Phenotype-Based Isolation of Antigen-Specific CD4 + T Cells in Autoimmunity: A Study of Celiac Disease.

The pathogenic immune response in celiac disease (CeD) is orchestrated by phenotypically distinct CD4 + T cells that recognize gluten epitopes in the context of disease-associated HLA-DQ allotypes. Cells with the same distinct phenotype, but with elusive specificities, are increased across multiple autoimmune conditions. Here, whether sorting of T cells based on their distinct phenotype (Tphe cells) yields gluten-reactive cells in CeD is tested. The method's efficiency is benchmarked by parallel isolation of gluten-reactive T cells (Ttet cells), using HLA-DQ:gluten peptide tetramers. From gut biopsies of 12 untreated HLA-DQ2.5 + CeD patients, Ttet + /Tphe + , Ttet - /Tphe + , and Ttet - /Tphe - cells are sorted for single-cell T-cell receptor (TCR)-sequencing (n = 8) and T-cell clone (TCC)-generation (n = 5). The generated TCCs are TCR sequenced and tested for their reactivity against deamidated gluten. Gluten-reactivity is observed in 91.2% of Ttet + /Tphe + TCCs, 65.3% of Ttet - /Tphe + TCCs and 0% of Ttet - /Tphe - TCCs. TCR sequencing reveals clonal expansion and sequence sharing across patients, features reflecting antigen-driven responses. The feasibility to isolate antigen-specific CD4 + T cells by the sole use of phenotypic markers in CeD outlines a potential avenue for characterizing disease-driving CD4 + T cells in autoimmune conditions.