IgA-Type Enterovirus Antibodies Are Increased among Adults and Children with Recently Diagnosed Type 1 Diabetes

Author:

Alnek Kristi1ORCID,Talja Ija1,Laht Brita1,Metsküla Kaja1,Mandel Maire1,Reppo Ingrid23,Lubi Maire23,Uibo Raivo1ORCID

Affiliation:

1. Department of Immunology, Institute of Bio- and Translational Medicine, University of Tartu, 19 Ravila, Tartu 50411, Estonia

2. Department of Internal Medicine, Institute of Clinical Medicine, University of Tartu, 8 L. Puusepa, Tartu 50406, Estonia

3. Internal Medicine Clinic of Tartu University Hospital, 8 L. Puusepa, Tartu 50406, Estonia

Abstract

Enteroviruses (EV) are among the leading environmental triggers of childhood-onset type 1 diabetes (T1D). Our aim was to determine the prevalence of antibodies against EV and their association with T1D in different age groups ( n = 62 ), including young adults, and to compare these data with results from HLA-matched control participants ( n = 62 ). IgA, IgG, and IgM antibodies against EV were detected. IgA EV antibodies were present in 46.8% of participants with T1D (median level 10.9 EIU) and in 11.3% of controls (median level 3.4 EIU). IgA EV positivity and higher level of IgA EV antibodies were both significant risk factors for T1D (odds ratio (OR) 8.33; 95% confidence interval (CI) 2.52–27.6; p = 0.0005 and OR 1.04; 95% CI 1.01–1.06; p = 0.0105 , respectively). Importantly, the prevalence of IgA EV antibodies in the subgroups of both children and young adults was also significantly different between participants with T1D and their matched controls ( p = 0.0089 and p = 0.0055 , respectively). Such differences were not seen for IgG and IgM EV antibodies. However, IgG EV antibodies were associated with 65 kDa glutamic acid decarboxylase antibodies, but not with zinc transporter 8 and protein tyrosine phosphatase IA2 antibodies. The genotype frequency of PTPN22 (rs2476601) and IFIH1 (rs1990760) was not associated with EV positivity. This study showed that EV infections may be an important disease-promoting factor of T1D not only in childhood-onset but also in adult-onset T1D. However, to further confirm this association, direct virological studies are needed in the latter T1D group.

Funder

Eesti Teadusagentuur

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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