Type 1 diabetes: Lessons for other autoimmune diseases?
Abstract Type 1 diabetes (T1D) satisfies many of the criteria for an autoimmune disease. The impact of the environment to promote the development of T1D and the ability to identify individuals at risk for T1D years before clinical presentation afford lessons for other autoimmune diseases, in regard...
Gespeichert in:
Veröffentlicht in: | Journal of autoimmunity 2008-11, Vol.31 (3), p.306-310 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 310 |
---|---|
container_issue | 3 |
container_start_page | 306 |
container_title | Journal of autoimmunity |
container_volume | 31 |
creator | Harrison, Leonard C Honeyman, Margo C Morahan, Grant Wentworth, John M Elkassaby, Shirley Colman, Peter G Fourlanos, Spiros |
description | Abstract Type 1 diabetes (T1D) satisfies many of the criteria for an autoimmune disease. The impact of the environment to promote the development of T1D and the ability to identify individuals at risk for T1D years before clinical presentation afford lessons for other autoimmune diseases, in regard to gene–environment interactions and the potential for rational approaches to pre-clinical diagnosis and prevention. Public health measures aimed at the modern pro-inflammatory environment are required to stem the rising tide not only of T1D but other autoimmune and chronic inflammatory disorders. In the non-obese diabetic (NOD) model of spontaneous autoimmune diabetes, compelling evidence indicates that adaptive autoimmunity to the pancreatic beta cell is initially targeted against proinsulin. Proof-of-principle studies in the NOD mouse, which established that insulin and proinsulin peptides could be applied as tools to induce immune tolerance and protect against diabetes development, await successful translation to at-risk humans. Initial trials of insulin-specific immunotherapy in humans show promise and reveal ways of optimising this approach that are also applicable to other autoimmune diseases. |
doi_str_mv | 10.1016/j.jaut.2008.04.026 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69827110</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0896841108000711</els_id><sourcerecordid>69827110</sourcerecordid><originalsourceid>FETCH-LOGICAL-c440t-114a7174d7ce3f90293622081e0d14cc69686b5f5956643ac1507bd2c28c46803</originalsourceid><addsrcrecordid>eNqFkU2L1EAQhhtR3NnVP-BBcvKWWNXpTxEXWVwVBjy4nptMp4Id8zF2J8L8ezvMgOBBT3V53reopxh7gVAhoHrdV32zLhUHMBWICrh6xHYIVpYWpX7MdmCsKo1AvGLXKfUAiFLKp-wKjZRGaL1j-uF0pAKLNjQHWii9KfaU0jyloptjMS_fKRZ5yRzGcZ0oY4maROn2GXvSNUOi55d5w77df3i4-1Tuv3z8fPd-X3ohYCkRRaNRi1Z7qjsL3NaKczBI0KLwXlll1EF20kqlRN14lKAPLffceKEM1Dfs1bn3GOefK6XFjSF5GoZmonlNTlnDNeL_QbQyX28xg_wM-jinFKlzxxjGJp4cgtu8ut5tXt3m1YFw2WsOvby0r4eR2j-Ri8gMvD0DlGX8ChRd8oEmT22I5BfXzuHf_e_-ivshTME3ww86UernNU5Zs0OXuAP3dfvs9lgwAJDvr38DSvKbbQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19511591</pqid></control><display><type>article</type><title>Type 1 diabetes: Lessons for other autoimmune diseases?</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Harrison, Leonard C ; Honeyman, Margo C ; Morahan, Grant ; Wentworth, John M ; Elkassaby, Shirley ; Colman, Peter G ; Fourlanos, Spiros</creator><creatorcontrib>Harrison, Leonard C ; Honeyman, Margo C ; Morahan, Grant ; Wentworth, John M ; Elkassaby, Shirley ; Colman, Peter G ; Fourlanos, Spiros</creatorcontrib><description>Abstract Type 1 diabetes (T1D) satisfies many of the criteria for an autoimmune disease. The impact of the environment to promote the development of T1D and the ability to identify individuals at risk for T1D years before clinical presentation afford lessons for other autoimmune diseases, in regard to gene–environment interactions and the potential for rational approaches to pre-clinical diagnosis and prevention. Public health measures aimed at the modern pro-inflammatory environment are required to stem the rising tide not only of T1D but other autoimmune and chronic inflammatory disorders. In the non-obese diabetic (NOD) model of spontaneous autoimmune diabetes, compelling evidence indicates that adaptive autoimmunity to the pancreatic beta cell is initially targeted against proinsulin. Proof-of-principle studies in the NOD mouse, which established that insulin and proinsulin peptides could be applied as tools to induce immune tolerance and protect against diabetes development, await successful translation to at-risk humans. Initial trials of insulin-specific immunotherapy in humans show promise and reveal ways of optimising this approach that are also applicable to other autoimmune diseases.</description><identifier>ISSN: 0896-8411</identifier><identifier>EISSN: 1095-9157</identifier><identifier>DOI: 10.1016/j.jaut.2008.04.026</identifier><identifier>PMID: 18558477</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Allergy and Immunology ; Animals ; Autoimmune ; Autoimmune Diseases - diagnosis ; Autoimmune Diseases - genetics ; Autoimmune Diseases - immunology ; Autoimmune Diseases - prevention & control ; Diabetes Mellitus, Type 1 - diagnosis ; Diabetes Mellitus, Type 1 - genetics ; Diabetes Mellitus, Type 1 - immunology ; Diabetes Mellitus, Type 1 - prevention & control ; Environment ; Genes ; Genetic Predisposition to Disease ; HLA-DR Antigens - genetics ; HLA-DR Antigens - immunology ; Humans ; Mice ; Prevention ; Risk Factors ; Type 1 diabetes</subject><ispartof>Journal of autoimmunity, 2008-11, Vol.31 (3), p.306-310</ispartof><rights>Elsevier Ltd</rights><rights>2008 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-114a7174d7ce3f90293622081e0d14cc69686b5f5956643ac1507bd2c28c46803</citedby><cites>FETCH-LOGICAL-c440t-114a7174d7ce3f90293622081e0d14cc69686b5f5956643ac1507bd2c28c46803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jaut.2008.04.026$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18558477$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harrison, Leonard C</creatorcontrib><creatorcontrib>Honeyman, Margo C</creatorcontrib><creatorcontrib>Morahan, Grant</creatorcontrib><creatorcontrib>Wentworth, John M</creatorcontrib><creatorcontrib>Elkassaby, Shirley</creatorcontrib><creatorcontrib>Colman, Peter G</creatorcontrib><creatorcontrib>Fourlanos, Spiros</creatorcontrib><title>Type 1 diabetes: Lessons for other autoimmune diseases?</title><title>Journal of autoimmunity</title><addtitle>J Autoimmun</addtitle><description>Abstract Type 1 diabetes (T1D) satisfies many of the criteria for an autoimmune disease. The impact of the environment to promote the development of T1D and the ability to identify individuals at risk for T1D years before clinical presentation afford lessons for other autoimmune diseases, in regard to gene–environment interactions and the potential for rational approaches to pre-clinical diagnosis and prevention. Public health measures aimed at the modern pro-inflammatory environment are required to stem the rising tide not only of T1D but other autoimmune and chronic inflammatory disorders. In the non-obese diabetic (NOD) model of spontaneous autoimmune diabetes, compelling evidence indicates that adaptive autoimmunity to the pancreatic beta cell is initially targeted against proinsulin. Proof-of-principle studies in the NOD mouse, which established that insulin and proinsulin peptides could be applied as tools to induce immune tolerance and protect against diabetes development, await successful translation to at-risk humans. Initial trials of insulin-specific immunotherapy in humans show promise and reveal ways of optimising this approach that are also applicable to other autoimmune diseases.</description><subject>Allergy and Immunology</subject><subject>Animals</subject><subject>Autoimmune</subject><subject>Autoimmune Diseases - diagnosis</subject><subject>Autoimmune Diseases - genetics</subject><subject>Autoimmune Diseases - immunology</subject><subject>Autoimmune Diseases - prevention & control</subject><subject>Diabetes Mellitus, Type 1 - diagnosis</subject><subject>Diabetes Mellitus, Type 1 - genetics</subject><subject>Diabetes Mellitus, Type 1 - immunology</subject><subject>Diabetes Mellitus, Type 1 - prevention & control</subject><subject>Environment</subject><subject>Genes</subject><subject>Genetic Predisposition to Disease</subject><subject>HLA-DR Antigens - genetics</subject><subject>HLA-DR Antigens - immunology</subject><subject>Humans</subject><subject>Mice</subject><subject>Prevention</subject><subject>Risk Factors</subject><subject>Type 1 diabetes</subject><issn>0896-8411</issn><issn>1095-9157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2L1EAQhhtR3NnVP-BBcvKWWNXpTxEXWVwVBjy4nptMp4Id8zF2J8L8ezvMgOBBT3V53reopxh7gVAhoHrdV32zLhUHMBWICrh6xHYIVpYWpX7MdmCsKo1AvGLXKfUAiFLKp-wKjZRGaL1j-uF0pAKLNjQHWii9KfaU0jyloptjMS_fKRZ5yRzGcZ0oY4maROn2GXvSNUOi55d5w77df3i4-1Tuv3z8fPd-X3ohYCkRRaNRi1Z7qjsL3NaKczBI0KLwXlll1EF20kqlRN14lKAPLffceKEM1Dfs1bn3GOefK6XFjSF5GoZmonlNTlnDNeL_QbQyX28xg_wM-jinFKlzxxjGJp4cgtu8ut5tXt3m1YFw2WsOvby0r4eR2j-Ri8gMvD0DlGX8ChRd8oEmT22I5BfXzuHf_e_-ivshTME3ww86UernNU5Zs0OXuAP3dfvs9lgwAJDvr38DSvKbbQ</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>Harrison, Leonard C</creator><creator>Honeyman, Margo C</creator><creator>Morahan, Grant</creator><creator>Wentworth, John M</creator><creator>Elkassaby, Shirley</creator><creator>Colman, Peter G</creator><creator>Fourlanos, Spiros</creator><general>Elsevier Ltd</general><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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20081101</creationdate><title>Type 1 diabetes: Lessons for other autoimmune diseases?</title><author>Harrison, Leonard C ; Honeyman, Margo C ; Morahan, Grant ; Wentworth, John M ; Elkassaby, Shirley ; Colman, Peter G ; Fourlanos, Spiros</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-114a7174d7ce3f90293622081e0d14cc69686b5f5956643ac1507bd2c28c46803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Allergy and Immunology</topic><topic>Animals</topic><topic>Autoimmune</topic><topic>Autoimmune Diseases - diagnosis</topic><topic>Autoimmune Diseases - genetics</topic><topic>Autoimmune Diseases - immunology</topic><topic>Autoimmune Diseases - prevention & control</topic><topic>Diabetes Mellitus, Type 1 - diagnosis</topic><topic>Diabetes Mellitus, Type 1 - genetics</topic><topic>Diabetes Mellitus, Type 1 - immunology</topic><topic>Diabetes Mellitus, Type 1 - prevention & control</topic><topic>Environment</topic><topic>Genes</topic><topic>Genetic Predisposition to Disease</topic><topic>HLA-DR Antigens - genetics</topic><topic>HLA-DR Antigens - immunology</topic><topic>Humans</topic><topic>Mice</topic><topic>Prevention</topic><topic>Risk Factors</topic><topic>Type 1 diabetes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harrison, Leonard C</creatorcontrib><creatorcontrib>Honeyman, Margo C</creatorcontrib><creatorcontrib>Morahan, Grant</creatorcontrib><creatorcontrib>Wentworth, John M</creatorcontrib><creatorcontrib>Elkassaby, Shirley</creatorcontrib><creatorcontrib>Colman, Peter G</creatorcontrib><creatorcontrib>Fourlanos, Spiros</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of autoimmunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harrison, Leonard C</au><au>Honeyman, Margo C</au><au>Morahan, Grant</au><au>Wentworth, John M</au><au>Elkassaby, Shirley</au><au>Colman, Peter G</au><au>Fourlanos, Spiros</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Type 1 diabetes: Lessons for other autoimmune diseases?</atitle><jtitle>Journal of autoimmunity</jtitle><addtitle>J Autoimmun</addtitle><date>2008-11-01</date><risdate>2008</risdate><volume>31</volume><issue>3</issue><spage>306</spage><epage>310</epage><pages>306-310</pages><issn>0896-8411</issn><eissn>1095-9157</eissn><abstract>Abstract Type 1 diabetes (T1D) satisfies many of the criteria for an autoimmune disease. The impact of the environment to promote the development of T1D and the ability to identify individuals at risk for T1D years before clinical presentation afford lessons for other autoimmune diseases, in regard to gene–environment interactions and the potential for rational approaches to pre-clinical diagnosis and prevention. Public health measures aimed at the modern pro-inflammatory environment are required to stem the rising tide not only of T1D but other autoimmune and chronic inflammatory disorders. In the non-obese diabetic (NOD) model of spontaneous autoimmune diabetes, compelling evidence indicates that adaptive autoimmunity to the pancreatic beta cell is initially targeted against proinsulin. Proof-of-principle studies in the NOD mouse, which established that insulin and proinsulin peptides could be applied as tools to induce immune tolerance and protect against diabetes development, await successful translation to at-risk humans. Initial trials of insulin-specific immunotherapy in humans show promise and reveal ways of optimising this approach that are also applicable to other autoimmune diseases.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>18558477</pmid><doi>10.1016/j.jaut.2008.04.026</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0896-8411 |
ispartof | Journal of autoimmunity, 2008-11, Vol.31 (3), p.306-310 |
issn | 0896-8411 1095-9157 |
language | eng |
recordid | cdi_proquest_miscellaneous_69827110 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Allergy and Immunology Animals Autoimmune Autoimmune Diseases - diagnosis Autoimmune Diseases - genetics Autoimmune Diseases - immunology Autoimmune Diseases - prevention & control Diabetes Mellitus, Type 1 - diagnosis Diabetes Mellitus, Type 1 - genetics Diabetes Mellitus, Type 1 - immunology Diabetes Mellitus, Type 1 - prevention & control Environment Genes Genetic Predisposition to Disease HLA-DR Antigens - genetics HLA-DR Antigens - immunology Humans Mice Prevention Risk Factors Type 1 diabetes |
title | Type 1 diabetes: Lessons for other autoimmune diseases? |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T11%3A53%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Type%201%20diabetes:%20Lessons%20for%20other%20autoimmune%20diseases?&rft.jtitle=Journal%20of%20autoimmunity&rft.au=Harrison,%20Leonard%20C&rft.date=2008-11-01&rft.volume=31&rft.issue=3&rft.spage=306&rft.epage=310&rft.pages=306-310&rft.issn=0896-8411&rft.eissn=1095-9157&rft_id=info:doi/10.1016/j.jaut.2008.04.026&rft_dat=%3Cproquest_cross%3E69827110%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=19511591&rft_id=info:pmid/18558477&rft_els_id=S0896841108000711&rfr_iscdi=true |