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Abstracts tagged "Inflammation"

  • Abstract Number: 782 • 2012 ACR/ARHP Annual Meeting

    Anti-TNF Therapy Slows Radiographic Progression of Ankylosing Spondylitis

    Nigil Haroon1, Robert D. Inman2, Thomas J. Learch3, Michael H. Weisman4, Michael M. Ward5, John D. Reveille6 and Lianne S. Gensler7, 1Medicine/Rheumatology, University Health Network, Toronto Western Research Institute, University of Toronto, Toronto, ON, Canada, 2Dept of Medicine/Rheumatology, Toronto Western Research Institute, University Health Network and University of Toronto, Toronto, ON, Canada, 3Cedars-Sinai, Los Angeles, CA, 4Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 5Bldg 10 CRC Rm 4-1339, NIAMS/NIH, Bethesda, MD, 6Internal Medicine/Rheumatology, Univ of Texas Health Science Center at Houston, Houston, TX, 7Medicine/Rheumatology, University of California, San Francisco, San Francisco, CA

    Background/Purpose: The influence of anti-TNF therapy on radiographic progression in ankylosing spondylitis (AS) is not well established. We studied this effect on radiographic progression in…
  • Abstract Number: 2669 • 2012 ACR/ARHP Annual Meeting

    TLR7 Ligation Contributes to Monocyte Migration in Rheumatoid Arthritis

    Nathan D. Chamberlain1, Seung-jae Kim1, Michael Volin2, William Swedler3, Suncica Volkov1 and Shiva Shahrara1, 1Medicine/Rheumatology, University of Illinois at Chicago, Chicago, IL, 2Department of Microbiology and Immunology, Chicago College of Osteopathic Medicine Midwestern University, Downers Grove, IL, 3Section of Rheumatology, University of Illinois at Chicago, Chicago, IL

    Background/Purpose: The aim of the study was to characterize the expression of TLR7 in rheumatoid arthritis (RA) peripheral blood (PB) cells and to examine the…
  • Abstract Number: 1516 • 2012 ACR/ARHP Annual Meeting

    TSLP Upregulation in Human SSc Skin and Induction of Overlapping Profibrotic Genes and Intracellular Signaling with IL-13 and TGFb

    Romy Christmann1, Allison Mathes2, Giuseppina Stifano2, Alsya J. Affandi3, Andreea Bujor3, Cristina Padilla3 and Robert Lafyatis3, 1Rheumatology, Boston University School of Medicine, Boston, MA, 2Rheumatology, Boston University Medical Center, Boston, MA, 3Rheumatology, Boston University, Boston, MA

    Background/Purpose: to investigate the expression of Thymic Stromal Lymphopoietin (TSLP) in diffuse cutaneous systemic sclerosis (dcSSc) patients and explore its effects in vivo and in vitro…
  • Abstract Number: 737 • 2012 ACR/ARHP Annual Meeting

    Citrullination of ENA-78/CXCL5 Results in Conversion From a Non-Monocyte Recruiting to a Monocyte Recruiting Chemokine

    Ken Yoshida1, Olex Korchynskyi2, Paul P. Tak3, Takeo Isozaki4, Jeffrey H. Ruth5, Phillip Campbell6, Dominique L. Baeten7, Danielle M. Gerlag7, M. Asif Amin8 and Alisa E. Koch9, 1Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, 2Department of Cellular Proliferation and Apoptosis, Institute of Cell Biology, Lviv, Ukraine, 3Departments of Experimental Immunology and Internal Medicine, GlaxoSmithKline U.K. and Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 4Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, 5Internal Medicine, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 6Department of Internal Medicine, University of Michigan, Ann Arbor, MI, 7Division of Clinical Immunology and Rheumatology, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 8Department of Medicine, University of Michigan, Ann Arbor, MI, 9Internal Medicine - Rheumatology, University of Michigan Medical School, Ann Arbor, MI

    Background/Purpose: Citrullination is a post-translational modification that is the conversion of arginine to citrulline in proteins mediated by peptidylarginine deiminase (PAD). Antibodies directed towards the…
  • Abstract Number: 1446 • 2012 ACR/ARHP Annual Meeting

    The Granulocyte Signature and Organ Inflammation in TLR7 Responsive Mice Is RNA and Type 1 Interferon Dependent

    Xizhang Sun1, Alice Wiedeman2, Thomas H. Teal3, Nalini Agrawal3, Jeffrey Duggan2, Matt B. Buechler4, Jeffrey A. Ledbetter3, Denny Liggitt5, Jessica A. Hamerman6 and Keith B. Elkon7, 1Division of Rheumatology, University of Washington, Seattle, WA, 2Department of Immunology, University of Washington, Seattle, WA, 3Rheumatology, University of Washington, Seattle, WA, 4Benaroya Research Institute at Virginia Mason, Seattle, WA, Seattle, 5Comparative Medicine, University of Washington, Seattle, WA, 6Benaroya Research Institute at Virginia Mason, Seattle, WA, 7Rheumatology Box 356428, University of Washington, Seattle, WA

    Background/Purpose: Microarray expression analysis of blood taken from patients with Systemic Lupus Erythematosus (SLE) has revealed two characteristic signatures: one that reflects exposure to type…
  • Abstract Number: 740 • 2012 ACR/ARHP Annual Meeting

    Select Soluble Inflammatory Mediators Are Detected Prior to and Increase At Systemic Lupus Erythematosus Classification

    Melissa E. Munroe1, Jourdan R. Anderson2, Julie M. Robertson3, Timothy B. Niewold4, George C. Tsokos5, Michael P. Keith6, John B. Harley7 and Judith A. James8, 1Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Section of Rheumatology and Gwen Knapp Center for Lupus and Immunology Research, University of Chicago, Chicago, IL, 5Medicine/Rheumatology, BIDMC, Harvard Medical School, Boston, MA, 6Rheumatology, Walter Reed National Military Medical Center, Bethesda, MD, 7Division of Rheumatology and The Center for Autoimmune Genomics & Etiology, University of Cincinnati, Cincinnati Children's Hospital Medical Center; US Department of Veterans Affairs Medical Center, Cincinnati, OH, 8Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation; Oklahoma University Health Sciences Center, Oklahoma City, OK

    Background/Purpose: The processes that lead to clinical illness in systemic lupus erythematosus (SLE) years before diagnosis are not well characterized.  Several cytokines have been associated…
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Embargo Policy

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.).

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].

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