Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA; Tumor Microenvironment Center, UPMC Hillman Cancer Center, Pittsburgh, PA 15232, USA.
Tumor Microenvironment Center, UPMC Hillman Cancer Center, Pittsburgh, PA 15232, USA; Department of Otolaryngology, University of Pittsburgh, Pittsburgh, PA 15213, USA; Department of Otorhinolaryngology, University Duisburg-Essen, 45147 Essen, Germany.
Immunity. 2020 Jan 14;52(1):183-199.e9. doi: 10.1016/j.immuni.2019.11.014. Epub 2020 Jan 7.
Head and neck squamous cell carcinoma (HNSCC) arises through exposure to environmental carcinogens or malignant transformation by human papillomavirus (HPV). Here, we assessed the transcriptional profiles of 131,224 single cells from peripheral and intra-tumoral immune populations from patients with HPV and HPV HNSCC and healthy donors. Immune cells within tumors of HPV and HPV HNSCC displayed a spectrum of transcriptional signatures, with helper CD4 T cells and B cells being relatively divergent and CD8+ T cells and CD4+ regulatory T cells being relatively similar. Transcriptional results were contextualized through multispectral immunofluorescence analyses and evaluating putative cell-cell communication based on spatial proximity. These analyses defined a gene expression signature associated with CD4 T follicular helper cells that is associated with longer progression-free survival in HNSCC patients. The datasets and analytical approaches herein provide a resource for the further study of the impact of immune cells on viral- and carcinogen-induced cancers.
头颈部鳞状细胞癌(HNSCC)是通过暴露于环境致癌物或人类乳头瘤病毒(HPV)的恶性转化而发生的。在这里,我们评估了来自 HPV 和 HPV HNSCC 患者以及健康供体的外周和肿瘤内免疫群体的 131224 个单细胞的转录谱。HPV 和 HPV HNSCC 肿瘤内的免疫细胞表现出一系列转录特征,辅助性 CD4 T 细胞和 B 细胞相对离散,而 CD8+T 细胞和 CD4+调节性 T 细胞则相对相似。通过多光谱免疫荧光分析和评估基于空间接近的潜在细胞间通信对转录结果进行了背景分析。这些分析定义了与 CD4 T 滤泡辅助细胞相关的基因表达特征,与 HNSCC 患者无进展生存期更长相关。本文提供的数据集和分析方法为进一步研究免疫细胞对病毒和致癌物诱导的癌症的影响提供了资源。