人源 CART22.19 治疗难治性儿童 B-ALL:指定患者队列的启示
Human CART22.19 therapy in refractory pediatric B-ALL: insights from a named-patient cohort.
CART22.19 疗法在高危儿科人群中显示出良好的安全性特征和有前景的临床活性,其双靶向设计使 CD19 阴性白血病获得疾病控制。
FRONTIER PAPERS
Human CART22.19 therapy in refractory pediatric B-ALL: insights from a named-patient cohort.
CART22.19 疗法在高危儿科人群中显示出良好的安全性特征和有前景的临床活性,其双靶向设计使 CD19 阴性白血病获得疾病控制。
CD19/CD22 targeting with cotransduced CAR T cells to prevent antigen-negative relapse after CAR T-cell therapy for B-cell ALL.
这些数据提示,通过共转导实现双靶向可能预防 CAR-T 细胞治疗后的抗原阴性复发。
CAR T cells with dual targeting of CD19 and CD22 in pediatric and young adult patients with relapsed or refractory B cell acute lymphoblastic leukemia
我们开展了一项针对复发或难治性B-ALL儿童及年轻成人患者(n = 15)的1期试验,以测试AUTO3——表达抗CD19和抗CD22 CAR的自体转导T细胞(AMELIA试验,EUDRA CT 2016-004680-39)。
Efficient manufacturing of CAR-T cells from whole blood: a scalable approach to reduce costs and enhance accessibility in cancer therapy.
可从全血中成功制备具有治疗相关剂量的 CD19/CD22 CAR-T 细胞。
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