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IJI-Iranian Journal of Immunology. 2006; 3 (4): 169-175
in English | IMEMR | ID: emr-76768

ABSTRACT

Autoimmune type 1 diabetes mellitus is caused by T-cell mediated immune destruction of the insulin-producing a-cell in pancreatic islets of Langerhans. Specificity of the auto-antibodies and of the auto-reactive T-cells has been investigated, in which several auto-antigens were proposed. To determine whether glutamic acid decarboxylase [GAD] feeding would induce oral tolerance of either T-cell or B-cell compartment in streptozotocin [STZ] diabetic rats. Rats in the experimental group were fed 2 mg/kg of GAD [extracted from Escherichia coli] 14 days before intra-peritoneal injections of streptozotocin [30 mg/kg body weight for 5 consecutive days]. Two control groups were considered: diabetic control group, which underwent STZ injections without receiving GAD, and normal control group. Systemic response was compared between the three groups. T-cells response was assessed by a proliferation assay of spleen cells and those of the B-cells by enzyme-linked immunosorbent assay [ELISA] for anti-GAD specific antibodies in serum. Compared with the diabetic control group, a significant reduction was observed only in the proliferative response of spleen cells, but not in the level of anti-GAD antibody. GAD feeding induces systemic T-cell tolerance in STZ-induced diabetes


Subject(s)
Animals, Laboratory , Glutamate Decarboxylase , Diabetes Mellitus, Experimental , Streptozocin , Rats , T-Lymphocytes , B-Lymphocytes
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