T-cell responses to enterovirus antigens in children with type 1 diabetes

Citation
S. Juhela et al., T-cell responses to enterovirus antigens in children with type 1 diabetes, DIABETES, 49(8), 2000, pp. 1308-1313
Citations number
35
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
DIABETES
ISSN journal
00121797 → ACNP
Volume
49
Issue
8
Year of publication
2000
Pages
1308 - 1313
Database
ISI
SICI code
0012-1797(200008)49:8<1308:TRTEAI>2.0.ZU;2-B
Abstract
Enterovirus infections, implicated in the pathogenesis of type 1 diabetes i n a number of studies, may precipitate the symptoms of clinical diabetes an d play a role in the initiation of the beta-cell damaging process. The aim of this study was to evaluate whether cellular immune responses to enterovi rus antigens are abnormal in children with type 1 diabetes. Lymphocyte prol iferation responses to enterovirus antigens were analyzed in 41 children wi th new-onset type 1 diabetes, 23 children with type I diabetes for 4-72 mon ths, and healthy control children in subgroups matched for HLA-DQB1 risk al leles, sex, and age. Children with diabetes for 4-72 months more often had T-cell responses to the Coxsackievirus B4-infected cell lysate antigen than children with new-onset diabetes (P < 0.01) or control children (P < 0.01) , Responses to recombinant nonstructural protein 2C of Coxsackievirus B4 we re also more frequent in children with type 1 diabetes for 4-72 months when compared with control subjects (P = 0.03), whereas the responses to purifi ed Coxsackieviras B4 and recombinant VP0 protein, which did not contain non structural proteins, did not differ. These data suggest that T-cell respons es to Coxsackievirus B4 proteins and particularly to the antigens containin g the nonstructural proteins of the virus are increased in children with ty pe 1 diabetes after the onset of the disease. However, in children with new -onset diabetes, responses were normal or even decreased. This phenomenon w as specific for enteroviruses and could be caused by trapping of enteroviru s-specific T-cells in the pancreas.