Islet autoimmunity in human type 1 diabetes: initiation and progression from the perspective of the beta cell

Type 1 diabetes results from the poorly understood process of islet autoimmunity, which ultimately leads to the loss of functional pancreatic beta cells. Mounting evidence supports the notion that the activation and evolution of islet autoimmunity in genetically susceptible people is contingent upon...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Diabetologia 2023-11, Vol.66 (11), p.1971-1982
Hauptverfasser: Thompson, Peter J., Pipella, Jasmine, Rutter, Guy A., Gaisano, Herbert Y., Santamaria, Pere
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1982
container_issue 11
container_start_page 1971
container_title Diabetologia
container_volume 66
creator Thompson, Peter J.
Pipella, Jasmine
Rutter, Guy A.
Gaisano, Herbert Y.
Santamaria, Pere
description Type 1 diabetes results from the poorly understood process of islet autoimmunity, which ultimately leads to the loss of functional pancreatic beta cells. Mounting evidence supports the notion that the activation and evolution of islet autoimmunity in genetically susceptible people is contingent upon early life exposures affecting the islets, especially beta cells. Here, we review some of the recent advances and studies that highlight the roles of these changes as well as antigen presentation and stress response pathways in beta cells in the onset and propagation of the autoimmune process in type 1 diabetes. Future progress in this area holds promise for advancing islet- and beta cell-directed therapies that could be implemented in the early stages of the disease and could be combined with immunotherapies. Graphical Abstract
doi_str_mv 10.1007/s00125-023-05970-z
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10542715</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2841881877</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-9e3e09732123ae4f47e0351ab85f12ec7644c989aa519aaf73ee1e7bff6e667a3</originalsourceid><addsrcrecordid>eNp9kU9v1DAQxS0EotvCF-CALHHhEvDYTuxwQaiiUKkSF5C4Wd7seNdVYgfbqbT99Hi7pfw5cLFlv9-8mdEj5AWwN8CYepsZA942jIuGtb1ize0jsgIpeMMk14_J6qA3oLvvJ-Q052vGmGhl95ScCCW1FpyvyHSZRyzULiX6aVqCL3vqA90tkw207GekQDferrFgflcVX7wtPgZqw4bOKW4T5nx4uxQnWnZIZ0x5xqH4G6TR3X3VaksHHMdn5ImzY8bn9_cZ-Xbx8ev55-bqy6fL8w9XzSBVW5oeBbJeCQ5cWJROKqyTg13r1gHHQXVSDr3urW2hHk4JREC1dq7DrlNWnJH3R995WU-4GTCUZEczJz_ZtDfRevO3EvzObOONAdZKrqCtDq_vHVL8sWAuZvL5sIINGJdsuJagNWilKvrqH_Q6LinU_SqlGKgeWF8pfqSGFHNO6B6mAWYOcZpjnKbGae7iNLe16OWfezyU_MqvAuII5CqFLabfvf9j-xMPZq2Y</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2870179109</pqid></control><display><type>article</type><title>Islet autoimmunity in human type 1 diabetes: initiation and progression from the perspective of the beta cell</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Thompson, Peter J. ; Pipella, Jasmine ; Rutter, Guy A. ; Gaisano, Herbert Y. ; Santamaria, Pere</creator><creatorcontrib>Thompson, Peter J. ; Pipella, Jasmine ; Rutter, Guy A. ; Gaisano, Herbert Y. ; Santamaria, Pere</creatorcontrib><description>Type 1 diabetes results from the poorly understood process of islet autoimmunity, which ultimately leads to the loss of functional pancreatic beta cells. Mounting evidence supports the notion that the activation and evolution of islet autoimmunity in genetically susceptible people is contingent upon early life exposures affecting the islets, especially beta cells. Here, we review some of the recent advances and studies that highlight the roles of these changes as well as antigen presentation and stress response pathways in beta cells in the onset and propagation of the autoimmune process in type 1 diabetes. Future progress in this area holds promise for advancing islet- and beta cell-directed therapies that could be implemented in the early stages of the disease and could be combined with immunotherapies. Graphical Abstract</description><identifier>ISSN: 0012-186X</identifier><identifier>EISSN: 1432-0428</identifier><identifier>DOI: 10.1007/s00125-023-05970-z</identifier><identifier>PMID: 37488322</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Antigen presentation ; Autoimmunity ; Autoimmunity - physiology ; Beta cells ; Cellular stress response ; Diabetes ; Diabetes mellitus (insulin dependent) ; Diabetes Mellitus, Type 1 - metabolism ; Genetic Predisposition to Disease ; Human Physiology ; Humans ; Immunotherapy ; Insulin-Secreting Cells - metabolism ; Internal Medicine ; Invited Review ; Islets of Langerhans - metabolism ; Medicine ; Medicine &amp; Public Health ; Metabolic Diseases</subject><ispartof>Diabetologia, 2023-11, Vol.66 (11), p.1971-1982</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-9e3e09732123ae4f47e0351ab85f12ec7644c989aa519aaf73ee1e7bff6e667a3</citedby><cites>FETCH-LOGICAL-c475t-9e3e09732123ae4f47e0351ab85f12ec7644c989aa519aaf73ee1e7bff6e667a3</cites><orcidid>0000-0001-5213-9168 ; 0000-0002-6851-8899 ; 0009-0005-9936-8386 ; 0000-0001-6360-0343 ; 0000-0003-3469-1586</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00125-023-05970-z$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00125-023-05970-z$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27903,27904,41467,42536,51298</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37488322$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thompson, Peter J.</creatorcontrib><creatorcontrib>Pipella, Jasmine</creatorcontrib><creatorcontrib>Rutter, Guy A.</creatorcontrib><creatorcontrib>Gaisano, Herbert Y.</creatorcontrib><creatorcontrib>Santamaria, Pere</creatorcontrib><title>Islet autoimmunity in human type 1 diabetes: initiation and progression from the perspective of the beta cell</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><addtitle>Diabetologia</addtitle><description>Type 1 diabetes results from the poorly understood process of islet autoimmunity, which ultimately leads to the loss of functional pancreatic beta cells. Mounting evidence supports the notion that the activation and evolution of islet autoimmunity in genetically susceptible people is contingent upon early life exposures affecting the islets, especially beta cells. Here, we review some of the recent advances and studies that highlight the roles of these changes as well as antigen presentation and stress response pathways in beta cells in the onset and propagation of the autoimmune process in type 1 diabetes. Future progress in this area holds promise for advancing islet- and beta cell-directed therapies that could be implemented in the early stages of the disease and could be combined with immunotherapies. Graphical Abstract</description><subject>Antigen presentation</subject><subject>Autoimmunity</subject><subject>Autoimmunity - physiology</subject><subject>Beta cells</subject><subject>Cellular stress response</subject><subject>Diabetes</subject><subject>Diabetes mellitus (insulin dependent)</subject><subject>Diabetes Mellitus, Type 1 - metabolism</subject><subject>Genetic Predisposition to Disease</subject><subject>Human Physiology</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Insulin-Secreting Cells - metabolism</subject><subject>Internal Medicine</subject><subject>Invited Review</subject><subject>Islets of Langerhans - metabolism</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Metabolic Diseases</subject><issn>0012-186X</issn><issn>1432-0428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kU9v1DAQxS0EotvCF-CALHHhEvDYTuxwQaiiUKkSF5C4Wd7seNdVYgfbqbT99Hi7pfw5cLFlv9-8mdEj5AWwN8CYepsZA942jIuGtb1ize0jsgIpeMMk14_J6qA3oLvvJ-Q052vGmGhl95ScCCW1FpyvyHSZRyzULiX6aVqCL3vqA90tkw207GekQDferrFgflcVX7wtPgZqw4bOKW4T5nx4uxQnWnZIZ0x5xqH4G6TR3X3VaksHHMdn5ImzY8bn9_cZ-Xbx8ev55-bqy6fL8w9XzSBVW5oeBbJeCQ5cWJROKqyTg13r1gHHQXVSDr3urW2hHk4JREC1dq7DrlNWnJH3R995WU-4GTCUZEczJz_ZtDfRevO3EvzObOONAdZKrqCtDq_vHVL8sWAuZvL5sIINGJdsuJagNWilKvrqH_Q6LinU_SqlGKgeWF8pfqSGFHNO6B6mAWYOcZpjnKbGae7iNLe16OWfezyU_MqvAuII5CqFLabfvf9j-xMPZq2Y</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Thompson, Peter J.</creator><creator>Pipella, Jasmine</creator><creator>Rutter, Guy A.</creator><creator>Gaisano, Herbert Y.</creator><creator>Santamaria, Pere</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5213-9168</orcidid><orcidid>https://orcid.org/0000-0002-6851-8899</orcidid><orcidid>https://orcid.org/0009-0005-9936-8386</orcidid><orcidid>https://orcid.org/0000-0001-6360-0343</orcidid><orcidid>https://orcid.org/0000-0003-3469-1586</orcidid></search><sort><creationdate>20231101</creationdate><title>Islet autoimmunity in human type 1 diabetes: initiation and progression from the perspective of the beta cell</title><author>Thompson, Peter J. ; Pipella, Jasmine ; Rutter, Guy A. ; Gaisano, Herbert Y. ; Santamaria, Pere</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-9e3e09732123ae4f47e0351ab85f12ec7644c989aa519aaf73ee1e7bff6e667a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antigen presentation</topic><topic>Autoimmunity</topic><topic>Autoimmunity - physiology</topic><topic>Beta cells</topic><topic>Cellular stress response</topic><topic>Diabetes</topic><topic>Diabetes mellitus (insulin dependent)</topic><topic>Diabetes Mellitus, Type 1 - metabolism</topic><topic>Genetic Predisposition to Disease</topic><topic>Human Physiology</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Insulin-Secreting Cells - metabolism</topic><topic>Internal Medicine</topic><topic>Invited Review</topic><topic>Islets of Langerhans - metabolism</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Metabolic Diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thompson, Peter J.</creatorcontrib><creatorcontrib>Pipella, Jasmine</creatorcontrib><creatorcontrib>Rutter, Guy A.</creatorcontrib><creatorcontrib>Gaisano, Herbert Y.</creatorcontrib><creatorcontrib>Santamaria, Pere</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thompson, Peter J.</au><au>Pipella, Jasmine</au><au>Rutter, Guy A.</au><au>Gaisano, Herbert Y.</au><au>Santamaria, Pere</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Islet autoimmunity in human type 1 diabetes: initiation and progression from the perspective of the beta cell</atitle><jtitle>Diabetologia</jtitle><stitle>Diabetologia</stitle><addtitle>Diabetologia</addtitle><date>2023-11-01</date><risdate>2023</risdate><volume>66</volume><issue>11</issue><spage>1971</spage><epage>1982</epage><pages>1971-1982</pages><issn>0012-186X</issn><eissn>1432-0428</eissn><abstract>Type 1 diabetes results from the poorly understood process of islet autoimmunity, which ultimately leads to the loss of functional pancreatic beta cells. Mounting evidence supports the notion that the activation and evolution of islet autoimmunity in genetically susceptible people is contingent upon early life exposures affecting the islets, especially beta cells. Here, we review some of the recent advances and studies that highlight the roles of these changes as well as antigen presentation and stress response pathways in beta cells in the onset and propagation of the autoimmune process in type 1 diabetes. Future progress in this area holds promise for advancing islet- and beta cell-directed therapies that could be implemented in the early stages of the disease and could be combined with immunotherapies. Graphical Abstract</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37488322</pmid><doi>10.1007/s00125-023-05970-z</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-5213-9168</orcidid><orcidid>https://orcid.org/0000-0002-6851-8899</orcidid><orcidid>https://orcid.org/0009-0005-9936-8386</orcidid><orcidid>https://orcid.org/0000-0001-6360-0343</orcidid><orcidid>https://orcid.org/0000-0003-3469-1586</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0012-186X
ispartof Diabetologia, 2023-11, Vol.66 (11), p.1971-1982
issn 0012-186X
1432-0428
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10542715
source MEDLINE; Springer Nature - Complete Springer Journals
subjects Antigen presentation
Autoimmunity
Autoimmunity - physiology
Beta cells
Cellular stress response
Diabetes
Diabetes mellitus (insulin dependent)
Diabetes Mellitus, Type 1 - metabolism
Genetic Predisposition to Disease
Human Physiology
Humans
Immunotherapy
Insulin-Secreting Cells - metabolism
Internal Medicine
Invited Review
Islets of Langerhans - metabolism
Medicine
Medicine & Public Health
Metabolic Diseases
title Islet autoimmunity in human type 1 diabetes: initiation and progression from the perspective of the beta cell
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T03%3A14%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Islet%20autoimmunity%20in%20human%20type%201%20diabetes:%20initiation%20and%20progression%20from%20the%20perspective%20of%20the%20beta%20cell&rft.jtitle=Diabetologia&rft.au=Thompson,%20Peter%20J.&rft.date=2023-11-01&rft.volume=66&rft.issue=11&rft.spage=1971&rft.epage=1982&rft.pages=1971-1982&rft.issn=0012-186X&rft.eissn=1432-0428&rft_id=info:doi/10.1007/s00125-023-05970-z&rft_dat=%3Cproquest_pubme%3E2841881877%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2870179109&rft_id=info:pmid/37488322&rfr_iscdi=true