Article
Author: Codet, Elisabeth ; Louis, Benjamin B V ; Rakhshandehroo, Taha ; Baral, Jessika ; Berland, Lea ; Nadeem, Omar ; Kuhnast, Adrien ; Rashidian, Mohammad ; Wucherpfennig, Kai W ; Khan, Radia M M ; Regan, Kathryn ; Tavakolpour, Soheil ; Nia, Hadi T ; Wolff, Alexandra ; Rowley, Jennifer E ; Munaretto, Leila ; Farkash, Zoe ; Shahbazian, Haneyeh ; Salehi Farid, Ali ; Nili, Ali ; Moravej, Heydar ; Jacobson, Caron A ; Allen, Harris H ; Uslu, Safak C ; Cong, Min ; Lee, Uk-Jae ; Simkova, Ester ; Pyrdol, Jason ; Mantri, Shreya R
Although chimeric antigen receptor (CAR) T cell therapies have demonstrated promising clinical outcomes, durable remissions remain limited. To extend the efficacy of CAR T cells, we develop a CAR enhancer (CAR-E), comprising a CAR T cell antigen fused to an immunomodulatory molecule. Here we demonstrate this strategy using B cell maturation antigen (BCMA) CAR T cells for the treatment of multiple myeloma, with a CAR-E consisting of the BCMA fused to a low-affinity interleukin 2 (IL-2). This selectively induces IL-2 signaling in CAR T cells upon antigen-CAR binding, enhancing T cell activation and antitumor activity while reducing IL-2-associated toxicities. We show that the BCMA CAR-E selectively binds CAR T cells and increases CAR T cell proliferation, clearance of tumor cells and development of memory CAR T cells. The memory cells retain the ability to re-expand upon restimulation, effectively controlling tumor growth upon rechallenge. Mechanistic studies reveal the involvement of both CAR and IL-2 receptor endodomains in the CAR-E mechanism of action. The CAR-E approach avoids the need for specific engineering and enables CAR T cell therapy with lower cell doses.