Investigating immune and non-immune cell interactions in head and neck tumors by single-cell RNA sequencing

Nat Commun. 2021 Dec 17;12(1):7338. doi: 10.1038/s41467-021-27619-4.

Abstract

Head and neck squamous cell carcinoma (HNSCC) is characterized by complex relations between stromal, epithelial, and immune cells within the tumor microenvironment (TME). To enable the development of more efficacious therapies, we aim to study the heterogeneity, signatures of unique cell populations, and cell-cell interactions of non-immune and immune cell populations in 6 human papillomavirus (HPV)+ and 12 HPV- HNSCC patient tumor and matched peripheral blood specimens using single-cell RNA sequencing. Using this dataset of 134,606 cells, we show cell type-specific signatures associated with inflammation and HPV status, describe the negative prognostic value of fibroblasts with elastic differentiation specifically in the HPV+ TME, predict therapeutically targetable checkpoint receptor-ligand interactions, and show that tumor-associated macrophages are dominant contributors of PD-L1 and other immune checkpoint ligands in the TME. We present a comprehensive single-cell view of cell-intrinsic mechanisms and cell-cell communication shaping the HNSCC microenvironment.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigen-Presenting Cells / metabolism
  • B7-H1 Antigen / metabolism
  • CD8-Positive T-Lymphocytes / immunology
  • Cancer-Associated Fibroblasts / pathology
  • Cell Communication*
  • Endothelial Cells / pathology
  • Epithelial Cells / pathology
  • Gene Expression Regulation, Neoplastic
  • Head and Neck Neoplasms / blood
  • Head and Neck Neoplasms / genetics
  • Head and Neck Neoplasms / immunology*
  • Head and Neck Neoplasms / pathology*
  • Humans
  • Immune Checkpoint Proteins / metabolism
  • Inflammation / blood
  • Inflammation / genetics
  • Ligands
  • Macrophages / pathology
  • Papillomaviridae / physiology
  • Pericytes / pathology
  • RNA-Seq*
  • Single-Cell Analysis*
  • Squamous Cell Carcinoma of Head and Neck / blood
  • Squamous Cell Carcinoma of Head and Neck / genetics
  • Squamous Cell Carcinoma of Head and Neck / immunology
  • Squamous Cell Carcinoma of Head and Neck / pathology
  • Stromal Cells / pathology
  • Survival Analysis
  • Transcriptome / genetics
  • Tumor Microenvironment / immunology

Substances

  • B7-H1 Antigen
  • CD274 protein, human
  • Immune Checkpoint Proteins
  • Ligands