ACR Meeting Abstracts

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  • Abstract Number: 27 • 2017 Pediatric Rheumatology Symposium

    Assessing the Safety of Kidney Biopsies Performed on Childhood-onset Systemic Lupus Erythmatosus Patients

    Shreya Goyal1, Daniel Ashton2,3, Kamlesh Kukreja3,4, Michael C. Braun5,6 and Scott E. Wenderfer5,7, 1Pediatrics, Baylor College of Medicine, Houston, TX, 2Interventional Radiology, Texas Children's Hospital, Houston, TX, 3Radiology, Baylor College of Medicine, Houston, TX, 4Interventional RAdiology, Texas Children's Hospital, Houston, TX, 5Texas Children's Hospital, Houston, TX, 6Pediatrics-Renal, Baylor College of Medicine, Houston, TX, 7Pediatrics-Renal, Baylor College of Medicine, Texas Children's Hospital, Houston, TX

    Title: Assessing the Safety of Kidney Biopsies Performed on Childhood-onset Systemic Lupus Erythematosus Patients Background/Purpose:                     There is very little data in the literature on…
  • Abstract Number: 2 • 2017 Pediatric Rheumatology Symposium

    Murine Model of Arthritis Flare Identifies CD8+ Tissue Resident Memory T Cells in Recurrent Synovitis

    Margaret H Chang1, Anais Levescot2, Allyn Morris2, Nathan Nelson-Maney3, Robert Fuhlbrigge4 and Peter A. Nigrovic2, 1Immunology, Boston Children's Hospital, Boston, MA, 2Rheumatology, Immunology, and Allergy, Brigham and Women’s Hospital, Boston, MA, 3Division of Rheumatology, Immunology, and Allergy, Brigham and Women’s Hospital, Boston, MA, 4Children's Hospital Colorado, Aurora, CO

    Background/Purpose: There are 75,000 children affected by JIA in the United States. Despite recent therapeutic advances, treatment often requires chronic therapy and is associated with…
  • Abstract Number: 109 • 2017 Pediatric Rheumatology Symposium

    Clinical features of pediatric Behçet’s disease patients in Japan

    Ken-ichi Yamaguchi1 and Satoshi Fujikawa2, 1Immuno-Rheumatology Center, St. Luke's International Hospital, Tokyo, Japan, 2Immuno-Rheumatology Center, St.luke's International Hospital, Tokyo, Japan

    Background/Purpose: To diagnose pediatric patients as Behçet’s disease (BD) is challenging. Sensitivity of four BD criteria, three BD criteria made for adult patients and Paediatric…
  • Abstract Number: 14 • 2017 Pediatric Rheumatology Symposium

    Efficacy and Safety of Canakinumab in Patients with Periodic Fever Syndromes (Colchicine-Resistant FMF, HIDS/MKD and TRAPS): Results from a Phase 3, Pivotal, Umbrella Trial

    Fabrizio De Benedetti1, Jordi Anton2, Eldad Ben-Chetrit3, Inmaculada Calvo4, Joost Frenkel5, Marco Gattorno6, Hal M. Hoffman7, Ozgur Kasapcopur8, Isabelle Koné-Paut9, Helen Lachmann10, Michel Moutschen11, Seza Ozen12, Pierre Quartier13, Anna Simon14, Andrew Zeft15, Karine Lheritier16, Antonio Speziale16 and Guido Junge16, 1IRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy, 2Unitat de Reumatologia Pediàtrica, Hospital Sant Joan de Déu, Barcelona, Spain, 3Rheumatology Unit, Hadassah—Hebrew University Medical Center, Jerusalem, Israel, 4Hospital Universitario y Polytecnico La Fe, Valencia, Spain, 5University Medical Center,Utrecht, Utrecht, Netherlands, 6Pediatric Rheumatology, G. Gaslini Institute, Genoa, Italy, 7Division of Rheumatology, Allergy, and Immunology, University of California at San Deigo, La Jolla, CA, 8Department of Pediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey, 9Hopital Kremlin Bicetre, University of Paris SUD, Paris, France, 10UK National Amyloidosis Centre, University College London Medical School, London, United Kingdom, 11CHU de Liège/ University of Liège, Liège, Belgium, 12Department of Pediatrics, Hacettepe University, Ankara, Turkey, 13Necker-Enfants Malades Hospital, Paris, France, 14National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 15Pediatrics Rheumatology, Cleveland Clinic, Cleveland, OH, 16Novartis Pharma AG, Basel, Switzerland

    Background/Purpose:  Open-label studies have suggested the efficacy of canakinumab (CAN), a fully human, highly specific anti-IL-1β neutralizing monoclonal antibody, in colchicine-resistant-FMF (crFMF), hyper-immunoglobulin (Ig) D…
  • Abstract Number: 8 • 2017 Pediatric Rheumatology Symposium

    Examination of Reported Risk Loci from Candidate Gene Studies of Systemic Juvenile Idiopathic Arthritis Identifies Link between IL1RN Variation and both Disease Susceptibility and Response to Interleukin-1 Directed Therapy

    Victoria Arthur1, Emily Shuldiner1, Anne Hinks2, The International Childhood Arthritis Genetics (INCHARGE) Consortium3, Patricia Woo4, Wendy Thomson2, Elaine F. Remmers5 and Michael J. Ombrello1, 1Translational Genetics and Genomics Unit, NIAMS, NIH, Bethesda, MD, 2Arthritis Research UK Centre for Genetics and Genomics,The University of Manchester, Manchester, United Kingdom, 3INCHARGE Consortium, Bethesda, MD, 4Paediatric Rheumatology Unit, University College London, London, United Kingdom, 5Inflammatory Disease Section, NHGRI, NIH, Bethesda, MD

    Background/Purpose: Systemic JIA (sJIA) is a childhood inflammatory disease whose pathophysiology is poorly understood. sJIA is phenotypically heterogeneous with variable manifestations and responses to treatment.…
  • Abstract Number: 18 • 2017 Pediatric Rheumatology Symposium

    Bridging the gap between GWAS and mechanism in juvenile idiopathic arthritis using a novel high-throughput experimental screen

    Gang Li1, Marta Martinez-Bonet1, Di Wu2, Jing Cui3 and Peter A. Nigrovic1,4, 1Brigham and Women's Hospital, Boston, MA, 2University of North Carolina, Chapel Hill, Chapel Hill, NC, 3Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 4Division of Immunology, Boston Children's Hospital, Boston, MA

    Background/Purpose:  Genome wide association studies (GWAS) have identified 27 non-HLA loci that convey risk for oligoarticular and seronegative polyarticular JIA. Most associated haplotypes bear no…
  • Abstract Number: 85 • 2017 Pediatric Rheumatology Symposium

    Characteristics of anti-MDA5 autoantibody-associated Juvenile Dermatomyositis (JDM) in North America

    Gulnara Mamyrova1, Takayuki Kishi2, Ira N Targoff3, Rodolfo V Curiel1, Frederick W Miller2, Lisa G Rider1,2 and The Childhood Myositis Heterogeneity Collaborative Study Group, 1Division of Rheumatology, Department of Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC, 2Environmental Autoimmunity Group, National Institute of Environmental Health Sciences, National Institute of Health, Bethesda, MD, 3VA Medical Center, University of Oklahoma Health Sciences Center, and Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Anti-MDA5 Abs have been reported to associate with clinically amyopathic and classic dermatomyositis (DM), with severe progressive interstitial lung disease (ILD) and poor prognosis…
  • Abstract Number: 157 • 2017 Pediatric Rheumatology Symposium

    Utility of Mailed Reminders for Uveitis Screening Guidelines in Patients with Juvenile Idiopathic Arthritis

    Laura Ballenger1 and Kyla Driest2, 1Nationwide Children's Hospital, Columbus, OH, 2Rheumatology, Nationwide Children's Hospital, Columbus, OH

    Background/Purpose: Uveitis is a major complication in patients with juvenile idiopathic arthritis (JIA) and can be completely asymptomatic until vision loss develops. In order to…
  • Abstract Number: 72 • 2017 Pediatric Rheumatology Symposium

    Systemic Juvenile Idiopathic Arthritis in a Colombian cohort: onset and clinical course

    Angela Mosquera, Clara Malagón and Christine Arango, Pediatric Rheumatology, Pediatric rheumatology post graduate program El Bosque University, Bogota, Colombia

    Background/Purpose: Juvenile idiopathic arthritis is the most prevalent rheumatic disease in children. The systemic form accounts for 10-15% of cases and is characterized by a…
  • Abstract Number: 40 • 2017 Pediatric Rheumatology Symposium

    Perspectives of young people with Juvenile Idiopathic Arthritis, their caregivers, and health care providers on transition to adult care: Informing development of a transition toolkit

    Nadia Luca1, Evelyn Rozenblyum2, April Elliott3, Lynn R. Spiegel4, Nicole Johnson5, Sara Ahola Kohut6, Yvonne Brandelli3, Carolyn Johns7, Stephanie Luca8, Dianne P. Mosher9, Gordon Soon10, Karine Toupin-April11, Gabriela Uifalusi3 and Jennifer N. Stinson12, 1Pediatric Rheumatology, University of Calgary, Alberta Children's Hospital, Calgary, AB, Canada, 2Royal University Hospital, Saskatoon, SK, Canada, 3Alberta Children's Hospital, Calgary, AB, Canada, 4Rheumatology/Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada, 5Pediatrics, University of Calgary, Alberta Children's Hospital, Calgary, AB, Canada, 6Hospital for Sick Children, Toronto, ON, Canada, 7Alberta Health Services, Calgary, AB, Canada, 8The Hospital for Sick Children, Toronto, ON, Canada, 9Med, University of Calgary, Calgary, AB, Canada, 10Pediatric Rheumatology, Hospital for Sick Children, Toronto, ON, Canada, 11Children’s Hospital of Eastern Ontario Research Institute, Ottawa, ON, Canada, 12Anesthesia and Pain Medicine, The Hospital for Sick Children, Toronto, ON, Canada

    Background/Purpose: A seamless transition from pediatric to adult care is critical to ensure optimal health outcomes in adolescents and young adults with Juvenile Idiopathic Arthritis…
  • Abstract Number: 47 • 2017 Pediatric Rheumatology Symposium

    Baseline characteristics of the first 123 patients enrolled in the Childhood Arthritis and Rheumatology Research Alliance Start Time Optimization of Biologic Therapy in Polyarticular JIA comparative effectiveness study

    Sarah Ringold1, George A. Tomlinson2, Pamela F. Weiss3, Laura E. Schanberg4, Brian M. Feldman5, Mary Ellen Riordan6, Anne C. Dennos7, Vincent Del Gaizo8, Kate Murphy9, Yukiko Kimura6 and the CARRA Registry Investigators, 1Seattle Children's Hospital, Seattle, WA, 2Medicine, Mount Sinai Hospital, Toronto, ON, Canada, 3Division of Rheumatology, Center for Pediatric Clincial Effectiveness, Children's Hospital of Philadelphia, Philadelphia, PA, 4Pediatrics, Duke Medical Center, Durham, NC, 5Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada, 6Hackensack University Medical Center, Hackensack, NJ, 7Duke Clinical Research Institute, Durham, NC, 8Parent Partner, Whitehouse Station, NJ, 9Patient Partner, San Francisco, CA

    Background/Purpose: Many new effective treatments for polyarticular JIA (p-JIA) are available, but there is significant variation among pediatric rheumatologists in the timing of when biologic…
  • Abstract Number: 105 • 2017 Pediatric Rheumatology Symposium

    Isolated Pediatric Pulmonary Capillaritis: A Comprehensive Single-Center Review of Disease Course, Management, and Prognosis

    William Lapin1, Saimun Singla2, Eyal Muscal3 and Manuel Silva-Carmona4, 1Department of Pediatrics, Division of Immunology, Allergy and Rheumatology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX, 2Department Pediatrics, Division of Immunology, Allergy and Rheumatology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX, 3Immunology, Allergy and Rheumatology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX, 4Department of Pediatrics, Pulmonology Section, Baylor College of Medicine, Texas Children's Hospital, Houston, TX

    Background/Purpose: Pediatric diffuse alveolar hemorrhage (DAH) is a life-threatening disorder characterized by pulmonary hemorrhage and respiratory insufficiency. Histologically, DAH with capillary inflammation is known as…
  • Abstract Number: 124 • 2017 Pediatric Rheumatology Symposium

    Underutilization of Social Workers for Mental Health Care of Adolescents in Pediatric Rheumatology: A Mixed Methods Study

    Andrea Knight1,2, Michelle Vickery3, Lauren Faust4, Eyal Muscal5, Alaina M. Davis6, Julia Harris7, Aimee O. Hersh8, Martha Rodriguez9, Karen Onel10, Laura E. Schanberg11, Tamar Rubinstein12, Nina Washington13,14, Elissa Weitzman15,16, Hana Conlon17, Dana Gerstbacher18, Jennifer Woo19 and Emily Von Scheven20, 1Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, 2Center for Pediatric Clinical Effectiveness & PolicyLab, Philadelphia, PA, 3PolicyLab, Children's Hospital of Philadelphia, Philadelphia, PA, 4Children's Hospital of Philadelphia, Philadelphia, PA, 5Immunology, Allergy and Rheumatology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX, 6Pediatric Rheumatology, Monroe Carell Junior Children's Hospital at Vanderbilt, Division of Pediatric Rheumatology, Nashville, TN, 7Children's Mercy Kansas City, Kansas City, MO, 8Pediatrics/Rheumatology, University of Utah, Salt Lake City, UT, 9Pediatrics, University of Chicago Medical Center, Chicago, IL, 10Hospital for Special Surgery, New York, NY, 11Pediatrics, Duke Medical Center, Durham, NC, 12Albert Einstein College of Medicine, Children's Hospital at Montefiore, New York, NY, 13University of Mississippi Medical Center, Jackson, MS, 14Dept. of Pediatric Rheumatology, University of Mississippi Medical Center, Jackson, MS, 15Boston Children's Hospital, Boston, MA, 16Harvard Medical School, Boston, MA, 17Columbia University, New York, NY, 18Stanford University, Palo Alto, CA, 19University of California Los Angeles, Los Angeles, CA, 20Dept of Pediatric Rheumatology, Univ of California San Francisco, San Francisco, CA

    Background/Purpose: Mental health problems are common, but undertreated in adolescents with rheumatologic conditions. As social workers help manage medical and psychosocial aspects of illness, we…
  • Abstract Number: 35 • 2017 Pediatric Rheumatology Symposium

    Kv1.3 Expression on Urinary Leukocytes in Lupus Nephritis:  Potential for Targeted Immunotherapy

    Anne Stevens1, Andrew Hinkle2, Megan Yuasa3, David Peckham4, Chelsea Olsen5, Craig Philips5, Shawn P. Iadonato4 and Peter Probst6, 1University of Washington, Pediatrics, Seattle, WA, 2Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, 3Seattle Children’s Research Institute, Seattle, WA, 4Kineta Inc, Seattle, WA, 5KPI Therapeutics, Inc., Seattle, WA, 6Kineta, Inc, Seattle, WA

    Background/Purpose: Lymphocyte activation depends upon a calcium signaling cascade that is regulated by voltage-gated potassium channels. Effector memory T cells (TEM), which are implicated in…
  • Abstract Number: 133 • 2017 Pediatric Rheumatology Symposium

    3-D Explant Method Facilitates the Study of Lymphocytes in Synovium and Reveals a Population of Resident Memory-Like T Cells in Rheumatoid Arthritis

    Lauren Henderson1, Deepak Rao2, Nikola Teslovich3,4, Sandra King5, Fumitaka Mizoguchi6, Sarah Ameri6, Allyn Morris7, Christopher Elco5, Margaret Chang8, Anais Levescot9, James Lederer10, Scott Martin11, Barry Simmons11, John Wright11, Michael Brenner2, Soumya Raychaudhuri12,13,14,15,16, Robert Fuhlbrigge17 and Peter Nigrovic1,18, 1Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, 2Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 3Program in Medical and Population Genetics, Broad Institute of Massachusetts Technical Institute and Harvard University, Cambridge, MD, 4Divisions of Genetics and Rheumatology, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA, 5Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 6Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 7Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, MA, 8Division of Immunology, Boston Children's Hospital, Boston, MA, 9Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, boston, MA, 10Department of Surgery, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 11Department of Orthopedic Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 12Divisions of Genetics and Rheumatology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, 13Program in Medical and Population Genetics, Broad Institute of Massachusetts Technical Institute, Harvard University, Cambridge, MA, 14Partners Center for Personalized Genetic Medicine, Boston, MA, 15Institute of Inflammation and Repair, University of Manchester, Manchester, United Kingdom, 16Rheumatology Unit, Karolinska Institutet, Karolinska University Hospital Solna, Stockholm, Sweden, 17Children's Hospital Colorado, Aurora, CO, 18Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA

    Background/Purpose:  Tissue resident memory T (TRM) cells survive indefinitely in barrier tissues and mediate swift immunologic memory responses at sites of microbe entry. TRM cells…
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