辐照 CD19 嵌合抗原受体 YTS 细胞保留抗肿瘤活性并可作为自体 CAR-T 疗法的可规模化替代方案
Irradiated CD19 chimeric antigen receptor YTS cells retain antitumor activity and offer a scalable alternative to autologous CAR-T therapy.
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Irradiated CD19 chimeric antigen receptor YTS cells retain antitumor activity and offer a scalable alternative to autologous CAR-T therapy.
Coexpression of GITRL confers resistance to Treg cell-mediated immunosuppression to anti-CD19 CAR-NK cells.
这些数据将 CAR19-GITRL-NK 细胞定位为一种有效的创新策略,将直接肿瘤靶向与主动破坏 Treg 驱动的免疫抑制结合起来,用于治疗 B 细胞白血病和淋巴瘤。
Durable response to CAR T is associated with elevated activation and clonotypic expansion of the cytotoxic native T cell repertoire.
2B4 co-stimulation and dasatinib modulation enhance anti-CD19 CAR-NK-92 cell cytotoxicity.
这些结果凸显了选择 NK 特异性共刺激结构域以及利用可逆的 Src 家族激酶抑制来优化 CAR-NK 性能的重要性。使用 NK-92 细胞使得能够对 CAR 信号传导和药理学效应进行可控的机制性剖析,为在原发性 NK 细胞中工程化下一代 CAR-NK 疗法提供了具有转化相关性的见解。嵌合抗原受体(CAR)为基础的疗法已经改变了癌症治疗,尤其是对血液系统恶性肿瘤。虽然共刺激结构域的选择是 CAR-T 成功的公认决定因素,但 CAR-自然杀
CAR-T cell therapy in cancer immunotherapy - Biology, clinical successes, and emerging challenges: A review.
Charting a killer course to the solid tumor: strategies to recruit and activate NK cells in the tumor microenvironment.
Engineering NK-CAR.19 cells with the IL-15/IL-15Rα complex improved proliferation and anti-tumor effect in vivo.
Lipid nanoparticle mediated delivery of Anti-CD19 CAR mRNA to umbilical cord blood NK cells for targeting CD19⁺ primary B-ALL cells.
Beyond CAR-T: The Rise of CAR-NK/T Cells for Haematological Cancer.
CAR-NK/T 细胞可能被证明是治疗血液系统恶性肿瘤的一种更安全、更灵活的细胞疗法。
Efficacy of chimeric antigen receptor engineered natural killer cells in the treatment of hematologic malignancies: a systematic review and meta-analy
在临床前模型中,CAR-NK 在血液系统恶性肿瘤的治疗中展现出前景。
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