CD2 共刺激桥接强效 CAR 诱导的细胞溶解与持久存续
CD2 costimulation bridges potent CAR-induced cytolysis and durable persistence.
CD2 胞质尾部与 CD3z 联合可提供平衡的共刺激,将快速的肿瘤减灭与 T 细胞持久性相偶联。
肿瘤细胞治疗研究
FRONTIER PAPERS
近 5 年肿瘤细胞治疗领域的研究论文。默认按评分排序(权威性 + 新鲜度)。
CD2 costimulation bridges potent CAR-induced cytolysis and durable persistence.
CD2 胞质尾部与 CD3z 联合可提供平衡的共刺激,将快速的肿瘤减灭与 T 细胞持久性相偶联。
Preparation and anti-tumor applications of universal umbilical cord blood-derived, mesothelin-targeted CAR-T cells.
Decoding the role of mesothelin in tumor dynamics and targeted treatment innovations.
Mesothelin antigen density influences anti-mesothelin chimeric antigen receptor T cell cytotoxicity.
这些数据凸显了针对一组表达不同水平靶肿瘤抗原的细胞(如同人类肿瘤中的情况)评估 CAR 构建体的价值。
Tumor resistance to anti-mesothelin CAR-T cells caused by binding to shed mesothelin is overcome by targeting a juxtamembrane epitope.
Development of Highly Effective Anti-Mesothelin hYP218 Chimeric Antigen Receptor T Cells With Increased Tumor Infiltration and Persistence for Treatin
Chimeric antigen receptor T cells engineered to recognize the P329G-mutated Fc part of effector-silenced tumor antigen-targeting human IgG1 antibodies
靶向 P329G 的 CAR-T 细胞联合含 P329G Fc 突变的人 IgG1 抗原结合抗体,在不同实体瘤模型中介导了显著的体外和体内效应功能,值得进一步推进该概念的临床转化。
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