使用人源化小鼠测量 CAR T 细胞激发的巨噬细胞和单核细胞系细胞在体外和体内分泌人类 IL-6 的方法。

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2024-12-20 Epub Date: 2024-11-01 DOI:10.1016/j.xpro.2024.103423
Thao Nguyen, Toshiaki Yoshikawa, Yusuke Ito, Hitomi Kasuya, Takahiro Nakashima, Sachiko Okamoto, Yasunori Amaishi, Haosong Zhang, Yang Li, Tetsuya Matsukawa, Satoshi Inoue, Yuki Kagoya
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引用次数: 0

摘要

嵌合抗原受体(CAR)T细胞疗法经常会引起严重的毒性反应,如细胞因子释放综合征(CRS),这主要是由单核细胞系细胞分泌的白细胞介素-6(IL-6)引起的。在此,我们介绍了一种生成抗 CD19 CAR T 细胞的方案,并对与 CAR T 细胞和靶肿瘤细胞体外共培养的人类单核细胞衍生 IL-6 进行了量化。我们进一步介绍了生成人源化小鼠模型并评估体内 CAR T 细胞相关血浆 IL-6 水平的方案。有关该方案使用和执行的完整细节,请参阅 Yoshikawa 等人的文章1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Protocol to measure human IL-6 secretion from CAR T cell-primed macrophage and monocyte lineage cells in vitro and in vivo using humanized mice.

Chimeric antigen receptor (CAR) T cell therapy often causes serious toxicities, such as cytokine release syndrome (CRS), mainly due to interleukin-6 (IL-6) secreted by monocyte lineage cells. Here, we describe a protocol to generate anti-CD19 CAR T cells and quantify human monocyte-derived IL-6 cocultured with CAR T cells and target tumor cells in vitro. We further describe a protocol to generate a humanized mouse model and evaluate CAR T cell-associated plasma IL-6 levels in vivo. For complete details on the use and execution of this protocol, please refer to Yoshikawa et al.1.

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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
期刊介绍:
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