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Abstracts tagged "pathogenesis"

  • Abstract Number: 2723 • 2015 ACR/ARHP Annual Meeting

    Basal STAT5 Signaling Is Elevated in Multiple Peripheral Blood Cell Subsets in Rheumatoid Arthritis and Is Markedly Downregulated By IFN-γ in T Lymphocytes

    Molly Boland1, Yanna Ding2, Surabhi Vinod3, S. Louis Bridges Jr.4 and Chander Raman1, 1Medicine/Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 2Medicine/Division of Clinical Immunology and Rheumatology, University of Alabama Birmingham, Birmingham, AL, 3University of Alabama at Birmingham, Birmingham, AL, 4Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: The importance of type I interferons (IFN-α and others) as a driver of pathogenesis in autoimmunity, including rheumatoid arthritis (RA) is well recognized.  However,…
  • Abstract Number: 519 • 2015 ACR/ARHP Annual Meeting

    In Indigenous North Americans at High Risk for RA Complement C5 Level Is Associated with ACPA Positivity and C5a with Transition to Synovitis Even after Correcting for in Vitro Complement Activation Found with Prolonged Sample Storage

    Ceri Richards1, Carol Hitchon2, Xiaobo Meng3, Irene Smolik4, David Robinson4 and Hani S. El-Gabalawy4, 1Internal Medicine, University of Manitoba, Winnipeg, MB, Canada, 2Department of Rheumatology, University of Manitoba, Winnipeg, MB, Canada, 3University of Manitoba, Winnipeg, MB, Canada, 4Arthritis Center, University of Manitoba, Winnipeg, MB, Canada

    Background/Purpose: Complement activation, a key component of innate immunity and activator of adaptive immunity has been linked to RA pathogenesis. Anti-citrullinated peptide antibody (ACPA) and…
  • Abstract Number: 3085 • 2015 ACR/ARHP Annual Meeting

    Platelet Activation and Endothelial Reactivity in the Pathogenesis of Tissue Inflammation/Injury in Systemic Lupus Erythematosus

    Robert Clancy1, Sokha Nhek2, Jonathan Newman3, Janet Nwaukoni1, Sara Rasmussen4, Jill P. Buyon1, Maya Rubin5, Kristen Lee1 and Jeffrey Berger5, 1Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY, 2New York University School of Medicine, New York, NY, 3Medicine, New York University School of Medicine, New York, NY, 4Department of Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY, 5Medicine, Division of Cardiology, New York University School of Medicine, New York, NY

    Background/Purpose: Patients with systemic lupus erythematosus (SLE) are at increased risk for widespread endothelial dysfunction, vascular thromboses, and premature cardiovascular disease.  Enhanced platelet activation and…
  • Abstract Number: 535 • 2015 ACR/ARHP Annual Meeting

    Taurine As a Biomarker for Prediction of Response to Biologic Therapy in Rheumatoid Arthritis

    Soshi Takahashi1, Jun Saegusa2, Ikuko Naka1, Kosaku Tsuda1, Takaichi Okano1, Kengo Akashi1, Miwa Nishida1, Keisuke Nishimura2, Sho Sendo2, Yo Ueda1, Akira Onishi3, Yoshinori Kogata2, Goichi Kageyama2 and Akio Morinobu2, 1Department of Rheumatology, Kobe University Hospital, Kobe, Japan, 2Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan, 3Rheumaology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan

    Background/Purpose: To identify a serum biomarker for prediction of the response to biologics (Bio) in patients with rheumatoid arthritis (RA), we performed serum metabolomics analysis…
  • Abstract Number: 3098 • 2015 ACR/ARHP Annual Meeting

    Synovial Lymphocytic Aggregates Associate with Highly Active RA and Predict Erosive Disease at 12 Months: Results from the Pathobiology of Early Arthritis Cohort

    Maria DiCicco1, Frances Humby1, Stephen Kelly2, Rebecca Hands1, nora ng3, Arti Mahto3, Illias Lazarou3, Vidalba Rocher1, Lu Zou3, Michele Bombardieri4, Christopher Buckley5, A.H.M. van der Helm- van Mil6, Robert B.M. Landewé7, Désirée van der Heijde8, Iain B. McInnes9, Peter C. Taylor10 and Costantino Pitzalis11, 1Centre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom, 2William Harvey Research Institute, Centre for Experimental Medicine and Rheumatology, Queen Mary University of London, London, United Kingdom, 3William Harvey Research Institute, Centre for Experimental Medicine and Rheumatology, London, United Kingdom, 4Experimental Medicine and Rheumatology, Queen Mary University of London, London, United Kingdom, 5University of Birmingham, Rheumatology Research Group, Birmingham, United Kingdom, 6Leiden University Medical Center, Leiden, Netherlands, 7University of Amsterdam and Atrium Medical Center, Amsterdam, Netherlands, 8Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 9Institute of Infection, Immunity and Inflammation, College of Medicine, Veterinary Medicine and Life Sciences, University of Glasgow, Glasgow, United Kingdom, 10Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford Botnar Research Centre, Oxford, United Kingdom, 11Centre for Experimental Medicine & Rheumatology, Queen Mary's School of Medicine and Dentistry, London, United Kingdom

    Background/Purpose: The inflammatory cell infiltrate in RA synovium has been recognised to organise into lymphocytic aggregates (Ags) with data to suggest that these structures are…
  • Abstract Number: 802 • 2015 ACR/ARHP Annual Meeting

    Identification of Cyclin-Dependent Kinase 1 As a Novel Regulator for Controlling Type I Interferon Signaling in Systemic Lupus Erythematosus

    Lingling Wu1, Bo Qu1, Yuting Qin1 and Nan Shen1,2, 1Shanghai Institute of Rheumatology,Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China, 2The Center for Autoimmune Genomics and Etiology (CAGE),Cincinnati Children’s Hospital Medical Center,Cincinnati, Ohio, United States of America, Cincinnati, OH

    Background/Purpose: Type I interferon (IFN) signaling has been  a central pathogenic pathway in systemic lupus erythematosus (SLE). The application of specific inhibitors of IFN  pathway has emerged…
  • Abstract Number: 3136 • 2015 ACR/ARHP Annual Meeting

    Impact of Prokinetic Agents on Systemic Sclerosis-Associated Gastrointestinal Disease: A Systematic Review

    Annaliese Tisseverasinghe1, Ahmad Kadhim2, Ambica Parmar2, Louis Liu2 and Sindhu R. Johnson1, 1Toronto Scleroderma Program, Division of Rheumatology, Toronto Western Hospital, Mount Sinai Hospital, Institue of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada, 2Division of Gastroenterology, Toronto Western Hospital, University of Toronto, Toronto, ON, Canada

    Background/Purpose: More than 90% of patients with Systemic Sclerosis (SSc) have gastroinstestinal (GI) involvement, commonly dysmotility causing complications such as gastroesophageal reflux and constipation. Treatment…
  • Abstract Number: 2448 • 2014 ACR/ARHP Annual Meeting

    DNA Methylation Analysis of Lymph Node Stromal Cells of Rheumatoid Arthritis Patients

    Emmanuel Karouzakis1, Caroline Ospelt1, Janine Hähnlein2, Renate E. Gay3, Paul Peter Tak4, Danielle Marie Gerlag5, Michel Neidhart1, Steffen Gay1 and Lisa G.M. van Baarsen2, 1Center of Experimental Rheumatology, University Hospital Zurich, Zurich, Switzerland, 2Division of Clinical Immunology and Rheumatology, Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands, 3Center of Experimental Rheumatology, Zurich University Hospital, Zurich, Switzerland, 4University of Cambridge,Cambridge and GlaxoSmithKline, Stevenage, United Kingdom, 5GSK,Clinical Unit Cambridge,R&D Projects Clinical Platforms & Sciences, Cambridge, United Kingdom

    Background/Purpose Lymph node stromal cells (LNSC) build the scaffold that enables migration and interaction of lymphocytes in the lymph node. More recently, it has been…
  • Abstract Number: 2449 • 2014 ACR/ARHP Annual Meeting

    Microrna-346 Regulation of Follicular Helper T Cells Is Involved in the Pathogenesis of rheumatoid Arthritis Disease

    Xinyi Tang1, Jie Ma2 and Shengjun Wang3, 1Department of Laboratory Medicine, Jiangsu University Affi�liated People’s Hospital, Zhenjiang, China, 2Department of Laboratory Medicine, Jiangsu University Affiliated People’s Hospital, Zhenjiang, China, 3Department of Laboratory Medicine, Jiangsu University Affiliated People’s Hospital, Zhenjiang, China

    Background/Purpose Follicular helper T (Tfh) cells have been identified as a new subset of effector helper T cells that are essential in regulating the development…
  • Abstract Number: 2165 • 2014 ACR/ARHP Annual Meeting

    Myeloid-Derived Suppressor Cells in Rheumatoid Arthritis: Friend or Foe?

    Fanlei Hu1, Chunqing Guo2, Xiang-Yang Wang2 and Zhanguo Li1, 1Department of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China, 2Department of Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA

    Background/Purpose Although myeloid-derived suppressor cells (MDSCs) have been linked to T-cell tolerance, their role in rheumatoid arthritis (RA) remains exclusive. Here, we investigated the potential…
  • Abstract Number: 1963 • 2014 ACR/ARHP Annual Meeting

    Hierarchical Role of PI3K/Akt/mTOR Signaling Cascade on: Tissue Inflammation, Organization and Angiogenesis in Autoimmune Arthritis

    Siba Raychaudhuri1, Anupam Mitra2, Ananya Datta Mitra3, Christine Abria4 and Smriti K. Raychaudhuri3, 1Med/Rheumatology, Univ California Davis/VA Sac, Davis, CA, 2Dermatology, VA Sacramento Medical Center, Mather, CA, 3Rheumatology, VA Sacramento Medical Center, Mather, CA, 4Research, VA Sacramento Medical Center, Mather, CA

    Background/Purpose: The PI3K/Akt/mTOR signaling proteins are pro-growth/pro-survival and thus likely to regulate inflammatory cascades in autoimmune diseases (1).  The key pathologic outcome in psoriatic arthritis…
  • Abstract Number: 1740 • 2014 ACR/ARHP Annual Meeting

    Predicting the Evolution of Inflammatory Arthritis in ACPA-Positive Individuals: Can T-Cell Subsets Model Help?

    Laura Hunt1, Agata Burska2, Elizabeth M.A. Hensor1, Jackie L. Nam1, Frederique Ponchel1 and Paul Emery1, 1NIHR-Leeds Musculoskeletal Biomedical Research Unit and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 2NIHR-Leeds Musculoskeletal Biomedical Research Unit and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds., Leeds, United Kingdom

    Background/Purpose: ACPA+ individuals with non-specific musculoskeletal symptoms are at high risk of developing rheumatoid arthritis (RA). We previously demonstrated dys-regulation of T-cell subsets with loss…
  • Abstract Number: 1466 • 2014 ACR/ARHP Annual Meeting

    Patients with Active Rheumatoid Arthritis Display an Expanded Population of GM-CSF Expressing Peripheral B Cells

    Sofia Adamidi, Anastasia Makris, Christos Koutsianas, Christina Tsalapaki, Emilia Hadziyannis and Dimitrios Vassilopoulos, 2nd Department of Medicine and Laboratory of Clinical Immunology-Rheumatology, Hippokration General Hospital, University of Athens Medical School, Athens, Greece

    Background/Purpose GM-CSF has been implicated in rheumatoid arthritis (RA) pathogenesis and is being investigated as a novel therapeutic target. B cells secreting GM-CSF have been…
  • Abstract Number: 1457 • 2014 ACR/ARHP Annual Meeting

    Stem Cell Growth Factor Expression in Rheumatoid Arthritis

    Youn Jung Woo1, Young Ae Baik1, Yong-Beom Park2, Soo-Kon Lee3, William H. Robinson4 and Jason Jungsik Song3, 1Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea, 2Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea, 3Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea, 4Division of Immunology and Rheumatology, Stanford University School of Medicine, Stanford, CA

    Background/Purpose: Stem cell growth factor (SCGF) is a member of the C-type lectin superfamily, encoded by gene CLEC11A. SCGF is not related to stem cell…
  • Abstract Number: 1434 • 2014 ACR/ARHP Annual Meeting

    The Longitudinal Association Between Inflammation and Blood Pressure in Rheumatoid Arthritis

    Chih-Chin Liu1, Daniel H. Solomon2, Rishi Desai3, Seoyoung C. Kim4 and Katherine Liao5, 1Rheumatology & Immunology, Brigham & Women's Hospital, Boston, MA, 2Brigham and Women's Hospital, Boston, MA, 3PharmacoEpidemiology & PharmacoEconomics, Brigham and Women's Hospital, Boston, MA, 4Div. of Pharmacoepidemiology and Pharmacoeconomics, Div. of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA, 5Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA

    Background/Purpose Inflammation is hypothesized to have direct effects on arterial endothelial and vasomotor function, functions which regulate blood pressure (BP).  While inflammation has been implicated…
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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 CT on October 25. 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.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

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