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嵌合抗原受体T细胞相关神经毒性的新型病理生理学见解。

Novel pathophysiological insights into CAR-T cell associated neurotoxicity.

作者信息

Genoud Vassilis, Migliorini Denis

机构信息

Department of Oncology, University Hospital of Geneva, Geneva, Switzerland.

Center for Translational Research in Onco-Haematology, University of Geneva, Geneva, Switzerland.

出版信息

Front Neurol. 2023 Mar 8;14:1108297. doi: 10.3389/fneur.2023.1108297. eCollection 2023.

Abstract

Chimeric antigen receptor (CAR) T cell therapy represents a scientific breakthrough in the treatment of advanced hematological malignancies. It relies on cell engineering to direct the powerful cytotoxic T-cell activity toward tumor cells. Nevertheless, these highly powerful cell therapies can trigger substantial toxicities such as cytokine release syndrome (CRS) and immune cell-associated neurological syndrome (ICANS). These potentially fatal side effects are now better understood and managed in the clinic but still require intensive patient follow-up and management. Some specific mechanisms seem associated with the development of ICANS, such as cytokine surge caused by activated CAR-T cells, off-tumor targeting of CD19, and vascular leak. Therapeutic tools are being developed aiming at obtaining better control of toxicity. In this review, we focus on the current understanding of ICANS, novel findings, and current gaps.

摘要

嵌合抗原受体(CAR)T细胞疗法是晚期血液系统恶性肿瘤治疗领域的一项科学突破。它依靠细胞工程技术,引导强大的细胞毒性T细胞活性作用于肿瘤细胞。然而,这些强大的细胞疗法会引发诸如细胞因子释放综合征(CRS)和免疫细胞相关神经综合征(ICANS)等严重毒性反应。目前,这些潜在的致命副作用在临床上已得到更好的理解和管理,但仍需要对患者进行密切随访和管理。一些特定机制似乎与ICANS的发生有关,例如活化的CAR-T细胞引起的细胞因子激增、CD19的脱瘤靶向作用以及血管渗漏。目前正在开发治疗工具,旨在更好地控制毒性。在这篇综述中,我们重点关注对ICANS的当前认识、新发现以及当前存在的差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b60/10031128/f5534c6f6cf1/fneur-14-1108297-g0001.jpg

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