CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:CAR T-Cell Therapy in Neurology: A Scoping Review of Neuro-Oncology, Autoimmune Diseases & Neurotoxicity.
CAR T-Cell Therapy in Neurology: A Scoping Review of Neuro-Oncology, Autoimmune Diseases & Neurotoxicity.
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嵌合抗原受体(CAR)T细胞疗法已在神经系统疾病中展开研究,涵盖中枢神经系统恶性肿瘤和自身免疫性疾病,从而将其应用范围扩展至血液系统癌症之外。本范围综述评估了CAR-T 细胞疗法在神经系统疾病中的应用,评价其治疗疗效、安全性特征及神经毒性管理策略。通过对四个数据库(2020年1月至2025年12月)进行文献检索,共识别出33项符合纳入标准的研究,涵盖来自国际中心的原创研究和二次研究。CAR-T 细胞疗法在多种神经系统疾病中展现出良好的疗效。在胶质母细胞瘤试验中,44%的患者(n = 128)实现了部分或完全的临床/影像学缓解,且安全性特征良好。
此外,视神经脊髓炎谱系疾病研究中也涌现出令人振奋的结果,92%的患者(11/12)在中位随访5.5个月内实现了持续无复发生存。多发性硬化、重症肌无力和僵人综合征病例表现出极佳的治疗耐受性,未出现显著的免疫效应细胞相关神经毒性综合征(ICANS),而ICANS是影响27%血液系统恶性肿瘤患者的主要关注问题。
总体而言,CAR-T 细胞疗法作为神经病学领域的一种新型治疗策略崭露头角,涵盖肿瘤性和自身免疫性疾病。神经系统CAR-T 细胞应用中的毒性特征与血液系统恶性肿瘤中观察到的毒性特征存在显著差异,凸显了制定针对特定疾病的风险评估框架和个体化管理方法的必要性。未来研究应优先开展更大规模的多中心试验并进行延长随访,以确立神经系统适应症中明确的疗效和安全性特征。
Chimeric antigen receptor (CAR) T-cell therapy has been investigated in neurological diseases, encompassing both central nervous system malignancies and autoimmune disorders, thereby extending its application beyond hematological cancers. This scoping review evaluates CAR T-cell therapy applications in neurological conditions, assessing therapeutic efficacy, safety profiles, and neurotoxicity management strategies.
A literature search across four databases (January 2020-December 2025) identified 33 studies meeting the inclusion criteria, encompassing original and secondary research from international centers. CAR T-cell therapy demonstrated promising efficacy across diverse neurological conditions. In glioblastoma trials, 44% of patients (n = 128) achieved partial or complete clinical/radiographic responses with favorable safety profiles.
Moreover, compelling results emerged from neuromyelitis optica spectrum disorder studies, in which 92% of patients (11/12) achieved sustained relapse-free remission over a median follow-up of 5. 5 months. Multiple sclerosis, myasthenia gravis, and stiff-person syndrome cases exhibited excellent treatment tolerance without significant immune effector cell-associated neurotoxicity syndrome (ICANS), which is a major concern affecting 27% of patients with hematological malignancies.
Overall, CAR T-cell therapy emerges as a novel therapeutic strategy in neurology, encompassing both oncological and autoimmune conditions. Toxicity profiles in neurological CAR T-cell applications differ substantially from those observed in hematologic malignancies, underscoring the need for condition-specific risk assessment frameworks and customized management approaches. Future research should prioritize larger multicenter trials with extended follow-up to establish definitive efficacy and safety profiles in neurological indications.
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