GPC3 嵌合抗原受体 (CAR)-NK 细胞联合 Enoblituzumab 增强抗肝细胞癌疗效
GPC3 chimeric antigen receptor (CAR)-NK cells combined with Enoblituzumab enhance the anti-tumor efficacy against hepatocellular carcinoma.
肿瘤细胞治疗研究
FRONTIER PAPERS
近 5 年肿瘤细胞治疗领域的研究论文,按发表时间由近到远排列。期刊指标供参考,不代表单项研究的证据强度。
GPC3 chimeric antigen receptor (CAR)-NK cells combined with Enoblituzumab enhance the anti-tumor efficacy against hepatocellular carcinoma.
Bispecific CAR-T cells targeting FAP and GPC3 have the potential to treat hepatocellular carcinoma.
Nonviral mcDNA-mediated bispecific CAR T cells kill tumor cells in an experimental mouse model of hepatocellular carcinoma.
我们的研究表明,通过非病毒 mcDNA 载体制备双特异性 CAR-T 细胞具有更高的效率和安全性。CoG133-CAR-T 细胞通过双抗原识别和内部激活增强了肿瘤抑制能力。这为 HCC 乃至实体瘤的 CAR-T 治疗提供了一种创新策略。
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