间皮素作为癌症免疫治疗的生物标志物和治疗靶点
Mesothelin as Biomarker and Therapeutic Target for Immunotherapy in Cancer.
癌症仍是一个关键的全球健康问题,原因在于发现晚、耐药和高死亡率。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A novel semi-quantitative scoring method for CD8+ tumor-infiltrating lymphocytes based on infiltration sites in gastric cancer.
A novel semi-quantitative scoring method for CD8+ tumor-infiltrating lymphocytes based on infiltration sites in gastric cancer.
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目前尚无既定方法用于评估胃癌(GC)中的TIL(肿瘤浸润淋巴细胞)(TILs),其在GC中基于浸润部位的临床意义仍不明确。
在本研究中,我们开发了一种根据浸润部位评估TILs的方法,作为GC的预后标志物。我们回顾性分析了103例接受根治性切除的晚期GC患者。位于浸润边缘(TIL IM)和肿瘤中心(TIL CT)的TILs通过CD8+ T细胞的免疫组化染色进行半定量评分。TIL IM和TIL CT评分之和被定义为TILs评分。基于该评分,患者被分为低TILs组和高TILs组。还评估了定量TILs以验证半定量评分方法。
此外,我们在体外证实了CD8+ T细胞在GC细胞系中共培养所产生的肿瘤抑制效应。在单因素分析中,与高TIL IM患者相比,低TIL IM患者显著更可能为女性、更年轻,并具有未分化组织学类型和更深的肿瘤浸润。同样,低TIL CT患者的淋巴结转移阳性显著多于高TIL CT患者。在多因素分析中,更深的肿瘤浸润和阳性淋巴结转移分别被确定为低TIL IM和低TIL CT患者的独立危险因素。根据我们的半定量TILs评分方法,低TILs组与高TILs组相比预后显著更差。该组具有显著更大的肿瘤直径、更深的肿瘤浸润和更多的阳性淋巴结转移。
此外,更深的肿瘤侵袭是低 TILs 组的独立危险因素。定量 TILs 分析显示,低 TILs 组的 TIL 水平显著低于高 TILs 组。在体外,CD8+ T 细胞以浓度依赖性方式诱导 GC 细胞凋亡。
此外,这些细胞显著抑制了 GC 细胞的增殖、迁移和侵袭能力。我们针对 CD8+ TILs 的简单且通用的半定量评分方法表明,CD8+ TILs 是敏感的预后标志物。低 TILs 组准确反映了低定量 TIL 水平,并与不良肿瘤学预后相关。
No established method currently exists for evaluating tumor-infiltrating lymphocytes (TILs) in gastric cancer (GC), and their clinical significance based on infiltration site in GC remains unclear. In this study, we developed a method to evaluate TILs according to their infiltration site as a prognostic marker for GC.
We retrospectively analyzed 103 patients with advanced GC who underwent curative resection. TILs located at the invasive margin (TIL IM ) and the center of tumors (TIL CT ) were scored semi-quantitatively using immunohistochemical staining of CD8+ T cells. The sum of the TIL IM and TIL CT scores was defined as the TILs score. Based on this score, patients were classified into low and high TILs groups. Quantitative TILs were also assessed to validate the semi-quantitative scoring method.
Furthermore, we confirmed a tumor suppressive effect due to CD8+ T cells co-cultured in GC cell lines in vitro . In the univariate analysis, patients with low TIL IM were significantly more likely to be female, younger, and have undifferentiated histological types and deeper tumor invasion compared to those with high TIL IM . Similarly, patients with low TIL CT had significantly more positive lymph node metastases than those with high TIL CT .
In the multivariate analysis, deeper tumor invasion and positive lymph node metastasis were identified as independent risk factors for patients with low TIL IM and low TIL CT , respectively. According to our semi-quantitative TILs scoring method, the low TILs group had significantly poorer prognoses compared to the high TILs group. This group had significantly larger tumor diameters, deeper tumor invasion, and more positive lymph node metastases.
Additionally, deeper tumor invasion was an independent risk factor for the low TILs group. Quantitative TILs analysis revealed that the low TILs group had significantly lower TIL levels compared to the high TILs group. In vitro , CD8+ T cells induced apoptosis in GC cells in a concentration-dependent manner.
Furthermore, these cells significantly suppressed the proliferative, migratory, and invasive capacities of GC cells.
Our simple and versatile semi-quantitative scoring method for CD8+ TILs indicates that CD8+ TILs are sensitive prognostic markers. The low TILs group accurately reflects the low quantitative TIL levels and is associated with poor oncological prognosis.
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