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:To BE or to PE: Prime editors provide more choices for epitope-editing-based immunotherapy.
表位编辑是一种有前景的策略,可保护造血细胞免受免疫治疗的清除。
表位编辑是一种有前景的策略,可保护造血细胞免遭免疫疗法清除。近期,Ji等人在《Cell Stem Cell》发表研究,将碱基编辑(BE)和先导编辑(PE)用于改变造血干细胞中的CD123表位,以配合CAR-T疗法治疗急性髓系白血病。
Epitope editing is a promising strategy for protecting hematopoietic cells from eradication by immunotherapies. Recently, in Cell Stem Cell, Ji et al. applied both base editing (BE) and prime editing (PE) to alter the epitope of CD123 in hematopoietic stem cells for CAR-T therapy against acute myeloid leukemia. 1 .
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