Discovery and validation of immunological biomarkers using an advanced flow cytometry platform
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POSTER PRESENTATION
Open Access
Discovery and validation of immunological biomarkers using an advanced flow cytometry platform F Villanova1*, P Di Meglio1, M Inokuma2, V C Maino2, F O Nestle1 From 5th European Workshop on Immune-Mediated Inflammatory Diseases Sitges-Barcelona, Spain. 1-3 December 2010 Introduction Immune mediated inflammatory diseases (IMIDs), such as rheumatoid arthritis, psoriasis and Crohn’s disease are a group of chronic conditions sharing common inflammatory pathways. Inflammatory cytokine imbalance is central in IMID pathophysiology suggesting a key role for CD4+ T cells in shaping the immune response via cytokine production. Given the phenotypic and functional complexity of the T-cell compartment, multiparameter flow cytometry represents one of the best experimental tools to study T cell biology. Aim The aim of our immuno-monitoring project is to develop a flow cytometry-platform to define and validate immune cell signatures in inflammatory diseases. In particular we want to simultaneously analyze the frequency and functional state (cytokine production, STAT protein phosphorylation) of T helper cell subsets relevant for IMIDs. Patients and methods Multicolour flow cytometry panels were developed for the simultaneous detection of up to 10 parameters both at surface and intracellular levels. PBMC are stimulated with PMA/Ionomycin and then stained in 96 well plates containing lyophilized reagents (lyoplates) to ensure consistency and reproducibility between different primary samples. Cellular activation and signalling was assessed by phosphoflow cytometry after ex vivo stimulation with relevant proinflammatory cytokines.
Results Three polychromatic (10 colours) flow cytometry panels using the lyoplate platform have been developed to analyse the number, cytokine production (IFNg, IL17A, IL22 and IL10) and transcription factor expression (T-Bet, RORC and FoxP3) of Th1, Th17 and Treg cells within PBMC. A fourth panel has been designed to study T cell activation by detecting constitutive and cytokine induced phosphorylation of Stat1 and Stat3. Conclusion The multicolour flow cytometry platform we have optimized is an excellent tool to characterize CD4+ T cell subsets in both healthy controls and patients with immune mediated inflammatory diseases. Author details 1 St. John’s Institute of Dermatology, King’s College London, London, UK. 2 Biological Research & Development, BD Biosciences, San Jose, CA, USA. Published: 25 November 2010
doi:10.1186/1479-5876-8-S1-P21 Cite this article as: Villanova et al.: Discovery and validation of immunological biomarkers using an advanced flow cytometry platform. Journal of Translational Medicine 2010 8(Suppl 1):P21.
1 St. John’s Institute of Dermatology, King’s College London, London, UK Full list of author information is available at the end of the article
© 2010 Villanova et al; licensee BioMed Central Ltd.
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