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