ACR Meeting Abstracts

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Abstracts tagged "B cells"

  • Abstract Number: 393 • 2017 ACR/ARHP Annual Meeting

    The Role of Follicular Helper 17 T Cells in Glucose-6-Phosphate Isomerase Induced Arthritis

    Izumi Kurata, Isao Matsumoto, Atsumu Osada, Hiroshi Ebe, Hoshimi Kawaguchi, Yuya Kondo, Hiroto Tsuboi and Takayuki Sumida, Department of Internal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

    Background/Purpose: Follicular helper T (Tfh) cell is a novel T cell subset which promotes follicular B cell activation, differentiation to plasma cell and antibody production.…
  • Abstract Number: 1917 • 2017 ACR/ARHP Annual Meeting

    A Novel Type I Interferon Biomarker on B Cell Predicts with Disease Activity in SLE and Can be Measured By Cell Surface Tetherin (CD317)

    Yasser M El-Sherbiny1,2,3, Md Yuzaiful Md Yusof1, Antonios Psarras1, Elizabeth M.A. Hensor1, Kumba Kabba1, Alaa Mohamed1,4, Miriam Wittmann5, Paul Emery5,6 and Edward M Vital1,5,7, 1Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 2NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals, NHS Trust, Leeds, United Kingdom, 3Clinical Pathology dept., School of Medicine, Mansoura University, Mansoura, Egypt, 4Faculty of Medicine, Assiut University, Department of Rheumatology and Rehabilitation, Assiut, Egypt, 5NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom, 6University of Leeds, Leeds Institute of Rheumatic and Musculoskeletal Medicine, Leeds, United Kingdom, 7University of Leeds, Leeds, United Kingdom

    Background/Purpose: SLE is an IFN-I-mediated disease with dysregulated handling of self-nuclear antigens triggering anti-viral immune mechanisms. The level of IFN-I activity appears to stratify for…
  • Abstract Number: 24 • 2017 ACR/ARHP Annual Meeting

    Trafficking of Innate B Cells to the Lungs As a Novel Mechanism in a Model of Pulmonary Lupus and Vasculitis

    Priti Prasad1, Michael Fishbein2, Rohan Sharma3, Ramesh Halder4, Isela Valera1 and Ram R. Singh5, 1Autoimmunity and Tolerance Laboratory, Division of Rheumatology, Department of Medicine, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA, 2Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at University of California Los Angeles, Los ángeles, CA, 3Autoimmunity and Tolerance Laboratory, Division of Rheumatology, Department of Medicine, David Geffen School of Medicine at University of California Los Angeles, Los angeles, CA, 4Autoimmunity and Tolerance Laboratory, Division of Rheumatology, Department of Medicine, David Geffen School of Medicine at University of California Los Angeles, Los ángeles, CA, 5Autoimmunity and Tolerance Laboratory, Department of Medicine/Rheumatology, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA

    Background/Purpose: Lung is involved in up to 50% patients with SLE. Among manifestations of pulmonary lupus, pneumonitis, vasculitis and diffuse pulmonary hemorrhage (DPH) carry a…
  • Abstract Number: 560 • 2017 ACR/ARHP Annual Meeting

    Clinical Relevance of Serum Free Light Chain Level As Biomarker in Primary Sjögren′s Syndrome

    Gwenny M. Verstappen1, Johan Bijzet1, Jolien F. van Nimwegen1, Martha S. van Ginkel1, Arjan Vissink2, Hendrika Bootsma1 and Frans G.M. Kroese1, 1Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, 2Oral and Maxillofacial Surgery, University of Groningen, University Medical Center Groningen, Groningen, Netherlands

    Background/Purpose: During immunoglobulin synthesis in B-cells, kappa and lambda light chains are produced in excess compared to heavy chains, and the surplus of light chains…
  • Abstract Number: 2562 • 2017 ACR/ARHP Annual Meeting

    Inhibition of Spleen Tyrosine Kinase Improves Renal Pathology and Reduces Lymphocyte Activation in the MRL/Lpr and NZB/NZW Murine Models of Systemic Lupus Erythematosus

    Julie Di Paolo1, Christopher Pohlmeyer1, Zhi-Hua Cui2, Gundula Min-Oo1, Igor Mikaelian3, Robert Brockett3, Bernard Murray4, Roy Bannister5, JiYun Kim6 and Franziska Matzkies7, 1Immunology and Inflammation Biology, Gilead Sciences, Foster City, CA, 2Fibrosis Biology, Gilead Sciences, Foster City, CA, 3Biology Core Support, Gilead Sciences, Foster City, CA, 4DMPK, Gilead Sciences, Foster City, CA, 5Drug Safety, Gilead Sciences, Foster City, CA, 6Biomarkers, Gilead Sciences, Foster City, CA, 7Gilead Sciences, Foster City, CA

    Background/Purpose: Spleen tyrosine kinase (SYK) mediates immunoreceptor signaling in hematopoietic cells important in the initiation and progression of systemic lupus erythematosus (SLE), including those from…
  • Abstract Number: 104 • 2017 Pediatric Rheumatology Symposium

    Rituximab Treatment for Chronic Steroid-Dependent Henoch-Schonlein Purpura

    Esraa M. A. Eloseily1,2, Courtney Crayne1, Melissa L Mannion3, Saji P Azerf4, Peter Weiser1, Timothy Beukelman1, Matthew L. Stoll1, Dan Feig5, Prescott Atkinson6 and Randy Q. Cron1, 1Pediatric Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 2Pediatrics, Assiut University, Assiut, Egypt, 3Pediatric rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4School of medicine, Univesity of Alabama at Birmingham,, Birmingham, AL, 5Pediatric Nephrology, University of Alabama at Birmingham, Birmingham, AL, 6Pediatric Allergy and Immunology, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Henoch-Schonlein purpura (HSP) is a small vessel vasculitis characterized by non-thrombocytopenic purpura, abdominal pain, arthritis, and glomerulonephritis. Typically, HSP is self-limited, but more severe…
  • Abstract Number: 19 • 2017 Pediatric Rheumatology Symposium

    The Lymphocyte Repertoire in Juvenile Dermatomyositis

    Kacie Hoyt1, Edwin Anderson1,2, Megan L. Curran3, Robert Fuhlbrigge4, Luigi Notarangelo5, Lauren M. Pachman6, Susan Kim7 and Lauren Henderson8, 1Division of Immunology, Boston Children's Hospital, Boston, MA, 2Clinical Research Center/Rheumatology, Boston Children's Hospital, Medford, MA, 3Pediatric Rheumatology, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, 4Children's Hospital Colorado, Aurora, CO, 5National Institute of Allergy and Infectious Diseases, Bethesda, MD, 6Cure JM Program of Excellence in Juvenile Myositis Research, Stanley Manne Children’s Research Institute, affiliated with Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL, 7Pediatric Rheumatology, University of California, San francisco School of Medicine, San Francisco, CA, 8Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA

    Background/Purpose: In adult dermatomyositis (DM), clonal populations of T and B cells with shared variable (V) gene usage have been identified in affected muscle, suggesting…
  • Abstract Number: 7 • 2017 Pediatric Rheumatology Symposium

    Activation of Immature, Transitional B cells by Integrated BCR, TLR and TACI signals promotes systemic autoimmunity in high BAFF settings

    Holly Jacobs, Samuel Du, Tanvi Arkatkar and Shaun Jackson, Seattle Children's Research Institute, Seattle, WA

    Background/Purpose: B cell activating factor of the TNF family (BAFF, also known as BLyS) promotes B cell survival and activation by binding distinct B cell…
  • Abstract Number: 816 • 2016 ACR/ARHP Annual Meeting

    Clinical Response to Treatment with Belimumab and Mycophenolate Mofetil Is Associated with Decrease in B Cell, TGF-β and PDGF Signaling in Systemic Sclerosis

    Viktor Martyanov1, Jessica K. Gordon2, Tammara A. Wood1, Robert F. Spiera2 and Michael L. Whitfield1, 1Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 2Rheumatology, Hospital for Special Surgery, New York, NY

    Background/Purpose: While B cell signaling is thought to be important in the pathogenesis of systemic sclerosis (SSc), the experience with B cell targeting therapies in…
  • Abstract Number: 1921 • 2016 ACR/ARHP Annual Meeting

    Evidence for Prevotella Copri As an Immune-Relevant Bacterium in Rheumatoid Arthritis

    Annalisa Pianta1, Sheila Arvikar1, Klemen Strle1, Elise E. Drouin2, Qi Wang3, Catherine E. Costello3 and Allen C. Steere4, 1Massachusetts General Hospital, Harvard Medical School, Boston, MA, 2Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 3Center for Biomedical Mass Spectrometry, Boston University School of Medicine, Boston, MA, 4Center for Immunolgy and Inflammatory Diseases, Massachusetts General Hospital, Harvard Medical School, Boston, MA

    Background/Purpose:  Prevotella copri Methods:  HLA-DR-presented peptides were identified directly from RA patients' synovial tissue or peripheral blood mononuclear cells (PBMC) by tandem mass spectrometry. P.…
  • Abstract Number: 2861 • 2016 ACR/ARHP Annual Meeting

    Proportions of Circulating Follicular Helper T Cells and Complement Levels, White Blood Cell Counts, and Skin Manifestations in Patients with Active Systemic Lupus Erythematosus

    Jun Kikuchi1, Masaru Takeshita1, Katsuya Suzuki2, Yoshiaki Kassai3, Takahiro Miyazaki3 and Tsutomu Takeuchi2, 1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 2Keio University School of Medcine, Division of Rheumatology, Department of Internal Medicine, Tokyo, Japan, 3Inflammation Drug Discovery Unit, Pharmaceutical Research Division, Takeda Pharmaceutical Company Ltd., Kanagawa, Japan

    Background/Purpose:  Although circulating B cells and T cells, including follicular helper T (Tfh) cells, are reported to be involved in systemic lupus erythematosus (SLE) 1,2),…
  • Abstract Number: 916 • 2016 ACR/ARHP Annual Meeting

    Novel Immunosignature Stratifies Patients with Rheumatoid Arthritis into Distinct Disease Sub-Groups and Predicts Response to Anti-Tnfα Therapies

    Laura Magill1, Marsilio Adriani1, Victoria Howard2, Jessica Manson2, Elizabeth Jury3 and Claudia Mauri4, 1University College London, London, United Kingdom, 2University College London Hospitals NHS Trust, London, United Kingdom, 3Division of Medicine, Centre for Rheumatology Research, University College London, London, United Kingdom, 4Division of Medicine, Centre for Rheumatology Research, University College London, University College London, London, United Kingdom

    Background/Purpose:  Autoimmune rheumatic diseases, including rheumatoid arthritis (RA), have multifactorial pathogenesis associated with failure of immune tolerance. Advances in understanding the disease immunopathology have led…
  • Abstract Number: 1937 • 2016 ACR/ARHP Annual Meeting

    Analysis of Innate and Adaptive Immune Responses in Eosinophilic Granulomatosis with Polyangiitis (Churg-Strauss)

    Jeremie Dion1,2, Jonathan London2,3, Benjamin Chaigne2,4, Nicolas Dumoitier2, Bertrand Dunogué5, Pascal Cohen3, Matthieu Groh4, Claire Le Jeunne4, Luc Mouthon2,5 and Benjamin Terrier2,5, 1Internal medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, 2INSERM U1016, Institut Cochin, Equipe Neutrophiles et Vascularites, Paris, France, 3Internal Medecine, National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, 4National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, 5Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France

    Background/Purpose: Eosinophilic granulomatosis with polyangiitis (EGPA, formerly called Churg-Strauss syndrome) belongs to ANCA-associated vasculitis and is characterized by late onset asthma, blood and tissue eosinophilia…
  • Abstract Number: 2872 • 2016 ACR/ARHP Annual Meeting

    SLE Subjects Express High Levels of Intracellular Interferon-β That Acts in an Autocrine Fashion to Promote Survival of Transitional Stage B Cells

    Jennie Hamilton1, Qi Wu2, PingAr Yang3, Bao Luo4, Shanrun Liu5, Jun Li6, Ignacio Sanz7, W. Winn Chatham8, Hui-Chen Hsu2 and John D. Mountz9, 1Medicine/Division of Clinical Immunology and Rhematology, University of Alabama at Birmingham, Birmingham, AL, 2Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 3Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 5Biochemistry & Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL, 6Medicine, University of Alabama at Birmingham, Birmingham, AL, 7Rheumatology and Lowance Center for Human Immunology, Emory University School of Medicine and Lowance Center for Human Immunology, Atlanta, GA, 8Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 9Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham and Birmingham VA Medical center, Birmingham, AL

    Background/Purpose:  Upregulation of interferon-β (IFNβ) is an important step in promoting maturation and survival of B cells. Secretion and autocrine action of IFNβ requires assembly…
  • Abstract Number: 124 • 2016 ACR/ARHP Annual Meeting

    Socioeconomic-Demographic, Disease Activity, Treatment and Immunologic Variables Affect B Cell Subtypes in Systemic Lupus Erythematosus

    Arlene Bravo1, Michelle T. Ngo2, Michael De Vera3, Karina Marianne D. Torralba2,4 and Abigail Benitez2,4, 1Internal Medicine, Loma Linda University, Loma Linda, CA, 2Rheumatology, Loma Linda University, Loma Linda, CA, 3Transplant Surgery, Loma Linda University, Loma Linda, CA, 4Transplantation Institute, Loma Linda University, Loma Linda, CA

    Background/Purpose: B cell subset proportions within the B cell pool, also known as B cell signatures (BCS), reflect not only systemic lupus erythematosus (SLE) disease…
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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 ET on November 14, 2024. 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].

ACR Abstract Embargo Policy

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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