A Fluorospot assay to detect single T lymphocytes simultaneously producing multiple cytokines

J Immunol Methods. 2003 Dec;283(1-2):91-8. doi: 10.1016/j.jim.2003.08.013.

Abstract

Various subpopulations of T lymphocytes-i.e. Type 1, Type 2, Tr1 T cells-play a major role in the homeostasis of the immune system and in the pathogenesis of many inflammatory and auto-immune diseases. At present, in the absence of specific surface markers, these T cells can only be reliably distinguished on the basis of their cytokine production profile. The Elispot assay detects cytokine-producing cells, but in most cases can detect only one secreted cytokine, which represents a major limitation of this technique. We have developed a Fluorospot assay to detect single cells that simultaneously produce multiple cytokines. The Fluorospot assay permits the detection of regulatory T cells with an immunosuppressive activity, identified by their coexpression of IL-10 and IFNgamma. Polarized type 1 and type 2 specific tetanus toxoid T cells are also directly detected using a dual color Fluorospot. This technique will therefore be useful for detailed analysis of T lymphocytes in various disease states in which an imbalance of T cell subpopulations is suspected, but will also provide a better characterization of polarized specific immune responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Polarity
  • Cytokines / analysis*
  • Cytokines / biosynthesis
  • Enzyme-Linked Immunosorbent Assay / methods*
  • Humans
  • Interferon-gamma / analysis
  • Interleukin-10 / analysis
  • Sensitivity and Specificity
  • T-Lymphocytes / metabolism*

Substances

  • Cytokines
  • Interleukin-10
  • Interferon-gamma