工程化 CAR-T 来源外泌体共递送 miR-145 与细胞毒性蛋白用于靶向实体瘤治疗
Engineered CAR-T-Derived Exosomes Co-Delivering miR-145 and Cytotoxic Proteins for Targeted Solid Tumour Therapy.
CAR-T 细胞疗法在血液系统恶性肿瘤中展现出显著疗效,但在实体瘤中仍受限于肿瘤渗透不足、免疫抑制微环境及细胞因子释放综合征(CRS)风险。
FRONTIER PAPERS
Engineered CAR-T-Derived Exosomes Co-Delivering miR-145 and Cytotoxic Proteins for Targeted Solid Tumour Therapy.
CAR-T 细胞疗法在血液系统恶性肿瘤中展现出显著疗效,但在实体瘤中仍受限于肿瘤渗透不足、免疫抑制微环境及细胞因子释放综合征(CRS)风险。
PVR Mediates Resistance to IL21.CD276.CAR-T Therapy in Esophageal Squamous Cell Carcinoma.
嵌合抗原受体(CAR)-T疗法在实体瘤中已取得部分疗效,但其整体有效性仍然有限。
Advances and challenges in immunotherapy for advanced esophageal squamous cell carcinoma.
尽管免疫治疗已显著改善晚期 ESCC 患者的预后并拓展了治疗前景,但仍需进一步研究以阐明耐药机制、优化治疗策略并识别可靠的预测性生物标志物。
Recent developments in immunotherapy for gastrointestinal tract cancers.
过去几十年见证了胃肠道(GI)肿瘤免疫治疗的兴起。
A novel microenvironment regulated system CAR-T (MRS.CAR-T) for immunotherapeutic treatment of esophageal squamous carcinoma.
CAR-T 细胞免疫治疗在血液系统恶性肿瘤的治疗中已取得令人鼓舞的疗效。
CAR T cells targeting B7H3 demonstrate potent preclinical activity against AML and ESCC.
本研究为AML和ESCC的CAR-T治疗提供了一个新靶点,以促进临床治疗策略的发展。
Harnessing NKG2D CAR-T cells with radiotherapy: a novel approach for esophageal squamous cell carcinoma treatment.
我们首次阐明了NKG2D CAR-T细胞在ESCC中的治疗疗效,以及其与放疗联合时的增强效应,为ESCC患者提供了一种新的治疗策略。
CCR5 and IL-12 co-expression in CAR T cells improves antitumor efficacy by reprogramming tumor microenvironment in solid tumors.
实体瘤的嵌合抗原受体(CAR)T 细胞治疗面临重大挑战,包括浸润不足、增殖有限、CAR T 细胞效应功能减弱以及免疫抑制性肿瘤微环境(TME)。
Immunotherapy resistance in esophageal cancer: Possible mechanisms and clinical implications.
然而,EC患者免疫治疗的总体缓解率(ORR)低于30%,且大多数初始接受免疫治疗的患者可能随时间推移出现获得性耐药(AR)。
Study on the in vitro and in vivo killing effects of PD-1 antibody-secreting c-Met-targeted CAR-T cells on esophageal cancer cell line ECA109.
c-Met/PD-1 CAR-T 细胞被成功构建,并表现出对 ECA109 食管癌细胞的显著体外和体内杀伤作用。
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