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Abstracts tagged "autoimmune diseases"

  • Abstract Number: 152 • 2017 Pediatric Rheumatology Symposium

    Characteristics of Patients With Juvenile Idiopathic Arthritis in a US Healthcare Claims Database

    TA Simon1, A Baheti2, N Ray2, S Kelly1 and Z Guo1, 1Bristol-Myers Squibb, Princeton, NJ, 2Mu Sigma, Bangalore, India

    Background/Purpose: Abatacept, the first selective co-stimulation modulator approved and used for the treatment of juvenile idiopathic arthritis (JIA), has a mechanism of action that is…
  • Abstract Number: 147 • 2017 Pediatric Rheumatology Symposium

    Epigenetic and Transcriptomic Profiling of Primary Juvenile Idiopathic Arthritis Patient Cells: Better Understanding of Disease Pathogenesis

    Lucas Picavet1, Janneke Peeters2, Sandra Coenen3, Arjan Boltjes4, Femke van Wijk5, Paul Coffer2, Bas Vastert6 and Jorg van Loosdregt7, 1Regenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, Netherlands, 2Center for Molecular Medicine and Regenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, Netherlands, 3University Medical Center Utrecht, Utrecht, Netherlands, 4Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 5Laboratory for Translational Immunity, University Medical Center Utrecht, Utrecht, Netherlands, 6Division of Pediatric Rheumatology, University Medical Center Utrecht, Utrecht, Netherlands, 7Division of Pediatrics, University Medical Center Utrecht, Utrecht, Netherlands

    Background/Purpose: For many autoimmune diseases, including Juvenile Idiopathic Arthritis (JIA), the molecular mechanisms remain elusive. JIA can be used as a model to study autoimmune…
  • Abstract Number: 12L • 2016 ACR/ARHP Annual Meeting

    Efficacy and Safety of Atacicept in Patients with Systemic Lupus Erythematosus: Results of a 24-Week Randomized, Placebo-Controlled, Phase IIb Study

    Joan T. Merrill1, Daniel J. Wallace2, Stephen Wax3, Amy Kao4, Patricia Fraser4, Wai Chin4 and David A. Isenberg5, 1Oklahoma Medical Research Foundation, Oklahoma City, OK, 2University of California Los Angeles, Los Angeles, CA, 3EMD Serono, BIllerica, MA, 4EMD Serono, Billerica, MA, 5University College Hospital, London, London, United Kingdom

    Background/Purpose: Atacicept targets B-cell stimulating factors BLyS and APRIL. In the APRIL-SLE trial, atacicept 150 mg was associated with reduced SLE flares in post-hoc analyses.1Methods:…
  • Abstract Number: 1179 • 2016 ACR/ARHP Annual Meeting

    The Impact of Autoimmune Disease in the Management and Prognosis of Acute Coronary Syndrome

    Nuria Lozano-Rivas1, Carlos Marras Fernandez-Cid2, Francisco Jose Pastor Perez3, Pedro Flores-Blanco4, Miriam Gomez-Molina4, Alberto Bermudez5, Luis Francisco Linares2, Javier Martinez Ferrin2, Francisco Andrés Martinez-Angosto1, Pablo Mesa del Castillo2 and Sergio Manzano-Fernandez4, 1Rheumatology, Hospital Virgen de la Arrixaca, murcia, Spain, 2Rheumatology, Hospital Virgen de la Arrixaca, Murcia, Spain, 3Cardiology, Hospital Virgen de la Arrixaca, Murcia, Spain, 4Cardiology, Hospital Virgen de la Arrixaca, murcia, Spain, 5Hospital Virgen de la Arrixaca, Molina de Segura (Mu, Spain

    Background/Purpose: Patients with autoimmune diseases (AID) have a high burden of cardiovascular disease leading to premature morbidity and mortality. But it is unclear if it…
  • Abstract Number: 1244 • 2016 ACR/ARHP Annual Meeting

    Establishing a Case Report Form (CRF) for Systemic Autoimmune Diseases Studies

    Lorenzo Beretta1, Laurence Laigle2, Ricard Cervera3, Alessandro Santaniello1, Julien Hervouet4, Chris Chamberlain5, Jacqueline Marovac5, Maria Juárez6, Javier Martín7, Sambasiva Rao8, Jacques-Olivier Pers9, Johan Frostegård10, Jerome Wojcik11, Bernard R. Lauwerys12 and Marta E. Alarcon Riquelme13,14, 1Scleroderma Unit, Referral Center for Systemic Autoimmune Diseases, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico di Milano, Milan, Italy, 2Institut de Recherches Internationales Servier, SURESNES CEDEX, France, 3Department of Autoimmune Diseases, Institut Clínic de Medicina i Dermatologia, Hospital Clínic de Barcelona, Barcelona, Spain, 4Institut de Recherches Internationales Servier, Suresnes cedex, France, 5UCB Pharma, Slough, United Kingdom, 6UCB, Slough, United Kingdom, 7Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, PTS-Granada, Granada, Spain, 8Sanofi Genzyme, Boston, MA, 9INSERM ERI29, EA2216, Université de Brest, Labex IGO, CHRU Morvan, Brest, France, 10Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden, 11QuartzBIO, SA, Geneva, Switzerland, 12Pôle de pathologies rhumatismales inflammatoires et systémiques, Institut de Recherche Expérimentale et Clinique, Université catholique de Louvain, Brussels, Belgium, 13Center for Genomics and Oncological Research, Pfizer-University of Granada-Junta de Andalucia, Granada, Spain and Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 14Institute for Environmental Medicine, Karolinska Institutet, Stockholm, Sweden

    Background/Purpose:  Systemic autoimmune diseases (SADs) are heterogeneous conditions with peculiar characteristics that share several clinical features. It is suspected that SADs share similar molecular abnormalities,…
  • Abstract Number: 1313 • 2016 ACR/ARHP Annual Meeting

    Rheumatologic Diseases in HIV-Infected Patients in the Post-Antiretroviral Therapy Era: The County Experience

    Muhsen Al-ani1, Yasir Abdulqader1, Robert Myers1, Napatkamon Ayutyanont‎2, Bikash Bhattarai2 and Konstantinos Parperis3, 1Internal Medicine, Maricopa Integrated Health System and University of Arizona College of Medicine, Phoenix Campus, phoenix, AZ, 2Research, Maricopa Integrated Health System, phoenix, AZ, 3Rheumatology, Maricopa Integrated Health System and University of Arizona College of Medicine, Phoenix Campus, phoenix, AZ

    Background/Purpose:  HIV infection has been associated with a plethora of rheumatologic diseases, however there are only few studies in the US analyzing the frequency of…
  • Abstract Number: 1359 • 2016 ACR/ARHP Annual Meeting

    New Markers for Celiac Disease: Anti-Neo-Epitope Human and Microbial Transglutaminases

    Torsten Matthias1, Sandra Neidhöfer2, Patricia Jeremias1 and Aaron Lerner3, 1Aesku.Kipp.Institute, Wendelsheim, Germany, 2AESKU.KIPP.Stitute, Wendelsheim, Germany, 3B. Rappaport School of Medicine, Technion-Israel Institute of Technology, Haifa, Israel

    Background/Purpose: Microbial transglutaminase (mTg) and human tissue Tg (tTg) complexed to gliadin peptides present neo-epitopes. Antibodies against these complexes are called tTg neo-epitope and mTg…
  • Abstract Number: 1428 • 2016 ACR/ARHP Annual Meeting

    Patient Attitudes Towards Being Prescribed Biosimilars in Inflammatory Autoimmune Diseases in Germany

    James Piercy1, John Waller1, Emma Sullivan1, Christopher Black2 and Sumesh Kachroo2, 1Adelphi Real World, Manchester, United Kingdom, 2CORE, Merck & Co., Inc., Kenilworth, NJ

    Background/Purpose: Our aim is to address the lack of understanding surrounding patient attitudes to being prescribed biosimilars in the real world for Rheumatoid Arthritis (RA),…
  • Abstract Number: 1610 • 2016 ACR/ARHP Annual Meeting

    Safety, Tolerability, and Dose-Dependent Inhibition of T-Cell-Dependent Antibody Response with MEDI4920, a Novel, Engineered CD40L Antagonist: Results of a Single-Ascending Dose Study in Healthy Volunteers

    Marius Albulescu1, Jim Bush2, Firas Almazedi2, Ethan Grant3, Alex Godwood1, Robert Miday4, Krista Arbaugh4, Lisa H. Butler1, Michele Gunsior4, Jing Li5 and David Howe1, 1MedImmune, Cambridge, United Kingdom, 2Covance Clinical Research Unit, Leeds, United Kingdom, 3Translational Medicine, MedImmune, Gaithersburg, MD, 4MedImmune, Gaithersburg, MD, 5MedImmune, Mountain View, CA

    Background/Purpose: The CD40L/CD40 co-stimulatory pathway is important for T-cell-dependent antibody production. Previous clinical programs with intact monoclonal antibodies against CD40L have been discontinued due to…
  • Abstract Number: 1912 • 2016 ACR/ARHP Annual Meeting

    A New Avenue of Immune Regulation Conferred By Self-Glycerophospholipids Via Mobilization and Migration of Myeloid-Derived Suppressor Cells

    Ramesh Halder1 and Ram R. Singh1,2,3, 1Autoimmunity and Tolerance Laboratory, Department of Medicine/Rheumatology, UCLA, Los Angeles, CA, 2Department of Pathology and Laboratory Medicine, UCLA, Los Angeles, CA, 3Jonsson Comprehensive Cancer Center, UCLA, Los Angeles, CA

    Background/Purpose: Lipids function as essential components of biological membranes, as signaling molecules, and as energy storage molecules. Glycerol-based phospholipids, called glycerophospholipids (GPL), are the most…
  • Abstract Number: 2150 • 2016 ACR/ARHP Annual Meeting

    Autoimmune Uveitis : Potential Role of  Interleukin-22 (IL-22) in Pathogenesis

    El-Desouki Fouda1, El-Sayed Mostafa Elewah2, Mona Elrayes3, Ghada Fouda4 and Mohamed Ahmed Bakry5, 1Al-Azhar University, Dokki Cairo, Egypt, 2Opthalmology, Faculty of Medicine, Al-Azhar University, Cairo, Egypt, 3Clinical Pathology, Faculty of Medicine, Al-Azhar University, Cairo, Egypt, 4Faculty of Medicine, Al-Azhar University, Cairo, Egypt, 5Al-Azhar University, Allergy & Immunology Center, Cairo, Egypt

    Background/Purpose:  : IL-22 is a member of IL-10 family, with both anti- inflammatory and pro- inflammatory functions, orchestrating the immune and inflammatory response.IL-22 is secreted…
  • Abstract Number: 2175 • 2016 ACR/ARHP Annual Meeting

    Comparisons of Patients Prescribed Biosimilars or BIO-Originators for Autoimmune Diseases in Germany

    Sumesh Kachroo1, Christopher Black1, Emma Sullivan2, John Waller2 and James Piercy2, 1CORE, Merck & Co., Inc., Kenilworth, NJ, 2Adelphi Real World, Manchester, United Kingdom

    Background/Purpose: To compare the characteristics of patients who receive biosimilars against patients receiving bio-originators. Methods: The Adelphi Biosimilars Programme 2016 is a cross-sectional survey of…
  • Abstract Number: 2428 • 2016 ACR/ARHP Annual Meeting

    Autoantibody Diversity in Pediatric Patients Undergoing Evaluation for Autoimmune Encephalitis: A Retrospective Investigation

    Anne E Tebo1, Thomas Haven2, Aimee O. Hersh3 and Eyal Muscal4, 1Pathology, University of Utah School of Medicine and ARUP Laboratories, Salt Lake City, UT, 2Department of Pathology, University of Utah, ARUP Institute of Clinical and Experimental Pathology, Salt Lake City, UT, 3Pediatrics/Rheumatology, University of Utah, Salt Lake City, UT, 4Immunology, allergy and Rheumatology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX

    Background/Purpose:  Antibodies directed against N-methyl-D-aspartate type glutamate receptor (NMDAR), voltage-gated potassium channel (VGKC) or glutamic acid decarboxylase (GAD65) are frequently associated with autoimmune encephalitis (AE)…
  • Abstract Number: 2857 • 2016 ACR/ARHP Annual Meeting

    Results from a Phase 0 Longitudinal Clinical Trial in Cutaneous Lupus Erythematosus: Analysis of the Type I IFN Signature in the Skin and Blood and Its Relationship with Disease Activity Scores and Autoantibody Profiles

    Jessica Schreiter1, Jarrat Jordan1, Matteo Cesaroni1, Marc Chevrier2, Alexa Piantone3, Ian Gourley3, Jacqueline Benson1 and Takahiro Sato1, 1Estrela Lupus Venture, Janssen Research and Development, LLC., Spring House, PA, 2Janssen Research and Development, LLC, Collegeville, PA, 3Immunology Translational Medicine, Janssen Pharmaceutical Research and Development, LLC, Spring House, PA

    Background/Purpose:  Type I IFN (IFN-I)-regulated gene expression is known to be elevated in blood and skin lesions of patients with two different forms of cutaneous…
  • Abstract Number: 2927 • 2016 ACR/ARHP Annual Meeting

    Mechanisms Regulating the Loss of Tregs in CD11c-Flip-KO Mice That Contribute to the Spontaneous Development of Inflammatory Arthritis

    Qi Quan Huang1, Renee E. Doyle2, Robert Birkett1, Deyu Fang3 and Richard M. Pope2, 1Medicine/Rheumatology, Northwestern University Feinberg school of Medicine, Chicago, IL, 2Medicine/Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 3Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: CD11c-Flip-KO (HUPO) mice spontaneously develop inflammatory, erosive arthritis. We previously demonstrated that T regulatory cells (Tregs) were reduced in HUPO mice and that the…
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Embargo Policy

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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