神经炎症
中枢神经系统
嵌合抗原受体
抗原
生物
细胞生物学
细胞外
细胞外基质
神经科学
间隙
受体
免疫学
免疫疗法
医学
炎症
免疫系统
生物化学
泌尿科
作者
Milos Simic,Payal Watchmaker,Sasha Gupta,Yuan Wang,Sharon A. Sagan,Jason Duecker,Chanelle Shepherd,David Diebold,Psalm Pineo-Cavanaugh,Jeffrey Haegelin,Robert Zhu,Ben Ng,Wei Yu,Yurie Tonai,Lia Cardarelli,Nishith R. Reddy,Sachdev S. Sidhu,Olga G. Troyanskaya,Stephen L. Hauser,Michael R. Wilson
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2024-12-05
卷期号:386 (6726): eadl4237-eadl4237
被引量:63
标识
DOI:10.1126/science.adl4237
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI