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:Effect of Neoadjuvant Chemotherapy on Tumor-Infiltrating Lymphocytes in Resectable Gastric Cancer: Analysis from a Western Academic Center.
Effect of Neoadjuvant Chemotherapy on Tumor-Infiltrating Lymphocytes in Resectable Gastric Cancer: Analysis from a Western Academic Center.
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TIL(肿瘤浸润淋巴细胞)是新兴生物标志物,可预测多种实体器官恶性肿瘤对免疫治疗的应答。对于接受当代多药新辅助化疗(NAC)的胃癌(GC),TIL特征尚未得到充分研究。本回顾性研究在一家西方医疗中心,对接受或未接受NAC后切除的GC标本进行免疫组化分析,评估TIL浸润程度、表型及空间分布。我们假设NAC具有免疫刺激作用,其证据是肿瘤微环境中抗肿瘤TIL数量增加。结果显示,与未经化疗的标本相比,化疗后肿瘤中常规和记忆CD8⁺ T细胞以及总TIL(CD4⁺、CD8⁺、调节性T细胞和B细胞)水平均显著升高。研究还发现,增强的TIL浸润与生存及病理应答存在重要关联。综上,研究结果支持化疗具有免疫刺激作用,并强调在可切除胃癌中化疗与免疫治疗可能产生协同效应。
Tumor-infiltrating lymphocytes (TILs) are an emerging biomarker predictive of response to immunotherapy across a spectrum of solid organ malignancies. The characterization of TILs in gastric cancer (GC) treated with contemporary, multiagent neoadjuvant chemotherapy (NAC) is understudied. In this retrospective investigation, we analyzed the degree of infiltration, phenotype, and spatial distribution of TILs via immunohistochemistry within resected GC specimens treated with or without NAC at a Western center.
We hypothesized that NAC executes immunostimulatory roles, as evidenced by an increased number of anti-tumor TILs in the tumor microenvironment.
We found significantly elevated levels of conventional and memory CD8+ T cells, as well as total TILs (CD4+, CD8+, T reg , B cells), within chemotherapy-treated tumors compared with chemotherapy-na ve specimens.
We also revealed important associations between survival and pathologic responses with enhanced TIL infiltration. Taken together, our findings advocate for an immunostimulatory role of chemotherapy and underscore the potential synergistic effect of combining chemotherapy with immunotherapy in resectable gastric cancer.
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