Fridberg Gil, Horn Galit, Globerson Levin Anat, Benisty Dan, Kay Sigi, Glait-Santar Chen, Perry Chava, Ram Ron, Avivi Irit, Katz Ben-Zion
The Hematology Division, Tel Aviv Sourasky Medical Center, Tel Aviv 6423906, Israel.
Immunology and Advanced CAR-T Therapy Laboratory, Tel Aviv Sourasky Medical Center, Dotan Center for Advanced Therapies, Tel Aviv Sourasky Medical Center, Tel Aviv University, Tel Aviv 6423906, Israel.
Cancers (Basel). 2023 Nov 28;15(23):5611. doi: 10.3390/cancers15235611.
Chimeric Antigen Receptor T-cell (CAR T) therapy has become the preferable treatment in relapsed/refractory diffuse large B-cell lymphomas (DLBCL) patients. Detection of CAR Ts in peripheral blood smear (PBS) is challenging due to insufficient data regarding their morphology and low sensitivity. The morphological evolution of CAR Ts along their production process, and in patients, was established by Full-Field Morphology (FFM), a novel digital microscopy approach that provides highly sensitive PBS analysis. At day 8 of production, 42.7 ± 10.8% of the CAR T transduced cells exhibited activated morphology compared with 9.3 ± 3.8% in untransduced cells. Moreover, engagement of transduced CAR Ts with target cells resulted in further morphological transformation into activated morphology (83 ± 5.6% of the cells). In patients, the average number of day 5 CAR Ts, and their sustained presence, were significantly higher in patients obtaining complete response. A high number of activated morphology CAR Ts at day 14 was associated with prolonged cytokine release storm. Overall, CAR Ts exhibited heterogeneous morphology, with the activated morphology attributed predominantly to transduced cells following engagement with target cells. Post-transfusion CAR T detection was associated with increased complete responses. FFM CAR T surveillance in PBS may serve as a simple inexpensive method to provide clinically relevant insights into this treatment modality.
嵌合抗原受体T细胞(CAR T)疗法已成为复发/难治性弥漫性大B细胞淋巴瘤(DLBCL)患者的首选治疗方法。由于关于CAR T细胞形态的数据不足且灵敏度较低,在外周血涂片(PBS)中检测CAR T细胞具有挑战性。通过全场形态学(FFM)建立了CAR T细胞在其生产过程中以及在患者体内的形态演变,FFM是一种新型数字显微镜方法,可提供高度灵敏的PBS分析。在生产第8天,42.7±10.8%的CAR T转导细胞呈现活化形态,而未转导细胞中这一比例为9.3±3.8%。此外,转导的CAR T细胞与靶细胞的结合导致其进一步形态转变为活化形态(83±5.6%的细胞)。在患者中,获得完全缓解的患者在第5天的CAR T细胞平均数量及其持续存在显著更高。第14天大量具有活化形态的CAR T细胞与细胞因子释放风暴延长相关。总体而言,CAR T细胞呈现出异质性形态,活化形态主要归因于与靶细胞结合后的转导细胞。输血后CAR T细胞检测与完全缓解率增加相关。PBS中的FFM CAR T细胞监测可作为一种简单廉价的方法,为这种治疗方式提供临床相关见解。