肿瘤细胞治疗研究
FRONTIER PAPERS
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。
Nicotinamide mononucleotide potentiates the anti-tumor efficacy of CAR-NK cell therapy targeting MSLN in ovarian cancer.
IL-15 boosts mesothelin- and CD70-CAR NK cell potency in PDAC without added benefit from dual targeting.
CD33(KO)-CD33-mesothelin Loop CAR design avoids fratricide and improves efficacy of iNK cells against acute myeloid leukemia.
Loop CAR 赋予 UCB-NK 细胞和 hPSC-iNK 细胞更强的针对 CD33 + MSLN + 肿瘤细胞的细胞毒性。
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。
Chimeric antigen receptor NK cells for breast cancer immunotherapy.
Neoleukin-2/15-armored CAR-NK cells sustain superior therapeutic efficacy in solid tumors via c-Myc/NRF1 activation.
An innovative strategy harnessing self-activating CAR-NK cells to mitigate TGF-β1-driven immune suppression.
MEMBER ACCOUNT
登录成功会直接打开下一页。
