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基于纵向阻抗肿瘤细胞活力测量的连续杀伤试验——评估 T 细胞性能的实用方法

英文原题:Serial Killing Assay Using Longitudinal Impedance-Based Tumor Cell Viability Measurement - A Useful Method to Assess T Cell Performance.

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Serial Killing Assay Using Longitudinal Impedance-Based Tumor Cell Viability Measurement - A Useful Method to Assess T Cell Performance.

PubMed 2025/12/30(内容时间) J Vis Exp Q3 · IF 1.2(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)细胞疗法革新了特定血液系统恶性肿瘤的治疗。然而,相当一部分患者会因抗原丢失、抗原下调或T细胞耗竭而复发。这些挑战凸显了开发功能实验的必要性,以评估慢性抗原刺激下CAR-T 细胞的杀伤能力和持久性。连续杀伤实验通过测量CAR-T 细胞反复清除肿瘤靶细胞的能力,可深入评估CAR-T 应答的持久性和效力。本文介绍一种采用实时细胞分析(RTCA)系统的基于阻抗实验,用于定量测定CAR-T 细胞在体外的连续杀伤能力。肿瘤细胞需反复接种于实验专用E-plate并贴壁,随后按设定效靶(E:T)比加入CAR-T 细胞。该平台无需标记即可连续监测肿瘤细胞活力,以较高时间分辨率记录动态细胞毒性。

核心读数包括细胞指数(CI)动力学、肿瘤细胞杀伤速率和靶细胞清除所需时间。随着肿瘤靶细胞反复刺激而观察到杀伤能力逐步下降,可作为CAR-T 细胞功能障碍(通常称为T细胞耗竭)的指标。这些指标有助于精确评估不同E:T比下CAR-T 细胞功能,并直接比较不同CAR-T 构建体或联合治疗随时间变化的表现。为提高成本效益,我们开发了实验板清洗流程,可在不影响实验性能或数据完整性的前提下重复使用E-plate。优化后的流程降低了实验成本,同时保持分析稳健性。该方法可经济、规模化地开展CAR-T 细胞功能临床前评估,促进细胞疗法设计改进。

展开英文摘要原文

Chimeric antigen receptor (CAR) cell therapy has revolutionized the treatment of specific hematologic malignancies.

However, a significant portion of patients experience relapse because of antigen loss, antigen downregulation, or T cell exhaustion. These challenges highlight the need for functional assays that can evaluate the killing capacity and persistence of CAR T cells under chronic antigen stimulation. Serial killing assays, which measure the ability of CAR T cells to repeatedly eliminate tumor targets, offer valuable insights into the durability and potency of CAR T cell responses.

Here, we present an impedance-based assay using the Real-Time Cell Analysis (RTCA) system to quantify CAR T cell-mediated serial killing in vitro. Tumor cells are repeatedly seeded and allowed to adhere to assay-specific E-plates before the addition of CAR T cells at defined effector-to-target (E:T) ratios.

The platform continuously monitors tumor cell viability without labels, capturing dynamic cytotoxicity with high temporal resolution. Core readouts include Cell Index (CI) kinetics, tumor-cell killing rate, and time-to-target clearance. The progressive decline in killing capacity observed upon repeated tumor-target engagements serves as a marker of acquired CAR T cell dysfunction, often termed T cell exhaustion.

Together, these metrics allow precise evaluation of CAR T cell function at various E:T ratios and enable direct comparison among different CAR T cell constructs or co-treatments over time. To enhance cost efficiency, we developed a plate-washing procedure that enables the reuse of assay E-plates without compromising assay performance or data integrity.

The optimized workflow reduces assay cost while preserving analytical robustness. This approach enables affordable and scalable preclinical assessment of CAR T cell function, facilitating improvements in cell-therapy design.

论文信息

作者
Tschaidse T、Trefny MP、Carlini E、Andreu-Sanz D、Michaelides S、Nguyen NTT、Kobold S
第一作者单位
Division of Clinical Pharmacology, LMU University Hospital; Department of General, Visceral and Transplantation Surgery, LMU University Hospital.
通讯作者单位
Division of Clinical Pharmacology, LMU University Hospital; German Cancer Consortium (DKTK), Partner Site Munich, a partnership between the DKFZ and the University Hospital of the LMU; German Center for Lung Research (DZL); Einheit für Klinische Pharmakologie (EKLiP), Helmholtz Zentrum München - German Research Center for Environmental Health Neuherberg; sebastian.kobold@med.uni-muenchen.de.Germany
文献类型
音视频资料 · 非美国政府资助研究
期刊
Journal of visualized experiments : JoVE2025 Dec 30
原文标识
PubMed 41554019 · DOI 10.3791/69623