ACR Meeting Abstracts

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Abstracts tagged "RNA"

  • Abstract Number: 0061 • ACR Convergence 2021

    Harnessing Spatially-Resolved Gene Expression to Characterize the Transcriptional Landscape of Psoriatic Skin

    Rochelle Castillo1, Ikjot Sidhu1, Di Yan1, Piotr Konieczny1, Rebecca Haberman1, Brandon Hsieh1, Andrea Neimann1, Shruti Naik1 and Jose Scher2, 1NYU Langone Health, New York, NY, 2New York University School of Medicine, New York, NY

    Background/Purpose: The skin is recognized as a window into the immunopathogenic mechanisms in the psoriatic arthritis (PsA) joint. This is evidenced by the fact that…
  • Abstract Number: 005 • 2020 Pediatric Rheumatology Symposium

    Single Cell Sequencing of the Skin to Define Cell Populations of Interest in Localized Scleroderma (LS)

    Emily Mirizio 1, Wei Chen 2, Tao Sun 2, Tracy Tabib 3, Kaila Schollaert-Fitch 1, Robert Lafyatis 4, Heidi Jacobe 5 and Kathryn Torok1, 1Pediatric Rheumatology, Univ of Pittsburgh Med Ctr, Pittsburgh, 2Research Computing Core at Children's Hospital of Pittsburgh, Pittsburgh, 3Univ of Pittsburgh Med Ctr, Pittsburgh, 4Univ of Pittsburgh Med Ctr, Pittsburgh, Pittsburgh, 5University of Texas Southwestern Medical Ctr, Dallas

    Background/Purpose: Scleroderma is an autoimmune disorder involving inflammatory driven fibrosis, which encompasses systemic sclerosis (SSc) and localized scleroderma (LS).  LS and SSc share histological characteristics,…
  • Abstract Number: 776 • 2019 ACR/ARP Annual Meeting

    Genetic Signatures Support Inflammation Driven Fibrosis in Localized Scleroderma

    Christina Schutt1, Emily Mirizio 2, Claudia Salgado 3, Miguel Reyes-Mugica 3, Kaila L. Schollaert 2 and Kathryn Torok 3, 1UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, 2University of Pittsburgh, Pittsburgh, 3UPMC Children's Hospital of Pittsburgh, Pittsburgh

    Background/Purpose: Localized scleroderma (LS) is a progressive autoimmune disease of the skin and underlying tissue that is characterized by an initial inflammatory infiltration which is…
  • Abstract Number: 2101 • 2018 ACR/ARHP Annual Meeting

    UV-Induced Skin Inflammation Is Exacerbated in Lupus-Prone Ro60 Knockout Female Mice with Interferon Priming

    Masaoki Kawasumi1, Daiki Rokunohe1, Xizhang Sun2, Lena Tanaka2, Sladjana Skopelja-Gardner3, Edward Chiou2, Anne Davidson4, Sandra L. Wolin5 and Keith B. Elkon2, 1Medicine/Dermatology, University of Washington, Seattle, WA, 2Medicine/Rheumatology, University of Washington, Seattle, WA, 3University of Washington, Seattle, WA, 4Feinstein Institute for Medical Research, Manhasset, NY, 5National Cancer Institute, Frederick, MD

    Background/Purpose: Photosensitivity is a major symptom of lupus, and excessive sunlight can cause skin rashes and flares of disease activity in systemic lupus erythematosus (SLE).…
  • Abstract Number: 2517 • 2018 ACR/ARHP Annual Meeting

    The JAK1-Selective Inhibitor Filgotinib Reverses the Disease-Associated Transcriptional Profile Found in the Blood of Patients with Active Rheumatoid Arthritis

    Peter C. Taylor1, Bryan Downie2, Luting Zhuo2, Yevgeniy Gindin2, Jacqueline Tarrant3, Jinfeng Liu2, René Galien4 and Amer M Mirza5, 1University of Oxford Botnar Research Centre, Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Oxford, United Kingdom, 2Bioinformatics, Gilead Sciences Inc., Foster City, CA, 3Gilead Sciences Inc., Foster City, CA, 4Galapagos SASU, Romainville, France, 5Biomarker Sciences, Gilead Sciences Inc., Foster City, CA

    Background/Purpose: Filgotinib (FIL), an oral JAK1- selective inhibitor, has shown good safety and efficacy in active rheumatoid arthritis (RA) patients with inadequate response to MTX…
  • Abstract Number: 2933 • 2018 ACR/ARHP Annual Meeting

    Non-Invasive Tape Sampling Reveals RNA Gene Clusters in Cutaneous Lupus Erythematosus That Discriminate Affected from Unaffected and Healthy Volunteer Skin

    Joseph F. Merola1, Wenting Wang2, Carrie Wager3, Stefan Hamann2, Xueli Zhang3, Alice Thai2, Chris Roberts2, Christina Lam4, Cristina Musselli2, Galina Marsh2, Dania Rabah2, Catherine Barbey5, Nathalie Franchimont2 and Taylor L. Reynolds2, 1Clinical Unit for Research Innovation & Trials, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 2Biogen, Cambridge, MA, 3Formerly of Biogen, Cambridge, MA, 4Boston University Medical School, Boston, MA, 5Biogen, Zug, Switzerland

    Background/Purpose: Punch biopsy, the standard diagnostic and monitoring procedure for patients with cutaneous lupus erythematosus (CLE), impedes patient recruitment and follow up due to risk…
  • Abstract Number: 2950 • 2018 ACR/ARHP Annual Meeting

    10X Genomics-Based Single-Cell RNA-Seq Analysis Identifies a Transcriptional Landscape of Inflammation and Fibrosis in Lupus Nephritis​

    Hemant Suryawanshi1, Evan Der2, Pavel Morozov1, Robert M. Clancy3, Beatrice Goilav4, H. Michael Belmont3, Peter M. Izmirly5, Nicole Bornkamp6, Nicole Jordan7, Ming Wu3, Judith A. James8, Joel M. Guthridge9, Soumya Raychaudhuri10, Jill P. Buyon3, Chaim Putterman2 and Thomas Tuschl1, 1Howard Hughes Medical Institute and The Rockefeller University, New York, NY, 2Albert Einstein College of Medicine, Bronx, NY, 3NYU School of Medicine, New York, NY, 4Division of Nephrology, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY, 5Rheumatology, NYU School of Medicine, New York, NY, 6Medicine, NYU School of Medicine, New York, NY, 7Division of Rheumatology, Albert Einstein College of Medicine, Bronx, NY, 8Oklahoma Medical Research Foundation, Oklahoma City, OK, 9Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 10Harvard Medical School, Boston, MA

    Background/Purpose: Renal histology remains a primary tool for classification and treatment decisions in lupus nephritis (LN). Single-cell RNA-seq (scRNA-seq) analysis may provide mechanistic insights into…
  • Abstract Number: 134 • 2018 ACR/ARHP Annual Meeting

    Exploration of T-Cell Signatures Following TCR Stimulation Using Single Cell RNA-Seq to Inform Treatment Response Studies in Rheumatoid Arthritis

    Paul Martin1, James Ding1, Ben Mulhearn1, Sebastien Viatte1 and Stephen Eyre1,2, 1Arthritis Research UK Centre for Genetics and Genomics, Centre for Musculoskeletal Research, Manchester Academic Health Science Centre, The University of Manchester, Manchester, United Kingdom, 2NIHR Manchester Musculoskeletal Biomedical Research Centre, Manchester University NHS Foundation Trust, Manchester, United Kingdom

    Background/Purpose: For rheumatoid arthritis (RA), as with many other rheumatic diseases, the importance of determining which therapy will work best, early in disease, to prevent…
  • Abstract Number: 924 • 2018 ACR/ARHP Annual Meeting

    10X Genomics-Based Single-Cell RNA-Seq and Low Input RNA-Seq Identify a Transcriptional Landscape Supporting Interferon in the Pathogenesis of Autoimmune-Associated Congenital Heart Block

    Hemant Suryawanshi1, Jill P. Buyon2, Miao Chang2, Thomas Tuschl1 and Robert M. Clancy2, 1Howard Hughes Medical Institute and The Rockefeller University, New York, NY, 2NYU School of Medicine, New York, NY

    Background/Purpose: Towards understanding the molecular mechanisms that link maternal anti-Ro antibodies to the development of conduction system disease in a second trimester fetus, single cell…
  • Abstract Number: 1119 • 2018 ACR/ARHP Annual Meeting

    Genetic Signatures from RNA Sequencing of Pediatric Localized Scleroderma (LS) Skin

    Emily Mirizio1, Roosha Mandal2, Qi Yan3, William Horne4, Kaila Schollaert-Fitch3 and Kathryn S. Torok5, 1Peds Rheum, University of Pittsburgh Med Ctr, Pittsburgh, PA, 2Carnegie Mellon University, Pittsburgh, PA, 3University of Pittsburgh Med Ctr, Pittsburgh, PA, 4Health Sciences Sequencing Core at Children's Hospital of Pittsburgh, Pittsburgh, PA, 5Pediatric Rheumatology, University of Pittsburgh Med Ctr, Pittsburgh, PA

    Background/Purpose: Localized scleroderma (LS) is a progressive disease of the skin and underlying tissue that causes significant functional disability and disfigurement, especially in developing children.…
  • Abstract Number: 1474 • 2018 ACR/ARHP Annual Meeting

    Circulating Transfer RNA-Derived Small RNAs Are Altered in Patients with Rheumatoid Arthritis

    Qiong Wu, Quanhu Sheng, Joseph F. Solus, Kasey Vickers, Ryan Allen, Shilin Zhao, Yan Guo, Fei Ye, C Michael Stein and Michelle J. Ormseth, Vanderbilt University Medical Center, Nashville, TN

    Background/Purpose: Small RNAs (sRNAs) are important gene regulators and markers of disease. Transfer RNA (tRNA)-derived sRNAs (tDRs), including tRNA fragments (tRFs) and halves (tRHs), are…
  • Abstract Number: 1832 • 2018 ACR/ARHP Annual Meeting

    Proteomic and Transcriptomic Profiling of Cells in Ankylosing Spondylitis Patients Identifies a Novel, Synovial-Resident CD8+ T Cell

    Zoya Qaiyum1, Eric Gracey2, Yuchen Yao2 and Robert D Inman3, 1Department of Immunology, University of Toronto, Toronto, ON, Canada, 2Krembil Research Institute, Toronto Western Hospital, Toronto, ON, Canada, 3Toronto Western Hospital, University of Toronto, Spondylitis Clinic, Toronto, ON, Canada

    Background/Purpose: Current data suggests that immune events in the gut may impact on joint inflammation in ankylosing spondylitis (AS) but what directs cells in the…
  • Abstract Number: 1897 • 2018 ACR/ARHP Annual Meeting

    Single Cell RNA Expression in Lupus Nephritis Comparing African-American and Caucasian Patients Identifies Differential Expression of Interferon Pathway

    Andrea Fava1, Yuji Zhang2, Nir Hacohen3, Arnon Arazi4, Celine C. Berthier5, Deepak Rao6, Michael Brenner7, David Wofsy8, Anne Davidson9, Matthias Kretzler10, David Hildeman11, E. Steve Woodle12, Betty Diamond13 and Michelle Petri14, 1Departement of Medicine - Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 2Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, MD, 3Harvard Medical School, Boston, MA, 4Broad Institute, Cambridge, MA, 5Nephrology, Division of Nephrology, University of Michigan Medical Center, Ann Arbor, MI, 6Human Immunology Center, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 7Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 8Rheumatology, University of California, San Francisco, San Francisco, CA, 9Center for Autoimmunity, Musculoskeletal & Hematopoietic Diseases, Feinstein Institute for Medical Research, Manhasset, NY, 10Division of Nephrology, University of Michigan, Ann Arbor, MI, 11University of Cincinnati, Cincinnati, OH, 12University of Cincinnati College of Medicine, Cincinnati, OH, 13The Feinstein Institute for Medical Research, Manhasset, NY, 14Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: African-American (AA) ethnicity is associated with a 3-fold higher risk of developing systemic lupus erythematosus (SLE). In addition, there is an increased risk of…
  • Abstract Number: 1899 • 2018 ACR/ARHP Annual Meeting

    Down-Regulation of RNA Processing Protein CFIm25 Amplifies Skin Fibrosis By up-Regulating Pro-Fibrotic Transcripts/Proteins in Systemic Sclerosis

    Tingting Mills1, Junsuk Ko1, Jingjing Huang1, Minghua Wu2, Ningyuan Chen1, Leng Han1, Yu Xiang1, Maureen D. Mayes3, Eric Wagner4, Michael Blackburn1 and Shervin Assassi2, 1Department of Biochemistry & Molecular Biology, University of Texas Health Science Center at Houston, Houston, TX, 2Rheumatology, University of Texas Health Science Center at Houston, Houston, TX, 3Rheumatology, University of Texas McGovern Medical School, Houston, TX, 4Department of Biochemistry & Molecular Biology, The University of Texas Medical Branch at Galveston, Galveston, TX

    Background/Purpose: Persistent myofibroblast activation and associated excessive extracellular matrix protein deposition are hallmarks of systemic sclerosis (SSc). However, the mechanisms that account for this excessive fibrotic response remain…
  • Abstract Number: 1903 • 2018 ACR/ARHP Annual Meeting

    Molecular Analysis of a Skin Equivalent Tissue Culture Model System of Systemic Sclerosis Using RNA Sequencing, Epigenetic Assays, Histology, and Immunoassays

    Diana M. Toledo1, Mengqi Huang2, Yue Wang2, Bhaven K. Mehta2, Tammara A. Wood3, Avi Smith4, Yolanda Nesbeth5, Irena Ivanovska6, Brock Christensen7, Patricia A. Pioli8, Jonathan Garlick4 and Michael L. Whitfield9, 1Department of Molecular & Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 2Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 3Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 4Tufts University School of Medicine, Boston, MA, 5Celdara Medical, LLC, Lebanon, NH, 6Celdara Medical, LLC, Hanover, NH, 7Geisel School of Medicine at Dartmouth, Hanover, NH, 8Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, NH, 9Biomedical Data Science, Geisel School of Medicine at Dartmouth, Hanover, NH

    Background/Purpose: The molecular mechanisms of systemic sclerosis (SSc) have been difficult to study outside of patient samples. Mouse models often lack key features of the…
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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

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