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  • Abstract Number: 0834 • ACR Convergence 2020

    Is Disease Severity Greater Among Patients with Rheumatoid Arthritis Who Receive a Newly Approved Biologic? Real-world US Experience with Sarilumab from the ACR RISE Registry

    Stefano Fiore1, Lang Chen2, Cassie Clinton2, Huifeng Yun2, Amy Praestgaard3, Kerri Ford3 and Jeffrey R Curtis2, 1Sanofi, Bridgewater, NJ, 2Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Sanofi, Cambridge, MA

    Background/Purpose: Patients with RA who have received multiple biologics or targeted therapies over time tend to have more refractory and more severe disease, which may…
  • Abstract Number: 0835 • ACR Convergence 2020

    Pathogenic Effect of Chronic Stress-induced interleukin-12/23p40 on Neuropsychiatric System in Lupus-prone Mouse

    Nobuya Abe1, Kenji Oku1, Yuichiro Fujieda1, Nobuhiko Takahashi2, Kohei Karino1, Michihito Kono1, Masaru Kato1, Yuki Tanaka3, Rie Hasebe4, Olga Amengual1, Miwako Yamasaki5, Masahiko Watanabe5, Masaaki Murakami3 and Tatsuya Atsumi6, 1Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan, 2Division of Molecular Psychoimmunology, Institute for Genetic Medicine, Graduate School of Medicine, Hokkaido University, Sapporo, Japan, 3Division of Molecular Psychoimmunology, Institute for Genetic Medicine, Graduate School of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan, 4Biomedical Animal Research Laboratory, Institute for Genetic Medicine, Hokkaido University, Sapporo, Hokkaido, Japan, 5Department of Anatomy, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan, 6Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine, Hokkaido University, Sapparo, Hokkaido, Japan

    Background/Purpose:Neuropsychiatric system is one of the major organs affected in systemic lupus erythematosus (SLE). However, the pathogenesis of neuropsychiatric SLE (NPSLE) has not been fully…
  • Abstract Number: 0836 • ACR Convergence 2020

    SH3BP2 Deficiency Ameliorates Murine Systemic Lupus Erythematosus

    Tomoyuki Mukai1, Kyoko Kawahara1, Masanori Iseki2, Akiko Nagasu1, Hajime Nagasu3, Takahiko Akagi1, Shoko Tsuji1, Yasuyoshi Ueki4, Katsuhiko Ishihara2, Naoki Kashihara3 and Yoshitaka Morita1, 1Department of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan, 2Department of Immunology and Molecular Genetics, Kawasaki Medical School, Kurashiki, Okayama, Japan, 3Department of Nephrology and Hypertension, Kawasaki Medical School, Kurashiki, Okayama, Japan, 4Department of Biomedical Sciences and Comprehensive Care, Indiana University School of Dentistry, Indianapolis, IN

    Background/Purpose: The adaptor protein, Src homology 3 domain-binding protein 2 (SH3BP2), is widely expressed in immune cells, such as myeloid cells, B cells, and T…
  • Abstract Number: 0837 • ACR Convergence 2020

    Deletion of miR-223 Exacerbates Lupus Nephritis by Targeting S1pr1 in Faslpr/lpr Mice

    Sumie Hiramatsu Asano1, Tomoyuki Mukai2, Yoshitaka Morita3 and Jun Wada4, 1Kawasaki Medical School/Department of Rheumatology, Kurashiki city, Japan, 2Kawasaki Medical School, Kurashiki-shi, Okayama, Japan, 3Kawasaki Medical School/Department of Rheumatology, Kurashiki, Okayama, Japan, 4Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences., Okayama city, Japan

    Background/Purpose: To identify new candidate genes regulated by micro RNAs (miRNAs) and involved in the pathogenesis of systemic lupus erythematosus (SLE), we integrated miRNA and…
  • Abstract Number: 0838 • ACR Convergence 2020

    T Cell–Specific CaMKIV Deficiency Protects Mice from Imiquimod-induced Glomerulonephritis

    Milena Vukelic1, Masataka Umeda1, Andrew Ferretti2, Rhea Bhargava1, Nobuya Yoshida1 and George Tsokos3, 1Beth Israel Deaconess Medical Center Harvard Medical School, Boston, MA, 2Beth Israel Deaconess Medical Center Harvard Medical School, Boston, 3Division of Rheumatology & Clinical Immunology/Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by autoantibody production, immune complex deposition and multisystem involvement.  Calcium/calmodulin-dependent protein kinase type IV…
  • Abstract Number: 0839 • ACR Convergence 2020

    Single-Cell Transcriptomics of Mouse and Human Lupus Nephritis Identifies Conserved Myeloid Populations Across Species

    Paul Hoover1, Michael Peters2, David Lieb3, Rakesh Mishra4, Nir Hacohen2 and Anne Davidson5, 1Brigham and Women's Hospital, Boston, MA, 2Broad Institute, Boston, 3Broad Institute, Boston, MA, 4Feinstein Institute, Manhasset, NY, 5Northwell Health, New York

    Background/Purpose: We recently identified novel immune cell states in the kidneys of lupus nephritis patients (Arazi et al, Nature Immunology 2019). To determine the similarities…
  • Abstract Number: 0840 • ACR Convergence 2020

    Amelioration of Immune Complex-Mediated Glomerulonephritis via CD6 Modulation

    Samantha Chalmers1, Sayra Garcia1, Leal Herlitz2, Jeanette Ampudia3, Cherie Ng4, Stephen Connelly3 and Chaim Putterman1, 1Albert Einstein College of Medicine, Bronx, NY, 2Cleveland Clinic, Cleveland, OH, 3Equillium, Inc, San Diego, CA, 4Equillium, Inc, La Jolla, CA

    Background/Purpose: CD6 is a co-stimulatory receptor, predominantly expressed on T cells, that binds to activated leukocyte cell adhesion molecule (ALCAM), a ligand expressed on antigen-presenting…
  • Abstract Number: 0841 • ACR Convergence 2020

    CD6 Modulation Ameliorates Kidney and Skin Disease in a Spontaneous Murine Lupus Model

    Samantha Chalmers1, Sayra Garcia1, Rajalakshmy Ayilam Ramachandran2, Chandra Mohan2, Leal Herlitz3, Dalena Chu4, Jeanette Ampudia4, Cherie Ng5, Stephen Connelly4 and Chaim Putterman1, 1Albert Einstein College of Medicine, Bronx, NY, 2University of Houston, Houston, TX, 3Cleveland Clinic, Cleveland, OH, 4Equillium, Inc, San Diego, CA, 5Equillium, Inc, La Jolla, CA

    Background/Purpose: T cells are an important contributor to the pathogenesis of SLE and lupus nephritis, and thus present themselves as interesting therapeutic targets. CD6 is…
  • Abstract Number: 0842 • ACR Convergence 2020

    mTOR Signaling Pathway Blockade and Rab4 Expression Affects Metabolism of Lupus T Cells

    Tamas Faludi1, Nick Huang1, Manuel Duarte1, Joshua Lewis1 and Andras Perl1, 1SUNY Upstate Medical University, Syracuse, NY

    Background/Purpose: Pro-inflammatory T-cell development underlies the pathogenesis of systemic lupus erythematosus (SLE). Activation of the mechanistic target of rapamycin (mTOR) plays a central role in…
  • Abstract Number: 0843 • ACR Convergence 2020

    Rab4A Activation Predisposes to Hepatitis in Spontaneous and Pristane-Induced Mouse Models of Systemic Lupus Erythematosus

    Nick Huang1, Akshay Patel1, Zachary Oaks1 and Andras Perl1, 1SUNY Upstate Medical University, Syracuse, NY

    Background/Purpose: HRES-1/Rab4 or Rab4A, a GTPase responsible for mitochondrial oxidative stress1 and activation of the mechanistic target of rapamycin2, is overexpressed in T cells of…
  • Abstract Number: 0844 • ACR Convergence 2020

    Rab4A Regulates Glomerulonephritis and Tryptophan Metabolism in Sle1.2.3. Lupus-prone Mice via Recycling of CD98

    Brandon Wyman1, Nick Huang1, Zhiwei Lai1, Mark Haas2, Manuel Duarte1, Joshua Lewis1 and Andras Perl1, 1SUNY Upstate Medical University, Syracuse, NY, 2Cedars-Sinai, Los Angeles, CA

    Background/Purpose: Systemic Lupus Erythematosus (SLE) is an autoimmune disease with an incompletely understood etiology. Previous work has identified Rab4A, a small GTPase responsible for endosomal…
  • Abstract Number: 0845 • ACR Convergence 2020

    Hematopoietic Specific Deficiency of Rho Kinase Attenuates Neutrophil NETosis and UVB-induced Skin Inflammation

    Minghui Li1, Xing Lyu1, Yubin Li2, James Liao3, Victoria Werth4 and Ming-Lin Liu1, 1University of Pennsylvania, philadelphia, 2University of Pennsylvania and the Michael J. Crescenz VA Medical Center, Philadelphia, PA, 3University of Chicago, Chicago, 4University of Pennsylvania and Corporal Michael J. Crescenz Veterans Administration Hospital, Philadelphia

    Background/Purpose: Neutrophils are the most abundant leukocytes and the first to be recruited to the site of photodamage after ultraviolet B (UVB) exposure. We have…
  • Abstract Number: 0846 • ACR Convergence 2020

    MHC Class I Epitopes Derived from Autoantibody Variable Regions, Conjugated to Synthetic Oligodeoxynuleotides, Induce Cytotoxic T Cells That Deplete Autoreactive B Cells and Ameliorate Murine Lupus

    Ram Singh1, 1UCLA David Geffen School of Medicine, Los Angeles, CA

    Background/Purpose: B cell depletion or modulation is emerging as a major treatment modality for autoimmune diseases. However, the current treatments to accomplish this non-specifically target…
  • Abstract Number: 0847 • ACR Convergence 2020

    Impact of Hydroxychloroquine Treatment on Immunologic Markers in SLE Depends on Ethnicity

    Laurence Magder1, Daniel Goldman2 and Michelle Petri2, 1University of Maryland, Baltimore, Baltimore, MD, 2Johns Hopkins University School of Medicine, Timonium, MD

    Background/Purpose: SLE patients with certain immunological markers (i.e., anti-DNA, low complement) are at higher risk of lupus nephritis and those with antiphospholipid antibodies are at…
  • Abstract Number: 0848 • ACR Convergence 2020

    Delineation of a Proinflammatory Cytokine Profile Targeted by Janus Kinase 1/2 Inhibition Using Baricitinib in a Phase 2 Systemic Lupus Erythematosus Trial

    Thomas Dörner1, Yoshiya Tanaka2, Michelle Petri3, Josef Smolen4, Daniel Wallace5, Brenda Crowe6, Ernst Dow6, Richard Higgs6, Guilherme Rocha6, Robert Benschop6, Maria Silk6, Stephanie de Bono6, Robert Hoffman6 and Damiano Fantini6, 1DRFZ and Charité University Hospitals, Berlin, Germany, 2The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan, 3Johns Hopkins University School of Medicine, Timonium, MD, 4Division of Rheumatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria, 5Cedars-Sinai Medical Center/UCLA, Los Angeles, CA, 6Eli Lilly and Company, Indianapolis, IN

    Background/Purpose: Given the unmet clinical needs in systemic lupus erythematosus (SLE), including poor disease control and drug toxicities, new therapies are needed. In a phase…
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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 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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