ACR Meeting Abstracts

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Abstracts tagged "T-Regulatory Cells"

  • Abstract Number: 2713 • 2013 ACR/ARHP Annual Meeting

    IL-21 Inhibited Follicular Regulatory T Cells To Promote Autoreactive Germinal Center Development In Autoimmune BXD2 Mice

    Yanna Ding1, Hui-Chen Hsu2,3, Jun Li4, PingAr Yang4, Qi Wu4, Allan J. Zajac5 and John D. Mountz3,6, 1University of Alabama at Birmingham, Birmingham, AL, 2Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Birmingham VA Medical Center, Birmingham, AL, 4Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 5Microbiology, University of Alabama at Birmingham, Birmingham, AL, 6Dept of Med/Rheumatology Div, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Follicular T helper (Tfh) cells have been correlated with germinal center (GC) formation, autoantibody production and disease severity in human systemic lupus erythematosus (SLE).…
  • Abstract Number: 2215 • 2013 ACR/ARHP Annual Meeting

    Apoptotic Cell-Based Therapy To Treat Collagen-Induced Experimental Arthritis. Rationale For The Use Of Apoptotic Cells In The Treatment Of Rheumatoid Arthritis

    Sylvain Perruche1, Amandine Clauzon1, Francis Bonnefoy1, Eric Toussirot2 and Philippe Saas3, 1UMR1098 INSERM, EFS Bourgogne Franche Comté, Besançon, France, 2Université de Franche Comté , CHRU, CIC Biotherapy 506 and Rheumatology and EA 4266 Pathogens and Inflammation, Besançon, France, 3Etablisement Français du Sang ; Université de Franche Comté, INSERM UMR1098, Besançon, France

    Background/Purpose: Most of the currently available biological agents used in the treatment of rheumatoid arthritis (RA) target a cellular or soluble factor involved in the…
  • Abstract Number: 1643 • 2013 ACR/ARHP Annual Meeting

    Ex Vivo Suppression Of RA Effector T Cells (Teff) By Mapc Media Is Synergistic With Treg

    Gali Malul1, David Soler2, Donald D. Anthony3, Hillard M. Lazarus4, Nicholas Lehman5, Thomas McCormick2, Julia M. Sugalski6, Anthony E. Ting5 and Nora G. Singer7, 1Rheumatology, MetroHealth Medical Center, Cleveland, OH, 2Dermatology, Case Medical Center, Cleveland, OH, 3Medicine, Case Western Reserve University, Cleveland, OH, 4Comprehensive Cancer Center, Case Medical Center, Cleveland, OH, 5Athersys, Inc., Cleveland, OH, 6Medicine/infectious disease, Case Western Reserve University, Cleveland, OH, 7Medicine, Division of Rheumatology, MetroHealth Medical Center, Cleveland, OH

    Background/Purpose: Use of mesenchymal/multipotent stem cells (MSCs/MAPCs) is an emerging immune modulatory therapeutic strategy promising for a number of human diseases. Multipotent adult progenitor cells…
  • Abstract Number: 1641 • 2013 ACR/ARHP Annual Meeting

    Bispecific Antibodies For Redirection Of Human Regulatory T Cells To Surface-Inducible Autoantigen La/SS-B

    Stefanie Koristka1, Marc Cartellieri2, Claudia Arndt2, Anja Feldmann2, Irene Michalk2, Claudia C. Bippes2, Nicole Berndt2, Anne Hermsdorf2, Slava Stamova2, Biji T. Kurien3, Robert Hal Scofield4, A. Darise Farris5, Judith A. James6, Holger Bartsch7 and Michael Bachmann2, 1Carl Gustav Carus TU-Dresden, Dresden, Germany, 2Inst. Immunology, Carl Gustav Carus TU-Dresden, Dresden, Germany, 3College of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 4Arthritis & 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, 5Arthritis & Immunology Program, Oklahoma Medical Research Foun, Oklahoma City, OK, 6Oklahoma Medical Research Foundation, Oklahoma City, OK, 7Inst. Immunol., Carl Gustav Carus TU-Dresden, Dresden, Germany

    Background/Purpose: Adoptive transfer of regulatory T cells (Tregs)  represents a promising strategy for treatment of auto- and alloimmunity. However, it is difficult to obtain therapeutically…
  • Abstract Number: 1412 • 2013 ACR/ARHP Annual Meeting

    Use Of a Biologic Marker For An Integrated Pharmacodynamic and Clinical Analysis To Inform Further Clinical Development, Including Dose Selection For The Phase 2b Trial – Treat 2b – Of Tregalizumab In Rheumatoid Arthritis

    Eva Dokoupilova1, Slawomir Jeka2, Jiri Vencovsky3, Janusz Badurski4, Klaas Prins5, Vibeke Strand6, Edward C. Keystone7, Ronald F van Vollenhoven8, Jurgen Wollenhaupt9, Andrea Wartenberg-Demand10, Gabriele Niemann10, Ahmed Abufarag10, Silke Aigner10, Sibylle Kaiser10, Faiza Rharbaoui10, Niklas Czeloth11, Ralf Wolter10, Benjamin Dälken10 and Thorsten Holzkämper10, 1Medical Plus s.r.o, Uherske Hradiste, Czech Republic, 2Clinic of Rheumatology and Connective Tissue Diseases University Hospital No 2 in Bydgoszcz Collegium Medicum UMK in Torun, Bydgoszcz, Poland, 3Institute of Rheumatology, Department of Clinical and Experimental Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic, 4Center of Osteoporosis and Osteo-articular Diseases, Bialystock, Poland, 5qPharmetra, Nijmegen, Netherlands, 6Adjunct, Division of Immunology / Rheumatology, Stanford University, Portola Valley, CA, 7Department of Medicine, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada, 8ClinTRID, Department of Medicine, Karolinska Institutet, Stockholm, Sweden, 9Schoen-Klinik Hamburg-Eilbek Teaching Hospital of the University of Hamburg, Hamburg, Germany, 10Biotest AG, Dreieich, Germany, 11Global Research Immunology, Biotest AG, Dreieich, Germany

    Background/Purpose: In patients with rheumatoid arthritis (RA) reduced numbers and functional impairment of regulatory T cells (Tregs) have been observed. Tregalizumab is a humanized, agonistic…
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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.).

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