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:The Clinical Significance of Circulating Lymphocytes Morphology in Diffuse Large B-Cell Lymphoma As Determined by a Novel, Highly Sensitive Microscopy.
The Clinical Significance of Circulating Lymphocytes Morphology in Diffuse Large B-Cell Lymphoma As Determined by a Novel, Highly Sensitive Microscopy.
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CAR-T 细胞疗法已成为复发/难治性弥漫大B细胞淋巴瘤(DLBCL)患者的优选治疗。由于缺少有关CAR-T 形态学的数据且检测灵敏度低,通过外周血涂片(PBS)识别CAR-T 具有挑战性。
本研究利用新型数字显微镜方法全视野形态学(FFM)开展高灵敏度PBS分析,确定CAR-T 在生产过程中及患者体内的形态演变。生产第8天,转导CAR-T 细胞中42.7±10.8%呈活化形态,而未转导细胞中为9.3±3.8%。
此外,转导CAR-T 与靶细胞接触后,呈活化形态的细胞进一步增加至83±5.6%。在患者中,获得完全缓解者第5天CAR-T 平均数量显著更高,且持续存在时间更长。第14天活化形态CAR-T 数量较高与细胞因子释放风暴持续时间延长相关。
总体而言,CAR-T 形态呈异质性;与靶细胞接触后,活化形态主要见于转导细胞。输注后检测到CAR-T 与完全缓解率增加相关。对PBS开展FFM CAR-T 监测可能是一种简便、低成本的方法,可为这种治疗提供具有临床意义的信息。
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.
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