ACR Meeting Abstracts

ACR Meeting Abstracts

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Abstracts tagged "Plasmablasts"

  • Abstract Number: 2798 • 2013 ACR/ARHP Annual Meeting

    Bone Marrow In Systemic Lupus Erythematosus Patients Contain a Highly Elevated Proportion Of Somatically Mutated, Activated Naive Cells Comprised Of Substantial Clonal Expansions

    Jennifer Hom1, Christopher Tipton2, Christopher Fucile3, Bridget Neary1, Chungwen Wei4, F. Eun-Hyung Lee1, Alex Rosenberg3 and Inaki Sanz2, 1Emory University, Atlanta, GA, 2Medicine/Rheumatology, Emory University, Atlanta, GA, 3University of Rochester, Rochester, NY, 4Rheumatology, Emory University, Atlanta, GA

    Background/Purpose: Systemic lupus erythematosus (SLE) is a disease where autoreactive antibodies are produced as a result of abnormal B cell activation and broken self-tolerance. This…
  • Abstract Number: 1647 • 2013 ACR/ARHP Annual Meeting

    An Altered Frequency Of Circulating Follicullar T Helper Cell Counterparts and Their Subsets Is Associated With Increased Circulating Plasmablasts In Seropositive RA Patients

    Irene Arroyo-Villa1, M. Belén Bautista-Caro1, Alejandro Balsa2, Pilar Aguado2, Alejandro Villalba1, Chamaida Plasencia2, Amaya Puig-Kröger3, Emilio Martín-Mola1 and Maria Eugenia Miranda-Carus1, 1Rheumatology, Hospital La Paz - IdiPaz, Madrid, Spain, 2Rheumatology, Hospital La Paz-IdiPaz, Madrid, Spain, 3Immuno-oncology, Hospital Gregorio Marañon, Madrid, Spain

    Background/Purpose: Follicular T helper (Tfh) cells, a CD4 T helper subset localized in lymphoid organs, help B cell differentiation and function. Circulating CD4 T cells…
  • Abstract Number: 42 • 2013 ACR/ARHP Annual Meeting

    Inhibition Of B Cell Differentiation To The Plasmablast and Plasma Cell Lineage By CC-220, a Potent Modulator Of The Cereblon E3 Ubiquitin Ligase Complex

    Peter Schafer1, Lori Capone2, Lei Wu1 and Rajesh Chopra3, 1Department of Translational Development, Celgene Corporation, Summit, NJ, 2Celgene Corporation, Summit, NJ, 3Translational Development, Celgene Corporation, Summit, NJ

    Background/Purpose: CC-220 is an immunomodulatory compound which binds to the CUL4 family E3 ubiquitin ligase complex protein cereblon (CRBN) with high affinity and modulates the…
  • Abstract Number: 24 • 2013 ACR/ARHP Annual Meeting

    Plasma Cells In Acute Systemic Lupus Erythematosus Flares Are Characterized By a Highly Diversified Repertoire Accentuated By Clonal Expansions Of VH4-34 Antibodies

    Christopher Tipton1, Christopher Fucile2, Alex Rosenberg2, Scott Jenks3, Jennifer Hom4, F. Eun-Hyung Lee4 and Inaki Sanz1, 1Medicine/Rheumatology, Emory University, Atlanta, GA, 2University of Rochester, Rochester, NY, 3Allergy, Immunology, and Rheumatology, Emory University School of Medicine, Atlanta, GA, 4Emory University, Atlanta, GA

    Background/Purpose :Systemic Lupus Erythematosus (SLE) is an autoimmune disease in which faulty B cell tolerance promotes the generation of multiple autoantibodies of which anti-ds DNA,…
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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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