Research Article: A novel region of the insulin B9–23 sequence is targeted by a HIP-reactive diabetogenic T cell clone
Abstract:
Type 1 Diabetes (T1D) is an organ-specific autoimmune disease in which T cells are major drivers, leading to the destruction of beta-cells and insulin deficiency. Although the B-chain of insulin is a critical target for islet-reactive CD4 T cells, the native sequence is poorly antigenic and in vivo , insulin elicits only a weak Th1 response. We previously reported that post-translational modification of proinsulin through hybrid insulin peptide (HIP) formation leads to the synthesis of potent epitopes for islet-reactive CD4 T cells, and that cathepsin D (catD), a protease present in beta-cells, can mediate the formation of HIPs through a transpeptidation process. In the present study, we defined the specificity of catD for the insulin B-chain and show a high specificity for proteolytic cleavage following the disease-critical tyrosine 16 residue. We therefore hypothesized that HIP formation occurs at this amino acid. We designed a panel of HIPs containing insB 9–16 fragments linked to different secretory granule proteins and challenged splenocytes isolated from diabetic NOD mice with insB 9–16 HIPs; ELISPOT analysis showed elevated inflammatory responses to several peptides. Among this panel of HIPs, we identified the 2.40HIP, a fusion peptide between insB 9–16 and the C-peptide, as a potent epitope recognized by PD12-2.40, a diabetogenic CD4 T cell clone isolated from the islets of a 12-week-old NOD mouse. These results define a new antigenic region of the insulin B:9–23 peptide and demonstrate that this sequence of the B-chain becomes dramatically more antigenic when post-translationally modified through HIP formation.
Introduction:
Type 1 diabetes (T1D) is an autoimmune disease in which autoreactive T cells selectively destroy insulin-producing pancreatic ?-cells in the islets of Langerhans where proinsulin is an important antigen. In the non-obese diabetic (NOD) mouse, a spontaneous model for T1D, the B-chain of insulin is one of the primary targets of both CD4 and CD8 T cells. Whereas both CD4 and CD8 T cells can react to the insB 15–23 sequence ( 1 , 2 ), it has been reported that CD4 T cells recognize three additional registers within…
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