| Literature DB >> 31924475 |
Anthony R Cillo1, Cornelius H L Kürten2, Tracy Tabib3, Zengbiao Qi3, Sayali Onkar1, Ting Wang4, Angen Liu5, Umamaheswar Duvvuri6, Seungwon Kim6, Ryan J Soose6, Steffi Oesterreich7, Wei Chen4, Robert Lafyatis3, Tullia C Bruno8, Robert L Ferris9, Dario A A Vignali10.
Abstract
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.Entities:
Keywords: cancer immunology; head and neck cancer; immunotherapy; multispectral immunofluorescence MC; mutagen-driven cancer; single-cell RNAseq; tertiary lymphoid structures; transcriptomics; viral-induced cancer
Mesh:
Year: 2020 PMID: 31924475 PMCID: PMC7201194 DOI: 10.1016/j.immuni.2019.11.014
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745