肿瘤细胞治疗研究
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Leukemic Stem Cell-Targeted Liposomal Nanoimmunotherapy Reverses Immune Evasion and Inhibits Fusion Oncoprotein-Driven Acute Myeloid Leukemia by Silen
急性髓系白血病（AML）是一种由白血病干细胞和免疫逃逸驱动的常见且侵袭性强的血液系统恶性肿瘤。
Ex vivo pretreatment with venetoclax boosts antileukemic efficacy of therapeutic γδ T cells in AML models.
这些结果表明，短期抑制BCL-2能增强γδ T细胞的细胞毒性和持久性。
Phase 1 Study of KITE-222, an Autologous CLL-1-Directed CAR T-cell Therapy in Patients with Relapsed/Refractory Acute Myeloid Leukemia.
尽管生产成功且安全性可接受，KITE-222缺乏初步疗效，需要未来研究解决CLL-1异质性并着重改善体内扩增和抗肿瘤活性。
The search for safe and effective CAR-T targets in AML.
急性髓系白血病（AML）仍是一种高度侵袭性的恶性肿瘤，治疗选择有限，长期生存较差。
Progress in reprogramming failed graft-versus-leukemia immunity in acute myeloid leukemia relapse after allogeneic transplantation.
急性髓系白血病（AML）异基因造血干细胞移植（allo-HSCT）后复发影响40-50%的受者，并且仍然是移植后死亡的主要原因；中位总生存期约为5个月，1年生存率低于20%。
Baiting-enhanced extravasation of lipid nanoparticles for targeted co-delivery of decitabine and siTNF-α to the bone marrow niche in leukemia therapy.
急性髓系白血病（AML）仍然是一种致命性恶性肿瘤，由于药物生物利用度有限以及保护性骨髓微环境内的治疗耐药性，其预后较差。
Venetoclax for elderly patients with acute myeloid leukaemia unfit for intensive chemotherapy: Prospects, resistance mechanisms and management strateg
然而，约30%的患者对基于venetoclax的联合方案无应答，且大多数初始应答者最终会复发。
Novel targeted therapy and cellular immunotherapy enabling allogeneic hematopoietic stem cell transplantation for relapsed/refractory acute myeloid le
复发或难治性（R/R）急性髓系白血病（AML）患者的预后极差。
Engineering CLL-1 CAR-NK cells via mRNA-LNP for potent antitumor activity and reversal of HLA-E-mediated resistance in acute myeloid leukemia.
瞬时、非整合的 mRNA LNP 转染的 CLL-1 CAR-NK 细胞为 MDR AML 提供了一种安全有效的策略。
Therapeutic ecology of the fiber-microbiota-barrier axis in leukemia: resilience, immune recovery and pharmacomicrobiomics.
白血病诊疗是生态系统压力下的一项临床实验。
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