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:Synchronous presentation of pH+ B cell acute lymphoblastic leukemia and chronic lymphocytic leukemia treated with blinatumomab.
采用单克隆抗体和CAR-T(CAR-T)细胞疗法的 CD19 靶向免疫治疗,已在复发/难治性非霍奇金淋巴瘤(NHL)和慢性淋巴细胞白血病(CLL)中显示出治疗疗效。
靶向CD19的单克隆抗体和CAR-T(CAR-T)细胞疗法已在非霍奇金淋巴瘤(NHL)和慢性淋巴细胞白血病(CLL)的复发/难治情境中显示疗效。然而,靶向CD19的T细胞接合双特异性抗体blinatumomab目前仅获批用于B细胞急性淋巴细胞白血病(ALL),在CLL等其他临床情境中的研究很少。我们报告一例同时患有费城染色体阳性(Ph+)ALL和CLL的患者,接受blinatumomab治疗后,两种疾病均达到微小残留病(MRD)阴性缓解。
CD19 directed immunotherapy with monoclonal antibodies and chimeric antigen receptor T (CAR-T) cell therapy has shown treatment efficacy in the relapsed/refractory setting for non-Hodgkin's lymphoma (NHL) and chronic lymphocytic leukemia (CLL). However, the CD19 directed bispecific T-cell engager, blinatumomab, is currently only approved in B-cell acute lymphoblastic leukemia (ALL) and has largely not been investigated in other clinical contexts for CLL. We report a case of a patient who presented with both Philadelphia chromosome positive (pH+) ALL and CLL who achieved measurable residual disease (MRD) negative remission for both diseases with blinatumomab.
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