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Detection of enterovirus RNA in peripheral blood mononuclear cells correlates with the presence of the predisposing allele of the type 1 diabetes risk gene IFIH1 and with disease stage

Locke Jonathan M.; Eichmann Martin; Lempainen Johanna; Nurminen Noora; Peakman Mark; Morgan Noel G.; Sioofy-Khojine Amir-Babak; Knip Mikael; Oikarinen Sami; Laine Antti-Pekka; Ilonen Jorma; Hyöty Heikki; Downes Kate; Veijola Riitta; Richardson Sarah J.; Todd John A.

Detection of enterovirus RNA in peripheral blood mononuclear cells correlates with the presence of the predisposing allele of the type 1 diabetes risk gene IFIH1 and with disease stage

Locke Jonathan M.
Eichmann Martin
Lempainen Johanna
Nurminen Noora
Peakman Mark
Morgan Noel G.
Sioofy-Khojine Amir-Babak
Knip Mikael
Oikarinen Sami
Laine Antti-Pekka
Ilonen Jorma
Hyöty Heikki
Downes Kate
Veijola Riitta
Richardson Sarah J.
Todd John A.
Katso/Avaa
s00125-022-05753-y.pdf (739.7Kb)
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SPRINGER
doi:10.1007/s00125-022-05753-y
URI
https://doi.org/10.1007/s00125-022-05753-y
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2022091258756
Tiivistelmä

Aims/hypothesis Enteroviral infection has been implicated consistently as a key environmental factor correlating with the appearance of autoimmunity and/or the presence of overt type 1 diabetes, in which pancreatic insulin-producing beta cells are destroyed by an autoimmune response. Genetic predisposition through variation in the type 1 diabetes risk gene IFIH1 (interferon induced with helicase C domain 1), which encodes the viral pattern-recognition receptor melanoma differentiation-associated protein 5 (MDA5), supports a potential link between enterovirus infection and type 1 diabetes.

Methods We used molecular techniques to detect enterovirus RNA in peripheral blood samples (in separated cellular compartments or plasma) from two cohorts comprising 79 children or 72 adults that include individuals with and without type 1 diabetes who had multiple autoantibodies. We also used immunohistochemistry to detect the enteroviral protein VP1 in the pancreatic islets of post-mortem donors (n=43) with type 1 diabetes.

Results We observed enhanced detection sensitivity when sampling the cellular compartment compared with the non-cellular compartment of peripheral blood (OR 21.69; 95% CI 3.64, 229.20; p<0.0001). In addition, we show that children with autoimmunity are more likely to test positive for enterovirus RNA than those without autoimmunity (OR 11.60; 95% CI 1.89, 126.90; p=0.0065). Furthermore, we found that individuals carrying the predisposing allele (946(Thr)) of the common variant in IFIH1 (rs1990760, Thr946Ala) are more likely to test positive for enterovirus in peripheral blood (OR 3.07; 95% CI 1.02, 8.58; p=0.045). In contrast, using immunohistochemistry, there was no correlation between the common variant in IFIH1 and detection of enteroviral VP1 protein in the pancreatic islets of donors with type 1 diabetes.Conclusions/interpretation Our data indicate that, in peripheral blood, antigen-presenting cells are the predominant source of enterovirus infection, and that infection is correlated with disease stage and genetic predisposition, thereby supporting a role for enterovirus infection prior to disease onset.

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