MR1-restricted T cell clonotypes are associated with “resistance” to Mycobacterium tuberculosis infection. MR1-restricted T cell clonotypes are associated with “resistance” to Mycobacterium tuberculosis infection

T cells are required for protective immunity against Mycobacterium tuberculosis. We recently described a cohort of Ugandan household contacts of tuberculosis cases who appear to “resist” M. tuberculosis infection (resisters; RSTRs) and showed that these individuals harbor IFN-γ–independent T cell responses to M. tuberculosis–specific peptide antigens. However, T cells also recognize nonprotein antigens via antigen-presenting systems that are independent of genetic background, known as donor-unrestricted T cells (DURTs). We used tetramer staining and flow cytometry to characterize the association between DURTs and “resistance” to M. tuberculosis infection. Peripheral frequencies of most DURT subsets were comparable between RSTRs and latently infected controls (LTBIs). However, we observed a 1.65-fold increase in frequency of MR1-restricted T (MR1T) cells among RSTRs in comparison with LTBIs. Single-cell RNA sequencing of 18,251 MR1T cells sorted from 8 donors revealed 5,150 clonotypes that expressed a common transcriptional program, the majority of which were private. Sequencing of the T cell receptor α/T cell receptor δ (TCRα/δ) repertoire revealed several DURT clonotypes were expanded among RSTRs, including 2 MR1T clonotypes that recognized mycobacteria-infected cells in a TCR-dependent manner. Overall, our data reveal unexpected donor-specific diversity in the TCR repertoire of human MR1T cells as well as associations between mycobacteria-reactive MR1T clonotypes and resistance to M. tuberculosis infection. Overall design: MR1-restricted T-cells (defined as live CD7+ MR1-5-OP-RU tetramer+ cells) were sorted from peripheral blood samples (n = 8). Surface protein expression, gene expression and paired T-cell receptor sequencing were performed on each sample. Samples from 4 ‘resistors’ (RSTR, defined as longitudinally negative for tuberculin skin test and IFNg release assay) and 4 latently infected donors (LTBI, defined as longitudinally positive for tuberculin skin test and IFNg release assay) have been included in this dataset. Samples were sequenced ex vivo without stimulation.