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流式细胞术检测与定量实体瘤内 CAR-T 细胞

英文原题:Flow cytometry detection and quantification of CAR T cells into solid tumors.

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Flow cytometry detection and quantification of CAR T cells into solid tumors.

PubMed 2021/08/11(内容时间) Methods Cell Biol

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中文摘要

过继T细胞治疗(ACT)是一种治疗方法,通过基因改造患者自体T细胞来靶向并清除恶性肿瘤。将靶向CD19表达B细胞的嵌合抗原受体(CAR)用于这一新型治疗方法后,急性B细胞淋巴细胞白血病治疗取得显著成功。然而,血液系统恶性肿瘤仅占影响患者的癌症的一部分。遗憾的是,ACT用于靶向实体恶性肿瘤仅取得有限成功。实体瘤患者CAR-T 细胞治疗存在许多已知障碍,其中一个突出障碍是CAR-T 细胞无法有效迁移至肿瘤部位。随着可增强CAR-T 细胞浸润实体瘤的新方法和靶点迅速发展,需要建立标准化方法评估和测量CAR-T 细胞浸润,以便跨平台比较不同方案。本文介绍一种流式细胞术方法,可快速检测并定量静脉注射后到达并进入肿瘤组织的CAR-T 细胞。要获得最佳结果,需要具备单细胞制备和流式细胞术操作能力。

展开英文摘要原文

Adoptive T cell therapy (ACT) is a therapeutic approach which employs genetically manipulated autologous T cells to target and eliminate a patient's malignancy. This novel therapeutic approach, when employing a chimeric antigen receptor (CAR) targeting CD19-expressing B cells, has shown remarkable success in treating acute B-cell lymphocytic leukemia.

However, blood born malignancies represent only a fraction of cancers which affect patients. Unfortunately, the utilization of ACT to target solid malignancies has only shown marginal success rates. There are many known obstacles which hinder CAR T cell therapy in patients suffering from solid cancer, one notable obstacle is the effective trafficking of CAR T cells to the tumor site.

With the rapid advancement of novel approaches and targets which may enhance CAR T cell infiltration into solid tumors, a standardized approach to assess and measure CAR T cell infiltration becomes imperative in order to compare these different approaches across platforms.

Here we describe a flow cytometry method which enables the rapid detection and quantification of CAR T cells which have reached and entered the tumor mass following intravenous injection. Competence with single cell preparation and flow cytometry is required for optimal results.

论文信息

作者
Tokarew NJA、Gosálvez JS、Nottebrock A、Briukhovestka D、Endres S、Cadilha BL、Kobold S
第一作者单位
Center of Integrated Protein Science Munich (CIPS-M) and Division of Clinical Pharmacology, Department of Medicine IV, Klinikum der Universität München, LMU, Munich, Germany.Germany
通讯作者单位
Center of Integrated Protein Science Munich (CIPS-M) and Division of Clinical Pharmacology, Department of Medicine IV, Klinikum der Universität München, LMU, Munich, Germany; German Center for Translational Cancer Research (DKTK), partner site Munich, Munich, Germany; Einheit für Klinische Pharmakologie (EKLiP), Helmholtz Zentrum München, German Research Center for Environmental Health (HMGU), Neuherberg, Germany. Electronic address: sebastian.kobold@med.uni-muenchen.de.Germany
文献类型
非美国政府资助研究
期刊
Methods in cell biology2022
原文标识
PubMed 35153001 · DOI 10.1016/bs.mcb.2021.06.015