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

Abstracts tagged "lymphocytes"

  • Abstract Number: 1825 • 2016 ACR/ARHP Annual Meeting

    the Non-Coding Genome and the Genetics of Systemic Lupus

    Joyce Hui-Yuen1, Lisha Zhu2, Lai Ping Wong3, Kaiyu Jiang4, Yanmin Chen4, Tao Liu5 and James Jarvis6, 1North Shore-Long Island Jewish Health System, Lake Success, NY, 2Biochemistry, University at Buffalo, Buffalo, NY, 3Pediatrics, University at Buffalo, Buffalo, NY, 4Pediatrics, The University at Buffalo, Buffalo, NY, 5Department of Biochemistry, University at Buffalo, Buffalo, NY, 6Pediatrics, SUNY Buffalo School of Medicine, Buffalo, NY

    Background/Purpose:  Systemic lupus erythematosus (SLE) is a multi-system, complex disease believed to be triggered by gene-environment interactions. While we have made considerable progress in investigation…
  • Abstract Number: 2569 • 2016 ACR/ARHP Annual Meeting

    Restoration of Decreased Lymphocyte Counts and the Shift to Th1 and Effector Memory CD8+T Cell Subsets Associate with Spontaneous Regression of Lympho-Proliferative Disorders Developed in RA Patients Treated with Methotrexate

    Shuntaro Saito1, Katsuya Suzuki1, Kunihiro Yamaoka1, Koichi Amano2, Michihide Tokuhira3 and Tsutomu Takeuchi1, 1Keio University School of Medcine, Division of Rheumatology, Department of Internal Medicine, Tokyo, Japan, 2Department of Rheumatology and Clinical Immunology, Saitama Medical Center, Saitama Medical University, Saitama, Japan, 3Department of Hematology, Saitama Medical Center, Saitama Medical University., Saitama, Japan

    Background/Purpose:  Methods:  Forty-three RA patients complicated with LPD were identified and 76 control patients were selected. Among the 43 LPD patients, 28 were regressive and…
  • Abstract Number: 538 • 2015 ACR/ARHP Annual Meeting

    Multidrug Resistant Lymphocytes of Patients with Rheumatoid Arthritis Are Predictive for DMARD and Glucocorticoid Treatment Response

    Jan Piet van Hamburg1, Sandra M.J. Paulissen2, Nadine Davelaar1, Mieke Hazes3 and Erik Lubberts1, 1Rheumatology and Immunology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands, 2Room Nb-84, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands, 3Rheumatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands

    Background/Purpose: A large fraction of patients with RA does not respond to treatment with glucocorticoids (GCs) and disease-modifying anti-rheumatic drugs (DMARDs), or becomes resistant in…
  • Abstract Number: 569 • 2015 ACR/ARHP Annual Meeting

    Neurophil to Lymphocyte Ratio Is a Reliable Marker of Treatment Response in Rheumatoid Arthritis Patients during Tocilizumab Therapy

    Byeongzu Ghang1, Doo-Ho Lim2, Soo Min Ahn3, Wook Jang Seo4, Seokchan Hong3, Yong-Gil Kim2, Chang-Keun Lee2 and Bin Yoo2, 1Division of Rheumatology, Department of Internal Medicine, Univerisy of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea, 2Division of Rheumatology, Department of Internal Medicine, Department of Rheumatology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea, 3Division of Rheumatology, Department of Internal Medicine, University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea, 4Internal Medicine, Seoul Veterans Hospital, Seoul, South Korea

    Background/Purpose: Tocilizumab, an interleukin-6 (IL-6) receptor antagonist, is an effective drug for the treatment of rheumatoid arthritis (RA). During administration of tocilizumab, previous studies have…
  • Abstract Number: 738 • 2015 ACR/ARHP Annual Meeting

    Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of the BCL-2 Inhibitor Venetoclax (ABT-199) in a Phase 1 Single and Multiple Ascending Dose Study in Female Patients with Systemic Lupus Erythematosus

    Peng Lu1, Roy Fleischmann2, Craig Curtis3, Stanislav Ignatenko4, Monali Desai5, Shekman L. Wong5, Kristie M. Grebe1, Jiewei Zeng5, Jeroen Medema5 and James Stolzenbach5, 1AbbVie Inc., Worcester, MA, 2University of Texas Southwestern Medical Center, Dallas, TX, 3Compass Research Center, Orlando, FL, 4Charité Research Organization, Berlin, Germany, 5AbbVie Inc., North Chicago, IL

    Background/Purpose: Apoptosis is needed to eliminate auto-reactive T and B cells during immune responses; failure of elimination is important in development of systemic lupus erythematosus…
  • Abstract Number: 1985 • 2015 ACR/ARHP Annual Meeting

    Abnormal B-Cell Distribution Is Improved By Tocilizumab Monotherapy in Patients with Polymyalgia Rheumatica

    Guillermo Carvajal Alegria1, Valerie Devauchelle2, Yves Renaudineau3, Alain Saraux4, Jacques-Olivier Pers5 and Divi Cornec6, 1Immunology, CHRU MORVAN, BREST, France, 2Service de Rhumatologie, CHU Brest, Brest, France, 3Immunology, Brest University Medical School Hospital, Brest, France, 4Rheumatology Department, CHU de la Cavale Blanche, Brest Cedex, France, 5EA2216/ERI29 UBO, Brest, France, 6Department of rheumatology, Brest Occidentale University, Brest, France

    Background/Purpose: Abnormalities in B-cell population distribution were recently reported in polymyalgia rheumatica (PMR) and giant cell arteritis, which improved with glucocorticoids. Our objective here was…
  • Abstract Number: 508 • 2014 ACR/ARHP Annual Meeting

    Relationship Between NK Cell Count and Important Safety Events in Rheumatoid Arthritis Patients Treated with Tofacitinib

    R. van Vollenhoven1, Y. Tanaka2, R. Riese3, M. Lamba3, T. Kawabata3, T. Hirose4, S. Toyoizumi4, A. Hazra3 and S. Krishnaswami3, 1The Karolinska Institute, Stockholm, Sweden, 2University of Occupational and Environmental Health, Kitakyushu, Japan, 3Pfizer Inc, Groton, CT, 4Pfizer Inc, Tokyo, Japan

    Background/Purpose: Tofacitinib is an oral Janus kinase (JAK) inhibitor for the treatment of rheumatoid arthritis (RA). Cytokines (e.g. interleukin [IL]-2, -4, -7, -15, -21) involved…
  • Abstract Number: 2330 • 2013 ACR/ARHP Annual Meeting

    Relationship Between Lymphocyte Count and Risk Of Infection In Rheumatoid Arthritis Patients Treated With Tofacitinib

    R. F. van Vollenhoven1, R. Riese2, S. Krishnaswami2, T. Kawabata2, C. Fosser2, S. Rottinghaus2, M. Lamba2 and S. H. Zwillich2, 1Clinical Trials Unit Department of Rheumatology, The Karolinska Institute, Stockholm, Sweden, 2Pfizer Inc, Groton, CT

    Background/Purpose: Tofacitinib is a novel oral Janus kinase (JAK) inhibitor for the treatment of rheumatoid arthritis (RA). Cytokines involved in lymphocyte development, function and homeostasis…
  • « Previous Page
  • 1
  • 2
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