ACR Meeting Abstracts

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Abstracts tagged "mouse model and systemic lupus erythematosus (SLE)"

  • Abstract Number: 2086 • 2018 ACR/ARHP Annual Meeting

    4-Phenylbutyric Acid Mediates Therapeutic Effect in Systemic Lupus Erythematosus: Observations in an Experimental Murine Lupus Model

    Yunjung Choi1, Ji-hyun Jung2, Eun-Kyeong Lee2, Myeung Su Lee3, Changhoon Lee4 and Wan-Hee Yoo5, 1Division of Rheumatology, Department of Internal Medicine, Research Institute of Clinical Medicine of chonbuk national university-Biomedical Research Institute of chonbuk national university hospital, jeonju, Korea, Republic of (South), 2Research Institute of Clinical Medicine of Chonbuk National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Korea, Republic of (South), 3Department of Rheumatology, Division of Rheumatology, Department of Internal Medicine, Wonkwang University Hospital, Iksan, Korea, Republic of (South), 4Division of Rheumatology, Department of Internal Medicine, Division of Rheumatology, Department of Internal Medicine, Wonkwang University Hospital, Iksan, Korea, Republic of (South), 5Division of Rheumatology, Department of Internal Medicine, Research Institute of Clinical Medicine of chonbuk national university-Biomedical Research Institute of chonbuk national university hospital, Jeonju, Korea, Republic of (South)

    Background/Purpose: The purpose of the present study was to investigate whether ER stress inhibition by 4-phenylbutyric acid (4-PBA) ameliorates lupus manifestations in an experimental lupus…
  • Abstract Number: 2573 • 2017 ACR/ARHP Annual Meeting

    Lack of CD137-CD137 Ligand Signalling Aggravates Glomerulonephritis and Reduces the Survival of Lupus-Prone B6.MRLlpr Mice

    Anselm Mak1, Bhushan Dharmadhikari2 and Herbert Schwarz2, 1Medicine, National University of Singapore, Singapore, Singapore, 2Physiology, National University of Singapore, Singapore, Singapore

    Background/Purpose: Costimulatory molecules, which are expressed on leukocytes that facilitate their cross-talks via stimulatory and inhibitory signalling, play a potentially important role in the inflammatory…
  • Abstract Number: 918 • 2016 ACR/ARHP Annual Meeting

    Anergic B Cells May Preserve Peripheral Tolerance in Lupus-Prone Congenic Mice

    Kieran Manion1,2, Yuriy Baglaenko1,2, Nan-Hua Chang2, Nafiseh Talaei3 and Joan Wither4, 1Immunology, University of Toronto, Toronto, ON, Canada, 2Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON, Canada, 3Genetics and Development, Krembil Research Institute, Toronto, ON, Canada, 4Krembil Research Institute, University Health Network, Toronto, ON, Canada

    Background/Purpose:  Anergic autoreactive B cells are thought to play a critical role in systemic lupus erythematosus (SLE), a chronic autoimmune disease where breach of tolerance…
  • Abstract Number: 1759 • 2015 ACR/ARHP Annual Meeting

    Activation of T-Follicular Helper Cells and B Cells in Ultraviolet Light-Induced Murine Model of Systemic Lupus Erythematosus

    Misha Zarbafian1, Mehran Ghoreishi2 and Jan Dutz2, 1Medicine, University of British Columbia Vancouver Fraser Medical Program, Vancouver, BC, Canada, 2University of British Columbia Department of Dermatology and Skin Science, Vancouver, BC, Canada

    Background/Purpose: Non-obese diabetic (NOD) mice repeatedly exposed to ultraviolet (UV) light and Toll-like receptor-7 (TLR7) agonist cream (imiquimod) develop lupus-like disease, modeling a possible cutaneous…
  • Abstract Number: 3084 • 2015 ACR/ARHP Annual Meeting

    Progression of Lupus Pathology Is Correlative with Cardiac Magnetic Resonance Imaging Abnormalities, Diminished Function, and Inflammatory Histopathology in an Animal Model

    Nicholas Young1, Jeffrey Hampton1, Saba Aqel1, Jessica Pyles2, Anna Bratasz2, Anuradha Kalyanasundaram3, Wael N. Jarjour4 and Stacy P. Ardoin5, 1Immunology and Rheumatology, The Ohio State University Medical Center, Columbus, OH, 2Small Animal Imaging Core, The Ohio State University Medical Center, Columbus, OH, 3Physiology and Cell Biology, The Ohio State University Medical Center, Columbus, OH, 4Department of Internal Medicine, Division of Immunology and Rheumatology, The Ohio State University Medical Center, Columbus, OH, 5Pediatric & Adult Rheumatology, Ohio State University, Columbus, OH

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease causing inflammation throughout the body and cardiovascular involvement is a significant contributor to morbidity and mortality…
  • Abstract Number: 1943 • 2014 ACR/ARHP Annual Meeting

    In Vivo Effects of Epratuzumab, a Monoclonal Antibody Targeting Human CD22, on B Cell Function in Human CD22 Knock-in (Huki) Mice

    Carolin Brandl*1, Lamia Özgör*1, Miriam Wöhner1,2, Anthony Shock3 and Lars Nitschke1, 1Division of Genetics, University of Erlangen, Erlangen, Germany, 2Research Institute of Molecular Pathology, Vienna, Austria, 3UCB Pharma, Slough, United Kingdom

    Background/Purpose Epratuzumab is a humanized monoclonal antibody that targets the B cell-specific protein CD22 currently in Phase 3 clinical trials in patients (pts) with systemic…
  • Abstract Number: 639 • 2014 ACR/ARHP Annual Meeting

    Lack of Response Gene to Complement-32 Impairs Th17 Differentiation and Attenuates Lupus-like Chronic Graft Versus Host Disease

    Vinh Nguyen1, Cosmin Tegla2, Cornelia Cudrici3, Tudor Badea4, Horea Rus2 and Violeta Rus1, 1Medicine, University of Maryland School of Medicine and Veteran Affairs Medical Center, Baltimore, MD, 2Neurology, University of Maryland School of Medicine and Veteran Affairs Medical Center, Baltimore, MD, 3Neurology, University of Maryland School of Medicine, Baltimore, MD, 4NIH, National Eye Institute, Bethesda, MD

    Background/Purpose . Response Gene to Complement (RGC)-32 was cloned and characterized by our group as one of the genes induced by complement activation. It encodes…
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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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