Author/Authors :
Krause، نويسنده , , Stephanie and Chmiel، نويسنده , , Ruth and Bonifacio، نويسنده , , Ezio and Scholz، نويسنده , , Marlon and Powell، نويسنده , , Michael and Furmaniak، نويسنده , , Jadwiga and Rees Smith، نويسنده , , Bernard and Ziegler، نويسنده , , Anette-G. and Achenbach، نويسنده , , Peter، نويسنده ,
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 107 to 1011 L/mol and was high (> 1.0 × 109 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.
Keywords :
epitopes , IA-2 autoantibodies , Type 1 diabetes , Diabetes risk , Affinity