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Distinct transcriptomic profiles in children prior to the appearance of type 1 diabetes-linked islet autoantibodies and following enterovirus infection

Lin, Jake (author)
University of Tampere
Moradi, Elaheh (author)
University of Tampere
Salenius, Karoliina (author)
University of Tampere
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Lehtipuro, Suvi (author)
University of Tampere
Häkkinen, Tomi (author)
University of Tampere
Laiho, Jutta E (author)
University of Tampere
Oikarinen, Sami (author)
University of Tampere
Randelin, Sofia (author)
University of Tampere
Parikh, Hemang M (author)
University of South Florida
Krischer, Jeffrey P (author)
University of South Florida
Toppari, Jorma (author)
University of Turku
Lernmark, Åke (author)
Lund University,Lunds universitet,Celiaki och diabetes,Forskargrupper vid Lunds universitet,Celiac Disease and Diabetes Unit,Lund University Research Groups,Skåne University Hospital
Petrosino, Joseph F (author)
Baylor College of Medicine
Ajami, Nadim J (author)
Baylor College of Medicine
She, Jin-Xiong (author)
Jinfiniti Precision Medicine
Hagopian, William A (author)
Pacific Northwest Research Institute
Rewers, Marian J (author)
Lloyd, Richard E (author)
Rautajoki, Kirsi J (author)
Hyöty, Heikki (author)
Nykter, Matti (author)
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 (creator_code:org_t)
 
2023
2023
English.
In: Nature Communications. - 2041-1723. ; 14, s. 1-13
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Although the genetic basis and pathogenesis of type 1 diabetes have been studied extensively, how host responses to environmental factors might contribute to autoantibody development remains largely unknown. Here, we use longitudinal blood transcriptome sequencing data to characterize host responses in children within 12 months prior to the appearance of type 1 diabetes-linked islet autoantibodies, as well as matched control children. We report that children who present with insulin-specific autoantibodies first have distinct transcriptional profiles from those who develop GADA autoantibodies first. In particular, gene dosage-driven expression of GSTM1 is associated with GADA autoantibody positivity. Moreover, compared with controls, we observe increased monocyte and decreased B cell proportions 9-12 months prior to autoantibody positivity, especially in children who developed antibodies against insulin first. Lastly, we show that control children present transcriptional signatures consistent with robust immune responses to enterovirus infection, whereas children who later developed islet autoimmunity do not. These findings highlight distinct immune-related transcriptomic differences between case and control children prior to case progression to islet autoimmunity and uncover deficient antiviral response in children who later develop islet autoimmunity.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Keyword

Humans
Child
Autoantibodies
Diabetes Mellitus, Type 1
Transcriptome
Autoimmunity/genetics
Insulin/metabolism
Enterovirus Infections/genetics
Islets of Langerhans/metabolism

Publication and Content Type

art (subject category)
ref (subject category)

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