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  • Abstract Number: 2675 • 2014 ACR/ARHP Annual Meeting

    The Selective Loss of SLAMF4+ CD8+ T Cells Contributes to the Decreased Cytotoxic Capacity Observed in Systemic Lupus Erythematosus

    Katalin Kis-Toth1, Denis Comte1, Maria Karampetsou1, Lakshmi Kannan2 and George C. Tsokos1, 1Rheumatology, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA, 2Rheumtology, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA

    Background/Purpose Signaling lymphocytic activation molecule family member 4 (SLAMF4) engagement by its ligand SLAMF2 can mediate the cytotoxicity of CD8+ T cells and natural killer…
  • Abstract Number: 2674 • 2014 ACR/ARHP Annual Meeting

    The Effect and Mechanisms of Icaritin on Regulating Foxp3/IL17a Expression in CD4+  T Cells from SLE

    Jieyue Liao1, Yu Liu2, Ming Zhao3, hai Jing Wu4 and Qianjin Lu5, 1Department of Dermatology, Department of Dermatology, Second Xiangya Hospital, Central South University, Changsha, China, 2Department of Dermatology, Second Xiangya Hospital, Central South University, shangcha, China, 3Department of Dermatology, Second Xiangya Hospital, Central South University, changsha, China, 4Department of Dermatology, Second Xiangya Hospital, Central South University, sahngsha, China, 5Department of Dermatology, Second Xiangya Hospital, Central South University, Changsha, China

    Background/Purpose : Systemic lupus erythematosus (SLE) is a female predominant autoimmune disease characterized by overproduction of autoantibodies. The pathogenesis of SLE is complex. Several studies…
  • Abstract Number: 2693 • 2014 ACR/ARHP Annual Meeting

    Hyporesponsiveness to TLR9 in Term of Cytokines Production By B Cells in SLE-Patients

    Julia Sieber1, Capucine Daridon1, Sarah J. Fleischer1, Vanessa Fleischer1, Falk Hiepe1, Tobias Alexander2, Guido Heine3, Gerd Burmester4, Simon Fillatreau5 and Thomas Dörner1, 1Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology/German Rheumatism Research Center (DRFZ), Berlin, Germany, 2Dept. Medicine/Rheumatology and Clinical Immunology, Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology/German Rheumatism Research Center (DRFZ), Berlin, Germany, 3Charité University Medicine, Dept. Dermatology, Venerology and Allergology, Berlin, Germany, 4Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology, Berlin, Germany, 5German Rheumatism Research Center (DRFZ), Berlin, Germany

    Background/Purpose The role of B cells in immunity has been mainly related to the generation of antibodies and formation of immune complexes. However, B cells…
  • Abstract Number: 2692 • 2014 ACR/ARHP Annual Meeting

    Up-Regulated Expression of CXCR4 on Circulating B Cells in Patients with Systemic Lupus Erythematosus

    Hironari Hanaoka1, Yuka Okazaki1, Akinori Hashiguchi2, Hidekata Yasuoka3, Tsutomu Takeuchi1 and Masataka Kuwana1, 1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 2Department of Pathology, Keio University School of Medicine, Tokyo, Japan, 3Rheumatology, Keio University School of Medicine, Tokyo, Japan

    Background/Purpose It is increasingly appreciated that circulating B cells are functionally altered and are involved in pathogenic process in patients with systemic lupus erythematosus (SLE).…
  • Abstract Number: 2690 • 2014 ACR/ARHP Annual Meeting

    Autoregulatory Function of IL-10 Producing Pre-Naïve B Cells Is Defective in Systemic Lupus Erythematosus

    Ji-Hyun Sim1, Hang-Rae Kim1, Soog-Hee Chang1, In Je Kim2, Peter E. Lipsky3 and Jisoo Lee4,5, 1Seoul National University, Seoul, South Korea, 2Rheumatology, Internal Medicine, Ewha Womans University School of Medicine, Seoul, South Korea, 3AMPEL BioSolutions, Charlottesville, VA, 4Internal Medicine, Ewha Womans Univeristy School of Medicine, Seoul, South Korea, 5Ewha Womans University School of Medicine, Seoul, South Korea

    Background/Purpose: Pre-naive B cells represent an intermediate stage in human B cell development with some functions of mature cells, but their involvement in immune responses…
  • Abstract Number: 2691 • 2014 ACR/ARHP Annual Meeting

    A Novel CD123–CD11c– Dendritic Cell Subset Increased in Relation to Disease Activity in Patients with Systemic Lupus Erythematosus

    Satoshi Kubo1, Shingo Nakayamada1, Naoki Yunoue1, Maiko Yoshikawa1, Kunihiro Yamaoka1 and Yoshiya Tanaka2, 1The First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2University of Occupational and Environmental Health, Japan, Kitakyushu, Japan

    Background/Purpose Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by overproduction of autoantibodies by B cells and breaking self-tolerance of T cells and dendritic…
  • Abstract Number: 2689 • 2014 ACR/ARHP Annual Meeting

    The CUL4CRBN E3 Ubiquitin Ligase Modulator CC-220 Induces Degradation of the Transcription Factors Ikaros and Aiolos: Immunomodulation in Healthy Volunteers and Relevance to Systemic Lupus Erythematosus

    Peter H. Schafer1, Ying Ye2, Lei Wu3, Jolanta Kosek4, Zhihong Yang5, Liangang Liu5, Michael Thomas5, Maria Palmisano5 and Rajesh Chopra5, 1Celgene Corporation, Celgene Corporation, Summit, NJ, 286 Morris Avenue, Celgene Corporation, Summit, NJ, 3Department of Translational Development, Celgene Corporation, Summit, NJ, 4Translational Development, Celgene Corporation, Summit, NJ, 5Celgene Corporation, Summit, NJ

    Background/Purpose: CC-220 is an immunomodulatory compound that binds to cereblon (CRBN), part of the CUL4CRBN E3 ubiquitin ligase complex, which has been shown to ubiquitinate…
  • Abstract Number: 2688 • 2014 ACR/ARHP Annual Meeting

    Comparison of Systemic Lupus Erythematosus and Healthy Anti-Nuclear Antibody Positive African-Americans Reveals Distinct Differences in T Cell and Progenitor Populations

    Rufei Lu1,2, Samantha Slight-Webb1, Holden T. Maecker3, Paul J. Utz4, Joel M. Guthridge1 and Judith A. James5,6, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Medicine and Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 3Division of Immunology and Rheumatology, Stanford University School of Medicine, Stanford, CA, 4Medicine, Stanford University School of Medicine, Stanford, CA, 5Clinical Arthritis and Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 6Rheumatology, University of Oklahoma Health Sciences Center, Oklahoma City, OK

    Background/Purpose Systemic lupus erythematosus (SLE) is a systemic autoimmune disorder which arises from both genetic and environmental factors that likely affect phenotypic and functional characteristics…
  • Abstract Number: 2687 • 2014 ACR/ARHP Annual Meeting

    Estrogen-Mediated STAT1 Activation By Estrogen Receptor a Induces TLR8 Expression: A Novel Pathogenic Mechanism in Systemic Lupus Erythematosus

    Nicholas Young1, Giancarlo Valiente2, Lai-Chu Wu3, Michael Bruss4, Stacy Ardoin2, Craig Burd5 and Wael N. Jarjour6, 1Ohio State University, Columbus, OH, 2Rheumatology and Immunology, The Ohio State University Wexner Medical Center, Columbus, OH, 3Immunology and Rheumatology, The Ohio State University Wexner Medical Center, Columbus, OH, 4Division of Rheumatology and Immunology, The Ohio State University Wexner Medical Center, Columbus, OH, 5Molecular & Cellular Biochemistry, The Ohio State University, Columbus, OH, 6Dept of Rheumatology/Medicine, The Ohio State University Wexner Medical Center, Columbus, OH

    Background/Purpose: Many autoimmune disorders, including Systemic Lupus Erythematosus (SLE) display female gender predominance.  Previous studies have demonstrated significant hormonal contributions to SLE pathogenesis, including estrogen,…
  • Abstract Number: 2686 • 2014 ACR/ARHP Annual Meeting

    Gene Array Analysis Reveals Unique Estrogen Signature in Peripheral Blood Mononuclear Cells of Patients with Systemic Lupus Erythematosus

    Stephanie Amici1, Nicholas A. Young2, Lai-Chu Wu2, Mireia Guerau1 and Wael N. Jarjour3, 1Health and Rehab Sciences, The Ohio State University, Columbus, OH, 2Immunology and Rheumatology, The Ohio State University Wexner Medical Center, Columbus, OH, 3Dept of Rheumatology/Medicine, The Ohio State University Wexner Medical Center, Columbus, OH

    Background/Purpose: Systemic Lupus Erythematosus (SLE) is an autoimmune disorder predominately affecting females in the reproductive age range.  Estrogen is present at higher levels in this…
  • Abstract Number: 2685 • 2014 ACR/ARHP Annual Meeting

    Ten-Eleven Translocation 2 Protein Down-Regulates DNA Methylation of Interleukin-17A Promoter and  Induces Its Expression in CD4+t Cells of Patients with Systemic Lupus Erythematosus

    Duo Li, Qian Tang, Lina Tan, Ming Zhao, Gongping Liang, Yang Yang and Qianjin Lu, Department of Dermatology, Second Xiangya Hospital, Central South University, Changsha, China

    Background/Purpose: Recent evidence indicates that IL-17A plays a key role in the pathogenesis of autoimmune diseases, such as systemic lupus erythematosus (SLE). SLE patients have…
  • Abstract Number: 2684 • 2014 ACR/ARHP Annual Meeting

    Association of Adam33 Polymorphisms with Systemic Lupus Erythematosus

    Seong-Wook Kang1, Seung-Taek Song1, Su-Jin Yoo2, Mi-Kyoung Lim3, Dong-Hyuk Sheen4, In-Seol Yoo5, Jinhyun Kim1 and Seung-Cheol Shim1, 1Department of Internal Medicine, Chungnam National University School of Medicine, Daejeon, South Korea, 2Rheumatology, Chungnam National University School of Medicine, Daejeon, South Korea, 3Rheumatology, Eulji University Hospital, Daejeon, South Korea, 4Department of Internal Medicine, Eulji University Hospital, Daejeon, South Korea, 5Departmen of Internal medicine, Chungnam National University School of Medicine, Daejeon, South Korea

    Background/Purpose A Disintegrin and Metalloprotease 33 (ADAM33) is a member of a family of genes that encode membrane-anchored proteins with a disintegrin and a metalloprotease…
  • Abstract Number: 2683 • 2014 ACR/ARHP Annual Meeting

    The Discovery of Novel Splicing Variants of Neurogranin and Their Role in the Pathogenesis of Systemic Lupus Erythematosus

    Xiaofang Luo1, Xuelan He1, Chaonan Wu1, Juan Ni1, Ling li Dong2 and Shouxin Li2, 1Department of Rheumatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China, 2Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

    Background/Purpose Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease with a diverse array of clinical manifestations that is characterized by the production of antibodies…
  • Abstract Number: 2682 • 2014 ACR/ARHP Annual Meeting

    Serine Arginine-Rich Splicing Factor 1 (SRSF1) Regulates Transcriptional Activation of the T Cell Receptor CD3 Zeta Chain in Human T Cells

    Vaishali Moulton1, Andrew R. Gillooly2 and George C. Tsokos3, 1Division of Rheumatology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 2Medicine/Rheumatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 3Rheumatology, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA

    Background/Purpose T cells from patients with systemic lupus erythematosus (SLE) express reduced amounts of the critical CD3 zeta signaling chain, and are poor producers of…
  • Abstract Number: 2681 • 2014 ACR/ARHP Annual Meeting

    Activated SLE-T Cells Enhance the Interferon-Alpha Production By Plasmacytoid Dendritic Cells Stimulated By RNA-IC

    Dag Leonard1, Maija-Leena Eloranta1, Niklas Hagberg1, Olof Berggren1, Karolina Tandre1, Gunnar Alm2 and Lars Rönnblom1, 1Department of Medical Sciences, SciLife Lab, Rheumatology, Uppsala University, Uppsala, Sweden, Uppsala, Sweden, 2Department of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, Uppsala, Sweden, Uppsala, Sweden

    Background/Purpose A prominent interferon-α (IFNα) signature is seen in several autoimmune diseases including systemic lupus erythematosus (SLE). Plasmacytoid dendritic cells (pDCs) are the main IFNα…
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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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