转移性上皮癌来源的 TIL(肿瘤浸润淋巴细胞)识别自体肿瘤类器官与临床疗效的相关性
Correlation between recognition of autologous tumor organoids by tumor-infiltrating lymphocytes from metastatic epithelial cancers and clinical respon
转移性上皮癌患者中,TIL 对自体肿瘤类器官的反应性似乎与客观临床缓解相关。
FRONTIER PAPERS
Correlation between recognition of autologous tumor organoids by tumor-infiltrating lymphocytes from metastatic epithelial cancers and clinical respon
转移性上皮癌患者中,TIL 对自体肿瘤类器官的反应性似乎与客观临床缓解相关。
Tightly bound T-cell clusters: A new class of hyper-effector tumor killers.
这些见解将T细胞聚类重新定位为有效抗肿瘤免疫的基本决定因素。
Going with the Flow: Circulating Tumor-Reactive Lymphocytes Stream into Cancer Therapy.
过继性细胞治疗(ACT),迄今最典型的代表是CAR-T 细胞、工程化 T 细胞受体和TIL(肿瘤浸润淋巴细胞)治疗,已成为癌症免疫治疗中一种具有变革性的方法。
Intentional heterogeneity in autologous cell-based gene therapies: strategic considerations for first-in-human trials.
基于细胞的基因疗法,包括CAR-T、TCR-T和TIL疗法,已经改变了某些癌症的治疗格局,但其在实体瘤中的疗效仍然有限。
Expert consensus guidelines on management and best practices for tumor-infiltrating lymphocyte cell therapy.
自体、体外扩增的TIL(肿瘤浸润淋巴细胞)过继性细胞疗法正在被研究用于治疗实体瘤,并在临床试验中显示出强劲的疗效。
Internal checkpoint regulates T cell neoantigen reactivity and susceptibility to PD1 blockade.
CISH 负向调控人 T 细胞效应功能,其基因敲除为提升过继性 TIL 疗法的疗效提供了新途径。
Targeting T-Cells for Cancer Treatment: Current Clinical Strategies and Challenges.
对靶向肿瘤细胞的免疫应答进行调节已被证明是一种成功的癌症治疗策略。
Algorithm guided personalized T cell therapy: machine learning unlocks next generation TCR engineered immunotherapy.
本研究旨在强调利用ML平台统一过继性T细胞疗法的多样性与精准性,从而实现快速、个性化地筛选肿瘤反应性克隆,用于下一代实体瘤免疫治疗。
The atypical IκB factor IκBδ enhances CD8 T cell accumulation and effector functions in solid tumors.
肿瘤抵御免疫控制的两个突出机制是:限制 T 细胞和 CAR T 细胞在肿瘤中存活和扩增的能力,以及抑制其维持完整细胞毒能力的能力。
Expansion of tumor-infiltrating and marrow-infiltrating lymphocytes from pediatric malignant solid tumors.
来自儿童实体瘤的TIL和MIL扩增成功,包括全规模扩增过程。这些数据支持在儿童人群中转化为ACT-TIL治疗策略,因此计划在儿童高危实体瘤中开展ACT-TIL的I期试验。
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