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dc.contributor.authorBoldison, J
dc.contributor.authorWong, FS
dc.date.accessioned2021-10-18T12:53:29Z
dc.date.issued2021-09-20
dc.description.abstractRegulatory B cells (Bregs) have an anti-inflammatory role and can suppress autoimmunity, by employing both cytokine secretion and cell-contact mediated mechanisms. Numerous Breg subsets have been described and have overlapping phenotypes in terms of their immune expression markers or cytokine production. A hallmark feature of Bregs is the secretion of IL-10, although IL-35 and TGFβ−producing B cells have also been identified. To date, few reports have identified an impaired frequency or function of Bregs in individuals with type 1 diabetes; thus our understanding of the role played by these Breg subsets in the pathogenesis of this condition is limited. In this review we will focus on how regulatory B cells are altered in the development of type 1 diabetes, highlighting both frequency and function and discuss both human and animal studies.en_GB
dc.description.sponsorshipResearch Englanden_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.identifier.citationVol. 12, article 746187en_GB
dc.identifier.doi10.3389/fimmu.2021.746187
dc.identifier.grantnumberMR/K021141/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/127497
dc.language.isoenen_GB
dc.publisherFrontiers Mediaen_GB
dc.rights© 2021 Boldison and Wong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en_GB
dc.subjectIL-10en_GB
dc.subjectB cellen_GB
dc.subjecttype 1 diabetesen_GB
dc.subjectfrequencyen_GB
dc.subjectfunctionen_GB
dc.titleRegulatory B Cells: Role in Type 1 Diabetesen_GB
dc.typeArticleen_GB
dc.date.available2021-10-18T12:53:29Z
dc.identifier.issn1664-3224
exeter.article-numberARTN 746187en_GB
dc.descriptionThis is the final version. Available on open access from Frontiers Media via the DOI in this recorden_GB
dc.identifier.journalFrontiers in Immunologyen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2021-09-02
exeter.funder::Research Englanden_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2021-09-20
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2021-10-18T12:52:26Z
refterms.versionFCDVoR
refterms.dateFOA2021-10-18T12:53:38Z
refterms.panelAen_GB


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© 2021 Boldison and Wong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Except where otherwise noted, this item's licence is described as © 2021 Boldison and Wong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.