Transient Insulin Autoantibody Expression Independent of Development of Diabetes: Comparison of NOD and NOR Strains

NOD mice spontaneously develop anti-insulin autoantibodies associated with the subsequent development of diabetes. NOD mice that express insulin autoantibodies at 8 weeks of age have a diabetes risk exceeding 90%, while mice that do not express autoantibodies by 16 weeks have a risk of less than 20%...

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Veröffentlicht in:Journal of autoimmunity 2001-08, Vol.17 (1), p.1-6
Hauptverfasser: Abiru, Norio, Yu, Liping, Miao, Dongmei, Maniatis, Aristides K, Liu, Edwin, Moriyama, Hiroaki, Eisenbarth, George S
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container_issue 1
container_start_page 1
container_title Journal of autoimmunity
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creator Abiru, Norio
Yu, Liping
Miao, Dongmei
Maniatis, Aristides K
Liu, Edwin
Moriyama, Hiroaki
Eisenbarth, George S
description NOD mice spontaneously develop anti-insulin autoantibodies associated with the subsequent development of diabetes. NOD mice that express insulin autoantibodies at 8 weeks of age have a diabetes risk exceeding 90%, while mice that do not express autoantibodies by 16 weeks have a risk of less than 20%. NOD female mice expressed insulin autoantibodies more often than male mice (13/15+vs. 6/15+). Autoantibodies characteristically developed between 8 and 20 weeks and then for most mice became negative at diabetes onset in NOD mice. In the diabetes-free strain NOR mice, spontaneous expression of insulin autoantibodies was observed in less mice (female 8/15+, male 3/10+) compared to NOD mice. The expression of autoantibodies was transient in NOR mice and followed the same time-course as for NOD mice and they were all negative by 28 weeks (without progression to diabetes). No correlation was found in NOR mice between the levels of autoantibodies and insulitis. The program of insulin autoantibody expression is regulated over approximately 5 months for both NOD and NOR mice with only NOD mice developing diabetes, indicating that depending upon genetic combination, the presence of insulin autoantibodies does not always predict diabetes development. In addition, this data is not consistent with the hypothesis that the time-course of autoantibodies simply reflects the destruction of β-cells with development of diabetes.
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NOD mice that express insulin autoantibodies at 8 weeks of age have a diabetes risk exceeding 90%, while mice that do not express autoantibodies by 16 weeks have a risk of less than 20%. NOD female mice expressed insulin autoantibodies more often than male mice (13/15+vs. 6/15+). Autoantibodies characteristically developed between 8 and 20 weeks and then for most mice became negative at diabetes onset in NOD mice. In the diabetes-free strain NOR mice, spontaneous expression of insulin autoantibodies was observed in less mice (female 8/15+, male 3/10+) compared to NOD mice. The expression of autoantibodies was transient in NOR mice and followed the same time-course as for NOD mice and they were all negative by 28 weeks (without progression to diabetes). No correlation was found in NOR mice between the levels of autoantibodies and insulitis. The program of insulin autoantibody expression is regulated over approximately 5 months for both NOD and NOR mice with only NOD mice developing diabetes, indicating that depending upon genetic combination, the presence of insulin autoantibodies does not always predict diabetes development. In addition, this data is not consistent with the hypothesis that the time-course of autoantibodies simply reflects the destruction of β-cells with development of diabetes.</description><identifier>ISSN: 0896-8411</identifier><identifier>EISSN: 1095-9157</identifier><identifier>DOI: 10.1006/jaut.2001.0530</identifier><identifier>PMID: 11488632</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Animals ; Autoantibodies - biosynthesis ; Autoantibodies - blood ; Biological and medical sciences ; Diabetes Mellitus, Type 1 - etiology ; Diabetes Mellitus, Type 1 - immunology ; Diabetes Mellitus, Type 1 - pathology ; Diabetes. 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NOD mice that express insulin autoantibodies at 8 weeks of age have a diabetes risk exceeding 90%, while mice that do not express autoantibodies by 16 weeks have a risk of less than 20%. NOD female mice expressed insulin autoantibodies more often than male mice (13/15+vs. 6/15+). Autoantibodies characteristically developed between 8 and 20 weeks and then for most mice became negative at diabetes onset in NOD mice. In the diabetes-free strain NOR mice, spontaneous expression of insulin autoantibodies was observed in less mice (female 8/15+, male 3/10+) compared to NOD mice. The expression of autoantibodies was transient in NOR mice and followed the same time-course as for NOD mice and they were all negative by 28 weeks (without progression to diabetes). No correlation was found in NOR mice between the levels of autoantibodies and insulitis. 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Target tissue resistance</subject><subject>Female</subject><subject>insulin</subject><subject>Insulin Antibodies - biosynthesis</subject><subject>Insulin Antibodies - blood</subject><subject>insulin autoantibody, NOD mouse, NOR mouse, diabetes, insulitis</subject><subject>Islets of Langerhans - immunology</subject><subject>Islets of Langerhans - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred NOD - immunology</subject><subject>Prospective Studies</subject><subject>Species Specificity</subject><subject>Time Factors</subject><issn>0896-8411</issn><issn>1095-9157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQQC0EotuFK0eUC9yyeGI7H9yqbSmVKipBOVuOPZZcJXHwJBX993i1i3pCXGbk8ZvRaB5j74DvgPP604NZl13FOey4EvwF2wDvVNmBal6yDW-7umwlwBk7J3rIFCilXrMzANm2tag2jO6TmSjgtBQ3E61DmIqLdYlmWkIf3VNx9XtOSBTilP8dzphDZqMvLvERhziPf5_B9LggfS72cZxNCpRbcv3b3WVhJpfz9-LHkkyY6A175c1A-PaUt-znl6v7_dfy9u76Zn9xW1pZN0vpwAvX277jpgED2ChT-64SUHHRGqm8RWmd7D1X1vdO1B4kr3LseaUsOLFlH49z5xR_rUiLHgNZHAYzYVxJNwAcaiH-C0LL26bL6JbtjqBNkSih13MKo0lPGrg--NAHH_rgQx985Ib3p8lrP6J7xk8CMvDhBBiyZvDZhg30zEkQvJNd5tojh_lgjwGTJputWXQhoV20i-FfO_wBlSOnrA</recordid><startdate>20010801</startdate><enddate>20010801</enddate><creator>Abiru, Norio</creator><creator>Yu, Liping</creator><creator>Miao, Dongmei</creator><creator>Maniatis, Aristides K</creator><creator>Liu, Edwin</creator><creator>Moriyama, Hiroaki</creator><creator>Eisenbarth, George S</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20010801</creationdate><title>Transient Insulin Autoantibody Expression Independent of Development of Diabetes: Comparison of NOD and NOR Strains</title><author>Abiru, Norio ; Yu, Liping ; Miao, Dongmei ; Maniatis, Aristides K ; Liu, Edwin ; Moriyama, Hiroaki ; Eisenbarth, George S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-d1f3dbcb90a71a1e75a6f92312038a45fce4cd4bf05cfbd36f14026f1b025c1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Autoantibodies - biosynthesis</topic><topic>Autoantibodies - blood</topic><topic>Biological and medical sciences</topic><topic>Diabetes Mellitus, Type 1 - etiology</topic><topic>Diabetes Mellitus, Type 1 - immunology</topic><topic>Diabetes Mellitus, Type 1 - pathology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Disease Progression</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>insulin</topic><topic>Insulin Antibodies - biosynthesis</topic><topic>Insulin Antibodies - blood</topic><topic>insulin autoantibody, NOD mouse, NOR mouse, diabetes, insulitis</topic><topic>Islets of Langerhans - immunology</topic><topic>Islets of Langerhans - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred NOD - immunology</topic><topic>Prospective Studies</topic><topic>Species Specificity</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abiru, Norio</creatorcontrib><creatorcontrib>Yu, Liping</creatorcontrib><creatorcontrib>Miao, Dongmei</creatorcontrib><creatorcontrib>Maniatis, Aristides K</creatorcontrib><creatorcontrib>Liu, Edwin</creatorcontrib><creatorcontrib>Moriyama, Hiroaki</creatorcontrib><creatorcontrib>Eisenbarth, George S</creatorcontrib><collection>Pascal-Francis</collection><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>Abiru, Norio</au><au>Yu, Liping</au><au>Miao, Dongmei</au><au>Maniatis, Aristides K</au><au>Liu, Edwin</au><au>Moriyama, Hiroaki</au><au>Eisenbarth, George S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transient Insulin Autoantibody Expression Independent of Development of Diabetes: Comparison of NOD and NOR Strains</atitle><jtitle>Journal of autoimmunity</jtitle><addtitle>J Autoimmun</addtitle><date>2001-08-01</date><risdate>2001</risdate><volume>17</volume><issue>1</issue><spage>1</spage><epage>6</epage><pages>1-6</pages><issn>0896-8411</issn><eissn>1095-9157</eissn><abstract>NOD mice spontaneously develop anti-insulin autoantibodies associated with the subsequent development of diabetes. 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subjects Animals
Autoantibodies - biosynthesis
Autoantibodies - blood
Biological and medical sciences
Diabetes Mellitus, Type 1 - etiology
Diabetes Mellitus, Type 1 - immunology
Diabetes Mellitus, Type 1 - pathology
Diabetes. Impaired glucose tolerance
Disease Progression
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Female
insulin
Insulin Antibodies - biosynthesis
Insulin Antibodies - blood
insulin autoantibody, NOD mouse, NOR mouse, diabetes, insulitis
Islets of Langerhans - immunology
Islets of Langerhans - pathology
Male
Medical sciences
Mice
Mice, Inbred C57BL
Mice, Inbred NOD - immunology
Prospective Studies
Species Specificity
Time Factors
title Transient Insulin Autoantibody Expression Independent of Development of Diabetes: Comparison of NOD and NOR Strains
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