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 in | Diabetes (New York, N.Y.) Vol. 45; no. 2; pp. 178 - 182 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
American Diabetes Association
01.02.1996
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Online Access | Get full text |
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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. |
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ISSN: | 0012-1797 1939-327X 0012-1797 |
DOI: | 10.2337/diabetes.45.2.178 |