通过非病毒工程与高度多重碱基编辑精准增强 CAR-NK 细胞
Precision enhancement of CAR-NK cells through non-viral engineering and highly multiplexed base editing.
我们观察到高效的单重和多重碱基编辑,导致NK细胞在体外和体内的功能显著增强。
FRONTIER PAPERS
Precision enhancement of CAR-NK cells through non-viral engineering and highly multiplexed base editing.
我们观察到高效的单重和多重碱基编辑,导致NK细胞在体外和体内的功能显著增强。
Enhancing human NK cell antitumor function by knocking out SMAD4 to counteract TGFβ and activin A suppression.
转化生长因子 β(TGF-β)和活化素 A 抑制自然杀伤(NK)细胞的功能和增殖,限制了过继性 NK 细胞治疗的疗效。
Integration of ζ-deficient CARs into the CD3ζ gene conveys potent cytotoxicity in T and NK cells.
嵌合抗原受体(CAR)重定向免疫细胞在肿瘤学、自身免疫性疾病、移植医学和感染领域具有重要的治疗潜力。
CAR-T cell therapy in cancer immunotherapy - Biology, clinical successes, and emerging challenges: A review.
癌症免疫疗法通过使复发或难治性恶性肿瘤患者能够靶向激活抗肿瘤免疫应答,已彻底改变了肿瘤学领域。
Delineating MYC-Mediated Escape Mechanisms from Conventional and T Cell-Redirecting Therapeutic Antibodies.
MYC 高表达的肿瘤细胞通过几种互不重叠的机制削弱了治疗性抗体的疗效。
Allogeneic CAR-T cells with of HLA-A/B and TRAC disruption exhibit promising antitumor capacity against B cell malignancies.
nU-CAR-T19细胞在R/R B-ALL中显示出强烈反应。nU-CAR-T19细胞有潜力成为治疗R/R B细胞恶性肿瘤的一种有前景的新方法。
Preclinical Evaluation of CRISPR-Edited CAR-NK-92 Cells for Off-the-Shelf Treatment of AML and B-ALL.
这些结果表明,CD19-CAR和CD276-CAR-NK-92细胞系的细胞毒性表现适合用于白血病杀伤,使其成为有前景的现货型治疗候选药物。
Current Anti-Myeloma Chimeric Antigen Receptor-T Cells: Novel Targets and Methods.
研究正在探索在更早期阶段使用CAR-T,包括在诊断时使用,以期替代ASCT。
Current Landscape of Adoptive Cell Therapy and Challenge to Develop "Off-The-Shelf" Therapy for Hepatocellular Carcinoma.
过继性细胞治疗(ACT)是一种免疫疗法,将自体或异体免疫细胞,如TIL(肿瘤浸润淋巴细胞)或工程化淋巴细胞,输注给癌症患者以清除恶性细胞。
CD45-Directed CAR-T Cells with CD45 Knockout Efficiently Kill Myeloid Leukemia and Lymphoma Cells In Vitro Even after Extended Culture.
我们报道了高效且持久活性的CD45 ko /CAR-T细胞的高效制备。CD45敲除并未损害CAR-T细胞的体外功能,无论靶抗原如何。如果其活性能在体内得到证实,CD45 ko /CD45CAR-T细胞可能例如作为干细胞移植前预处理方案的组成部分而有用。
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