一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Granzyme B (GZMB)-Positive Tumor-Infiltrating Lymphocytes in Lung Adenocarcinoma: Significance as a Prognostic Factor and Association with Immunosuppressive Proteins.
Granzyme B (GZMB)-Positive Tumor-Infiltrating Lymphocytes in Lung Adenocarcinoma: Significance as a Prognostic Factor and Association with Immunosuppressive Proteins.
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我们分析了肺腺癌中的 GZMB+ TIL 计数,并阐明了其预后意义及其与 PD-L1 和 IDO1 的关联。
颗粒酶 B(GZMB)是细胞毒性淋巴细胞产生的一种丝氨酸蛋白酶,可反映TIL(肿瘤浸润淋巴细胞)中的抗肿瘤免疫反应活性;然而,GZMB⁺ TIL 在肺腺癌中的预后意义尚未得到充分了解。
分析了 2003 至 2012 年间在九州大学接受手术治疗的 273 例病理分期(pStage)I–IIIA 期肺腺癌患者。采用免疫组织化学评估 GZMB⁺ TIL 数量,以每 0.04 mm² 12 个细胞作为 GZMB⁺ TIL 的截断值,并将患者分为 GZMB 高表达组(n = 171)和低表达组(n = 102)。比较两组的临床病理特征及临床结局,同时评估肿瘤细胞中的程序性死亡配体-1(PD-L1)和吲哚胺 2,3-双加氧酶 1(IDO1)表达,并联合分析 GZMB⁺ TIL 与 PD-L1 或 IDO1 的预后关系。
GZMB 低表达与 pStage II–III、PD-L1 阳性及 IDO1 阳性显著相关。GZMB 低表达组的无病生存期(DFS)和总生存期(OS)均显著短于高表达组。多变量分析显示,GZMB 低表达是 DFS 和 OS 的独立预后因素。此外,GZMB⁺ TIL 与 PD-L1 或 IDO1 的联合预后分析显示,GZMB 低表达且这些免疫抑制蛋白高表达的患者预后最差。
本研究分析了肺腺癌中的 GZMB⁺ TIL 数量,阐明其预后意义及其与 PD-L1、IDO1 的关联。GZMB⁺ TIL 数量可能反映患者针对癌细胞的免疫状态,可作为肺腺癌有用的预后标志物。
Granzyme B (GZMB) is a serine protease produced by cytotoxic lymphocytes that reflects the activity of anti-tumor immune responses in tumor-infiltrating lymphocytes (TILs); however, the prognostic significance of GZMB+ TILs in lung adenocarcinoma is poorly understood.
We analyzed 273 patients with pathological stage (pStage) I-IIIA lung adenocarcinoma who underwent surgery at Kyushu University from 2003 to 2012. We evaluated GZMB+ TIL counts by immunohistochemistry. We set the cut-off values at 12 cells/0.04 mm 2 for GZMB+ TILs and divided the patients into GZMB-High (n = 171) and GZMB-Low (n = 102) groups. Then, we compared the clinicopathological characteristics of the two groups and clinical outcomes. Programmed cell death ligand-1 (PD-L1) and indoleamine 2,3-dioxygenase 1 (IDO1) expression in tumor cells was also evaluated, and combined prognostic analyses of GZMB+ TILs with PD-L1 or IDO1 were performed.
GZMB-Low was significantly associated with pStage II-III, PD-L1 positivity, and IDO1 positivity. Disease-free survival (DFS) and overall survival (OS) in the GZMB-Low group were significantly worse than in the GZMB-High group. In multivariable analysis, GZMB-Low was an independent prognostic factor for both DFS and OS. Furthermore, combined prognostic analyses of GZMB+ TILs with PD-L1 or IDO1 showed that GZMB-Low with high expression of these immunosuppressive proteins had the worst prognosis.
We analyzed GZMB+ TIL counts in lung adenocarcinoma and elucidated its prognostic significance and association with PD-L1 and IDO1. GZMB+ TIL counts might reflect the patient's immunity against cancer cells and could be a useful prognostic marker of lung adenocarcinoma.
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