TIL 治疗进展:拓展黑色素瘤之外的视野
Advances in TIL therapy: Expanding the horizons beyond melanoma.
TIL(肿瘤浸润淋巴细胞)疗法代表着实体瘤治疗的突破,满足了选择有限患者的未满足需求。
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Advances in TIL therapy: Expanding the horizons beyond melanoma.
TIL(肿瘤浸润淋巴细胞)疗法代表着实体瘤治疗的突破,满足了选择有限患者的未满足需求。
Lung Cancer Adoptive Cell Therapy: Inspiring TIL ACT Comes Center Stage.
Schoenfeld 及其同事在本期报告中指出,在接受 lifileucel(一种基于自体 TIL(肿瘤浸润淋巴细胞)的细胞治疗产品)治疗的晚期非小细胞肺癌患者中,6/28 例(21.4%)取得了可测量的客观缓解率。
Novel growth pattern-specific digital marker of TILs improves stratification of lung adenocarcinoma patients.
我们的研究结果显示,GPS-TILs 对总生存期具有强大的预后价值(p < 0.0001,C-index = 0.59),优于传统的基于 TIL 的指标和基于形态学的分层方法。
CD4(+) tumor-infiltrating lymphocytes secreting T cell-engagers induce regression of autologous patient-derived non-small cell lung cancer xenografts.
TIL(肿瘤浸润淋巴细胞)的过继转移在黑色素瘤中显示出显著效果,但在其他癌症中临床获益有限,即使在 TIL 经过基因改造以改善其肿瘤归巢、细胞毒性潜力或克服细胞耗竭之后也是如此。
Tertiary lymphoid structure-related immune infiltrates in NSCLC tumor lesions correlate with low tumor-reactivity of TIL products.
NSCLC 肿瘤中免疫细胞浸润的组成与扩增 TIL 产物的功能性相关。
Functional and molecular characterization of PD1(+) tumor-infiltrating lymphocytes from lung cancer patients.
抗体介导的肿瘤免疫治疗靶向抑制性表面分子,如 PD1、PD-L1 和 CTLA-4,旨在重新激活功能失调的 T 细胞。
Mechanisms of resistance to adoptive cell therapy with tumor-infiltrating lymphocytes.
TIL-ACT 在特定用途之外显示出前景,但其成功取决于能否克服由患者、肿瘤和产品因素驱动的耐药性。要提高其疗效,需要精细的患者选择、TIL 优化以及机制性见解,以指导新的、改进的治疗方法。
A hexamerization-enhanced, Fc-silenced agonistic CD27 antibody amplifies T-cell effector functions as single agent and in combination with PD-1 blocka
HexaBody-CD27 以不依赖 Fc R 交联的方式增强 T 细胞活化和效应功能,且不诱导 T 细胞耗竭。
Tumor-Infiltrating Lymphocytes and Adoptive Cell Therapy: State of the Art in Colorectal, Breast and Lung Cancer.
我们对 TIL(肿瘤浸润淋巴细胞)(TILs)的认识正在迅速扩展。
Cardiac Toxicity Associated with Cancer Immunotherapy and Biological Drugs.
癌症免疫治疗显著改善了癌症患者的预后。
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