2018
DOI: 10.1101/351130
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Defining Inflammatory Cell States in Rheumatoid Arthritis Joint Synovial Tissues by Integrating Single-cell Transcriptomics and Mass Cytometry

Abstract: Wei, Slowikowski, Fonseka, Rao et al A single cell map of the RA joint Abstract 78 To define the cell populations in rheumatoid arthritis (RA) driving joint inflammation, we applied 79 single-cell RNA-seq (scRNA-seq), mass cytometry, bulk RNA-seq, and flow cytometry to sorted 80 T cells, B cells, monocytes, and fibroblasts from 51 synovial tissue RA and osteoarthritis (OA) 81 patient samples. Utilizing an integrated computational strategy based on canonical correlation 82 analysis to 5,452 scRNA-seq profiles, … Show more

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Cited by 169 publications
(400 citation statements)
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“…These synovial DCs are generally mature and NF-κB is over-expressed. Multiple subsets of MHC class II + APCs are present in RA synovial tissue, including Toll-like receptor (TLR)-activated myeloid-derived cells, CD11c + CD20 + activated B cells and MHC class II hi fibroblast-like synoviocytes [30]. Multiple subsets of MHC class II + APCs are present in RA synovial tissue, including Toll-like receptor (TLR)-activated myeloid-derived cells, CD11c + CD20 + activated B cells and MHC class II hi fibroblast-like synoviocytes [30].…”
Section: Autoantigen Presentation In Ramentioning
confidence: 99%
“…These synovial DCs are generally mature and NF-κB is over-expressed. Multiple subsets of MHC class II + APCs are present in RA synovial tissue, including Toll-like receptor (TLR)-activated myeloid-derived cells, CD11c + CD20 + activated B cells and MHC class II hi fibroblast-like synoviocytes [30]. Multiple subsets of MHC class II + APCs are present in RA synovial tissue, including Toll-like receptor (TLR)-activated myeloid-derived cells, CD11c + CD20 + activated B cells and MHC class II hi fibroblast-like synoviocytes [30].…”
Section: Autoantigen Presentation In Ramentioning
confidence: 99%
“…In rheumatoid arthritis (RA), analysis of synovial tissue with single‐cell RNA sequencing and cytometry by time‐of‐flight mass spectrometry have revealed discrete cell subpopulations with transcriptomic and cell surface expression profiles linked to functional activities . These analyses, focused on the synovium and not the peripheral blood, provided new insights regarding key pathogenic cell–cell interactions and underscore the necessity of examining cellular and molecular events in the target tissue.…”
Section: Characteristics Of Tissue‐resident Memory T Cellsmentioning
confidence: 99%
“…The ABF is defined as the likelihood ratio of the probability of observing an effect size according to a normal distribution (mean 0, variance equal to the variance of all effect sizes) to the probability of observing the same effect size according to a normal distribution with wider variance, eg adjusted for a prior of observing an odds ratio of 1.5. Of the RA‐associated putatively causal variants, we rediscovered missense variants in PTPN22 and TYK2 and found a novel missense variant rs35677470 in DNASE1L3 (expressed in stromal fibroblasts) and noncoding variants in CD28‐CTLA4 (rs55686954, rs117701653) and TNFAIP3 (rs35926684). The noncoding variants rs117701653 and rs35926684, near CD28‐CTLA4 and TNFAIP3 , respectively, exhibited allele‐specific protein binding activity (electrophoretic mobility shift assay (EMSA)) and CD4 + T cell specific differential enhancer activity (Luciferase reporter assay).…”
Section: Identifying Causal Variants Among Genome‐wide Associations Wmentioning
confidence: 99%
“…One such initiative is the Accelerating Medicines Partnership, which in its first phase profiled more than 5000 cells in 36 RA patients and 15 osteoarthritis (OA) controls. Our group developed a CCA graph‐based clustering strategy to identify single cell populations by leveraging correlated regulatory structure with bulk reference samples . As a result, 3 CD4 + T cell subtypes were identified with distinct expression profiles, CCR7+ T cells, Tregs, and a mix of T peripheral (Tph) and follicular (Tfh) helper cells.…”
Section: Single Cell Transcriptomic and Epigenomic Advancesmentioning
confidence: 99%
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