Résumé
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 IFNγ. 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.
langue originale | Anglais |
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Pages (de - à) | 91-98 |
Nombre de pages | 8 |
journal | Journal of Immunological Methods |
Volume | 283 |
Numéro de publication | 1-2 |
Les DOIs | |
état | Publié - 1 janv. 2003 |
Modification externe | Oui |