Tracking the role of Aire in immune tolerance to the eye with a TCR transgenic mouse model

Abstract

Roughly one-half of mice with partial defects in two immune tolerance pathways (Aire GW/+ Lyn −/− mice) spontaneously develop severe damage to their retinas due to T cell reactivity to Aire-regulated interphotoreceptor retinoid–binding protein (IRBP). Single-cell T cell receptor (TCR) sequencing of CD4 + T cells specific for a predominate epitope of IRBP showed a remarkable diversity of autoantigen-specific TCRs with greater clonal expansions in mice with disease. TCR transgenic mice made with an expanded IRBP-specific TCR (P2.U2) of intermediate affinity exhibited strong but incomplete negative selection of thymocytes. This negative selection was absent in IRBP −/− mice and greatly defective in Aire GW/+ mice. Most P2.U2 +/− mice and all P2.U.2 +/− Aire GW/+ mice rapidly developed inflammation of the retina and adjacent uvea (uveitis). Aire-dependent IRBP expression in the thymus also promoted Treg differentiation, but the niche for this fate determination was small, suggesting differences in antigen presentation leading to negative selection vs. thymic Treg differentiation and a stronger role for negative selection in preventing autoimmune disease in the retina.