Cellular immune responses to β casein : elevated in but not specific for individuals with Type I diabetes mellitus
Elevated cellular immune responses against the cows' milk protein beta casein have been reported in individuals with Type I diabetes mellitus, a finding supportive of the concept that cows' milk consumption may be causative for the disease. We analysed cellular immune reactivities against...
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Veröffentlicht in: | Diabetologia 1998-06, Vol.41 (6), p.731-735 |
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description | Elevated cellular immune responses against the cows' milk protein beta casein have been reported in individuals with Type I diabetes mellitus, a finding supportive of the concept that cows' milk consumption may be causative for the disease. We analysed cellular immune reactivities against beta casein in newly-diagnosed Type I diabetic patients, their immediate autoantibody negative relatives, and unrelated healthy individuals in order to further elucidate the role of anti-beta casein immunity in the pathogenesis of Type I diabetes mellitus. Peripheral blood mononuclear cells were stimulated in vitro with various concentrations of three different beta casein preparations, control antigens (tetanus toxoid, mumps extract) and a mitogen (phytohemagglutinin). The frequency and/or mean simulation index of cellular proliferation against two of the beta casein preparations at high antigen concentrations (i.e. 10 or 50 microg/ml) were significantly higher in newly-diagnosed Type I diabetic subjects compared with autoantibody negative healthy control subjects. However, reactivities against beta casein in the Type I diabetic probands and their autoantibody negative relatives, individuals with a very low-rate of disease development, were almost identical. Cellular immune reactivities to other antigens were similar between the subject groups. In addition to indicating the need for appropriately matched subject populations (e.g. human leukocyte antigen (HLA) matched relatives) when analysing cellular immune responses, these findings support our previous contention that individuals genetically prone to autoimmunity may be deficient in forming tolerance to dietary antigens. However, the significance of anti-beta casein immunity as a specific causative factor in the pathogenesis of Type I diabetes mellitus remains unclear. |
doi_str_mv | 10.1007/s001250050976 |
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M ; OTTENDORFER, E ; JODOIN, E ; SALISBURY, P. J ; SHE, J. X ; SCHATZ, D. A ; ATKINSON, M. A</creator><creatorcontrib>ELLIS, T. M ; OTTENDORFER, E ; JODOIN, E ; SALISBURY, P. J ; SHE, J. X ; SCHATZ, D. A ; ATKINSON, M. A</creatorcontrib><description>Elevated cellular immune responses against the cows' milk protein beta casein have been reported in individuals with Type I diabetes mellitus, a finding supportive of the concept that cows' milk consumption may be causative for the disease. We analysed cellular immune reactivities against beta casein in newly-diagnosed Type I diabetic patients, their immediate autoantibody negative relatives, and unrelated healthy individuals in order to further elucidate the role of anti-beta casein immunity in the pathogenesis of Type I diabetes mellitus. Peripheral blood mononuclear cells were stimulated in vitro with various concentrations of three different beta casein preparations, control antigens (tetanus toxoid, mumps extract) and a mitogen (phytohemagglutinin). The frequency and/or mean simulation index of cellular proliferation against two of the beta casein preparations at high antigen concentrations (i.e. 10 or 50 microg/ml) were significantly higher in newly-diagnosed Type I diabetic subjects compared with autoantibody negative healthy control subjects. However, reactivities against beta casein in the Type I diabetic probands and their autoantibody negative relatives, individuals with a very low-rate of disease development, were almost identical. Cellular immune reactivities to other antigens were similar between the subject groups. In addition to indicating the need for appropriately matched subject populations (e.g. human leukocyte antigen (HLA) matched relatives) when analysing cellular immune responses, these findings support our previous contention that individuals genetically prone to autoimmunity may be deficient in forming tolerance to dietary antigens. However, the significance of anti-beta casein immunity as a specific causative factor in the pathogenesis of Type I diabetes mellitus remains unclear.</description><identifier>ISSN: 0012-186X</identifier><identifier>EISSN: 1432-0428</identifier><identifier>DOI: 10.1007/s001250050976</identifier><identifier>PMID: 9662058</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Adolescent ; Adult ; Age Factors ; Analysis of Variance ; Antibody Formation - immunology ; Antigens - immunology ; Antigens - pharmacology ; Autoantibodies - blood ; Biological and medical sciences ; Caseins - administration & dosage ; Caseins - immunology ; Caseins - pharmacology ; Cell Division - drug effects ; Cell Division - immunology ; Child ; Child, Preschool ; Diabetes Mellitus, Type 1 - etiology ; Diabetes Mellitus, Type 1 - genetics ; Diabetes Mellitus, Type 1 - immunology ; Diabetes. Impaired glucose tolerance ; Dose-Response Relationship, Drug ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Female ; HLA Antigens - genetics ; HLA Antigens - immunology ; Humans ; Immunity, Cellular ; Leukocytes, Mononuclear - cytology ; Leukocytes, Mononuclear - drug effects ; Leukocytes, Mononuclear - immunology ; Male ; Medical sciences ; Phytohemagglutinins - immunology ; Phytohemagglutinins - pharmacology ; Sex Factors ; Tetanus Toxoid - immunology ; Tetanus Toxoid - pharmacology</subject><ispartof>Diabetologia, 1998-06, Vol.41 (6), p.731-735</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-9a25f36fbe7e664ff5fe837151d355dbc94fa5584b9c17caf617923ccb9028183</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2267843$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9662058$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ELLIS, T. M</creatorcontrib><creatorcontrib>OTTENDORFER, E</creatorcontrib><creatorcontrib>JODOIN, E</creatorcontrib><creatorcontrib>SALISBURY, P. J</creatorcontrib><creatorcontrib>SHE, J. X</creatorcontrib><creatorcontrib>SCHATZ, D. A</creatorcontrib><creatorcontrib>ATKINSON, M. A</creatorcontrib><title>Cellular immune responses to β casein : elevated in but not specific for individuals with Type I diabetes mellitus</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><description>Elevated cellular immune responses against the cows' milk protein beta casein have been reported in individuals with Type I diabetes mellitus, a finding supportive of the concept that cows' milk consumption may be causative for the disease. We analysed cellular immune reactivities against beta casein in newly-diagnosed Type I diabetic patients, their immediate autoantibody negative relatives, and unrelated healthy individuals in order to further elucidate the role of anti-beta casein immunity in the pathogenesis of Type I diabetes mellitus. Peripheral blood mononuclear cells were stimulated in vitro with various concentrations of three different beta casein preparations, control antigens (tetanus toxoid, mumps extract) and a mitogen (phytohemagglutinin). The frequency and/or mean simulation index of cellular proliferation against two of the beta casein preparations at high antigen concentrations (i.e. 10 or 50 microg/ml) were significantly higher in newly-diagnosed Type I diabetic subjects compared with autoantibody negative healthy control subjects. However, reactivities against beta casein in the Type I diabetic probands and their autoantibody negative relatives, individuals with a very low-rate of disease development, were almost identical. Cellular immune reactivities to other antigens were similar between the subject groups. In addition to indicating the need for appropriately matched subject populations (e.g. human leukocyte antigen (HLA) matched relatives) when analysing cellular immune responses, these findings support our previous contention that individuals genetically prone to autoimmunity may be deficient in forming tolerance to dietary antigens. However, the significance of anti-beta casein immunity as a specific causative factor in the pathogenesis of Type I diabetes mellitus remains unclear.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Analysis of Variance</subject><subject>Antibody Formation - immunology</subject><subject>Antigens - immunology</subject><subject>Antigens - pharmacology</subject><subject>Autoantibodies - blood</subject><subject>Biological and medical sciences</subject><subject>Caseins - administration & dosage</subject><subject>Caseins - immunology</subject><subject>Caseins - pharmacology</subject><subject>Cell Division - drug effects</subject><subject>Cell Division - immunology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Diabetes Mellitus, Type 1 - etiology</subject><subject>Diabetes Mellitus, Type 1 - genetics</subject><subject>Diabetes Mellitus, Type 1 - immunology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Dose-Response Relationship, Drug</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>HLA Antigens - genetics</subject><subject>HLA Antigens - immunology</subject><subject>Humans</subject><subject>Immunity, Cellular</subject><subject>Leukocytes, Mononuclear - cytology</subject><subject>Leukocytes, Mononuclear - drug effects</subject><subject>Leukocytes, Mononuclear - immunology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Phytohemagglutinins - immunology</subject><subject>Phytohemagglutinins - pharmacology</subject><subject>Sex Factors</subject><subject>Tetanus Toxoid - immunology</subject><subject>Tetanus Toxoid - pharmacology</subject><issn>0012-186X</issn><issn>1432-0428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkMtKLTEQRYMoenwMHV7IQJy15tFJOnd2OfgCwYmCsyadrmAu_bIrrfhbfojfZMSD4Kgo9mJVsQk55uyMM2bOkTEuFGOKWaO3yIqXUhSsFNU2WX1FBa_04x7ZR_zPGJOq1Ltk12otmKpWBNfQdUvnZhr7fhmAzoDTOCAgTSP9eKfeIcSB_qXQwYtL0NK8NUuiw5goTuBjiJ6GMQuGNr7EdnEd0teYnuj92wT0hrbRNZCysM-nYlrwkOyEDMHRZh6Qh8uL-_V1cXt3dbP-d1t4qXQqrBMqSB0aMKB1GYIKUEnDFW-lUm3jbRmcUlXZWM-Nd0FzY4X0vrFMVLySB-T02zvN4_MCmOo-os9PuAHGBWtjrVVSmgwW36CfR8QZQj3NsXfzW81Z_VVy_avkzP_ZiJemh_aH3rSa85NN7tC7Lsxu8BF_MCG0qUopPwESzYVr</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>ELLIS, T. 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A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-9a25f36fbe7e664ff5fe837151d355dbc94fa5584b9c17caf617923ccb9028183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Analysis of Variance</topic><topic>Antibody Formation - immunology</topic><topic>Antigens - immunology</topic><topic>Antigens - pharmacology</topic><topic>Autoantibodies - blood</topic><topic>Biological and medical sciences</topic><topic>Caseins - administration & dosage</topic><topic>Caseins - immunology</topic><topic>Caseins - pharmacology</topic><topic>Cell Division - drug effects</topic><topic>Cell Division - immunology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Diabetes Mellitus, Type 1 - etiology</topic><topic>Diabetes Mellitus, Type 1 - genetics</topic><topic>Diabetes Mellitus, Type 1 - immunology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Dose-Response Relationship, Drug</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>HLA Antigens - genetics</topic><topic>HLA Antigens - immunology</topic><topic>Humans</topic><topic>Immunity, Cellular</topic><topic>Leukocytes, Mononuclear - cytology</topic><topic>Leukocytes, Mononuclear - drug effects</topic><topic>Leukocytes, Mononuclear - immunology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Phytohemagglutinins - immunology</topic><topic>Phytohemagglutinins - pharmacology</topic><topic>Sex Factors</topic><topic>Tetanus Toxoid - immunology</topic><topic>Tetanus Toxoid - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ELLIS, T. M</creatorcontrib><creatorcontrib>OTTENDORFER, E</creatorcontrib><creatorcontrib>JODOIN, E</creatorcontrib><creatorcontrib>SALISBURY, P. J</creatorcontrib><creatorcontrib>SHE, J. X</creatorcontrib><creatorcontrib>SCHATZ, D. A</creatorcontrib><creatorcontrib>ATKINSON, M. A</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>MEDLINE - Academic</collection><jtitle>Diabetologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ELLIS, T. M</au><au>OTTENDORFER, E</au><au>JODOIN, E</au><au>SALISBURY, P. J</au><au>SHE, J. X</au><au>SCHATZ, D. A</au><au>ATKINSON, M. A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular immune responses to β casein : elevated in but not specific for individuals with Type I diabetes mellitus</atitle><jtitle>Diabetologia</jtitle><addtitle>Diabetologia</addtitle><date>1998-06-01</date><risdate>1998</risdate><volume>41</volume><issue>6</issue><spage>731</spage><epage>735</epage><pages>731-735</pages><issn>0012-186X</issn><eissn>1432-0428</eissn><abstract>Elevated cellular immune responses against the cows' milk protein beta casein have been reported in individuals with Type I diabetes mellitus, a finding supportive of the concept that cows' milk consumption may be causative for the disease. We analysed cellular immune reactivities against beta casein in newly-diagnosed Type I diabetic patients, their immediate autoantibody negative relatives, and unrelated healthy individuals in order to further elucidate the role of anti-beta casein immunity in the pathogenesis of Type I diabetes mellitus. Peripheral blood mononuclear cells were stimulated in vitro with various concentrations of three different beta casein preparations, control antigens (tetanus toxoid, mumps extract) and a mitogen (phytohemagglutinin). The frequency and/or mean simulation index of cellular proliferation against two of the beta casein preparations at high antigen concentrations (i.e. 10 or 50 microg/ml) were significantly higher in newly-diagnosed Type I diabetic subjects compared with autoantibody negative healthy control subjects. However, reactivities against beta casein in the Type I diabetic probands and their autoantibody negative relatives, individuals with a very low-rate of disease development, were almost identical. Cellular immune reactivities to other antigens were similar between the subject groups. In addition to indicating the need for appropriately matched subject populations (e.g. human leukocyte antigen (HLA) matched relatives) when analysing cellular immune responses, these findings support our previous contention that individuals genetically prone to autoimmunity may be deficient in forming tolerance to dietary antigens. However, the significance of anti-beta casein immunity as a specific causative factor in the pathogenesis of Type I diabetes mellitus remains unclear.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>9662058</pmid><doi>10.1007/s001250050976</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Age Factors Analysis of Variance Antibody Formation - immunology Antigens - immunology Antigens - pharmacology Autoantibodies - blood Biological and medical sciences Caseins - administration & dosage Caseins - immunology Caseins - pharmacology Cell Division - drug effects Cell Division - immunology Child Child, Preschool Diabetes Mellitus, Type 1 - etiology Diabetes Mellitus, Type 1 - genetics Diabetes Mellitus, Type 1 - immunology Diabetes. Impaired glucose tolerance Dose-Response Relationship, Drug Endocrine pancreas. Apud cells (diseases) Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Female HLA Antigens - genetics HLA Antigens - immunology Humans Immunity, Cellular Leukocytes, Mononuclear - cytology Leukocytes, Mononuclear - drug effects Leukocytes, Mononuclear - immunology Male Medical sciences Phytohemagglutinins - immunology Phytohemagglutinins - pharmacology Sex Factors Tetanus Toxoid - immunology Tetanus Toxoid - pharmacology |
title | Cellular immune responses to β casein : elevated in but not specific for individuals with Type I diabetes mellitus |
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