ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 919 • 2013 ACR/ARHP Annual Meeting

    B Cell Derived IFN-γ Contributes To The Negative Regulation Of T-Regulatory Cell Differentiation In Arthritis

    Susan Olalekan1, Yanxia Cao2 and Alison Finnegan2, 1Immunology, Rush University Medical Center, Chicago, IL, 2Dept of Medicine, Rush University Medical Center, Chicago, IL

    Background/Purpose: Depletion of B cells using a monoclonal antibody against CD20 expressed on mature B cells has proven efficacious in patients with rheumatoid arthritis (RA).…
  • Abstract Number: 920 • 2013 ACR/ARHP Annual Meeting

    Fms-Like Tyrosine Kinase 3 Signaling Is Essential For Differentiation Of Antigen Specific Plasma Cells During Experimental Arthritis

    Mattias Svensson1, Kersti Månsson1, Karin Andersson1, Mats Bemark2, Mikael Brisslert1 and Maria Bokarewa1, 1Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, Sweden, 2Microbiology and Immunology, University of Gothenburg, Gothenburg, Sweden

    Background/Purpose: Signaling through the tyrosine kinase receptor Flt3 plays an important role in early B-cell development. Mice lacking either Flt3 or its ligand (Flt3L) have…
  • Abstract Number: 921 • 2013 ACR/ARHP Annual Meeting

    Blocking The Complement Receptor 2 (CR2) Ligand-Receptor Interaction With a Novel Mouse Anti-Mouse CR2 Monoclonal Antibody Decreases Antigen-Specific Humoral Immune Responses and The Evolution Of Collagen-Induced Arthritis

    Rosa Rodriguez1, Liudmila Kulik1, Joshua Thurman2, Jonathan Hannan1, Steve Tomlinson3 and V. Michael Holers1, 1Rheumatology Division, University of Colorado School of Medicine, Aurora, CO, 2Renal Division, University of Colorado School of Medicine, Aurora, CO, 3Microbiology and Immunology, Medical University of South Carolina, Charleston, NC

    Background/Purpose: The CR2/CD19 complex on B cells serves as a co-receptor for membrane IgM and amplifies B cell responses through physical associations of the bound…
  • Abstract Number: 922 • 2013 ACR/ARHP Annual Meeting

    Role Of B Cells and/Or Autoantibodies In Pulmonary Manifestations Of Inflammatory Arthritis

    Lisa K. Peterson1, Jeremy Sokolove2, Paul Jedlicka3, Lauren J. Lahey4, William H. Robinson5 and Leonard L. Dragone6, 1Pediatrics, National Jewish Health, Denver, CO, 2VA Palo Alto Healthcare System and Stanford University, Palo Alto, CA, 3Pathology, University of Colorado Denver, Aurora, CO, 4Medicine, VA Palo Alto Health Care System and Stanford University, Palo Alto, CA, 5VA Palo Alto Health Care System and Stanford University, Palo Alto, CA, 6Dept of Pediatrics, National Jewish Health, Denver, CO

    Background/Purpose: RA is a systemic condition affecting approximately 1% of the general population leading to progressive arthritis and extra-articular manifestations (ExRA), including interstitial lung disease…
  • Abstract Number: 923 • 2013 ACR/ARHP Annual Meeting

    Redox Dependent Conformational Changes Of The Autoantigen La Are Responsible For Its Shuttling, Translocation and a Pathophysiological Role Of Anti-La Autoantibodies

    Irene Michalk1, Nicole Berndt1, Claudia C. Bippes1, Holger Bartsch2, Stefanie Koristka3, Claudia Arndt1, Anja Feldmann1, Biji T. Kurien4, Robert Hal Scofield5, A. Darise Farris6, Judith A. James7, Marc Cartellieri1 and Michael Bachmann1, 1Inst. Immunology, Carl Gustav Carus TU-Dresden, Dresden, Germany, 2Inst. Immunol., Carl Gustav Carus TU-Dresden, Dresden, Germany, 3Carl Gustav Carus TU-Dresden, Dresden, Germany, 4College of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 5Arthritis & Clinical Immunology Program, Oklahoma Medical Research Foundation; Department of Medicine, University of Oklahoma Health Sciences Center; US Department of Veterans Affairs Medical Center, Oklahoma City, OK, 6Arthritis & Immunology Program, Oklahoma Medical Research Foun, Oklahoma City, OK, 7Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Since their detection a pathophysiological role of antibodies (abs) to extractable nuclear autoantigens including anti-La abs has been controversially discussed. Stainings of anti-La abs…
  • Abstract Number: 924 • 2013 ACR/ARHP Annual Meeting

    B Cell Subsets and Dysfunction Of Regulatory B Cells In IgG4-Related Diseases and Primary Sjögren Syndrome: The Similarities and Differences

    Wei Lin1, Lixia Jin2, Wen Zhang1, Hua Chen3, QingJun Wu4, Yunyun Fei1, Yan Zhao1, Xiaofeng Zeng5 and Fengchun Zhang3, 1Peking Union Medical College Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Beijing, China, 2Tsinghua University, Beijing, China, 3Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China, 4Department of Rheumatology, Peking Union Medical College Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Beijing, China, 5Department of Rheumatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

    Background/Purpose: IgG4 related disease (IgG4-RD) is a chronic, multisystem-involved autoimmune disease. Abnormally activated and differentiated B cells may play important roles. Regulatory B cells (Breg)…
  • Abstract Number: 925 • 2013 ACR/ARHP Annual Meeting

    B Cell Subset Phenotypes In Patients With Granulomatosis With Polyangiitis (Wegener’s)

    Atul A. Khasnis1, Carol A. Langford2, Leonard H. Calabrese3, Julia M. Sugalski4, Michael Lederman5 and Donald D. Anthony6, 1Rheumatology, Cleveland Clinic Foundation, Cleveland, OH, 2Center for Vasculitis Care and Research, Cleveland Clinic, Cleveland, OH, 3Cleveland Clinic Foundation, Cleveland, OH, 4Medicine/infectious disease, Case Western Reserve University, Cleveland, OH, 5Infectious Diseases, Case Western Reserve University, Cleveland, OH, 6Medicine, Case Western Reserve University, Cleveland, OH

    Background/Purpose: B cells are pathogenic in granulomatosis with polyangiitis (Wegener’s) (GPA). Rituximab (RTX), an anti-CD20 monoclonal antibody, is effective therapy however B cell reconstitution patterns…
  • Abstract Number: 926 • 2013 ACR/ARHP Annual Meeting

    Autoantibodies to the Th/To Complex Are the Most Common Antibodies in Systemic Sclerosis (SSc) Patients Without Other Autoantibodies

    Michael Mahler1, Jason Y.F. Chan2, Edward K.L. Chan3, Minoru Satoh2, Marie Hudson4, Murray Baron5, James Wick6 and Marvin J. Fritzler7, 1Research, INOVA Diagnostics, San Diego, CA, 2Medicine, University of Florida, Gainesville, FL, 3Oral Biology, University of Florida, Gainesville, FL, 4Jewish General Hospital, McGill University, Montreal, QC, Canada, 5Pavillion A, Rm 216, Lady David Institute for Medical Research and Jewish General Hospital, Montreal, QC, Canada, 6Department of medicine, Faculty of Medicine, University of Calgary, Calgary, AB, Canada, 7Medicine, University of Calgary, Calgary, AB, Canada

    Background/Purpose: Antinuclear antibodies (ANA) play an important role in the diagnosis of systemic sclerosis (SSc) being present in about 80-90% of the patients. In the…
  • Abstract Number: 927 • 2013 ACR/ARHP Annual Meeting

    The Role of HIF-1 and HIF-2 During Angiogenesis and Metabolic Adaptation of Human Microvascular Endothelial Cells Towards Hypoxia

    Martin Hahne1, Cindy Strehl1, Manuela Jakstadt1, Paula Hoff1, Timo Gaber1, Gerd Burmester2 and Frank Buttgereit3, 1Department of Rheumatology and Clinical Immunology, Charité University Medicine, Berlin, Germany, 2Rheumatology and Clinical Immunology, Campus Mitte, Charite University Hospital, Berlin, Germany, 3Charité - Universitätsmedizin Berlin, Berlin, Germany

    Background/Purpose: Hypoxia is a feature of RA synovitis. In the present study, we focused on the two transcription factors Hypoxia inducible factor (HIF)-1 and (HIF)-2.…
  • Abstract Number: 888 • 2013 ACR/ARHP Annual Meeting

    Role of Calcium/Calmodulin Kinase IV On Podocyte Function in Lupus Nephritis

    Kunihiro Ichinose1, Takeshi Ushigusa2, Tomohiro Koga3, George C. Tsokos4 and Atsushi Kawakami5, 1Department of Immunology and Rheumatology, Unit of Translational Medicine, Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan, 2Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan, 3Medicine/Rheumatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 4Medicine/Rheumatology, BIDMC, Harvard Medical School, Boston, MA, 5Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan

    Role of calcium/calmodulin kinase IV on podocyte function in lupus nephritis Background/Purpose: Kidney podocytes and their slit diaphragms settle the integrity of renal basement membrane…
  • Abstract Number: 889 • 2013 ACR/ARHP Annual Meeting

    Podocytes Take Up Adsdna Autoantibody Complexes

    Anja Hillmann1, Elisabeth Jung2, Annika Engbers1, Hedda Wardemann3, Annett M. Jacobi2 and Thomas Pap4, 1Institute of Experimental Musculoskeletal Medicine, University Hospital Münster, Münster, Germany, 2Rheumatology Internal Medicine D, University Hospital Münster, Münster, Germany, 3Max Planck Research Group Molecular Immunology, Max Planck Institute for Infection Biology, Berlin, Germany, 4Institute of Experimental Muskuloskeletal Medicine, University Hospital Münster, Münster, Germany

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease, resulting in inflammation and tissue damage in several organs. This autoimmune reaction is caused by autoantibodies,…
  • Abstract Number: 890 • 2013 ACR/ARHP Annual Meeting

    Quantitative Cell Distance Mapping In Human Nephritis Reveals Organization Of In Situ Adaptive Immune Responses

    Marcus R. Clark1, Vladimir M. Liarski1, Natalya Kavernia2, Maryellen L. Giger3, Anthony Chang4, Yahui Peng3 and Daniel F. Brandt2, 1Rheumatology and Knapp Center for Lupus Research, University of Chicago, Chicago, IL, 2Rheumatology, University of Chicago, Chicago, IL, 3Radiology, University of Chicago, Chicago, IL, 4Pathology, University of Chicago, Chicago, IL

    Background/Purpose: Inflammatory infiltrates contain multiple cell types that could interact in myriad ways to amplify in situ immune responses. However, there currently are no methods…
  • Abstract Number: 891 • 2013 ACR/ARHP Annual Meeting

    A Single Amino Acid In The β1 Chain Of HLA-DR Explains The Majority Of The HLA Association With Giant Cell Arteriti

    Javier Martin1, F. David Carmona2, Jose Ezequiel Martin3, Aurora Serrano1, Lara Bossini-Castillo4, Roser Solans5, Jose A. Miranda-Filloy6, Santos Castañeda7, Maria C. Cid8, Jose A. Hernandez9, Inmaculada C. Morado10, Javier Narvaez11, Ricardo Blanco12, Bernardo Sopeña13, M. Jesus García-Villanueva14, Jordi Monfort15, Norberto Ortego-Centeno16, Ainhoa Unzurrunzaga17, Begoña Marí-Alfonso18, Cesar Magro19, Ana Hidalgo-Conde20, Marta Conde-Jaldon21, María F. González-Escribano21, Paul de Bakker22, Bobby P.C. Koeleman23 and Miguel A. González-Gay24, 1Instituto de Parasitologia y Biomedicina Lopez-Neyra (IPBLN-CSIC), Granada, Spain, 2Instituto de Parasitología y Biomedicina López-Neyra, Consejo Superior de Investigaciones Científicas, Armilla (Granada), Spain, 3Immunology, Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Armilla (Granada), Spain, 4Immunology, Instituto de Parasitologia y Biomedicina Lopez-Neyra (IPBLN-CSIC), Granada, Spain, 5Department of Internal Medicine, Hospital Vall d'Hebron, Barcelona, Spain, 6Rheumatology, Division of Rheumatology, Hospital Lucus Augusti, Lugo, Spain, 7Rheumatology, Hospital Universitario de La Princesa, IIS Princesa, Madrid, Spain, 8Vasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic University of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain, 9Hospital Clinic. University of Barcelona, IDIBAPS,, Barcelona, Spain, 10Rheumatology, Hospital Clínico San Carlos, Madrid, Spain, 11Rheumatology, Hospital Universitario de Bellvitge, Barcelona, Spain, 12Rheumatology, Hospital Universitario Marqués de Valdecilla, IFIMAV, Santander, Spain, 13Thrombosis and Vasculitis Unit-Internal Medicine, Complejo Hospitalario Universitario de Vigo (CHUVI), Vigo, Spain, 14Rheumatology, Hospital Ramón y Cajal, Madrid, Spain, 15Reumatologia, Hospital del Mar, Barcelona, Spain, 16Internal Medicine, Hospital Clínico San Cecilio, Granada, Spain, 17Internal Medicine, Hospital de Galdakano, Vizcaya, Spain, 18Internal Medicine, Corporació Sanitaria Parc Taulí, Instituto Universitario Parc Taulí, UAB, Sabadell, Spain, 19Rheumatology, Hospital Clínico San Cecilio, Granada, Spain, 20Internal Medicine, Hospital Universitario Virgen de la Victoria, Málaga, Spain, 21Immunology, Hospital Universitario Virgen del Rocío, Sevilla, Spain, 22Medical Genetics, University Medical Center Utrecht, Utrecht, Netherlands, 23Department of Medical Genetics, University Medical Center Utrecht, Utrecht, Netherlands, 24Rheumatology, Hospital Universitario Marqués de Valdecilla. IDIVAL. Santander. Spain, Santander, Spain

    Background/Purpose: Giant cell arteritis (GCA) is a polygenic inflammatory disease affecting medium- and large-sized blood vessels in people elder than 50-years old. Although it is…
  • Abstract Number: 892 • 2013 ACR/ARHP Annual Meeting

    The Functional PTPN22 Variant R620W Is Strongly Associated With Giant Cell Artetitis Predisposition

    F. David Carmona1, Sarah L. Mackie2, Aurora Serrano3, Ana Marquez4, Roser Solans5, Jose A. Miranda-Filloy6, Jose Hernández-Rodríguez7, Maria C. Cid8, Santos Castañeda9, Inmaculada C. Morado10, Javier Narvaez11, Ricardo Blanco12, Bernardo Sopeña13, M. Jesus García-Villanueva14, Jordi Monfort15, Norberto Ortego-Centeno16, Ainhoa Unzurrunzaga17, Begoña Marí-Alfonso18, Julio Sánchez-Martín19, Eugenio de Miguel20, Cesar Magro21, Enrique Raya22, Niko Braun23, Joerg Latus24, Øyvind Molberg25, Benedicte A. Lie26, Frank Moosig27, Torsten Witte28, Ann W. Morgan2, Miguel A. González-Gay29 and Javier Martin3, 1Instituto de Parasitología y Biomedicina López-Neyra, Consejo Superior de Investigaciones Científicas, Armilla (Granada), Spain, 2NIHR-Leeds Musculoskeletal Biomedical Research Unit and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 3Instituto de Parasitologia y Biomedicina Lopez-Neyra (IPBLN-CSIC), Granada, Spain, 4Instituto de Parasitología y Biomedicina 'López-Neyra' (IPBLN-CSIC), Granada, Spain, 5Department of Internal Medicine, Hospital Vall d'Hebron, Barcelona, Spain, 6Rheumatology, Division of Rheumatology, Hospital Lucus Augusti, Lugo, Spain, 7Hospital Clínic. University of Barcelona. IDIBAPS, Barcelona, Spain, 8Vasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic University of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain, 9Rheumatology, Hospital Universitario de La Princesa, IIS Princesa, Madrid, Spain, 10Rheumatology, Hospital Clínico San Carlos, Madrid, Spain, 11Rheumatology, Hospital Universitario de Bellvitge, Barcelona, Spain, 12Rheumatology, Hospital Universitario Marqués de Valdecilla. IFIMAV. Santander. Spain, Santander, Spain, 13Thrombosis and Vasculitis Unit-Internal Medicine, Complejo Hospitalario Universitario de Vigo (CHUVI), Vigo, Spain, 14Rheumatology, Hospital Ramón y Cajal, Madrid, Spain, 15Reumatologia, Hospital del Mar, Barcelona, Spain, 16Systemic Autoimmune Diseases Unit, Hospital Clínico San Cecilio, Granada, Spain, 17Internal Medicine, Hospital de Galdakano, Vizcaya, Spain, 18Internal Medicine, Corporació Sanitaria Parc Taulí, Instituto Universitario Parc Taulí, UAB, Sabadell, Spain, 19Rheumatology,, Hospital Universitario 12 de Octubre, Madrid, Spain, 20Rheumatology, University Hospital La Paz - IdiPaz, Madrid, Spain, 21Rheumatology, Hospital Clínico San Cecilio, Granada, Spain, 22Rheumatology, University Hospital San Cecilio, Granada, Spain, 23Department of Internal Medicine, Division of Nephrology, Robert-Bosch-Hospital, Stuttgart, Germany, 24Internal Medicine, Division of Nephrology, Robert-Bosch-Hospital, Stuttgart, Germany, 25Oslo University Hospital, Oslo, Norway, 26Department of Medical Genetics, University of Oslo and Oslo University Hospital, Oslo, Norway, 27Department of Clinical Immunology and Rheumatology, University of Luebeck, Bad Bramstedt, Germany, 28Clinical Immunology and Rheumatology, Medical University Hannover, Hanover, Germany, 29Rheumatology, Hospital Universitario Marqués de Valdecilla. IDIVAL. Santander. Spain, Santander, Spain

    Background/Purpose: The PTPN22/CSK signaling represents one of the common susceptibility pathways in autoimmunity. Considering that the genetic basis of giant cell arteritis (GCA), an autoimmune…
  • Abstract Number: 893 • 2013 ACR/ARHP Annual Meeting

    Association Between Human Leukocyte Antigen-B’s Amino Acid Variation and Disease-Susceptibility To Takayasu’s Arteritis

    Hajime Yoshifuji1, Chikashi Terao2, Kosaku Murakami3, Daisuke Kawabata3, Koichiro Ohmura1, Takao Fujii4, Yasushi Kawaguchi5, Hisashi Yamanaka5 and Tsuneyo Mimori1, 1Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 2Center for Genomic Medicine, Kyoto University, Kyoto, Japan, 3Dept of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 4Department of the Control for Rheumatic Diseases, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 5Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan

    Background/Purpose: HLA-B52 and HLA-B51 are frequently seen in Asian population and are almost identical except two amino acid residues(the 63rd and 67th), but HLA-B52 is…
  • « Previous Page
  • 1
  • …
  • 2187
  • 2188
  • 2189
  • 2190
  • 2191
  • …
  • 2425
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology