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:TA-TMA occurring after sequential CD7 CAR-T cell therapy and allogeneic hematopoietic stem cell transplantation: a case report.
目前,CAR-T细胞治疗桥接异基因造血干细胞移植(allo-HSCT)已成为难治/复发性血液系统恶性肿瘤的关键治疗策略。
目前,CAR-T细胞治疗桥接异基因造血干细胞移植(allo-HSCT)已成为难治/复发性血液系统恶性肿瘤的关键治疗策略。CD7CAR-T(CAR-T)细胞联合allo-HSCT的序贯治疗,为T淋巴系恶性肿瘤、CD7高表达急性髓系白血病(AML)及混合表型急性白血病(MPAL)提供了一种新的治疗途径。该策略规避了传统清髓性预处理化疗和免疫抑制剂的毒性,同时实现肿瘤清除、造血重建及移植物抗宿主病(GVHD)的预防。移植相关血栓性微血管病(TA-TMA)是allo-HSCT后罕见但危及生命的并发症,与非复发死亡率(NRM)升高相关。本文报道1例MPAL患者在接受CD7 CAR-T桥接allo-HSCT后发生早发性TA-TMA的病例。本研究旨在提高临床医生对CAR-T桥接allo-HSCT后TA-TMA诊断与管理的认识,为早期识别和及时干预提供参考,进一步改善患者预后。
Currently, CAR-T cell therapy bridging to allogeneic hematopoietic stem cell transplantation (allo-HSCT) has become a pivotal therapeutic strategy for refractory/relapsed hematologic malignancies. Sequential therapy with CD7 chimeric antigen receptor T (CAR-T) cells combined with allo-HSCT provides a novel therapeutic approach for T-lymphoid malignancies, CD7-highly expressed acute myeloid leukemia (AML), and mixed phenotype acute leukemia (MPAL). This strategy circumvents the toxicities of conventional myeloablative conditioning chemotherapy and immunosuppressive agents, while achieving tumor eradication, hematopoietic reconstitution, and prevention of graft-versus-host disease (GVHD). Transplant-associated thrombotic microangiopathy (TA-TMA) is a rare but life-threatening complication following allo-HSCT, associated with elevated non-relapse mortality (NRM). This article reports a case of early-onset TA-TMA in a patient with MPAL after CD7 CAR-T bridging to allo-HSCT. This study aims to enhance clinicians' awareness of the diagnosis and management of TA-TMA following CAR-T bridging to allo-HSCT, provide a reference for early identification and timely intervention, and further improve patient outcomes.
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