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 S. 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,Scott S. Zamvil,Hideho Okada,Wendell A. Lim
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2024-12-05
卷期号:386 (6726)
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.
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