MSLN-CAR-T 细胞中开关受体 PD1/IL15Rβ 的表达克服实体瘤中的 PD1/PDL1 信号
Expression of the switch receptor PD1/IL15Rβ in MSLN-CAR-T cells overcomes PD1/PDL1 signaling in solid tumors.
FRONTIER PAPERS
Expression of the switch receptor PD1/IL15Rβ in MSLN-CAR-T cells overcomes PD1/PDL1 signaling in solid tumors.
Genome editing of immune checkpoints: CRISPR-mediated PD-1 inhibition in cancer.
Simultaneous targeting of Tim3 and A2a receptors modulates MSLN-CAR T cell antitumor function in a human cervical tumor xenograft model.
这些发现凸显了同时基因靶向 Tim3 和 A2a 受体以增强 CAR-T 细胞治疗实体瘤疗效的潜力。
CRISPR/Cas9-mediated TGFβRII disruption enhances anti-tumor efficacy of human chimeric antigen receptor T cells in vitro.
TGF RII KO 方法可能成为实体瘤免疫治疗中不可或缺的工具,因为它可能克服 T 细胞中一个关键的负调控信号通路。
Biogenic Selenium Nanoparticles Potentiate Anti-Mesothelin CAR-T Cell Therapy in a Syngeneic TNBC Model.
Current Developments of CAR-T and CAR-NK Cell Therapies for Ovarian Cancer.
Systematic Review of Available CAR-T Cell Trials around the World.
共 7 条
MEMBER ACCOUNT
登录成功会直接打开下一页。