ACR Meeting Abstracts

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Abstracts tagged "lupus nephritis and mouse model"

  • Abstract Number: 2094 • 2018 ACR/ARHP Annual Meeting

    Examining T Cell Exhaustion in Murine Systemic Lupus Erythematosus

    Jeremy Tilstra1, Lyndsay Avery2, Ashley Menk2, Rachael Gordon2, Shuchi Smita3, Lawrence Kane3, Maria Chikina2, Greg Delgoffe3 and Mark Shlomchik4, 1Rheumatology, Univ of Pittsburgh Medical Center, Pittsburgh, PA, 2University of Pittsburgh, Pittsburgh, PA, 3Department of Immunology, University of Pittsburgh, Pittsburgh, PA, 4Immunology, University of Pittsburgh, Pittsburgh, PA

    Background/Purpose: While T cells are important for the pathogenesis of systemic lupus erythematosus (SLE) and lupus nephritis, little is known about how T cells function…
  • Abstract Number: 2104 • 2018 ACR/ARHP Annual Meeting

    Glomerular and Tubular Transcriptional Profiles Reveal Gene Clusters Specific for Different Stages of Glomerulonephritis in NZM2328 Mice

    Hongyang Wang1, Nick Geraci2, Prathyusha Bachali2, Brian Kegerreis3, Michelle Catalina2, Erika Hubbard2, Sun-sang Sung4, Felicia Gaskin5, Amrie Grammer2, Peter Lipsky2 and Shu Man Fu6, 1Center for Immunity, Inflammation, and Regenerative Medicine, University of Virginia, Charlottesville, VA, 2AMPEL BioSolutions and RILITE Research Institute, Charlottesville, VA, 3AMPELBioSolutions and RILITE Research Institute, Charlottesville, VA, 4Center for Immunity, Inflammation, and Regenerative Medicine, University of Virginia School of Medicine, Charlottesville, VA, 5Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA, 6Department of Medicine, University of Virginia, Charlottesville, VA

    Background/Purpose: NZM2328 mice spontaneously develop glomerulonephritis (GN) and females commonly progress to renal failure. Our previous study showed that acute GN (aGN) and chronic GN…
  • Abstract Number: 2839 • 2014 ACR/ARHP Annual Meeting

    BCL-2 As a Potential Therapeutic Target in Human Lupus Tubulointerstitial Inflammation

    Kichul Ko1, Denisse Yanez1, Natalya Kaverina1, Vladimir M. Liarski1, Yahui Peng2, Li Lan3, Stuart Perper4, Annette Schwartz5, Liz O'connor6, Andrew Souers7, Steven Elmore7, Lisa Olson5, Maryellen L. Giger3, Li Chun Wang4 and Marcus R. Clark1, 1Rheumatology and Knapp Center for Lupus Research, University of Chicago, Chicago, IL, 2School of Electronic and Information Engineering, Beijing Jiaotong University, Beijing, China, 3Radiology, University of Chicago, Chicago, IL, 4Immunology, AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 5AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 6Toxicology, AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 7AbbVie Inc, North Chicago, IL

    Background/Purpose Lupus nephritis (LuN) is the most common, severe manifestation of systemic lupus erythematosus (SLE). We have previously shown that glomerulonephritis appears to be a…
  • Abstract Number: 558 • 2013 ACR/ARHP Annual Meeting

    Fli-1 Regulates Immune Cell Infiltration Through Affecting Local Chemokine Expression and IL-6 Expression In The Kidney Of Lupus Prone Mice

    Shuzo Sato1, Sarah Williams2, Eva Karam3 and Xian Zhang4, 1Rheumatology and Immunology, Medical University of South Carolina, Charleston, SC, 2Ralph H. Johnson VA Medical Center, Charleston, SC, 3Medicine, Medical University of South Carolina, Charleston, SC, 4Medicine, Medical University of South Carolina and Ralph H. Johnson VA Medical Center, Charleston, SC

    Background/Purpose: Fli-1 expression level, a member of the Ets family of transcription factors, is a mitigating factor in the development of nephritis in murine models…
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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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