An IFIH1 gene polymorphism associated with risk for autoimmunity regulates canonical antiviral defence pathways in Coxsackievirus infected human pancreatic islets

dc.contributor.authorErna Domsgen
dc.contributor.authorKatharina Lind
dc.contributor.authorLingjia Kong
dc.contributor.authorMichael H. Hühn
dc.contributor.authorOmid Rasool
dc.contributor.authorFrank van Kuppeveld
dc.contributor.authorOlle Korsgren
dc.contributor.authorRiitta Lahesmaa
dc.contributor.authorMalin Flodström-Tullberg
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organization-code2609200
dc.converis.publication-id18615123
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/18615123
dc.date.accessioned2022-10-27T11:56:35Z
dc.date.available2022-10-27T11:56:35Z
dc.description.abstract<p>The IFIH1 gene encodes the pattern recognition receptor MDA5. A common polymorphism in IFIH1 (rs1990760, A946T) confers increased risk for autoimmune disease, including type 1-diabetes (T1D). Coxsackievirus infections are linked to T1D and cause beta-cell damage in vitro. Here we demonstrate that the rs1990760 polymorphism regulates the interferon (IFN) signature expressed by human pancreatic islets following Coxsackievirus infection. A strong IFN signature was associated with high expression of IFNλ1 and IFNλ2, linking rs1990760 to the expression of type III IFNs. In the high-responding genotype, IRF-1 expression correlated with that of type III IFN, suggesting a positive-feedback on type III IFN transcription. In summary, our study uncovers an influence of rs1990760 on the canonical effector function of MDA5 in response to an acute infection of primary human parenchymal cells with a clinically relevant virus linked to human T1D. It also highlights a previously unrecognized connection between the rs1990760 polymorphism and the expression level of type III IFNs.</p>
dc.identifier.olddbid172975
dc.identifier.oldhandle10024/156069
dc.identifier.urihttps://www.utupub.fi/handle/11111/30769
dc.identifier.urnURN:NBN:fi-fe2021042716451
dc.language.isoen
dc.okm.affiliatedauthorKong, Lingjia
dc.okm.affiliatedauthorRasool, Omid
dc.okm.affiliatedauthorLahesmaa, Riitta
dc.okm.discipline1184 Genetics, developmental biology, physiologyen_GB
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumber39378
dc.relation.doi10.1038/srep39378
dc.relation.ispartofjournalScientific Reports
dc.relation.volume6
dc.source.identifierhttps://www.utupub.fi/handle/10024/156069
dc.titleAn IFIH1 gene polymorphism associated with risk for autoimmunity regulates canonical antiviral defence pathways in Coxsackievirus infected human pancreatic islets
dc.year.issued2016

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