靶向白血病干细胞的脂质体纳米免疫疗法通过沉默 B 细胞淋巴瘤 2 逆转免疫逃逸并抑制融合癌蛋白驱动的急性髓系白血病
Leukemic Stem Cell-Targeted Liposomal Nanoimmunotherapy Reverses Immune Evasion and Inhibits Fusion Oncoprotein-Driven Acute Myeloid Leukemia by Silen
FRONTIER PAPERS
Leukemic Stem Cell-Targeted Liposomal Nanoimmunotherapy Reverses Immune Evasion and Inhibits Fusion Oncoprotein-Driven Acute Myeloid Leukemia by Silen
A phase 1 trial of CD123-directed chimeric antigen receptor T-cell therapy in adults with relapsed/refractory acute myeloid leukemia or blastic plasma
CD123 靶向 CAR-T 细胞疗法在 r/r AML 和 BPDCN 患者中是可行的,并显示出良好的安全性特征,包括既往接受过 alloHCT 的患者。尽管估计的总体完全缓解率不高,但这些发现为进一步优化 CD123 CAR-T 细胞设计、患者选择和联合策略提供了基础。
The search for safe and effective CAR-T targets in AML.
Antibody format matters: A comparative analysis of VHH and scFv domains reveals superior in vivo CAR T cell function with VHH domains.
Exploring CAR cell therapies beyond CAR-T for myeloid malignancies.
Progress in reprogramming failed graft-versus-leukemia immunity in acute myeloid leukemia relapse after allogeneic transplantation.
Novel targeted therapy and cellular immunotherapy enabling allogeneic hematopoietic stem cell transplantation for relapsed/refractory acute myeloid le
Quantifying target antigen-dependent CAR T-cell performance against AML.
Evaluation of multi-antigen targeting ADCC strategies in pediatric BCP-ALL.
因此,CD24 成为 BCP-ALL 中的一个有效靶点,而 CD24 与 CD123 的联合则是一种潜在的有效双靶向策略。应测试不同识别模式(例如 CAR 和 CD16)的联合,以确定其是否在三靶向中提供协同的细胞毒性活性。
Emerging strategies in CAR-T cell therapy for acute myeloid leukemia: overcoming heterogeneity and improving safety through dual-antigen targeting.
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