RORing CAR-T 细胞在实体瘤与血液肿瘤中:相同却不同
RORing CAR T Cells in Solid and Hematologic Cancers: Same but Different.
FRONTIER PAPERS
RORing CAR T Cells in Solid and Hematologic Cancers: Same but Different.
Immunotherapies for Breast Cancer: From Checkpoint Inhibition to Emerging Cellular Therapies.
Inducible localized delivery of an anti-PD-1 scFv enhances anti-tumor activity of ROR1 CAR-T cells in TNBC.
我们下一代靶向 ROR1 的诱导型装甲 CAR 平台,仅在靶肿瘤细胞存在时释放免疫刺激载荷,从而增强 CAR-T 细胞的治疗活性。
Tumour assessment of ROR1 levels in various adult leukaemia and lymphoma types.
CAR-T cell therapy for triple-negative breast cancer and other solid tumors: preclinical and clinical progress.
CAR-T 细胞治疗的一个挑战是选择最佳靶点以尽量减少靶向/脱靶毒性。抗原丢失和内在异质性导致的肿瘤逃逸是进一步的障碍。TROP2、GD2、ROR1、MUC1 和 EpCAM 是有前景的靶点。通过应用带有趋化因子受体和/或组成性激活的白细胞介素受体的 CAR,可能增强持久性和向肿瘤细胞的迁移。第四代 CAR(TRUCKs)可能重定向 T 细胞以实现通用的细胞因子介导的杀伤。联合策略以及将 CAR 应用于其他免疫细胞可能逆转实体肿瘤所特有
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