Department of Microbiology and Immunology, Medical University of South Carolina, 173 Ashley Avenue, Charleston, SC 29425, USA.
Department of Otolaryngology, Head and Neck Surgery, Medical University of South Carolina, 135 Rutledge Avenue, Charleston, SC 29425, USA.
Cancers (Basel). 2014 Apr 2;6(2):756-70. doi: 10.3390/cancers6020756.
Head and neck squamous cell carcinoma (HNSCC) is marked by immunosuppression, a state in which the established tumor escapes immune attack. However, the impact of the premalignant and tumor microenvironments on immune reactivity has yet to be elucidated. The purpose of this study was to determine how soluble mediators from cells established from carcinogen-induced oral premalignant lesions and HNSCC modulate immune cell cytokine production. It was found that premalignant cells secrete significantly increased levels of G-CSF, RANTES, MCP-1, and PGE2 compared to HNSCC cells. Splenocytes incubated with premalignant supernatant secreted significantly increased levels of Th1-, Th2-, and Th17-associated cytokines compared to splenocytes incubated with HNSCC supernatant. These studies demonstrate that whereas the premalignant microenvironment elicits proinflammatory cytokine production, the tumor microenvironment is significantly less immune stimulatory and may contribute to immunosuppression in established HNSCC.
头颈部鳞状细胞癌 (HNSCC) 的特点是免疫抑制,即已建立的肿瘤逃避免疫攻击的状态。然而,癌前病变和肿瘤微环境对免疫反应的影响尚未阐明。本研究旨在确定来自致癌物诱导的口腔癌前病变和 HNSCC 细胞的可溶性介质如何调节免疫细胞细胞因子的产生。结果发现,与 HNSCC 细胞相比,癌前病变细胞分泌的 G-CSF、RANTES、MCP-1 和 PGE2 水平显著增加。与用 HNSCC 上清液孵育的脾细胞相比,用癌前病变上清液孵育的脾细胞分泌的 Th1、Th2 和 Th17 相关细胞因子水平显著增加。这些研究表明,虽然癌前病变微环境引发促炎细胞因子的产生,但肿瘤微环境的免疫刺激性显著降低,可能导致已建立的 HNSCC 中的免疫抑制。