CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Serial Killing Assay Using Longitudinal Impedance-Based Tumor Cell Viability Measurement - A Useful Method to Assess T Cell Performance.
Serial Killing Assay Using Longitudinal Impedance-Based Tumor Cell Viability Measurement - A Useful Method to Assess T Cell Performance.
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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。
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.
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