Single-cell profiling identifies T cell subsets associated with control of tuberculosis dissemination

Abstract

To identify T cell subsets associated with control of tuberculosis, single-cell transcriptome and T cell receptor sequencing were performed on total T cells from patients with tuberculosis and healthy controls. Fourteen distinct subsets of T cells were identified by unbiased UMAP clustering. A GZMK-expressing CD8⁺ cytotoxic T cell cluster and a SOX4-expressing CD4⁺ central memory T cell cluster were depleted, while a MKI67-expressing proliferating CD3⁺ T cell cluster was expanded in patients with tuberculosis compared with healthy controls. The ratio of Granzyme K-expressing CD8⁺CD161^-Ki-67^- and CD8⁺Ki-67⁺ T cell subsets was significantly reduced and inversely correlated with the extent of TB lesions in patients with TB. In contrast, ratio of Granzyme B-expressing CD8⁺Ki-67⁺ and CD4⁺CD161⁺Ki-67^- T cells and Granzyme A-expressing CD4⁺CD161⁺Ki-67^- T cells were correlated with the extent of TB lesions. It is concluded that granzyme K-expressing CD8⁺ T cell subsets might contribute to protection against tuberculosis dissemination.

Keywords: Cellular immunity; Infection and immunity; Single-cell transcriptome; T-lymphocytes; Tuberculosis.