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Enteral virus infections in early childhood and an enhanced type 1 diabetes-associated antibody response to dietary insulin

Mäkelä, Miia (författare)
Immunogenetics Lab, University of Turku, Finland
Vaarala, Outi, 1962- (författare)
Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Pediatrik,Barn- och ungdomskliniken i Linköping
Hermann, Robert (författare)
Immunogenomics Lab, Cell Screen Applied Biomedi cal Res Center, Budapest. Hungary
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Salminen, Kimmo (författare)
Dept of Virology, Turku, Finland
Vahlberg, Tero (författare)
Dept of Biostatistics University of Turku, Finland
Veijola, Riita (författare)
Dept of Pediatrics, University of Oulu, Finland
Hyöty, Heikki (författare)
Dept of Virology, University of Tampere, Finland
Knip, Mikael (författare)
Hospital for Children and Adolescents, University of Helsinki, Finland
Simell, Olli (författare)
Immunogenetics Lab, University of Turku, Finland
Ilonen, Jorma (författare)
Dept of Clin Microbiology, University of Kuopio, Finland
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 (creator_code:org_t)
Elsevier BV, 2006
2006
Engelska.
Ingår i: Journal of Autoimmunity. - : Elsevier BV. - 0896-8411 .- 1095-9157. ; 27:1, s. 54-61
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Enteral virus infections may trigger the development of β-cell-specific autoimmunity by interacting with the gut-associated lymphoid system. We analyzed the effect of three different virus infections on immunization to dietary insulin in children carrying increased genetic risk for type 1 diabetes. Forty-six of 238 children developed multiple diabetes-associated autoantibodies and 31 clinical diabetes (median follow-up time 75 months). Insulin-binding antibodies were measured with EIA method (median follow-up time 24 months). Antibodies to enteroviruses, rotavirus and adenovirus were measured with EIA in samples drawn at birth and the ages of 3 and 6 months. Nineteen enterovirus, 14 rotavirus and 8 adenovirus infections were diagnosed. At the ages of 6, 12, and 18 months, the concentrations of insulin-binding antibodies were higher in children with postnatal entero-, rota- and/or adenovirus infections than in children without these infections. Children who subsequently developed ICA or IA-2 antibodies or clinical type 1 diabetes had higher concentrations of insulin-binding antibodies than children who remained autoantibody negative. Our data suggest that enteral virus infections can enhance immune response to insulin, induced primarily by bovine insulin in cow's milk. An enhanced antibody response to dietary insulin preceded the development of β-cell specific autoimmunity and type 1 diabetes. © 2006 Elsevier Ltd. All rights reserved.

Nyckelord

Immunization
insulin
type 1 diabetes
virus infection
MEDICINE
MEDICIN

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