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Abstracts tagged "complement"

  • Abstract Number: 2338 • ACR Convergence 2023

    Results of Single-Arm, Phase 1b Study of Anti-C1q Treatment (ANX009) Show That the Classical Pathway Is a Key Driver of Complement Activation and Consumption in Patients with Active Lupus Nephritis

    Maria Dall'Era1, Juan Lichauco2, Hsiang Chen3, Harold Gomez4, Michael Tee5, Caroline Arroyo6, Joung-Liang Lan7, Yao-Fan Fang8, Edmund Chang9, Noosha Yousefpour9, Julian Low9, Min Bao9, Qing Chang9, Jeannette Osterloh9, Ann Mongan9, Ted Yednock9, Dean Artis9, Yaisa Andrews-Zwilling9 and Henk-Andre Kroon9, 1University of California San Francisco, San Francisco, CA, 2St. Luke’s Medical Center, Quezon City, Philippines, 3Tri-service General Hospital, Taipei City, Taiwan, 4Angeles University Foundation Medical Center, Pampanga, Philippines, 5Medical Center Manila and University of the Philippines Manila, Manila, Philippines, 6Iloilo Doctors Hospital, Iloilo City, Philippines, 7China Medical University Hospital, Taichung, Taiwan, 8Chang Gung Memorial Hospital, Linkou, Taiwan, 9Annexon Biosciences, Brisbane, CA

    Background/Purpose: Lupus nephritis (LN) is an autoantibody-mediated disease involving glomerular deposition of immune complexes containing pathogenic anti-C1q antibodies, leading to C1q binding and activation of…
  • Abstract Number: 0684 • ACR Convergence 2023

    Report on Twelve Patients with Diffuse Alveolar Hemorrhage in the Phase 3 Trial of Avacopan for the Treatment of ANCA-Associated Vasculitis

    Ulrich Specks1, David Jayne2 and Peter Merkel3, 1Mayo Clinic, Rochester, MN, 2University of Cambridge, Cambridge, United Kingdom, 3University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Although respiratory tract involvement in ANCA-associated vasculitis (AAV) is frequent and associated with increased mortality, studies focusing on diffuse alveolar hemorrhage (DAH) in AAV…
  • Abstract Number: 2370 • ACR Convergence 2023

    C5 as a Genetic Marker for Discriminating Between IgA Vasculitis and IgA Nephropathy?

    JOAO CARLOS BATISTA LIZ1, Vanesa Calvo Río2, María Sebastián Mora-Gil1, Belén Sevilla-Pérez3, María Teresa Leonardo4, Ana Peñalba4, María Jesús Cabero4, Javier Narvaez5, luis martin penagos6, Emilio Rodrigo6, Lara Belmar-Vega6, Cristina Gomez-Fernandez7, Luis Caminal-Montero8, Paz Collado9, Antonio Fernandez-Nebro10, gisela Díaz-Cordovés11, Maryia Nikitsina12, Esther Vicente Rabaneda13, secundino Cigarrán14, jesús Calviño15, carmen cobelo15, Manuel León Luque16, Esteban Rubio16, Juan María Blanco-Madrigal17, Eva Galindez-Agirregoikoa18, Santos Castañeda19, Ricardo Blanco20, Verónica Pulito-Cueto1 and Raquel López-Mejías1, 1Rheumatology Department, Immunopathology Group, Hospital Universitario Marqués de Valdecilla-IDIVAL, Santander, Spain, 2Valdecilla Hospital, Santander, Spain, 3Division of Pediatrics, Hospital Universitario San Cecilio, Granada, Spain, 4Division of Pediatrics, Hospital Universitario Marqués de Valdecilla, Santander, Spain, 5Hospital Universitario de Bellvitge, Barcelona, Spain, 6Division of Nephrology, Immunopathology Group, Hospital Universitario Marqués de Valdecilla-DIVAL, Santander, Spain, 7Division of Dermatology,Immunopathology Group, Hospital Universitario Marqués de Valdecilla-IDIVAL, Santander, Spain, 8Internal Medicine Department, Hospital Universitario Central de Asturias, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain, 9Division of Rheumatology, Hospital Universitario Severo Ochoa, Madrid, Spain, 10Hospital Regional Universitario de Málaga, Malaga, Spain, 11Division of Rheumatology, Hospital Regional Universitario Carlos Haya, Málaga, Spain, 12Division of Rheumatology, Hospital Universitario de La Princesa, Madrid, Spain, 13Rheumatology, Hospital Universitario de La Princesa, Madrid, Spain, 14Division of Nephrology, Hospital da Costa Burela, Lugo, Spain, 15Division of Nephrology, Hospital Universitario Lucus Augusti, Lugo, Spain, 16Division of Rheumatology, Hospital Universitario Virgen del Rocío, Sevilla, Spain, 17Division of Rheumatology, Hospital Universitario de Basurto, Bilbao, Spain, 18Basurto University Hospital, Bilbao, Spain, 19Hospital Universitario de la Princesa, Madrid, Spain, 20Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain

    Background/Purpose: Immunoglobulin-A vasculitis (IgAV) and IgA nephropathy (IgAN) are inflammatory conditions that share pathophysiological mechanisms1,2. Similar features are also described between IgAV nephritis (IgAVN) and…
  • Abstract Number: 0685 • ACR Convergence 2023

    Efficacy and Safety of Avacopan in Patients with ANCA-Associated Vasculitis Receiving Rituximab in a Phase 3 Trial

    Duvuru Geetha1, Anisha Dua2, Huibin Yue3, Carlo Salvarani4, David Jayne5 and Peter Merkel6, 1Johns Hopkins University, Baltimore, MD, 2Northwestern University, Chicago, IL, 3Amgen, Inc., Thousand Oaks, CA, 4Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy, 5University of Cambridge, Cambridge, United Kingdom, 6University of Pennsylvania, Philadelphia, PA

    Background/Purpose: The randomized, double-blind, double-dummy, controlled Phase 3 ADVOCATE trial tested whether avacopan, an oral selective C5a receptor inhibitor approved for the treatment of ANCA-associated…
  • Abstract Number: 2494 • ACR Convergence 2023

    Complement mRNA Expression in Patients with ANCA-associated Glomerulonephritis

    Salem Almaani1, Arnon Arazi2, Huijuan Song3, Pearlly Yan3, Estela Puchulu-Campanella3, Hubao Wang3, Lynn Fussner3, Samir Parikh3 and Brad Rovin3, 1Ohio State University Medical Center, Columbus, OH, 2Broad Institute of MIT and Harvard, Melrose, MA, 3Ohio State University, Columbus, OH

    Background/Purpose: The role of complement in patients with ANCA-associated vasculitis (AAV) has been increasingly appreciated and led to the use of complement system antagonists as…
  • Abstract Number: 0686 • ACR Convergence 2023

    Safety and Efficacy of Avacopan in Patients 65 Years and Older with ANCA-Associated Vasculitis

    David Jayne1, Duvuru Geetha2, Christian Pagnoux3, Sebastian Sattui4 and Peter Merkel5, 1University of Cambridge, Cambridge, United Kingdom, 2Johns Hopkins University, Baltimore, MD, 3Mount Sinai Hospital, Toronto, ON, Canada, 4University of Pittsburgh, Pittsburgh, PA, 5University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Older adults are at increased risk of glucocorticoid (GC)-related toxicity; minimization of GCs is a major focus for treatment of patients with ANCA-associated vasculitis…
  • Abstract Number: 0687 • ACR Convergence 2023

    Avacopan for the Treatment of ANCA-associated Vasculitis. Real World Experience in Spain

    Georgina Espigol-Frigole1, Maria C Cid2, Juliana Bordignon Draibe3, Maria Carmen Prados4, Elena Guillen5, Ana Huerta6, Javier Villacorta7, Cristina Vega8, Judith Martins9, Borja Gracia10 and Enrique Morales11, 1Autoimmune Diseases. Hospital Clinic Barcelona, Barcelona, Spain, 2Hospital Clinic Barcelona, Barcelona, Spain, 3Hospital Bellvitge, Barcelona, Spain, 4Hospital Torrecárdenas, Almeria, Spain, 5Hospital Clínic de Barcelona, Barcelona, Spain, 6Hospital Puerta de Hierro, Madrid, Spain, 7Hospital Ramón y Cajal, Madrid, Spain, 8Hospital La Paz, Madrid, Spain, 9Hospital de Getafe, Madrid, Spain, 10Hospital Lozano Blesa, Zaragoza, Spain, 11Hospital 12 de Octubre, Madrid, Spain

    Background/Purpose: ANCA-associated vasculitis are chronic and relapsing diseases. Relapses are frequently associated with organ damage accrual as a consequence of disease activity or treatment-related side…
  • Abstract Number: 0688 • ACR Convergence 2023

    Efficacy and Safety Experience with Avacopan Beyond 52 Weeks in the Early Access Program (EAP)

    Federico Alberici1, Carlo Salvarani2, Christine Chan3, Achim Obergfell4 and Tamara Popov4, 1Universita degli Studi di Brescia, Brescia, Italy, 2Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy, 3CSL Vifor, Redwood City, CA, 4CSL Vifor, Glattbrugg, Switzerland

    Background/Purpose: Avacopan, a selective C5aR1 inhibitor, has demonstrated efficacy and safety over 52 weeks in patients with anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis. However, efficacy and…
  • Abstract Number: 0736 • ACR Convergence 2023

    Deciphering Complement System-dependent Cellular Pathways in Human Rheumatoid Arthritis Synovial Tissue Using Large Single-cell Computational Omics

    Juan Vargas1, Ian Mantel2, Nirmal Banda1, Anna Helena Jonsson3, Kevin Wei4, Deepak Rao3, Susan Goodman5, Kevin Deane1, The Accelerating Medicines Partnership SLE/RA1, Jennifer Anolik6, Michael Brenner4, Soumya Raychaudhuri3, Jennifer Seifert7, Michael Holer1, Laura Donlin5 and Fan Zhang8, 1University of Colorado Anschutz Medical Campus, Aurora, CO, 2Weill Cornell Medicine, New York, NY, 3Brigham and Women's Hospital, Boston, MA, 4Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 5Hospital for Special Surgery, New York, NY, 6University of Rochester Medical Center, Rochester, NY, 7the Accelerating Medicines Partnership (AMP) RA/SLE Network, Boston, MA, 8University of Colorado, Aurora, CO

    Background/Purpose: The complement system is a major component of innate immunity and plays a vital role in autoimmune disease pathogenesis. In patients with rheumatoid arthritis…
  • Abstract Number: 0094 • ACR Convergence 2023

    Granzyme K Elicits a New Pathway for Complement Activation in RA Synovium

    Anna Helena Jonsson1, Carlos Donado2, Erin Theisen2, Dominique Jones1, Aparna Nathan3, Fan Zhang4, Accelerating Medicines Partnership (AMP): RA/SLE1, Soumya Raychaudhuri1 and Michael Brenner2, 1Brigham and Women's Hospital, Boston, MA, 2Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 3Harvard Medical School, Boston, MA, 4University of Colorado, Aurora, CO

    Background/Purpose: T cells are major drivers of rheumatoid arthritis (RA) pathogenesis. While most research has focused on CD4+ T cells, we have found that CD8+…
  • Abstract Number: 0857 • ACR Convergence 2023

    Change in Albuminuria in Patients with ANCA-Associated Vasculitis Treated with Avacopan

    Duvuru Geetha1, Frank Cortazar2, alexandre Karras3, Annette Bruchfeld4, Huibin Yue5, Peter Merkel6 and David Jayne7, 1Johns Hopkins University, Baltimore, MD, 2New York Nephrology, Watervliet, NY, 3HEGP - APHP, Paris, France, 4Karolinska Institutet, Stockholm, Sweden, 5Amgen, Inc., Thousand Oaks, CA, 6University of Pennsylvania, Philadelphia, PA, 7University of Cambridge, Cambridge, United Kingdom

    Background/Purpose: Urinary albumin:creatinine ratio (UACR) is an important biomarker of active glomerulonephritis, a common complication of antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV). In most glomerular…
  • Abstract Number: 0099 • ACR Convergence 2023

    Cell-bound Complement Activation Products in Antiphospholipid Antibody-positive Patients Without Other Systemic Autoimmune Diseases

    Doruk Erkan1, JoAnn Vega1, Tyler O'Malley2 and Andrew Concoff3, 1Hospital for Special Surgery, New York, NY, 2Exagen, Vista, CA, 3Exagen, Los Angeles, CA

    Background/Purpose: Based on animal models, complement activation is part of Antiphospholipid Syndrome (APS) pathogenesis. However, studies investigating complement activation in antiphospholipid antibody (aPL)-positive patients are…
  • Abstract Number: 0899 • ACR Convergence 2023

    Complement Factor I (CFI) Gene Expression by Kidney Tubular Cells Is Increased in Lupus Nephritis Patients with Interstitial Fibrosis and Tubular Atrophy

    Shudan Wang1, John Greally2, Masako Suzuki3, Jee-Young Moon2, Tao Wang2, Yvonne M Saenger2, Brad Rovin4 and J. Michelle Kahlenberg5, 1Albert Einstein College of Medicine / Montefiore Medical Center, New York, NY, 2Albert Einstein College of Medicine, Bronx, NY, 3Texas A&M University, College Station, TX, 4Ohio State University, Columbus, OH, 5University of Michigan, Ann Arbor, MI

    Background/Purpose: Tubulointerstitial injury is a strong predictor of progression to kidney failure in lupus nephritis (LN). Prior animal studies suggest intrarenal complement activation has an…
  • Abstract Number: 0257 • ACR Convergence 2023

    Activity of IgG4-related Disease Differs Depending on the Presence or Absence of Concomitant Hypocomplementemia

    Risa Wakiya1, Hiroki Ozaki2, Hiromi Shimada1, Shusaku Nakashima1, Taichi Miyagi3, Yusuke Ushio4, Koichi Sugihara5, Mao Mizusaki1, Rina Mino6, Kanako Chujo7, Ryoko Kagawa4, Hayamasa Yamaguchi4, Tomohiro Kameda1 and Hiroaki Dobashi1, 1Division of Hematology, Rheumatology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Kagawa University, Kagawa, Japan, 2Department of Rheumatology, KKR Takamatsu Hospital, Kagawa, Japan, 3Division of Hematology, Rheumatology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Kagawa University, Kidagun, Japan, 4Division of Hematology, Rheumatology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Kagawa University, Miki-cho, Kita-gun, Japan, 5Kagawa University, Miki-cho, Kita-gun, Japan, 6Kagawa University, Division of Hematology, Rheumatology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Kagawa, Japan, 7Kagawa University, Miki, Kita District, Kagawa, Japan

    Background/Purpose: Hypocomplementemia (HC) is often observed in IgG4-related diseases (IgG4-RD), but there are also IgG4-RD without HC. This study aimed to clarify the difference of…
  • Abstract Number: 0900 • ACR Convergence 2023

    Complement Deposition on Extracellular Mitochondria Induces Platelet Activation in Vitro

    Marina Barguil Macedo and Christian Lood, University of Washington, Seattle, WA

    Background/Purpose: Mitochondria are extruded upon cell death and platelet activation, being elevated in several inflammatory conditions, including systemic lupus erythematosus (SLE). Mitochondria are immunogenic, with…
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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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