Whole blood flow cytometric measurement of NFATc1 and IL-2 expression to analyze cyclosporine A-mediated effects in T cells
Autor: | Karin Mueller, Petra Reinke, Ria Baumgrass, Peter Liman, Hanna Bendfeldt, Margitta Worm, Andreas Radbruch, Claudia Brandt |
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Rok vydání: | 2010 |
Předmět: |
CD4-Positive T-Lymphocytes
Interleukin 2 Histology medicine.medical_treatment Biology Pharmacology Pathology and Forensic Medicine Flow cytometry medicine Animals Humans Whole blood Ionophores NFATC Transcription Factors medicine.diagnostic_test Ionomycin Reproducibility of Results NFAT Cell Biology Flow Cytometry Calcineurin Cytokine Blood Preservation Toxicity Cyclosporine Interleukin-2 Tetradecanoylphorbol Acetate Cytometry Biomarkers Immunosuppressive Agents medicine.drug |
Zdroj: | Cytometry Part A. :607-613 |
ISSN: | 1552-4930 1552-4922 |
DOI: | 10.1002/cyto.a.20928 |
Popis: | The calcineurin inhibitor Cyclosporine A (CsA) is one of the crucial immunosuppressive drugs given after organ transplantation. The small therapeutic window of CsA generates the dilemma that efficient and toxic drug doses differ only slightly. Moreover, these threshold concentrations differ considerably between individuals; therefore, functional assays are urgently needed. We explored whether the transcription factor NFATc1, a direct as well as indirect target of CsA, can be used as a potential biomarker to determine the individual immunosuppressive activity of CsA. First, in isolated human T cells we showed that flow cytometry is practicable to measure NFATc1, the most abundant NFATc isoform in activated T cells. Second, for whole blood we developed a flow cytometric assay to determine in parallel the inducible transcription factor NFATc1 and the cytokine IL-2 in stimulated T cells. We found that added CsA inhibits both the expression of NFATc1 and IL-2 in T cells of stimulated whole blood samples with IC50 values of 200 and 150 nM, respectively. The intra- and inter-assay variability was low, and clinical practicability was good. Further experiments have to demonstrate whether the parallel cytometric measurement of NFATc1 and IL-2 in whole blood is a good predictor of individual CsA efficacy and toxicity in CsA-treated patients. © 2010 International Society for Advancement of Cytometry. |
Databáze: | OpenAIRE |
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