肿瘤细胞治疗研究
MODALITY HUB
FOR TREATMENT
按「中国试验优先 → 正在招募 → 更新更近」排序。信息来自 ClinicalTrials.gov 与 CDE 公开登记。能否入组、费用与可及性，以登记原文和主治医生判断为准。
FOR RESEARCH
Erratum to "CircRNA-based CD19-targeted CAR-NK therapy for B-cell acute lymphoblastic leukemia using a Coccidioides immitis-derived group II intron pl
Pluripotent stem cell-derived CAR-NK progenitor therapy targets minimal residual disease and prevents relapse in leukemia models.
降低化疗后的复发率仍是提高肿瘤治疗疗效的一大挑战。
Donor-derived CD19-targeted CAR-NK cells induce complete remission in a child with relapsed B-ALL after failure of blinatumomab and autologous CD19-ta
复发仍是儿童 B 细胞急性淋巴细胞白血病（B-ALL）治疗失败和死亡的主要原因。
CircRNA-based CD19-targeted CAR-NK therapy for B-cell acute lymphoblastic Leukemia using a Coccidioides immitis-derived group II intron platform.
这些结果支持基于circRNA的CAR-NK疗法作为提高癌症免疫治疗安全性和有效性的一种有效方法的潜力。
Overcoming Resistance and Relapse in CAR-T and CAR-NK Cell Therapies: From Bench to Bedside.
作为开创性的免疫治疗手段，CAR-T 细胞与NK 细胞（CAR-NK）疗法在治疗多种血液系统恶性肿瘤时已显示出显著的临床疗效。
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。
Combination of targeted pharmacotherapy and immunotherapy with anti-CD19 CAR NK cells in acute lymphoblastic leukemia.
这些数据表明 aCD19 CAR NK 细胞作为 BCP-ALL 联合治疗组成部分的潜力，应在临床试验中进一步评估。
Tumor-priming CD8(+) natural killer T-like cells as an efficient novel cell therapy for relapsed/refractory multiple myeloma.
TPNC 是一种通过肿瘤驱动的致敏产生的新型细胞毒性淋巴细胞产品。
Constitutive IL-7 signaling promotes CAR-NK cell survival in the solid tumor microenvironment but impairs tumor control.
C7R在不依赖外源性信号的情况下促进了CAR-NK细胞在恶劣TMEs中的存活，但在体内导致抗肿瘤功能不佳。我们的数据揭示了持续性IL-7信号传导对CAR-NK细胞的有害作用，并为在尝试增强CAR-NK细胞抗肿瘤活性时合理应用细胞因子信号提供了见解。
iPSC-derived NK cells with site-specific integration of CAR19 and IL24 at the multi-copy rDNA locus enhanced antitumor activity and proliferation.
利用诱导多能干细胞（iPSC）制备嵌合抗原受体修饰的自然杀伤（CAR-NK）细胞，已成为生产现货型通用免疫疗法的范式之一。
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