Flow Cytometric Characterization of Antigen-Specific T Cells Based on RNA and Its Advantages in Detecting Infections and Immunological Disorders

Crit Rev Immunol. 2016;36(5):359-378. doi: 10.1615/CritRevImmunol.2017018316.

Abstract

Fluorescence in situ hybridization coupled with flow cytometry (FISH-Flow) is a highly quantitative, high-throughput platform allowing precise quantification of total mRNA transcripts in single cells. In undiagnosed infections posing a significant health burden worldwide, such as latent tuberculosis or asymptomatic recurrent malaria, an important challenge is to develop accurate diagnostic tools. Antigen-specific T cells create a persistent memory to pathogens, making them useful for diagnosis of infection. Stimulation of memory response initiates T-cell transitions between functional states. Numerous studies have shown that changes in protein levels lag real-time T-cell transitions. However, analysis at the single-cell transcriptional level can determine the differences. FISH-Flow is a powerful tool with which to study the functional states of T-cell subsets and to identify the gene expression profiles of antigen-specific T cells during disease progression. Advances in instrumentation, fluorophores, and FISH methodologies will broaden and deepen the use of FISH-Flow, changing the immunological field by allowing determination of functional immune signatures at the mRNA level and the development of new diagnostic tools.

MeSH terms

  • Animals
  • Antigens / immunology
  • Cell Separation
  • Flow Cytometry / methods*
  • High-Throughput Screening Assays
  • Humans
  • Immune System Diseases / diagnosis*
  • Immune System Diseases / immunology
  • Immunologic Memory
  • In Situ Hybridization, Fluorescence / methods*
  • Infections / diagnosis*
  • Infections / immunology
  • RNA / analysis*
  • T-Cell Antigen Receptor Specificity
  • T-Lymphocyte Subsets / physiology*
  • T-Lymphocytes / physiology*
  • Transcriptome

Substances

  • Antigens
  • RNA