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

被引:6
|
作者
Nie, Esther H. [1 ,5 ]
Ahmadian, Saman S. [2 ]
Bharadwaj, Sushma N. [3 ,4 ]
Acosta-Alvarez, Lehi [1 ]
Threlkeld, Zachary D. [1 ]
Frank, Matthew J. [3 ,4 ]
Miklos, David B. [3 ,4 ]
Monje, Michelle [1 ]
Scott, Brian J. [1 ]
Vogel, Hannes [2 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA USA
[2] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA USA
[3] Stanford Univ, Sch Med, Dept Med, Div Blood & Marrow Transplantat & Cellular Therapy, Stanford, CA USA
[4] Stanford Univ, Sch Med, Dept Med, Div Hematol Oncol, Stanford, CA USA
[5] Stanford Hlth Care, Ctr Acad Med CAM, Dept Neurol & Neurol Sci, 453 Quarry Rd, Palo Alto, CA 94304 USA
来源
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY | 2023年 / 82卷 / 02期
关键词
Chimeric antigen receptor T-cell (CAR T) therapy; Immune effector cell-associated neurotoxicity syndrome (ICANS); Immunotherapy; Mantle cell lymphoma; Multifocal demyelinating leukoencephalopathy; Neurotoxicity; Oligodendrocyte progenitor cell; IMMUNOTHERAPY;
D O I
10.1093/jnen/nlac121
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:160 / 168
页数:9
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