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- W2130796878 abstract "<h3>Abstract</h3> To define the cell populations in rheumatoid arthritis (RA) driving joint inflammation, we applied single-cell RNA-seq (scRNA-seq), mass cytometry, bulk RNA-seq, and flow cytometry to sorted T cells, B cells, monocytes, and fibroblasts from 51 synovial tissue RA and osteoarthritis (OA) patient samples. Utilizing an integrated computational strategy based on canonical correlation analysis to 5,452 scRNA-seq profiles, we identified 18 unique cell populations. Combining mass cytometry and transcriptomics together revealed cell states expanded in RA synovia: <i>THY1</i><sup>+</sup><i>HLA</i><sup><i>high</i></sup> sublining fibroblasts (OR=33.8), <i>IL1B</i><sup>+</sup> pro-inflammatory monocytes (OR=7.8), <i>CD11c</i><sup>+</sup><i>T-bet</i><sup>+</sup> autoimmune-associated B cells (OR=5.7), and <i>PD-1</i><sup>+</sup>Tph/Tfh (OR=3.0). We also defined CD8<sup>+</sup> T cell subsets characterized by <i>GZMK</i><sup>+</sup>, <i>GZMB</i><sup>+</sup>, and <i>GNLY</i><sup>+</sup> expression. Using bulk and single-cell data, we mapped inflammatory mediators to source cell populations, for example attributing <i>IL6</i> production to <i>THY1</i><sup>+</sup><i>HLA</i><sup><i>high</i></sup> fibroblasts and naïve B cells, and <i>IL1B</i> to pro-inflammatory monocytes. These populations are potentially key mediators of RA pathogenesis." @default.
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- W2130796878 date "2007-04-01" @default.
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- W2130796878 title "Comparison of 1 and 2 weeks of omeprazole, amoxicillin and clarithromycin treatment for Helicobacter pylori eradication: the HYPER Study" @default.
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- W2130796878 doi "https://doi.org/10.1136/gut.2006.102269" @default.
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