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Abstracts tagged "Late-Breaking 2016"

  • Abstract Number: 13L • 2016 ACR/ARHP Annual Meeting

    Low-Dose IL-2 Therapy in Refractory SLE: Results from Single Center Phase I/IIa Clinical Trial

    Jens Humrich1, Caroline von Spee-Mayer2, Elise Siegert3, Angelika Rose2, Martina Bertolo4, Philipp Enghard5, Falk Hiepe6, Tobias Alexander7, Eugen Feist8, Andreas Radbruch9, Gerd R. Burmester10 and Gabriela Riemekasten11, 1Department of Rheumatology, University Hospital Schleswig-Holstein - Campus Lübeck, Lübeck, Germany, 2Rheumatology and Clinical Immunology, Charité – University Hospital, Berlin, Germany, 3Rheumatology and Clinical Immunology, Charité – University Medicine Berlin, Berlin, Germany, 4Department of Rheumatology, Charité – University Medicine Berlin, Berlin, Germany, 5Department of Nephrology, Charité – University Medicine Berlin, Berlin, Germany, 6Charité – Universitätsmedizin, Berlin, Germany, 7Rheumatology and Clinical Immunology, Charité - University Medicine Berlin, Berlin, Germany, 8Charité-Universitätsmedizin Berlin, Berlin, Germany, 9Deutsches Rheumaforschungszentrum, Berlin, Germany, 10Charité – University Medicine Berlin, Berlin, Germany, 11Department of Rheumatology, Universitatsklinikum Schleswig-Holstein, Lubeck, Germany

    Background/Purpose: Interleukin-2 (IL-2) is crucial for the growth and survival of regulatory T cells (Treg), and thus for the control of autoimmunity. In previous studies…
  • Abstract Number: 14L • 2016 ACR/ARHP Annual Meeting

    Use of Intravenous Epoprostenol As a Treatment for the Digital Vasculopathy Associated with the Scleroderma Spectrum of Diseases

    Shing Law1, Robert W. Simms2 and Harrison W. Farber3, 1Rheumatology, Boston Medical Center, Boston, MA, 2Rheumatology, Boston University School of Medicine, Boston, MA, 3Pulmonary Center, Boston University Medical Center, Boston, MA

    Background/Purpose: Intravenous prostanoid therapy is recommended for severe systemic sclerosis related digital vasculopathy. Evidence to support this recommendation is limited. Our objective is to evaluate…
  • Abstract Number: 15L • 2016 ACR/ARHP Annual Meeting

    Selective Oral ROCK2 Inhibitor Reduces Clinical Scores in Patients with Psoriasis vulgaris and Normalizes Skin Pathology Via Concurrent Regulation of IL-17 and IL-10 Levels

    Alexandra Zanin-Zhorov1, Jonathan Weiss1, Alissa Trzeciak1, Carmen Arencibia1, Seetharam Polimera1, Wei Chen1, Jingya Zhang1, Melanie Nyuydzefe1, Judilyn Fuentes-Duculan2, Kathleen Bonifacio2, Norma Kunjravia2, Inna Cueto2, Mark Berger1, James Krueger2, Samuel Waksal1 and John Ryan1, 1Kadmon, New York, NY, 2Rockefeller University, New York, NY

    Background/Purpose: Rho-associated kinase 2 (ROCK2) was shown to be implicated in regulation of autoimmunity in mice and humans1. Previous findings demonstrated that oral administration of…
  • Abstract Number: 16L • 2016 ACR/ARHP Annual Meeting

    Comparison of Systematic Vs Individually Tailored Rituximab Regimen to Maintain ANCA-Associated–Vasculitis Remission: Results of a Prospective, Randomized–Controlled, Phase 3 Trial

    Pierre Charles1, Benjamin Terrier2, Pascal Cohen3, Stanislas Faguer4, Antoine Huart5, Mohamed Hamidou6, Christian Agard7, Bernard Bonnotte8, Maxime Samson8, Alexandre Karras9, Noémie Jourde-Chiche10, François Lifermann11, Pierre Gobert12, Catherine Hanrotel-Saliou13, Pascal Godmer14, Nicolas Martin Silva15, Grégory Pugnet16, Marie Matignon17, Olivier Aumaître18, Estibaliz Lazaro19, Luc Mouthon20, Loïc Guillevin21 and French Vasculitis Study Group, 1Service de Médecine Interne, Hôpital Cochin, Paris, France, 2Internal Medicine, Cochin University Hospital, Paris, France, 3Department of Internal Medicine, Referral Center for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, Paris, France, 42Service de Néphrologie et Immunologie Clinique, Centre Hospitalier Universitaire (CHU) de Toulouse, Toulouse, France, 5CHU, Toulouse, France, 6Internal Medicine Department, Internal Medicine Department, Nantes University Hospital, Nantes, France, 7Internal Medicine Department, Nantes University Hospital, Nantes, France, 8Department of Internal Medicine and Clinical Immunology, Hôpital François Mitterrand, CHU de Dijon, Dijon, France, 9Nephrology, HEGP, Paris, France, 10Vascular Research Center of Marseille, Aix-Marseille Univ., Vascular Research Center of Marseille, Marseille, France, 11CH Dax, Dax, France, 12Nephrology, Centre Hospitalier d'Avignon, Avignon, France, 13CHU Cavale Blanche, Brest, Brest, France, 14CH Vannes, Vannes, France, 15Department of Internal Medicine, Caen University Hospital, Caen, France, 16Service de Médecine Interne, CHU de Toulouse, Toulouse, Toulouse, France, 17Service de Néphrologie, Hôpital Henri-Mondor, Créteil, Créteil, France, 18CHU Pitié-Salpêtrière - Department of Internal Medicine 2. Referal center for SLE/APS, Paris, France, 19Service de Médecine Interne et Maladies Infectieuses, CHU de Bordeaux, Pessac, France, 20Internal Medicine, Referral Center for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, Paris, France, 21National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France

    Background/Purpose: Remission of ANCA-associated vasculitides (AAVs) can be induced with combined glucocorticoids and cyclophosphamide or rituximab (RTX) with comparable efficacy.1 RTX superiority to azathioprine was…
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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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