Remote control of therapeutic T cells through a small molecule–gated chimeric receptor

Abstract
Keeping a leash on cancer-killing cells: Redirecting the immune system to attack tumor cells is proving to be an effective therapy against cancer. However, when patients are exposed to T cells engineered to recognize and attack cancer cells, there is a risk of runaway or excessive activity or of off-target effects, both of which can themselves be deadly. Wu et al. designed T cells expressing chimeric antigen receptors that recognize and attack cancer cells with an additional control system. This mechanism would allow a doctor administering the therapy to turn the engineered T cell “on” or “off” by administering a small molecule that is required along with cancer cell antigen to stimulate the T cells and activate their tumor cell–killing properties. Science , this issue p. 10.1126/science.aab4077
Funding Information
  • NIH (F32 GM101782, PN2 EY016546, P50 GM081879, R01 GM055040, R01 CA196277)
  • Jane Coffin Childs Memorial Fund (A121505)
  • HHMI