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dc.contributor.authorRichardson, SJ
dc.contributor.authorPugliese, A
dc.date.accessioned2022-01-26T15:23:29Z
dc.date.issued2021-12-09
dc.date.updated2022-01-26T14:22:18Z
dc.description.abstractWe review the current knowledge of pancreas pathology in type 1 diabetes. During the last two decades, dedicated efforts toward the recovery of pancreas from deceased patients with type 1 diabetes have promoted significant advances in the characterization of the pathological changes associated with this condition. The implementation of autoantibody screening among organ donors has also allowed examining pancreas pathology in the absence of clinical disease, but in the presence of serological markers of autoimmunity. The assessment of key features of pancreas pathology across various disease stages allows driving parallels with clinical disease stages. The main pathological abnormalities observed in the pancreas with type 1 diabetes are beta-cell loss and insulitis; more recently, hyperexpression of HLA class I and class II molecules have been reproduced and validated. Additionally, there are changes affecting extracellular matrix components, evidence of viral infections, inflammation, and ER stress, which could contribute to beta-cell dysfunction and the stimulation of apoptosis and autoimmunity. The increasing appreciation that beta-cell loss can be less severe at diagnosis than previously estimated, the coexistence of beta-cell dysfunction, and the persistence of key features of pancreas pathology for years after diagnosis impact the perception of the dynamics of this chronic process. The emerging information is helping the identification of novel therapeutic targets and has implications for the design of clinical trials.en_GB
dc.description.sponsorshipEuropean Union FP7en_GB
dc.description.sponsorshipDiabetes Research Wellness Foundationen_GB
dc.description.sponsorshipJDRFen_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.format.extentR41-R57
dc.format.mediumElectronic
dc.identifier.citationVol. 252 (2), pp. R41-R57en_GB
dc.identifier.doihttps://doi.org/10.1530/JOE-21-0358
dc.identifier.grantnumber261441en_GB
dc.identifier.grantnumber5-CDA-2014-221-A-Nen_GB
dc.identifier.grantnumber25-2012-516en_GB
dc.identifier.grantnumberMR/P010695/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/128583
dc.identifierORCID: 0000-0002-1160-6062 (Richardson, Sarah J)
dc.identifierScopusID: 24601185100 (Richardson, Sarah J)
dc.language.isoenen_GB
dc.publisherBioscientifica / Society for Endocrinology / European Society of Endocrinologyen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/34755679en_GB
dc.rights© Society for Endocrinology 2021en_GB
dc.subjectbeta cellen_GB
dc.subjectinsulitisen_GB
dc.subjectislet autoimmunityen_GB
dc.subjectpancreasen_GB
dc.subjecttype 1 diabetesen_GB
dc.subjectAutoimmunityen_GB
dc.subjectAutopsyen_GB
dc.subjectDiabetes Mellitus, Type 1en_GB
dc.subjectDisease Progressionen_GB
dc.subjectEndocrinologyen_GB
dc.subjectHistory, 20th Centuryen_GB
dc.subjectHistory, 21st Centuryen_GB
dc.subjectHumansen_GB
dc.subjectPancreasen_GB
dc.title100 years of insulin: Pancreas pathology in type 1 diabetes: an evolving storyen_GB
dc.typeArticleen_GB
dc.date.available2022-01-26T15:23:29Z
dc.identifier.issn0022-0795
exeter.place-of-publicationEngland
dc.descriptionThis is the author accepted manuscript. The final version is available from Bioscientifica via the DOI in this recorden_GB
dc.identifier.eissn1479-6805
dc.identifier.journalJournal of Endocrinologyen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2021-11-09
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2021-12-09
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-01-26T15:20:13Z
refterms.versionFCDAM
refterms.dateFOA2022-01-26T15:23:40Z
refterms.panelAen_GB


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