T细胞受体
细胞毒性T细胞
T细胞
表位
生物
嵌合抗原受体
癌症研究
免疫学
细胞生物学
抗原
免疫系统
体外
生物化学
作者
Enric Vercher,Ángela Covo-Vergara,Enrique Conde,Mercedes Hernández-Rueda,Edurne Elizalde,Uxua Mancheño,Javier Glez‐Vaz,Ibón Tamayo,Maritza Roxana García-García,Marta Ferrer-Roig,Javier Marañón-Lopez,David Repáraz,Marta Ruiz,Ascensión López-Díaz de Cerio,Susana Inogés,Mercedes Iñarrairaegui,Juan José Lasarte,Bruno Sangro,Pablo Sarobe,Sandra Hervás‐Stubbs
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2024-11-26
标识
DOI:10.1097/hep.0000000000001175
摘要
Glypican-3 (GPC3) is a promising target for T-cell therapy in hepatocellular carcinoma (HCC). While chimeric antigen receptor (CAR) T cells targeting GPC3 have demonstrated therapeutic efficacy, their effectiveness is limited by challenges such as low persistence and shedding of surface GPC3. Natural T-cell receptors (TCRs) may serve as an alternative, though identifying GPC3-specific TCRs within the endogenous repertoire is difficult.
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