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使用造血人源化模型评估脑癌的细胞免疫疗法的安全性。

Assessing the Safety of a Cell-Based Immunotherapy for Brain Cancers Using a Humanized Model of Hematopoiesis.

机构信息

Department of Biochemistry, McMaster University, Hamilton, ON L8S 4L8, Canada.

Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON L8S 4L8, Canada.

出版信息

STAR Protoc. 2020 Oct 7;1(3):100124. doi: 10.1016/j.xpro.2020.100124. eCollection 2020 Dec 18.

Abstract

Despite a surge in the preclinical development of immunotherapies, current models are unable to predict putative toxicity, particularly the "on-target, off-tumor" effects of these therapeutics. To address this gap, we used a humanized mouse model of hematopoiesis to examine the toxicity profile of CAR-Ts targeting brain tumor-antigens also expressed in the hematopoietic system. In assessing the safety of cell-based therapies, we aim to develop and integrate a preclinical evaluation protocol as a necessary step in the clinical development pathway. For complete details on the use and execution of this protocol, please refer to Vora et al. (2020).

摘要

尽管免疫疗法的临床前发展迅速,但目前的模型仍无法预测潜在的毒性,特别是这些治疗方法的“靶内、肿瘤外”效应。为了解决这一差距,我们使用了一种人源化造血小鼠模型,研究了针对也在造血系统中表达的脑肿瘤抗原的 CAR-T 细胞的毒性特征。在评估细胞治疗的安全性时,我们旨在开发并整合一个临床前评估方案,作为临床开发途径中的必要步骤。有关该方案的使用和执行的详细信息,请参阅 Vora 等人(2020 年)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4067/7756979/0f532fd09f6b/fx1.jpg

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