更正:B7-H3 CAR T 细胞清除肝内胆管癌并诱导持久应答
Correction: B7-H3 CAR T cells eradicate intrahepatic cholangiocarcinoma and induce durable response.
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Correction: B7-H3 CAR T cells eradicate intrahepatic cholangiocarcinoma and induce durable response.
B7-H3 CAR T cells eradicate intrahepatic cholangiocarcinoma and induce durable response.
这些结果为在晚期 ICC 患者的临床试验中评估 iCas9.B7-H3 CAR T 细胞策略提供了有力依据。
Immunotherapy in advanced biliary tract cancer: current status and future directions.
3期TOPAZ-1和KEYNOTE-966试验现已确立免疫检查点抑制剂联合化疗作为新的标准一线方案,而2期IMbrave151试验正在评估增加抗血管生成治疗是否能提供进一步获益。
Advances and challenges in immunotherapy for intrahepatic cholangiocarcinoma based on the tumour immune microenvironment.
通过整合机制、临床证据、分子亚型和转化局限性,本综述为ICC中生物标志物指导的精准免疫治疗提供了一个平衡的框架。对肝内胆管癌免疫治疗的临床证据和局限性进行了批判性评估,重点强调了对更广泛胆道癌试验的ICC特异性解读。将ICC肿瘤免疫微环境整合到涉及基质、髓系、淋巴系和代谢调节的功能性免疫轴中。分子亚型和免疫相关生物标志物为ICC中生物标志物指导的精准免疫治疗提供了框架。当前ICC免疫治疗试验仍受限于异质性设计、ICC特异性队列较小以及临
Cellular and molecular networks governing precursor exhausted CD8+ T cells in chronic liver disease: Implications for immunotherapy.
多种病因引起的慢性肝病以及原发性肝癌构成了全球主要的健康负担,且治愈性治疗选择有限。
CAR-T cells directed toward PD-L1 demonstrate potent, antigen-specific activity against cholangiocarcinoma: A proof of concept study.
这些发现证明了第二代 PD-L1 CAR-T 细胞的可行性,展示了其临床前疗效和特异性,并验证了一种针对这些棘手癌症、靶向肿瘤微环境的治疗策略。
Current Status of Drug Treatment of Cholangiocarcinoma-Updated Progress and Critical Limitations.
胆管癌(CCA)是一种起源于胆道系统的高度致死性、异质性恶性肿瘤。
Overcoming heterogeneity and immunosuppression: novel strategies in adoptive therapy for biliary tract cancer.
本综述总结了过继性细胞疗法治疗胆道癌的最新进展,并讨论了促进临床转化的优化策略。
Enhancement of CAR-T cell activity against cholangiocarcinoma by simultaneous knockdown of six inhibitory membrane proteins.
我们的结果显示,敲低六重抑制分子的 PTG-T16R-scFV-CAR-T 细胞在体外和体内均表现出对胆管癌的强大免疫力和长期疗效。该策略为胆管癌提供了一种有效且个性化的免疫细胞治疗。
Preclinical development of mesothelin-targeting CAR T cells for the treatment of cholangiocarcinoma.
我们的结果提示,MSLN 是 CCA 中 CAR-T 细胞治疗一个有前景的靶点。
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