Krum David, Rösch Saskia, Warta Rolf, Mogler Carolin, Yılmaz Topçuoğlu Miray-Su, Grabe Niels, Schuler Patrick J, Dyckhoff Gerhard, Herold-Mende Christel
Department of Otorhinolaryngology, Head and Neck Surgery, Medical Faculty of Heidelberg, University of Heidelberg, INF 400, 69120 Heidelberg, Germany.
Division of Experimental Neurosurgery, Department of Neurosurgery, Medical Faculty of Heidelberg, University of Heidelberg, INF 400, 69120 Heidelberg, Germany.
Cells. 2025 May 27;14(11):789. doi: 10.3390/cells14110789.
Patients with head and neck squamous cell carcinoma (HNSCC) suffer from severe morbidity and mortality. Immunotherapy represents a novel promising treatment option. Therefore, a better understanding of the immune niche is needed. This study focuses on the spatial distribution and prognostic value of different T cell subtypes in 84 HNSCC specimens as well as chemokine and cytokine levels associated with spatial T cell infiltration. Density of T helper (T), cytotoxic (CTL), and regulatory T cells (T) was quantified by multicolor tissue cytometry on a single cell level in whole tissue sections, discriminating between T cells located in epithelial tumor cell nests or tumor stroma, respectively. In addition, quantitative levels of 27 immune-related factors were assessed. Survival analysis of patients with p16-negative HNSCC revealed higher stromal T densities to be an independent prognostic factor for better progression-free and overall survival. Furthermore, high levels of CXCL10, IL-9, and CCL4 were associated with significantly higher numbers of T cells, especially for CTL with direct contact to tumor cells, whereas for VEGF the opposite effect was observed in the tumor stroma. In conclusion, T cell infiltration as well as distinct cytokine levels could serve as new immune biomarkers in p16-negative HNSCC to predict survival and the spatial distribution of T cells.
头颈部鳞状细胞癌(HNSCC)患者的发病率和死亡率都很高。免疫疗法是一种有前景的新型治疗选择。因此,需要更好地了解免疫微环境。本研究聚焦于84例HNSCC标本中不同T细胞亚型的空间分布和预后价值,以及与T细胞空间浸润相关的趋化因子和细胞因子水平。通过多色组织细胞术在全组织切片的单细胞水平上对辅助性T细胞(Th)、细胞毒性T细胞(CTL)和调节性T细胞(Treg)的密度进行定量分析,区分位于上皮肿瘤细胞巢或肿瘤基质中的T细胞。此外,还评估了27种免疫相关因子的定量水平。对p16阴性HNSCC患者的生存分析显示,较高的基质T细胞密度是无进展生存期和总生存期更好的独立预后因素。此外,高水平的CXCL10、IL-9和CCL4与显著更多的T细胞相关,尤其是与肿瘤细胞直接接触的CTL,而在肿瘤基质中观察到VEGF有相反的作用。总之,T细胞浸润以及不同的细胞因子水平可作为p16阴性HNSCC中预测生存和T细胞空间分布的新免疫生物标志物。