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与 CD19 靶向嵌合抗原受体 T 细胞疗法相关的神经毒性。

Neurotoxicity Associated with CD19-Targeted CAR-T Cell Therapies.

机构信息

Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.

Division of Pediatric Neurology, Department of Neurology, University of Washington, Seattle, WA, USA.

出版信息

CNS Drugs. 2018 Dec;32(12):1091-1101. doi: 10.1007/s40263-018-0582-9.

Abstract

Neurotoxicity is an important and common complication of chimeric antigen receptor-T cell therapies. Acute neurologic signs and/or symptoms occur in a significant proportion of patients treated with CD19-directed chimeric antigen receptor-T cells for B-cell malignancies. Clinical manifestations include headache, confusion, delirium, language disturbance, seizures and rarely, acute cerebral edema. Neurotoxicity is associated with cytokine release syndrome, which occurs in the setting of in-vivo chimeric antigen receptor-T cell activation and proliferation. The mechanisms that lead to neurotoxicity remain unknown, but data from patients and animal models suggest there is compromise of the blood-brain barrier, associated with high levels of cytokines in the blood and cerebrospinal fluid, as well as endothelial activation. Corticosteroids, interleukin-6-targeted therapies, and supportive care are frequently used to manage patients with neurotoxicity, but high-quality evidence of their efficacy is lacking.

摘要

神经毒性是嵌合抗原受体-T 细胞疗法的一个重要且常见的并发症。在接受 CD19 导向的嵌合抗原受体-T 细胞治疗 B 细胞恶性肿瘤的患者中,相当一部分会出现急性神经体征和/或症状。临床表现包括头痛、意识混乱、谵妄、语言障碍、癫痫发作,极少数情况下还会出现急性脑水肿。神经毒性与细胞因子释放综合征有关,后者发生于嵌合抗原受体-T 细胞在体内激活和增殖的情况下。导致神经毒性的确切机制尚不清楚,但来自患者和动物模型的数据表明,血脑屏障受到损害,血液和脑脊液中细胞因子水平升高,以及内皮细胞激活。经常使用皮质类固醇、针对白细胞介素-6 的治疗和支持性护理来治疗神经毒性患者,但缺乏其疗效的高质量证据。

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