Treg cells are essential for 'tuning' appropriate immune responses; however, the extent to which their numerical or functional impairment contributes to allergy in humans is unclear. In Cell, Scheffold and colleagues use a technique for isolating and functionally examining minute populations of antigen-reactive human T cells to investigate the role of Treg cells in allergy. In normal volunteers, both conventional T cells and Treg cells are found to react to self, non-self and commensal antigens. People allergic to aeroantigens also show normal Treg cell numbers and functionality but fail to control allergic responses of the TH2 subset of helper T cells. This relative inability to suppress allergen-specific responses arises because the Treg cells and TH2 cells target different sets of antigens. The data suggest that rather than there being an inherent wholesale loss of Treg cell functionality, allergy can arise by a failure of the suppressive cells to overlap in time and/or space with the pathogenic T cells.

Cell (20 October 2016) doi:10.1016/j.cell.2016.09.050