Department of Biochemistry, McMaster University, Hamilton, ON L8S 4L8, Canada.
Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON L8S 4L8, Canada.
STAR Protoc. 2020 Oct 7;1(3):100124. doi: 10.1016/j.xpro.2020.100124. eCollection 2020 Dec 18.
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).
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)。