Exploration of T-Cell Diversity Using Mass Cytometry

Methods Mol Biol. 2020:2111:1-20. doi: 10.1007/978-1-0716-0266-9_1.

Abstract

T-cell diversity is multifactorial and includes variability in antigen specificity, differentiation, function, and cell-trafficking potential. Spectral overlap limits the ability of traditional flow cytometry to fully capture the diversity of T-cell subsets and function. The development of mass cytometry permits deep immunoprofiling of T-cell subsets, activation state, and function simultaneously from even small volumes of blood. This chapter describes our methods for mass cytometry and high-throughput data analysis of T cells in patient cohorts. We provide a pipeline that includes practical considerations when customizing a panel for mass cytometry. We also provide protocols for the conjugation and titration of metal-labeled antibodies (including two T-cell panels) and a staining procedure. Finally, with the aim to support translational science, we provide R scripts that contain a detailed workflow for initial evaluation of high-dimensional data generated from cohorts of patients.

Keywords: Clustering; CyTOF; Data processing; High-throughput analysis; Mass cytometry; R; Systems biology; T cells.

MeSH terms

  • Antibodies / chemistry
  • Antibodies / metabolism*
  • Cohort Studies
  • Flow Cytometry / methods*
  • High-Throughput Screening Assays
  • Humans
  • Immunophenotyping
  • Lymphocyte Activation
  • Metals, Heavy / chemistry*
  • Single-Cell Analysis / methods
  • Staining and Labeling
  • Systems Biology
  • T-Lymphocyte Subsets / immunology*
  • Workflow

Substances

  • Antibodies
  • Metals, Heavy