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:Acute T-cell lymphoblastic leukemia: chimeric antigen receptor technology may offer a new hope.
急性淋巴细胞白血病(ALL)是一种累及造血系统的常见恶性肿瘤,包括B细胞ALL(B-ALL)和T细胞ALL(T-ALL)。
急性淋巴细胞白血病(ALL)是一种累及造血系统的常见恶性肿瘤,包括B细胞ALL(B-ALL)和T细胞ALL(T-ALL)。T-ALL以骨髓中T细胞祖细胞增殖为特征,治疗面临重大挑战,尽管化疗和造血干细胞移植(HSCT)取得了进展,患者仍常出现高复发率和较差的长期生存。本综述探讨了T-ALL的发病机制和传统治疗策略,强调了嵌合抗原受体(CAR)技术在克服当前治疗局限性方面的广阔前景。CAR疗法利用基因修饰的免疫细胞靶向白血病特异性抗原,为T-ALL治疗提供了一种新颖且精准的方法。本综述批判性地分析了CAR-T和CAR-NK细胞疗法的最新进展、其常见靶点、优化策略、临床结局及相关挑战,全面概述了其在T-ALL治疗中的临床前景。
Acute lymphoblastic leukemia (ALL) is a prevalent malignancy affecting the hematopoietic system, encompassing both B-cell ALL (B-ALL) and T-cell ALL (T-ALL). T-ALL, characterized by the proliferation of T-cell progenitors in the bone marrow, presents significant treatment challenges, with patients often experiencing high relapse rates and poor long-term survival despite advances in chemotherapy and hematopoietic stem cell transplantation (HSCT). This review explores the pathogenesis and traditional treatment strategies of T-ALL, emphasizing the promising potential of chimeric antigen receptor (CAR) technology in overcoming current therapeutic limitations. CAR therapy, leveraging genetically modified immune cells to target leukemia-specific antigens, offers a novel and precise approach to T-ALL treatment. The review critically analyzes recent developments in CAR-T and CAR-NK cell therapies, their common targets, optimization strategies, clinical outcomes, and the associated challenges, providing a comprehensive overview of their clinical prospects in T-ALL treatment.
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