- Simic, Milos S;
- Watchmaker, Payal B;
- Gupta, Sasha;
- Wang, Yuan;
- Sagan, Sharon A;
- Duecker, Jason;
- Shepherd, Chanelle;
- Diebold, David;
- Pineo-Cavanaugh, Psalm;
- Haegelin, Jeffrey;
- Zhu, Robert;
- Ng, Ben;
- Yu, Wei;
- Tonai, Yurie;
- Cardarelli, Lia;
- Reddy, Nishith R;
- Sidhu, Sachdev S;
- Troyanskaya, Olga;
- Hauser, Stephen L;
- Wilson, Michael R;
- Zamvil, Scott S;
- Okada, Hideho;
- Lim, Wendell A
To engineer cells that can specifically target the central nervous system (CNS), we identified extracellular CNS-specific antigens, including components of the CNS extracellular matrix and surface molecules expressed on neurons or glial cells. Synthetic Notch receptors engineered to detect these antigens were used to program T cells to induce the expression of diverse payloads only in the brain. CNS-targeted T cells that induced chimeric antigen receptor expression efficiently cleared primary and secondary brain tumors without harming cross-reactive cells outside of the brain. Conversely, CNS-targeted cells that locally delivered the immunosuppressive cytokine interleukin-10 ameliorated symptoms in a mouse model of neuroinflammation. Tissue-sensing cells represent a strategy for addressing diverse disorders in an anatomically targeted manner.