not associated with epitope specificity or HLA class II haplotype. On follow-up, affinity increased or remained high, and IA-2A were commonly against epitopes within the protein tyrosine phosphatase-like IA-2 domain and the homologue protein IA-2β. IA-2A were preceded or accompanied by other islet autoantibodies in 49 (98%) children, of which 34 progressed to diabetes. IA-2A affinity did not stratify diabetes risk. In conclusion, the IA-2A response in children is intense with rapid maturation against immunogenic epitopes and a strong association with diabetes development.Entities:
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Year: 2012 PMID: 23110943 DOI: 10.1016/j.clim.2012.09.010
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969