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Diabetes ; 63(2): 446-55, 2014 Feb.
Article in English | MEDLINE | ID: mdl-23974921

ABSTRACT

The rapidly increasing incidence of type 1 diabetes implies that environmental factors are involved in the pathogenesis. Enteroviruses are among the suspected environmental triggers of the disease, and the interest in exploring the possibilities to develop vaccines against these viruses has increased. Our objective was to identify enterovirus serotypes that could be involved in the initiation of the disease process by screening neutralizing antibodies against 41 different enterovirus types in a unique longitudinal sample series from a large prospective birth-cohort study. The study participants comprised 183 case children testing persistently positive for at least two diabetes-predictive autoantibodies and 366 autoantibody-negative matched control children. Coxsackievirus B1 was associated with an increased risk of ß-cell autoimmunity. This risk was strongest when infection occurred a few months before autoantibodies appeared and was attenuated by the presence of maternal antibodies against the virus. Two other coxsackieviruses, B3 and B6, were associated with a reduced risk, with an interaction pattern, suggesting immunological cross-protection against coxsackievirus B1. These results support previous observations suggesting that the group B coxsackieviruses are associated with the risk of type 1 diabetes. The clustering of the risk and protective viruses to this narrow phylogenetic lineage supports the biological plausibility of this phenomenon.


Subject(s)
Diabetes Mellitus, Type 1/etiology , Diabetes Mellitus, Type 1/immunology , Enterovirus B, Human/immunology , Enterovirus Infections/immunology , Enterovirus Infections/virology , Insulin-Secreting Cells/immunology , Animals , Autoantibodies/blood , Autoimmunity , Case-Control Studies , Cell Line , Child , Child, Preschool , Diabetes Mellitus, Type 1/virology , Enterovirus B, Human/genetics , Enterovirus Infections/complications , Gene Expression Regulation/physiology , Genotype , HLA-DQ beta-Chains/genetics , HLA-DQ beta-Chains/metabolism , Humans , Phylogeny , Risk Factors
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