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Abstracts tagged "B-Cell Targets"

  • Abstract Number: 0009 • ACR Convergence 2022

    Pharmacokinetics, Receptor Occupancy, and Pharmacodynamics of Obexelimab Following Intravenous Administration in Adult Healthy Volunteers and in Patients with Rheumatoid Arthritis

    Xiaodong Wang, Mark Matijevic, Allen Poma, Shauna Quinn, Minggeng Gao, Lisa Crockett, Jessica Karnes, Keith Wilcoxen and Hua Mu, Zenas BioPharma, Waltham

    Background/Purpose: Obexelimab is a novel bifunctional antibody that inhibits B-cell, CD19 expressing plasma cell, and plasmablast activity and is expected to provide clinical benefit across…
  • Abstract Number: 1428 • ACR Convergence 2022

    Molecular and Clinical Profiling of Rheumatoid Arthritis Patients Predicts the Response to Rituximab

    Daniel Toro-Domínguez1, José Linares-Blanco1, Raúl López-Domínguez2, Pilar S. López-Garrido2, Georgina Galicia-Rosas1, Pedro Carmona-Sáez2 and Marta Alarcon-Riquelme1, 1Center for Genomics and Oncological Research (GENYO), Granada, Spain, 2University of Granada, Granada, Spain

    Background/Purpose: Rheumatoid arthritis (RA) is one of the most prevalent rheumatic diseases, mainly characterized by chronically painful, swollen joints that can severely impair physical function…
  • Abstract Number: 0045 • ACR Convergence 2022

    Rheumatoid Arthritis Patient-derived Anti-citrullinated Protein Antibodies (ACPAs) Ameliorate Joint Inflammation in Early Collagen-antibody Induced Arthritis (CAIA)

    Alejandro Gomez1, Camille Brewer1, Jae-Seung Moon2, Suman Acharya1, Tobias V. Lanz1, Qian Wang1, Gundula Min-Oo3, Anita Niedziela-Majka3 and William Robinson4, 1Stanford University, Stanford, CA, 2Stanford University, Palo Alto, CA, 3Gilead Sciences, Foster City, CA, 4Stanford University School of Medicine, Palo Alto, CA

    Background/Purpose: ACPAs are present in two-thirds of patients with rheumatoid arthritis (RA) and are associated with higher risks for severe bone erosions. The pathogenic role…
  • Abstract Number: 1572 • ACR Convergence 2022

    CD40, BLK and BANK1 in the Pathogenesis of Immunoglobulin-A Vasculitis

    Fernanda Genre1, Sara Remuzgo-Martinez1, Veronica Pulito-Cueto1, JOAO CARLOS BATISTA LIZ2, Diana Prieto-Peña1, Belén Atienza-Mateo1, Belén Sevilla-Pérez3, Javier Llorca4, Norberto Ortego5, María Teresa Leonardo6, Ana Peñalba6, F. Javier Narváez7, Luis Martín-Penagos8, Emilio Rodrigo8, Cristina Gomez-Fernandez9, Lara Belmar-Vega8, José A. Miranda-Filloy10, Luis Caminal-Montero11, Paz Collado12, Pedro Rodriguez-Jimenez13, Diego De Argila14, Patricia Quiroga-Colina15, Esther Vicente-Rabaneda16, Enrique Rubio17, Manuel León Luque17, Juan María Blanco-Madrigal18, Eva Galíndez-Agirregoikoa19, Javier Martín20, Santos Castañeda16, Ricardo Blanco21, Miguel Ángel González-Gay22 and Raquel Lopez Mejias23, 1Research Group on Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Bone Diseases of the Musculoskeletal System, IDIVAL; and Department of Rheumatology, Hospital Universitario Marqués de Valdecilla, Santander, Spain, 2Ilerna, Madrid, Spain, 3Division of Pediatrics, Hospital Universitario San Cecilio, Granada, Spain, 4Department of Epidemiology and Computational Biology, School of Medicine, University of Cantabria, and CIBER Epidemiología y Salud Pública (CIBERESP), Santander, Spain, 5Medicine Department, Universidad de Granada, Granada, Spain, 6Division of Pediatrics, Hospital Universitario Marqués de Valdecilla, Santander, Spain, 7Rheumatology Department, Hospital Universitario de Bellvitge, Barcelona, Spain, 8Division of Nephrology, Hospital Universitario Marqués de Valdecilla, Santander, Spain, 9Division of Dermatology, Hospital Universitario Marqués de Valdecilla, Santander, Spain, 10Division of Rheumatology, Hospital Universitario Lucus Augusti, Lugo, Spain, 11Division of Rheumatology, Hospital Universitario Central de Asturias, Oviedo, Spain, 12Division of Rheumatology, Hospital Universitario Severo Ochoa, Madrid, Spain, 13Dermatology Department, Hospital Universitario de La Princesa, Madrid, 14Dermatology Department, Hospital Universitario de La Princesa, Madrid, Spain, 15Division of Rheumatology, Hospital Universitario de La Princesa, Madrid, Spain, 16Division of Rheumatology, Hospital Universitario de La Princesa, IIS-Princesa, Madrid, Spain, 17Division of Rheumatology, Hospital Universitario Virgen del Rocío, Sevilla, Spain, 18Division of Rheumatology, Hospital Universitario de Basurto, Bilbao, Spain, 19Basurto University Hospital, Bilbao, Spain, 20Instituto de Parasitología y Biomedicina ‘López-Neyra’, CSIC, PTS Granada, Granada, Spain, 21Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain, 22Department of Medicine and Psychiatry, Universidad de Cantabria; Rheumatology Division, Hospital Universitario Marqués de Valdecilla; Research group on genetic epidemiology and atherosclerosis in systemic diseases and in metabolic diseases of the musculoskeletal system, IDIVAL, Santander, Spain. Cardiovascular Pathophysiology and Genomics Research Unit, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa, 23IDIVAL, Santander, Spain

    Background/Purpose: CD40 is a membrane glycoprotein expressed on B cells surface that activates antigen presenting cells [1]. BLK and BANK1 are components of B cells…
  • Abstract Number: 0335 • ACR Convergence 2022

    Multiplexed Mass Cytometry of Cutaneous Lupus Erythematosus and Dermatomyositis Skin: An In-depth B Cell Directed Immunoprofile

    Mariko Ogawa-Momohara1, Thomas Vazquez2, Meena Sharma2, Josh Dan3, Grant Sprow3 and Victoria Werth3, 1Nagoya University Graduate School of Medicine, Nagoya, Japan, 2Philadelphia VAMC, Philadelphia, PA, USA and Department of Dermatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, 3Philadelphia VAMC, Philadelphia, PA, USA and Department of Dermatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia

    Background/Purpose: Cutaneous lupus erythematosus (CLE) and dermatomyositis (DM) are both characterized histologically by interface dermatitis with a perivascular and periadnexal lymphocytic infiltrate, requiring clinical correlation…
  • Abstract Number: 1629 • ACR Convergence 2022

    AUR200: An Improved BAFF/APRIL Inhibitor with Increased Potency and Safety for the Treatment of B Cell-Mediated Diseases

    Shawn Morales, Jennifer Cross and Robert Huizinga, Aurinia Pharmaceuticals, Inc., Victoria, BC, Canada

    Background/Purpose: AUR200 targets both B cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL), which are key mediators in the pathogenesis of B cell-mediated autoimmune…
  • Abstract Number: 0351 • ACR Convergence 2022

    The Effect of Belimumab to Achieve Low Disease Activity or Remission Based on SLE-DAS in Systemic Lupus Erythematosus: A Single-center Retrospective Study

    Yasuhiro Hasegawa1, Yoshiyuki Arinuma2, Yu Matsueda1, Kenji Oku3 and Kunihiro Yamaoka4, 1Kitasato University School of Medicine, Sagamihara, Japan, 2Kitasato University, Kanagawa, Japan, 3Kitasato University, Chigasaki, Japan, 4Department of Rheumatology and Infectious Diseases, Kitasato University School of Medicine, Kanagawa, Japan

    Background/Purpose: Low disease activity (LDA) and remission in patients with systemic lupus erythematosus (SLE) can reduce organ damage accrual and improve prognosis. We investigated the…
  • Abstract Number: 1631 • ACR Convergence 2022

    Phospholipase D 4 Is a Novel Surface Marker of a Distinctive B Cell Population Overlapping with Double Negative 2 B Cells

    Ken Yasaka1, Tomohide Yamazaki2, Hiroko Sato1, Tsuyoshi Shirai1, Hiroshi Fujii1, Tomonori Ishii3 and Hideo Harigae4, 1Department of Rheumatology, Tohoku University Hospital, Sendai, Japan, 2SBI Biotech, Tokyo, Japan, 3Clinical Research, Innovation and Education Center, Tohoku University Hospital, Sendai, Japan, 4Department of Hematology, Tohoku University Hospital, Sendai, Japan

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by various autoantibodies. In particular, targeting autoreactive B cells could be a promising therapy with…
  • Abstract Number: 0527 • ACR Convergence 2022

    Rituximab as Maintenance Therapy for ANCA-associated Vasculitides: Pooled Analysis and Long-term Outcome of MAINRITSAN Trials

    Florence Delestre1, Pierre Charles2, Loïc Guillevin3, Raphaël Porcher4 and Benjamin Terrier3, 1cochin Hospital, Paris, France, 2Institut Mutualiste Montsouris, Paris, France, 3National Referral Center for Rare Systemic Autoimmune Diseases, Cochin Hospital, Paris, France, 4Université Paris Cité, Hôtel-Dieu, Paris, France

    Background/Purpose: Maintenance therapy after induction of remission has been shown to reduce relapse rate and mortality in anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis. The three MAINRITSAN…
  • Abstract Number: 1632 • ACR Convergence 2022

    Novel Autoantibodies Identify Sjögren’s Disease in Patients Lacking Serum IgG Specific for Ro/SS-A and La/SS-B

    Sherri Longobardi1, Charmaine Lopez-Davis1, Bhuwan Khatri1, Constantin Georgescu1, Christina Lawrence1, Astrid Rasmussen1, Lida Radfar2, R. Hal Scofield2, Robert C. Axtell1, Gabriel Pardo1, Jonathan Wren1, Kristi A Koelsch1, Joel Guthridge1, Judith James1, Christopher Lessard1 and A. Darise Farris1, 1Oklahoma Medical Research Foundation, Oklahoma City, OK, 2University of Oklahoma Health Sciences Center, Oklahoma City, OK

    Background/Purpose: Classification of Sjögren's disease (SjD) requires either Ro/SS-A autoantibodies or minor salivary gland biopsy positive for focal lymphocytic infiltrates. Up to 40% of SjD…
  • Abstract Number: 0624 • ACR Convergence 2022

    CD20+ T Cells in the Synovial Fluid of Patients with Rheumatoid Arthritis Suggest a Role for Trogocytosis in Disease Pathogenesis and Activity

    Maria De Santis1, Natasa Isailovic2, Giacomo Maria Guidelli3, Daniela Renna4, Arianna Sonaglia3, Nicoletta Luciano3, Marta Caprioli5, Angela Ceribelli1, Francesca Motta6, Matteo Vecellio1, Enrico Brunetta3 and Carlo Selmi1, 1Humanitas University, IRCCS Humanitas Research Hospital, Rheumatology and Clinical Immunology, Pieve Emanuele, Italy, 2IRCCS Humanitas Research Hospital, Rozzano (MI), Italy, Rozzano, Italy, 3IRCCS Humanitas Research Hospital, Rheumatology and Clinical Immunology, Rozzano, Italy, 4IRCCS Humanitas Research Hospital, Rheumatology and Clinical Immunology, Milano, Italy, 5IRCCS Humanitas Research Hospital, Rheumatology and Clinical Immunology, Pavia, Italy, 6Humanitas University, IRCCS Humanitas Research Hospital, Rheumatology and Clinical Immunology, Rozzano, Italy

    Background/Purpose: Approximately 1-2% of peripheral blood T cells express CD20, a marker of the B lineage, in both healthy individuals and patients with rheumatoid arthritis…
  • Abstract Number: 1677 • ACR Convergence 2022

    Chimeric Autoantigen-T Cell Receptor (CATCR)-T Cell Therapies to Selectively Target Autoreactive B Cells

    Brian J. Mog1, Elana R. Shaw1, Michael S. Hwang1, Alexander H. Pearlman1, Sarah R. DiNapoli1, Suman Paul1, Chetan Bettegowda1, Nickolas Papadopoulos1, Sandra B. Gabelli1, Michelle Petri2, Antony Rosen1, Shibin Zhou1, Kenneth W. Kinzler1, Bert Vogelstein1 and Maximilian F. Konig1, 1The Johns Hopkins University School of Medicine, Baltimore, MD, 2Johns Hopkins University School of Medicine, Division of Rheumatology, Baltimore, MD

    Background/Purpose: Chimeric antigen receptor (CAR)-T cell therapies have revolutionized the treatment of cancer and can be curative. CD19-targeted CAR-T cells hold promise for the treatment…
  • Abstract Number: 0644 • ACR Convergence 2022

    Long-lived Plasma Cells in the Lupus Bone Marrow Are Imprinted by Interferon

    Jennifer Barnas1, Diana Alzamareh2, Neha Nandedkar-Kulkarni2, Jennifer Albrecht2, Nida Meednu2, Cameron Baker2, Andrew McDavid1 and Jennifer Anolik2, 1University of Rochester, Rochester, NY, 2University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Systemic lupus erythematous (SLE) is a complex autoimmune disorder with heterogeneous disease presentation and a multi-pronged pathogenesis. Although autoreactive plasma cells (PC) play a…
  • Abstract Number: 1869 • ACR Convergence 2022

    Looking for BlyS(BAFF) in Juvenile Dermatomyositis: A New Biomarker of Disease Activity

    Christopher Costin1, Gabrielle Morgan2, Amer Khojah3 and Lauren Pachman4, 1Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, 2Ann & Robert H. Lurie Children's Hospital of Chicago and Northwestern University Feinberg School of Medicine, Chicago, IL, 3Umm Al-Qura University, Makkah, Saudi Arabia, 4Northwestern's Feinberg School of Medicine. Ann and Robert H. Lurie Children's Hospital of Chicago; Stanley Manne Children's Research Institute of Chicago, Lake Forest, IL

    Background/Purpose: B Cell Activating Factor (BAFF) is a cytokine that drives B Cell proliferation and maturation. B Cells remain an important factor in JDM immune…
  • Abstract Number: 0720 • ACR Convergence 2022

    Risk-Benefit Assessment of Primary Prophylaxis for Pneumocystis Pneumonia in Patents with Rheumatic Diseases Exposed to Rituximab: A Multicenter Cohort Study

    Jun Won Park1, Jeffrey Curtis2, Min Jung Kim3, You-Jung Ha4, Yun Jong Lee4 and Eun Bong Lee1, 1Seoul National University Hospital, Seoul, Republic of Korea, 2Division of Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Seoul Metropolitan Government Boramae Medical center, Dongjak-gu, Seoul, Republic of Korea, 4Seoul National University Bundang Hospital, Seongnam, Republic of Korea

    Background/Purpose: Although previous studies suggested that primary prophylaxis for pneumocystis pneumonia (PJP) during rituximab treatment could be beneficial, it is uncertain whether this strategy should…
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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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