可扩展生成靶向实体瘤的造血干细胞工程化现成单特异性细胞毒性 T 细胞
Scalable generation of hematopoietic stem cell-engineered off-the-shelf mono-specific cytotoxic T cells targeting solid tumors.
实体瘤的过继性T细胞治疗受到自体制造复杂性的限制,而在异体环境中还存在移植物抗宿主病(GvHD)、HLA限制和供者变异性等风险。
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Scalable generation of hematopoietic stem cell-engineered off-the-shelf mono-specific cytotoxic T cells targeting solid tumors.
实体瘤的过继性T细胞治疗受到自体制造复杂性的限制,而在异体环境中还存在移植物抗宿主病(GvHD)、HLA限制和供者变异性等风险。
Human cancer-targeted immunity via transgenic hematopoietic stem cell progeny.
这些结果表明,转基因HSCs可用于在人类参与者中生成自我更新的肿瘤特异性细胞免疫治疗来源。
Human cDC1 enhance cytotoxic function of CD226+ terminally exhausted tumor-infiltrating lymphocytes.
预防或逆转T细胞耗竭是癌症免疫治疗的主要目标。
Downregulation of HLA class II is associated with relapse after allogeneic stem cell transplantation and alters recognition by antigen-specific T cell
白血病细胞中供受者错配 HLA 等位基因的基因组缺失是异基因造血干细胞移植(HSCT)后复发的主要原因。
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