Control of autoimmune diabetes in NOD mice by CAD expression or suppression in beta cells

Glutamic acid decarboxylase (GAD) is a pancreatic beta cell autoantigen in humans and nonobese diabetic (NOD) mice. beta Cell-specific suppression of GAD expression in two Lines of antisense CAD transgenic NOD mice prevented autoimmune diabetes, whereas persistent GAD expression in the beta cells in the other four Lines of antisense CAD transgenic NOD mice resulted in diab etes, similar to that seen in transgene-negative NOD mice. Complete suppres sion of beta cell GAD expression blocked the generation of diabetogenic T c ells and protected islet grafts from autoimmune injury. Thus, beta cell-spe cific CAD expression is required for the development of autoimmune diabetes in NOD mice, and modulation of GAD might, therefore, have therapeutic valu e in type 1 diabetes.