Department of Immunology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Department of Oto-rhino-laryngology and Head-and-neck-surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Int J Cancer. 2019 Jun 1;144(11):2811-2822. doi: 10.1002/ijc.32024. Epub 2018 Dec 16.
FOXP3 regulatory T (Treg) cells suppress anti-tumor immunity. The suppression of Treg cells is regulated by cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4), whose expression on the cell surface is tightly regulated. Here we found that Treg cells expressing abundant CTLA-4 on the cell surface (surface-CTLA-4 Treg) were expanded in human head and neck cancer tissues. RNA sequencing of surface-CTLA-4 and surface-CTLA-4 Treg cells infiltrating human head and neck cancer tissues revealed that surface-CTLA-4 Treg cells have a previously undescribed gene expression profile correlating to cell cycle, cell proliferation, and DNA replication. Moreover, surface-CTLA-4 Treg cells were PD-1 , actively proliferated and associated with CD45RA FOXP3 Treg cells with strong suppressive function. Thus, surface-CTLA-4 Treg cells with a proliferative gene expression signature and phenotype are key features of head and neck cancer. Targeting surface-CTLA-4 Treg cells might be new strategies to evoke effective immune responses to head and neck cancer.
叉头框蛋白 3(FOXP3)调节性 T(Treg)细胞抑制抗肿瘤免疫。Treg 细胞的抑制作用受细胞毒性 T 淋巴细胞相关抗原-4(CTLA-4)调控,其细胞表面表达受到严格调控。在这里,我们发现表面 CTLA-4 表达丰富的 Treg 细胞(表面 CTLA-4 Treg)在人类头颈部癌组织中扩增。对浸润人类头颈部癌组织的表面 CTLA-4 和表面 CTLA-4 Treg 细胞进行 RNA 测序显示,表面 CTLA-4 Treg 细胞具有以前未描述的基因表达谱,与细胞周期、细胞增殖和 DNA 复制相关。此外,表面 CTLA-4 Treg 细胞表达 PD-1,处于活跃增殖状态,并与具有强大抑制功能的 CD45RA FOXP3 Treg 细胞相关。因此,具有增殖基因表达特征和表型的表面 CTLA-4 Treg 细胞是头颈部癌的关键特征。靶向表面 CTLA-4 Treg 细胞可能是引发对头颈部癌有效免疫反应的新策略。