决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Minimal/Measurable Disease Analysis in Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma by Flow Cytometry.
本文详细介绍了在纪念斯隆-凯特琳癌症中心开发的一种流式细胞术检测方法,该方法已证实在骨髓和外周血中能够持续达到高灵敏度(<0.01%的有核细胞),即使在CD19丢失或无法进行分析的情况下也是如此。
慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)是西方国家最常见的白血病。疾病进展缓慢,但多数患者在病程某个阶段需要治疗。除异基因移植外,治疗很少能治愈疾病,但通常可多年控制CLL/SLL表现。患者可能依次接受多线治疗以延长临床缓解。由于病程漫长,在承担造血系统肿瘤诊断和监测工作的流式细胞术实验室中,CLL/SLL监测占据相当大的工作量。微小/可测量残留病(MRD)监测已成为治疗监测和方案排序的关键环节。随着疗法日益有效,临床实验室需要以高精度和准确性监测比例越来越低的MRD。近期新增抗体和CAR-T细胞等靶向表面抗原的生物制剂后,由于流式分析常用抗原不再可用,检测任务变得更加复杂。本文详细介绍纪念斯隆凯特琳癌症中心开发的一项流式细胞术检测方法;即使CD19缺失或无法检测,该方法在骨髓和外周血中仍可稳定达到高灵敏度(低于有核细胞的0.01%)。此外,该检测有助于区分CLL与其他CD5阳性B细胞肿瘤。基础操作方案详细说明样本处理、染色和流式采集步骤;辅助方案介绍CLL/SLL MRD数据分析,以及区分CLL/SLL、其他B细胞肿瘤和正常CD5阳性B细胞的常用步骤及注意事项。©2022 Wiley Periodicals LLC。基础方案:处理、染色和流式分析骨髓或外周血细胞以检测CLL/SLL MRD。辅助方案:CLL MRD检测的分析与解释。
CLL/SLL is the most common leukemia in the western world. The disease is indolent; however, most patients require treatment at some point of the disease course. Outside of allogeneic transplants, the treatment is rarely curative but often controls CLL/SLL manifestations for many years. Several lines of therapy may be used sequentially to prolong clinical remission. Because of the prolonged disease course, CLL/SLL monitoring represents a sizable portion of the workload in a typical flow cytometry laboratory involved in the diagnosis and monitoring of hematopoietic neoplasms. Minimal/measurable disease monitoring of CLL/SLL has emerged as a key component in treatment monitoring and sequencing. In the face of effective therapies, clinical laboratories are tasked with monitoring ever smaller proportions of MRD with high precision and accuracy. With the recent addition of surface antigen-targeting biologics such as antibodies and CAR-T cells, the task has become more complex due to the unavailability of commonly analyzed antigens for flow cytometric analysis. This article details a flow cytometric test developed at Memorial Sloan Kettering Cancer Center that has proven to consistently achieve high sensitivity (<0.01% of nucleated cells) in the bone marrow and peripheral blood, even when CD19 is lost or unavailable for analysis. Moreover, the test helps distinguish between CLL and other CD5-positive B cell neoplasms. The Basic Protocol provides a detailed operational procedure for processing, staining, and cytometric acquisition of samples. The Support Protocol provides typical steps and caveats for MRD data analysis in CLL/SLL and in distinguishing CLL/SLL from other B cell neoplasms and normal CD5-positive B cells. 2022 Wiley Periodicals LLC. Basic Protocol: Processing, staining, and cytometric analysis of bone marrow or peripheral blood cells for MRD analysis of CLL/SLL Support Protocol: Analysis and interpretation of CLL MRD assay.
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