TCR-JANUS 衔接蛋白实现双特异性靶向以克服 TCR-T 细胞治疗中的肿瘤异质性
TCR-JANUS engager proteins enable bispecific targeting to overcome tumor heterogeneity in TCR-T cell therapy.
基于 T 细胞受体(TCR)的免疫疗法受限于肿瘤抗原异质性,后者常导致复发。
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TCR-JANUS engager proteins enable bispecific targeting to overcome tumor heterogeneity in TCR-T cell therapy.
基于 T 细胞受体(TCR)的免疫疗法受限于肿瘤抗原异质性,后者常导致复发。
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。
A modular γδ TCR-T platform combining KRAS pMHC targeting with re-dosable mRNA engager redirection.
当抗原表达发生变化或限制性人类白细胞抗原(HLA)等位基因丢失时,实体瘤常能逃逸TCR工程化T细胞的攻击。
Programmable engineered bacteria manipulate metabolism and remodel the TME in situ for enhancing adoptive cell therapy.
我们的研究结果共同表明,工程化细菌是可编程的免疫代谢调节剂,能够在实体瘤中实现有效且安全的 ACT。
Advances and prospects in cell therapy for cancer: explorations from T cells to stem cells.
全球癌症负担日益加重,亟需创新的治疗策略。
Extracellular ATP-P2RY2 signaling drives intratumoral prostaglandin E2 accumulation and adaptive resistance to immunotherapy in solid tumors.
细胞外 ATP(eATP)在肿瘤微环境(TME)中蓄积,其代谢产物腺苷被认为可促进免疫抑制通路。
Breathing new life into T-cell receptor-engineered T-cell therapy in solid tumors: enhancing strategies to expand the universality of precision therap
过继性 T 细胞转移疗法(ACT)显著推动了肿瘤免疫治疗的进展。
De novo engineered disulfide bond supersedes native interchain linkage to enhance TCR pairing and anti-tumor efficacy in T cell therapy.
T 细胞受体工程化 T 细胞(TCR-T)疗法被认为在治疗实体瘤方面极具前景。
Engineered TCR-T cells secreting IFNα/anti-PD-L1 potentiate endogenous immunity to synergistically bolster the efficacy against solid tumors.
T 细胞受体工程化 T 细胞(TCR-T)疗法是治疗实体瘤的一种有前景的方法。
Clonotype-Resolved Single-Cell Multi-Omics Unlocks the Profile of Tumor-Infiltrating CD39⁺CD8⁺ T Cells and Enables Adoptive Cell Therapy for Solid Tum
肿瘤反应性T细胞是肿瘤免疫治疗的核心,而免疫检查点抑制剂(ICI)通过解除对肿瘤反应性T细胞的免疫抑制,彻底改变了治疗格局,但应答率仍不尽如人意。
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