| Literature DB >> 14659902 |
Agnès Gazagne1, Emmanuel Claret, John Wijdenes, Hans Yssel, François Bousquet, Eric Levy, Philippe Vielh, Florian Scotte, Thierry Le Goupil, Wolf H Fridman, Eric Tartour.
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.Entities:
Mesh:
Substances:
Year: 2003 PMID: 14659902 DOI: 10.1016/j.jim.2003.08.013
Source DB: PubMed Journal: J Immunol Methods ISSN: 0022-1759 Impact factor: 2.303