TRANSGENIC MICE EXPRESSING CONSTITUTIVE LEVELS OF IL-2 IN ISLET BETA-CELLS DEVELOP DIABETES

被引:18
作者
ELLIOTT, EA [1 ]
FLAVELL, RA [1 ]
机构
[1] YALE UNIV, SCH MED, HOWARD HUGHES MED INST, IMMUNOBIOL SECT, NEW HAVEN, CT 06510 USA
关键词
ANERGY; AUTOIMMUNE DISEASE; IL-2; INFLAMMATION; ISLETS; NATURAL KILLER CELLS; PERIPHERAL TOLERANCE; TRANSGENIC MICE;
D O I
10.1093/intimm/6.11.1629
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
IL-2 plays an important role in the clonal expansion of T cells during an immune response and it has been implicated in autoimmune disease. To examine the role of IL-2 in the regulation of peripheral tolerance we produced transgenic mice in which the expression of murine IL-2 was directed by the rat insulin II promoter. The IL-2 transgene was expressed specifically in the pancreas. Islets from transgenic mice synthesized biologically active IL-2. Expression of IL-2 in the pancreas resulted in a massive inflammatory response directed at the beta cells of the pancreas. The infiltrate consisted primarily of B cells and CD4(+) and CD8(+) T cells. The infiltrate resulted in destruction of the insulin-producing beta cells and diabetes, but there was no evidence for antigen specificity. The results suggest that local IL-2 production elicits the recruitment and activation of cells capable of destroying beta cells by non-antigen-specific mechanisms.
引用
收藏
页码:1629 / 1637
页数:9
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