肿瘤细胞治疗研究
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Quantitative assessment of extravasation of IL-15-secreting MSLN-CAR-NK-92 cells using tumor transparency imaging.
结合这些结果，抗癌免疫细胞的血管外渗效率可被视为评估为靶向胰腺癌的 NK 细胞所设计的 CAR 结构有效性的一个有价值指标。
Rapid CAR screening and circRNA-driven CAR-NK cells for persistent shed-resistant immunotherapy.
One-step knock-in CAR constructs in human NK cells enable scalable, TGFβ1-resistant immunotherapy for solid tumors.
我们采用无病毒、一步工程化策略，设计了稳健的、抗 TGF 1 的同种异体 CAR-NK 细胞，建立了一种通用且临床可规模化的方法，用于工程化改造代谢增强的 CAR-NK 细胞，使其能够克服实体瘤中 TME 介导的免疫抑制。
Synergistic immunotherapeutic effects of irreversible electroporation and CAR-NK cell therapy against hepatocellular carcinoma.
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。
Chemical priming potentiates mesothelin-targeting chimeric antigen receptor-engineered NK-92 antitumor activity by improving tumor trafficking and cyt
这些发现表明，化学预处理可增强 CAR-NK 细胞功能，并提供了一种有前景的非基因策略来提升 CAR-NK 细胞对实体瘤模型的活性。
Natural killer cell membrane manipulation for augmented immune synapse and anticancer efficacy.
A chimeric antigen receptor tailored to integrate complementary activation signals potentiates the antitumor activity of NK cells.
因此，基于 NK 受体的结构域为 NK-CAR 设计的未来带来了巨大希望，可能具有显著的治疗益处。
IL-7Rα signaling potentiates the anti-tumor activity of NK92 cells.
IL-7R-IM 的表达赋予 NK 和 CAR-NK 细胞细胞因子非依赖性以及强效的抗肿瘤活性。该策略为提高用于临床应用的现货型 NK 细胞疗法的持久性与疗效提供了一种切实可行的解决方案。
An innovative strategy harnessing self-activating CAR-NK cells to mitigate TGF-β1-driven immune suppression.
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