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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Multifocal demyelinating leukoencephalopathy and oligodendroglial lineage cell loss with immune effector cell-associated neurotoxicity syndrome (ICANS) following CD19 CAR T-cell therapy for mantle cell lymphoma.
Multifocal demyelinating leukoencephalopathy and oligodendroglial lineage cell loss with immune effector cell-associated neurotoxicity syndrome (ICANS) following CD19 CAR T-cell therapy for mantle cell lymphoma.
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免疫效应细胞相关神经毒性综合征(ICANS)是CAR-T 细胞治疗及其他癌细胞治疗后常见的一种病症。由于患者病例脑组织评估的可用性有限,且缺乏用于转化研究的高保真临床前动物模型,该临床综合征的潜在病理生理学和神经病理学尚未被完全理解。在此,我们报告了一例因套细胞淋巴瘤接受抗CD19 CAR-T 治疗后发生4级ICANS的患者的细胞和组织神经病理学分析。我们的病理学评估揭示了一种多灶性脱髓鞘性脑白质病的模式,与严重ICANS的临床病程相关。对胶质细胞亚型的聚焦分析进一步提示,区域特异性的少突胶质细胞谱系细胞丢失是严重ICANS中潜在的细胞和病理生理学关联因素。我们提出了一个迄今为止在ICANS病例中所报告的神经病理学变化连续谱的框架。未来阐明ICANS背后的机制过程,对于最大限度地减少CAR-T 细胞及相关免疫治疗在肿瘤和自身免疫性疾病后的神经毒性将至关重要。
Immune effector cell-associated neurotoxicity syndrome (ICANS) is a prevalent condition seen after treatment with chimeric antigen receptor T-cell (CAR T) therapy and other cancer cell therapies. The underlying pathophysiology and neuropathology of the clinical syndrome are incompletely understood due to the limited availability of brain tissue evaluation from patient cases, and a lack of high-fidelity preclinical animal models for translational research.
Here, we present the cellular and tissue neuropathologic analysis of a patient who experienced grade 4 ICANS after treatment with anti-CD19 CAR T therapy for mantle cell lymphoma.
Our pathologic evaluation reveals a pattern of multifocal demyelinating leukoencephalopathy associated with a clinical course of severe ICANS. A focused analysis of glial subtypes further suggests region-specific oligodendrocyte lineage cell loss as a potential cellular and pathophysiologic correlate in severe ICANS.
We propose a framework for the continuum of neuropathologic changes thus far reported across ICANS cases. Future elucidation of the mechanistic processes underlying ICANS will be critical in minimizing neurotoxicity following CAR T-cell and related immunotherapy treatments across oncologic and autoimmune diseases.
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