Cellular immune response to cow's milk beta-lactoglobulin in patients with newly diagnosed IDDM

Cellular immune response to cow's milk beta-lactoglobulin in patients with newly diagnosed IDDM. O Vaarala , P Klemetti , E Savilahti , H Reijonen , J Ilonen and H K Akerblom Children's Hospital, University of Helsinki, Finland. Abstract Elevated levels of antibodies to cow's milk pro...

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Published inDiabetes (New York, N.Y.) Vol. 45; no. 2; pp. 178 - 182
Main Authors Vaarala, O., Klemetti, P., Savilahti, E., Reijonen, H., Ilonen, J., Akerblom, H. K.
Format Journal Article
LanguageEnglish
Published American Diabetes Association 01.02.1996
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Summary:Cellular immune response to cow's milk beta-lactoglobulin in patients with newly diagnosed IDDM. O Vaarala , P Klemetti , E Savilahti , H Reijonen , J Ilonen and H K Akerblom Children's Hospital, University of Helsinki, Finland. Abstract Elevated levels of antibodies to cow's milk proteins, i.e., beta-lactoglobulin (BLG) and bovine serum albumin (BSA), have been associated with IDDM. We observed enhanced cellular immune response by a proliferation test of peripheral blood mononuclear cells to BLG in 22 of 40 (55%) patients with newly diagnosed IDDM compared with 7 of 32 healthy children (22%) (P = 0.004, chi 2 test). The median stimulation index to BLG was 3.3 in patients and 1.5 in healthy children (P = 0.003, Mann-Whitney U test). No difference was found in cellular reactivity to other cow's milk proteins, such as BSA or alpha-casein, or to a dietary immunogenic protein, ovalbumin. Cellular responsiveness to BLG was not associated with HLA-DQB1* risk alleles of IDDM, which suggests that immune response to the protein does not only reflect the accumulation of these HLA alleles in the patients with IDDM. We suggest that enhanced cellular immune response to dietary BLG may reflect a disturbance in the regulation of immune response to oral antigens in IDDM. This kind of defect may play a fundamental role in the development of beta-cell autoimmunity in IDDM.
ISSN:0012-1797
1939-327X
0012-1797
DOI:10.2337/diabetes.45.2.178