Genetic risk for autoimmunity is associated with distinct changes in the human gut microbiome

dc.contributor.authorRussell JT
dc.contributor.authorRoesch LFW
dc.contributor.authorOrdberg M
dc.contributor.authorIlonen J
dc.contributor.authorAtkinson MA
dc.contributor.authorSchatz DA
dc.contributor.authorTriplett EW
dc.contributor.authorLudvigsson J
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id42011802
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/42011802
dc.date.accessioned2025-08-27T21:25:39Z
dc.date.available2025-08-27T21:25:39Z
dc.description.abstractSusceptibility to many human autoimmune diseases is under strong genetic control by class II human leukocyte antigen (HLA) allele combinations. These genes remain by far the greatest risk factors in the development of type 1 diabetes and celiac disease. Despite this, little is known about HLA influences on the composition of the human gut microbiome, a potential source of environmental influence on disease. Here, using a general population cohort from the All Babies in Southeast Sweden study, we report that genetic risk for developing type 1 diabetes autoimmunity is associated with distinct changes in the gut microbiome. Both the core microbiome and beta diversity differ with HLA risk group and genotype. In addition, protective HLA haplotypes are associated with bacterial genera Intestinibacter and Romboutsia. Thus, general population cohorts are valuable in identifying potential environmental triggers or protective factors for autoimmune diseases that may otherwise be masked by strong genetic control.
dc.identifier.eissn2041-1723
dc.identifier.jour-issn2041-1723
dc.identifier.olddbid200349
dc.identifier.oldhandle10024/183376
dc.identifier.urihttps://www.utupub.fi/handle/11111/46449
dc.identifier.urlhttps://www.nature.com/articles/s41467-019-11460-x
dc.identifier.urnURN:NBN:fi-fe2021042822188
dc.language.isoen
dc.okm.affiliatedauthorIlonen, Jorma
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherNATURE PUBLISHING GROUP
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumber3621
dc.relation.doi10.1038/s41467-019-11460-x
dc.relation.ispartofjournalNature Communications
dc.relation.volume10
dc.source.identifierhttps://www.utupub.fi/handle/10024/183376
dc.titleGenetic risk for autoimmunity is associated with distinct changes in the human gut microbiome
dc.year.issued2019

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