Article
作者: Merghoub, Taha ; Hackett, Christopher S ; Hirschhorn, Daniel ; Hackett, Christopher S. ; Purdon, Terence J ; Rafiq, Sarwish ; Wolchok, Jedd D. ; Agaram, Narasimhan P. ; Marouf, Yacine ; Schad, Sara E ; Brentjens, Renier J. ; Purdon, Terence J. ; de Stanchina, Elisa ; Agaram, Narasimhan P ; Monette, Sebastien ; Tang, Meixian S ; Piersigilli, Alessandra ; Wolchok, Jedd D ; Brentjens, Renier J ; Tang, Meixian S. ; Schad, Sara E. ; Liu, Cailian
Despite therapeutic efficacy observed with immune checkpoint blockade in advanced melanoma, many tumors do not respond to treatment, representing a need for new therapies. Here, we have generated chimeric antigen receptor (CAR) T cells targeting TYRP1, a melanoma differentiation antigen expressed on the surface of melanomas, including rare acral and uveal melanomas. TYRP1-targeted CAR T cells demonstrate antigen-specific activation and cytotoxic activity in vitro and in vivo against human melanomas independent of the MHC alleles and expression. In addition, the toxicity to pigmented normal tissues observed with T lymphocytes expressing TYRP1-targeted TCRs was not observed with TYRP1-targeted CAR T cells. Anti-TYRP1 CAR T cells provide a novel means to target advanced melanomas, serving as a platform for the development of similar novel therapeutic agents and as a tool to interrogate the immunobiology of melanomas.