Human self-reactive T cell clones expressing identical T cell receptor β chains differ in their ability to recognize a cryptic self-epitope

Abstract

Recognition of self-antigens by T lymphocytes is a central event in autoimmunity. Understanding of the molecular interactions between T cell receptors (TCR) and self-epitopes may explain how T cells escape thymic education and initiate an autoimmune reaction. We have studied five human in vivo activated T cell clones specific for the region 535-551 of human thyroid peroxidase (TPO) established from a Graves' patient. Three clones (37, 72, and 73) expressed identical TCR β and α chains rearranging Vβ 1.1 and Vα 15.1, and were considered sister clones. Clone 43 differed from clone 37 and its sisters in the Jα region only. Clone NP-7 expressed Vβ 6.5 but rearranged two in-frame TCR α chain, both using the Vα 22.1 segment. Fine epitope mapping using nested peptides showed that clones using identical TCR β chains, identical Vα, but a different Jα recognized distinct, nonoverlapping epitopes in the TPO 535-551 region. This finding shows that a different Jα region alone leads to a heterogeneous pattern of recognition. This indicates that the 'restricted' TCR V region usage sometimes found in autoimmune diseases may not always correspond to identical epitope recognition. To confirm that clones 37 (and its sisters) and 43 recognize different epitopes, the T cell clones were stimulated with a TPO-transfected autologous Epstein-Barr virus (EBV) cell line (TPO-EBV) that presents TPO epitopes after endogenous processing. Only clone 37 and its sisters recognizes the TPO-EBV cell line, suggesting that the epitope recognized by clone 43 is not presented upon endogenous processing. We have shown that thyroid epithelial cells (TEC), the only cells that produce TPO, express HLA class II molecules in Graves' disease and can act as antigen- presenting cells, presenting TPO after endogenous processing to autoantigen- reactive T cell clones. We tested, therefore, whether autologous TEC induced the same pattern of stimulation as TPO-EBV; T cell clone 37 recognizes the TEC, whereas it is stimulated poorly by the TPO loaded to autologous peripheral blood mononuclear cells (PBMC). Clone 43, which fails to recognize the TPO-EBV, also fails to recognize the TEC, but is activated by exogenous TPO presented by autologous PBMC. These results show that exogenous versus endogenous processing in vivo generates a different TPO epitope repertoire, producing a 'cryptic' epitope (epitope not always available for recognition). Our findings define a route by which human self- reactive T cells may escape thymic selection and become activated in vivo, thus possibly leading to autoimmunity.