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:Richter transformation: emerging immunologic strategies beyond chemoimmunotherapy.
Richter转化(RT)是一种侵袭性淋巴瘤,发生于慢性淋巴细胞白血病(CLL)患者,最常见为弥漫大B细胞淋巴瘤(DLBCL-RT)。
Richter转化(RT)是一种侵袭性淋巴瘤,发生于慢性淋巴细胞白血病(CLL)患者,最常见为弥漫大B细胞淋巴瘤(DLBCL-RT)。传统化学免疫治疗下结局仍然不佳,反映了基因组不稳定性增加和DNA修复受损在RT发病机制中的作用。用于CLL的靶向治疗(BTK或BCL2抑制)在RT中显示出疗效;然而,持久疾病控制仍然难以实现,凸显了免疫学方法的必要性。本综述讨论了支持免疫学方法用于RT的临床证据,重点关注异基因干细胞移植、嵌合抗原T细胞(CAR T细胞)治疗、双特异性T细胞导向抗体和检查点抑制。异基因干细胞移植可在选定患者中提供长期缓解;然而,存在相当大的障碍,如需要患者具备足够的体能状态和移植前疾病控制。上市后观察性研究提供了CAR T细胞治疗疗效和安全性的证据,以及免疫毒性风险的证据。双特异性抗体和检查点抑制的早期阶段研究已证明具有疾病活性,多项联合策略研究正在进行中。未来优先事项包括优化免疫治疗前的疾病控制、测试新型联合方法以及开展相关性研究以优化未来治疗策略。
Richter transformation (RT) is an aggressive lymphoma that arises in patients with chronic lymphocytic leukemia (CLL), most commonly diffuse large B-cell lymphoma (DLBCL-RT). Outcomes remain poor with conventional chemoimmunotherapy, reflecting the role of increased genomic instability and impaired DNA repair in the pathogenesis of RT.. Targeted therapies used in CLL (BTK or BCL2 inhibition) have shown efficacy in RT; however, durable disease control remains elusive, highlighting the need for immunological approaches. This review discusses the clinical evidence supporting immunologic approaches in RT, focusing on allogeneic stem cell transplantation, chimeric antigen T-cell (CAR T-cell) therapy, bispecific T-cell directing antibodies, and checkpoint inhibition. Allogeneic stem cell transplantation can provide long-term remission in selected patients; however, there are considerable barriers, such as the requirement for adequate patient fitness and pre-transplant disease control. Post-approval observational studies have provided evidence of the efficacy and safety of CAR T-cell therapy, as well as the risk of immunologic toxicity. Early phase studies on bispecific antibodies and checkpoint inhibition have demonstrated disease activity, and multiple studies on combination strategies are ongoing. Future priorities include optimizing disease control prior to immunologic therapy, testing novel combination approaches and conducting correlative studies to optimize future therapeutic strategies.
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