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  • Abstract Number: 2861 • 2017 ACR/ARHP Annual Meeting

    Treat-to-Target in Rheumatoid Arthritis: What Level of Treatment Response Is Necessary By 3 Months in Order to Achieve the Treatment Target By 6 Months? Results from the Real Life NOR-DMARD Study

    Vibeke Norvang1, Inge C Olsen2, Joseph Sexton1, Eirik K Kristianslund1, Till Uhlig1, Tore Kvien3, Daniel Aletaha4, Josef S. Smolen4 and Espen A. Haavardsholm1, 1Dept. of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 2Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 3Diakonhjemmet Hospital, Oslo, Norway, 4Medical University Vienna, Division of Rheumatology, Department of Internal Medicine III, Vienna, Austria

    Background/Purpose : In a treat-to-target strategy in rheumatoid arthritis (RA) treatment adoptions are recommended in case of poor improvement in disease activity 3 months after…
  • Abstract Number: 2862 • 2017 ACR/ARHP Annual Meeting

    Diverse Disease Activity Measures Demonstrate That the Routine Assessment of Patient Index Data with 3 Measures (Rapid-3) Assesses Only Non Inflammatory Components of Disease and Should Not be Utilized in a Treat to Target Strategy in Rheumatoid Arthritis

    Craig Wiesenhutter, Coeur d'Alene Arthritis Clinic, Coeur D Alene, ID

    Background/Purpose: Treating Rheumatoid Arthritis (RA) patients to target (T2T) has been shown to result in better outcomes in patients with RA. Surrogate measures of disease…
  • Abstract Number: 2863 • 2017 ACR/ARHP Annual Meeting

    Serum Proteomic Signatures Predict Relapse in Rheumatoid Arthritis Patients Undergoing DMARD Withdrawal

    Liam O'Neil1, Victor Spicer2, Carol A Hitchon2, Juergen Rech3, Axel J. Hueber4, John Wilkins2, Hani El-Gabalawy1 and Georg Schett3, 1Rheumatology, University of Manitoba, Winnipeg, MB, Canada, 2University of Manitoba, Winnipeg, MB, Canada, 3Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Department of Internal Medicine 3 – Rheumatology and Immunology, Universitätsklinikum Erlangen, Erlangen, Germany., Erlangen, Germany, 4Department of Medicine 3, Rheumatology and Immunology, University of Erlangen-Nuremberg, Erlangen, Germany

    Background/Purpose: Early and targeted treatment strategies have led to increasing numbers of patients with RA achieving sustained clinical remission. If and when to taper Disease…
  • Abstract Number: 2864 • 2017 ACR/ARHP Annual Meeting

    Anti-Acetylated Peptide Antibodies Positive Rheumatoid Arthritis Patients Show a More Favorable Response to Tumor-Necrosis-Factor Inhibitor Treatment and Better Disease Activity Control over Time

    Paul Studenic1, Stephan Blüml1, Holger Bang2, Daniela Sieghart1, Daniel Aletaha1, Helmuth Haslacher3, Josef S. Smolen1,4 and Günter Steiner1, 1Medical University Vienna, Division of Rheumatology, Department of Internal Medicine III, Vienna, Austria, 2Orgentec Diagnostika GmbH, Mainz, Germany, 3Medical University Vienna, Department of Laboratory Medicine, Vienna, Austria, 4Department of Internal Medicine, Hietzing Hospital, Vienna, Austria

    Background/Purpose: Anti-acetylated-peptide antibodies (AAPA) have been found in rheumatoid arthritis (RA) patients and may be additional markers for diagnosis, particularly in rheumatoid factor (RF)/ anti-citrullinated…
  • Abstract Number: 2865 • 2017 ACR/ARHP Annual Meeting

    The Utility and Limitations of Serum C-Reactive Protein in Appraising Synovial Inflammation

    Carl Orr1, Aurélie Najm2, Francis Young1, Trudy McGarry3, Monika Biniecka4, Ursula Fearon5 and Douglas J. Veale6, 1Centre for Arthritis and Rheumatic Diseases, Dublin Academic Medical Centre, University College Dublin, Dublin 4, Ireland, 2INSERM U1238 University of medicine, PHY-OS Laboratory, Nantes, France, 3St. Vincent's University Hospital, Dublin, Ireland, 4Dublin Academic Medical Centre, Dublin, Ireland, 5Trinity College Dublin, Department of Molecular Rheumatology, Trinity College Dublin, Dublin, Ireland, 6Rheumatology, St. Vincent's University Hospital, Dublin 4, Ireland

    Background/Purpose: Despite the clinical role of synovial histology in the differential diagnosis of arthritis, there are still profound unmet needs regarding predictors for diagnosis, disease…
  • Abstract Number: 2866 • 2017 ACR/ARHP Annual Meeting

    Microarray Pathway Analysis Comparing Baricitinib and Adalimumab in Moderate to Severe Rheumatoid Arthritis Patients, from a Phase 3 Study

    Paul Emery1, Peter C. Taylor2, Michael Weinblatt3, Yoshiya Tanaka4, Edward C. Keystone5, Ernst R. Dow6, Richard Higgs6, William L. Macias6, Guilherme Rocha6, Terence P. Rooney6, Douglas E. Schlichting6, Steven H. Zuckerman6 and Iain B. McInnes7, 1Leeds MSK Biomed/Chapel Allerton Hospital, Leeds, United Kingdom, 2NDORMS, University of Oxford, Oxford, United Kingdom, 3Brigham and Women’s Hospital, Boston, MA, 4The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan, 5University of Toronto, Toronto, ON, Canada, 6Eli Lilly and Company, Indianapolis, IN, 7University of Glasgow, Glasgow, United Kingdom

    Background/Purpose: In RA-BEAM (NCT01710358), baricitinib (BARI), an oral selective inhibitor of Janus kinase (JAK) 1 and JAK 2, yielded significant improvements in patients (pts) with…
  • Abstract Number: 2867 • 2017 ACR/ARHP Annual Meeting

    CD39 Positive Regulatory T Cells As a Biomarker of Responsiveness to Methotrexate in Rheumatoid Arthritis

    Vikas Gupta1, Shobhita Katiyar2, Ankita Singh2, Ramnath Misra1 and Amita Aggarwal1, 1Clinical Immunology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India, 2Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India

    Background/Purpose: About 30-40% of patients with RA do not respond to MTX, the first-line therapy in RA. Early identification of responders may allow the use…
  • Abstract Number: 2868 • 2017 ACR/ARHP Annual Meeting

    Pharmacodynamic Analysis of Whole Blood Gene Expression over 2 Years in a Phase IIIb Head-to-Head Trial of Abatacept and Adalimumab in Patients with RA

    O Jabado1, MA Maldonado1, Michael Schiff2, Michael Weinblatt3, Roy Fleischmann4, William H. Robinson5, A Greenfield1 and SE Connolly1, 1Bristol-Myers Squibb, Princeton, NJ, 2University of Colorado, Denver, CO, 3Brigham and Women’s Hospital, Boston, MA, 4Metroplex Clinical Research Center Dallas, Dallas, TX, 5Stanford University, Palo Alto, CA

    Background/Purpose: The head-to-head AMPLE study compared the safety and efficacy of abatacept (co-stimulatory modulator) versus adalimumab (TNFα inhibitor) for treatment of RA over 2 years.…
  • Abstract Number: 2869 • 2017 ACR/ARHP Annual Meeting

    Significant Decrease of T-Cells but Not Macrophages in the Synovium of Patients with Active Rheumatoid Arthritis after Treatment with Tocilizumab

    Katerina Chatzidionysiou1, Marianne Engström1, Erik af Klint1, Aase Hensvold1 and Anca I Catrina2, 1Rheumatology Unit, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden, 2Department of Medicine, Rheumatology Unit, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden

    Background/Purpose: Tocilizumab (TCZ) is an anti-IL6R monoclonal antibody approved for the treatment of Rheumatoid Arthritis (RA). There is limited data on synovial tissue histology changes.…
  • Abstract Number: 2870 • 2017 ACR/ARHP Annual Meeting

    Ex Vivo Comparison of Baricitinib, Upadacitinib, Filgotinib, and Tofacitinib for Cytokine Signaling in Human Leukocyte Subpopulations

    Iain B. McInnes1, Richard Higgs2, Jonathan Lee2, William L. Macias2, Songqing Na2, Robert A. Ortmann2, Guilherme Rocha2, Thomas Wehrman3, Xin Zhang2, Steven H. Zuckerman2 and Peter C. Taylor4, 1University of Glasgow, Glasgow, United Kingdom, 2Eli Lilly and Company, Indianapolis, IN, 3Primity Bio, Fremont, CA, 4NDORMS, University of Oxford, Oxford, United Kingdom

    Background/Purpose: Baricitinib (bari), an oral selective Janus kinase (JAK) 1/2 inhibitor, has been approved in the EU for the treatment of adults with moderately to…
  • Abstract Number: 2871 • 2017 ACR/ARHP Annual Meeting

    Anti-RA33 (hnRNP-A2/B1) Autoantibodies Are Associated with the Therapeutic Response to Methotrexate and Anti-TNF Treatment in Patients with Rheumatoid Arthritis

    Daniela Sieghart1, Paul Studenic1, Farideh Alasti2, Daniel Aletaha3, Josef S. Smolen1 and Günter Steiner2, 1Medical University Vienna, Division of Rheumatology, Department of Internal Medicine III, Vienna, Austria, 2Rheumatology, Medical University of Vienna, Vienna, Austria, 3Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria

    Background/Purpose: Besides the determination of rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPA), anti-RA33 antibodies (which are directed to the nuclear antigen hnRNP-A2/B1) could be…
  • Abstract Number: 2872 • 2017 ACR/ARHP Annual Meeting

    Elevated mTORC1 Signature in B Cells from Sjögren’s Syndrome Patients: mTOR Inhibition As a Novel Therapeutic Strategy to Halt B Cell Hyperactivity

    Sofie L.M. Blokland1,2, Maarten R. Hillen3,4, Rina G.K. Kommer-Wichers4, Aike A. Kruize2, Timothy R.D.J. Radstake2,5, Jasper C.A. Broen2,4 and Joel A.G. van Roon2,4, 1Rheumatology & Clinical Immunology/ Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 2Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 3Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 4Laboratory of Translational Immunology, UMC Utrecht, Utrecht, Netherlands, 5Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands

    Background/Purpose: A hallmark feature of primary Sjögren’s syndrome (pSS) is B cell hyperactivity, including presence of autoantibodies, aberrant presence of B cells and plasma cells…
  • Abstract Number: 2873 • 2017 ACR/ARHP Annual Meeting

    DNA Microarray Analysis Identifies Nuclear Receptor Subfamily 4 Group a Member 2 (NR4A2) As a Novel Molecule Involved in the Pathogenesis of Sjogren’s Syndrome

    Hiroyuki Takahashi, Hiroto Tsuboi, Hiromitsu Asashima, Hanae Kudo, Yuko Ono, Saori Abe, Yuya Kondo, Isao Matsumoto and Takayuki Sumida, Department of Internal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

    Background/Purpose:Some reports on DNA microarray analysis in labial salivary glands (LSGs) of Sjögren’s syndrome (SS) and healthy controls (HCs) showed that the genes associated with…
  • Abstract Number: 2874 • 2017 ACR/ARHP Annual Meeting

    Thymic Stromal Lymphopoietin (TSLP) Expression Is Associated with Lymphoproliferation and Lymphoma in Primary Sjögren’s Syndrome

    Saviana Gandolfo1, Cinzia Fabro1, Michela Bulfoni2, Sabino Russi3, Luca Quartuccio1, Domenico Ettore Sansonno3, Carla Di Loreto2, Daniela Cesselli2 and Salvatore De Vita1, 1Rheumatology Clinic, Academic Hospital S. M. della Misericordia, Medical Area Department, University of Udine, Italy, Udine, Italy, 2Institute of Anatomic Pathology, Academic Hospital S. M. della Misericordia, Medical Area Department, University of Udine, Italy, Udine, Italy, 3Department of Biomedical Sciences and Human Oncology, University of Bari, Italy, Bari, Italy

    Background/Purpose: Primary Sjögren’s syndrome (pSS) is an autoimmune and lymphoproliferative systemic disease with B cell hyperactivity and increased risk of non-Hodgkin lymphoma (NHL) evolution. In…
  • Abstract Number: 2875 • 2017 ACR/ARHP Annual Meeting

    Molecular Features Define Unique Sjögren’s Syndrome Patient Subsets

    Judith A. James1, Joel M. Guthridge2, Hua Chen3, Rufei Lu3, Rebecka L. Bourn3, Alan N. Baer4, Ghaith Noaiseh5, Anne Parke6, Andreea Coca7, Tammy Utset8, Mark C. Genovese9, Teresa Aberle3, Daniel J. Wallace10, Karen Boyle11, Lynette Keyes-Elstein12, Nathalie Franchimont13, Eugene St. Clair14, Virginia Pascual15, Paul J. Utz16 and Kathy L. Sivils2, 1Arthritis & Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Medicine (Rheumatology), Johns Hopkins University School of Medicine, Baltimore, MD, 5University of Pittsburgh Medical Center, Pittsburgh, PA, 6University of Connecticut, Farmington, CT, 7University of Rochester Medical Center, Rochester, NY, 8University of Chicago, Chicago, IL, 9Stanford University Medical Center, Palo Alto, CA, 10UCLA, Beverly Hills, CA, 11Rho Federal Systems, Inc, Chapel Hill, NC, 12Rho Federal Systems, Inc., Chapel Hill, NC, 13Biogen, Cambridge, MA, 14Department of Medicine, Duke University Medical Center, Durham, NC, 15Baylor Institute for Immunology Research, Baylor Research Institute, Dallas, TX, 16Medicine, Stanford University School of Medicine, Stanford, CA

    Background/Purpose: Immunologic heterogeneity in primary Sjogren’s syndrome (pSS) poses a challenge when selecting a therapeutic for a given patients or when assembling patient cohorts for…
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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.).

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