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.
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
Cellular and molecular networks governing precursor exhausted CD8+ T cells in chronic liver disease: Implications for immunotherapy.
CAR-T cells directed toward PD-L1 demonstrate potent, antigen-specific activity against cholangiocarcinoma: A proof of concept study.
Current Status of Drug Treatment of Cholangiocarcinoma-Updated Progress and Critical Limitations.
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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