OR7A10 GPCR 工程增强 CAR-NK 疗法对抗实体瘤
OR7A10 GPCR engineering boosts CAR-NK therapy against solid tumours.
我们确定并全面验证了OR7A10,一种G蛋白偶联受体(GPCR),作为最佳候选。
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OR7A10 GPCR engineering boosts CAR-NK therapy against solid tumours.
我们确定并全面验证了OR7A10,一种G蛋白偶联受体(GPCR),作为最佳候选。
A new immunotherapy ROR: Proximal ROR1 domain targeting breast cancer via monoclonal antibodies and CAR NK cells.
Harnessing immunity against breast cancer: from checkpoints to cell therapies.
乳腺癌(BC)仍是全球女性癌症相关死亡的首要原因,也是疾病负担的主要贡献者。
Evaluation of Efficacy and Safety of Chimeric Antigen Receptor-Natural Killer (CAR-NK) Cells in Breast Cancer: A Systematic Review and Meta-Analysis.
在汇总的临床前分析中,CAR-NK 相较于未处理对照和未修饰/模拟对照显著降低了肿瘤负荷(ROM 分别为 0.311 [0.22-0.44] 和 0.42 [0.33-0.53],p < 0.001)。
Engineering Human MAIT Cells with Chimeric Antigen Receptors for Cancer Immunotherapy.
用嵌合Ag受体(CAR)工程化免疫细胞是癌症免疫治疗中一项有前景的技术。
Redirecting cytotoxic lymphocytes to breast cancer tumors via metabolite-sensing receptors.
细胞毒性淋巴细胞向实体瘤的浸润不足,限制了免疫疗法与细胞疗法的疗效。
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