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对可向大脑输送治疗的组织感知T细胞进行编程。

Programming tissue-sensing T cells that deliver therapies to the brain.

作者信息

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

机构信息

UCSF Cell Design Institute and Department of Cellular & Molecular Pharmacology, University of California San Francisco, San Francisco, CA, USA.

Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.

出版信息

Science. 2024 Dec 6;386(6726):eadl4237. doi: 10.1126/science.adl4237.

Abstract

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.

摘要

为了构建能够特异性靶向中枢神经系统(CNS)的细胞,我们鉴定了细胞外CNS特异性抗原,包括CNS细胞外基质的成分以及神经元或神经胶质细胞上表达的表面分子。经过工程改造以检测这些抗原的合成Notch受体被用于对T细胞进行编程,使其仅在大脑中诱导多种有效载荷的表达。高效诱导嵌合抗原受体表达的靶向CNS的T细胞有效清除了原发性和继发性脑肿瘤,而不会损害脑外的交叉反应性细胞。相反,局部递送免疫抑制细胞因子白细胞介素-10的靶向CNS的细胞在神经炎症小鼠模型中改善了症状。组织传感细胞代表了一种以解剖学靶向方式解决多种疾病的策略。

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