为肝细胞癌武装 GPC3 CAR T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
FRONTIER PAPERS
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
Large language model-guided CAR-T in silico platform for cytokine optimization in liver cancer with low antigen density.
CAR-T 细胞疗法在血液系统恶性肿瘤中已取得显著成功,但由于抗原异质性、靶抗原密度低以及免疫抑制性肿瘤微环境(TME),其在肝癌等实体瘤中仍然受限。
CAR-T cell therapy in hepatocellular carcinoma: from mechanistic insights to clinical translation.
嵌合抗原受体(CAR)-T细胞疗法已经改变了肿瘤免疫治疗,在血液系统肿瘤中实现了持久的完全缓解。
Interleukin-15-armoured GPC3 CAR T cells for patients with solid cancers.
这些结果共同表明,IL-15 可增强 GPC3 CAR T 细胞在患者体内的扩增、瘤内存活和抗肿瘤活性。
rhIL-7-hyFc, a long-acting interleukin-7, improves efficacy of CAR-T cell therapy in solid tumors.
本研究为 NT-I7 联合 CAR-T 细胞治疗人类实体瘤提供了依据。
Targeting Lin28 axis enhances glypican-3-CAR T cell efficacy against hepatic tumor initiating cell population.
我们的结果表明,抑制Lin28B可降低IDO1和PD-L1表达,并增强GPC3-CART细胞对HCC的免疫治疗潜力。
Integrated therapies for targeting the microenvironment of hepatocellular carcinoma.
肝细胞癌(HCC)微环境(MEs)由免疫和非免疫成分组成,这些成分驱动肿瘤进展和治疗耐药。
Cell surface oncofetal antigens in prostate cancer: therapeutic potential and radioligand targeting.
CEACAM5、Trop-2、5T4、GPC3和ROR1癌胚蛋白在晚期前列腺癌中表达各异。针对这些蛋白的治疗药物和放射性药物显像剂正在研发中。尽管已出现令人振奋的发现,但仍需大量临床研究来确定靶向这些蛋白的价值。
Non-coding RNAs in cancer immunotherapy: Predictive biomarkers and targets.
本综述总结了在接受不同免疫治疗模式(包括单克隆抗体、小分子抑制剂、癌症疫苗和 CAR-T 细胞)治疗的癌症患者中报道的重要预测性 ncRNA 生物标志物。
Human VH-based chimeric antigen receptor T cells targeting glypican 3 eliminate tumors in preclinical models of HCC.
我们的发现表明,与靶向近膜表位相比,改变靶向 GPC3 远端表位的纳米抗体 CAR 的铰链区和跨膜结构域,可导致强健的 T 细胞信号传导,并诱导快速且持久地清除肝细胞癌(HCC)肿瘤。
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