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
Hauptverfasser: ELLIS, T. M, OTTENDORFER, E, JODOIN, E, SALISBURY, P. J, SHE, J. X, SCHATZ, D. A, ATKINSON, M. A
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container_end_page 735
container_issue 6
container_start_page 731
container_title Diabetologia
container_volume 41
creator ELLIS, T. M
OTTENDORFER, E
JODOIN, E
SALISBURY, P. J
SHE, J. X
SCHATZ, D. A
ATKINSON, M. A
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.
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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. 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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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