Tuberculosis (TB), caused by Mycobacterium tuberculosis (Mtb), remains the leading cause of death from infection globally, yet the contribution of non-classical T-cell pathways to human immunity remains poorly defined. CD1c-autoreactive T-cells, which recognise self-lipids presented by the antigen-presenting molecule CD1c, are frequent in human blood, but their role during infection is unclear. Here, we investigate how CD1c-expressing antigen-presenting cells (APCs) and Mtb infection shape CD1c-
Human CD1c-autoreactive T cells recognise Mycobacterium tuberculosis–infected antigen-presenting cells and display cytotoxic effector programmes
Matthew Milton·Salah Mansour·Rita Szoke-kovacs·Patrick Trimby-Smith·Alex Look·Diana Garay-Baquero·Daniel Burns·Laura Denney·Liku B. Tezera·Richard J Stopforth·Marco Lepore·David K. Cole·Andrew White·Sally Sharpe·Alasdair Leslie·Andrés F. Vallejo·Sahar Farag·Paul T Elkington·Jennie Gullick
