NOD background genes influence T cell responses to GAD 65 in HLA-DQ8 transgenic mice

The major histocompatibility complex (MHC) genes play a significant role in the predisposition to insulin-dependent diabetes mellitus or type 1 diabetes. HLA-DQ8 (DQB1∗0302, DQA1∗0301) genes have been shown to have the highest relative risk for human type 1 diabetes. To develop a “humanized” mouse model of diabetes, HLA-DQ8 was transgenically expressed in mice lacking endogenous class II genes. Since non-MHC background genes of the NOD influence the disease process, Aβo/DQ8 mice were mated with the NOD strain and backcrossed to generate Aβo/DQ8/NOD mice. These mice have DQ8 as the sole MHC class II restriction element with NOD background genes at the N 2 generation. The DQ8 transgenic mice were used to identify T cell epitopes on glutamic acid decarboxylase (GAD 65), an important putative autoantigen in type 1 diabetes. The NOD background genes strongly influenced antigen processing, that is, different T cell epitopes were generated from the processing of GAD 65 in vivo in the Aβo/DQ8 and in the Aβo/DQ8/NOD mice.