RhoB Mediates Phosphoantigen Recognition by Vγ9Vδ2 T Cell Receptor

Human V gamma 9V delta 2 T cells respond to tumor cells by sensing elevated levels of phosphorylated intermediates of the dysregulated mevalonate pathway, which is translated into activating signals by the ubiquitously expressed butyrophilin A1 (BTN3A1) through yet unknown mechanisms. Here, we developed an unbiased, genome-wide screening method that identified RhoB as a critical mediator of V gamma 9V delta 2 TCR activation in tumor cells. Our results show that V gamma 9V delta 2 TCR activation is modulated by the GTPase activity of RhoB and its redistribution to BTN3A1. This is associated with cytoskeletal changes that directly stabilize BTN3A1 in the membrane, and the subsequent dissociation of RhoB from BTN3A1. Furthermore, phosphoantigen accumulation induces a conformational change in BTN3A1, rendering its extracellular domains recognizable by V gamma 9V delta 2 TCRs. These complementary events provide further evidence for inside-out signaling as an essential step in the recognition of tumor cells by a V gamma 9V delta 2 TCR.