Recognition of Multiple Hybrid Insulin Peptides by a Single Highly Diabetogenic T-Cell Receptor

Abstract

The mechanisms underlying the major histocompatibility complex class II (MHCII) type 1 diabetes (T1D) association remain incompletely understood. We have previously shown that thymocytes expressing the highly diabetogenic, I-A^g7-restricted 4.1-T-cell receptor (TCR) are MHCII-promiscuous, and that, in MHCII-heterozygous mice, they sequentially undergo positive and negative selection/Treg deviation by recognizing pro- and anti-diabetogenic MHCII molecules on cortical thymic epithelial cells and medullary hematopoietic antigen-presenting cells (APCs), respectively. Here, we use a novel autoantigen discovery approach to define the antigenic specificity of this TCR in the context of I-A^g7. This was done by screening the ability of random epitope-GS linker-I- ${\text{A}}_{\beta }^{\text{g}7}$ chain fusion pools to form agonistic peptide-MHCII complexes on the surface of I- ${\text{A}}_{\alpha }^{\text{d}}$ chain-transgenic artificial APCs. Pool deconvolution, I-A^g7-binding register-fixing, TCR contact residue mapping, and alanine scanning mutagenesis resulted in the identification of a 4.1-TCR recognition motif XL(G/A)XEXE(D/E)X that was shared by seven agonistic hybrid insulin peptides (HIPs) resulting from the fusion of several different chromogranin A and/or insulin C fragments, including post-translationally modified variants. These data validate a novel, highly sensitive MHCII-restricted epitope discovery approach for orphan TCRs and suggest thymic selection of autoantigen-promiscuous TCRs as a mechanism for the murine T1D-I-A^g7-association.

Keywords: TCR-transgenic NOD mice; antigenic promiscuity; autoimmunity; epitope discovery; genetic susceptibility and resistance; hybrid insulin peptides; major histocompatibility complex; type 1 diabetes.