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dc.contributor.authorSioofy-Khojine, A-B
dc.contributor.authorRichardson, SJ
dc.contributor.authorLocke, JM
dc.contributor.authorOikarinen, S
dc.contributor.authorNurminen, N
dc.contributor.authorLaine, A-P
dc.contributor.authorDownes, K
dc.contributor.authorLempainen, J
dc.contributor.authorTodd, JA
dc.contributor.authorVeijola, R
dc.contributor.authorIlonen, J
dc.contributor.authorKnip, M
dc.contributor.authorMorgan, NG
dc.contributor.authorHyöty, H
dc.contributor.authorPeakman, M
dc.contributor.authorEichmann, M
dc.date.accessioned2022-07-28T12:18:59Z
dc.date.issued2022-07-22
dc.date.updated2022-07-28T11:44:28Z
dc.description.abstractAIMS/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 (946Thr) 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.en_GB
dc.description.sponsorshipJDRFen_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.description.sponsorshipWellcome Trusten_GB
dc.description.sponsorshipEuropean Union FP7en_GB
dc.format.extent1-9
dc.identifier.citationPublished online 22 July 2022en_GB
dc.identifier.doihttps://doi.org/10.1007/s00125-022-05753-y
dc.identifier.grantnumber1-2007-1803en_GB
dc.identifier.grantnumber5-CDA-2014-221-A-Nen_GB
dc.identifier.grantnumberJDRF 25-2012-516en_GB
dc.identifier.grantnumber4-SRA-2017-473-A-Nen_GB
dc.identifier.grantnumberMR/P010695/1en_GB
dc.identifier.grantnumber07212/A/15/Zen_GB
dc.identifier.grantnumber261441en_GB
dc.identifier.urihttp://hdl.handle.net/10871/130435
dc.identifierORCID: 0000-0002-1160-6062 (Richardson, Sarah J)
dc.identifierScopusID: 24601185100 (Richardson, Sarah J)
dc.identifierORCID: 0000-0001-9516-5251 (Locke, Jonathan M)
dc.identifierORCID: 0000-0003-1537-8113 (Morgan, Noel G)
dc.identifierORCID: 0000-0002-8675-2822 (Eichmann, Martin)
dc.language.isoenen_GB
dc.publisherSpringeren_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/35867130en_GB
dc.rights© The Author(s) 2022. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.en_GB
dc.subjectAutoimmunityen_GB
dc.subjectEnterovirusen_GB
dc.subjectGenetic risken_GB
dc.subjectIFIH-1en_GB
dc.subjectInterferon induced with helicase C domain 1en_GB
dc.subjectMDA5en_GB
dc.subjectMelanoma differentiation-associated protein 5en_GB
dc.subjectPancreatic isletsen_GB
dc.subjectType 1 diabetesen_GB
dc.subjectrs1990760en_GB
dc.titleDetection 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 stageen_GB
dc.typeArticleen_GB
dc.date.available2022-07-28T12:18:59Z
dc.identifier.issn0012-186X
exeter.place-of-publicationGermany
dc.descriptionThis is the final version. Available on open access from Springer via the DOI in this recorden_GB
dc.descriptionData availability: The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.en_GB
dc.identifier.eissn1432-0428
dc.identifier.journalDiabetologiaen_GB
dc.relation.ispartofDiabetologia
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2022-05-16
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2022-07-22
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-07-28T12:14:37Z
refterms.versionFCDVoR
refterms.dateFOA2022-07-28T12:19:00Z
refterms.panelAen_GB
refterms.dateFirstOnline2022-07-22


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© The Author(s) 2022. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Except where otherwise noted, this item's licence is described as © The Author(s) 2022. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.