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Dual Targeting with CAR T Cells to Limit Antigen Escape in Multiple Myeloma

机译:与CAR T细胞的双重靶向限制多发性骨髓瘤的抗原逃逸

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摘要

Adoptive T-cell therapy targeting a single tumor antigen can induce remissions of hematologic cancers but relapses often occur due to the outgrowth of tumor cells with absent or low expression of the antigen. Strategies to simultaneousy target multiple antigens are needed to fully capitalize on the promise of this therapeutic strategy. In this issue of Blood Cancer Discovery, Fernandez de Larrea and colleagues demonstrate in preclinical models of multiple myeloma that targeting BCMA and GPRC5D simultaneously with T cells engineered to express chimeric antigen receptors specific for these antigens may prevent tumor cell escape.
机译:靶向单个肿瘤抗原的产物T细胞疗法可以诱导血液学癌症的缓解,但由于肿瘤细胞的生长而经常发生复发,而肿瘤细胞的生长没有抗原的表达或低表达。 需要同时靶向多种抗原的策略,以充分利用这种治疗策略的承诺。 在这一问题的发现中,Fernandez de Larrea和同事在多发性骨髓瘤的临床前模型中证明,与设计用于表达针对这些抗原特有的嵌合抗原受体的T细胞同时靶向BCMA和GPRC5D可能会预防肿瘤细胞逃逸。

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