ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2530

Anti-Ribosomal P Antibodies in a Large Cohort of Autoimmune Hepatitis with No Evidence of Lupus: A Common Underlying Mechanism Targeting Liver?

Ana Luisa Calich1, Vilma S. T. Viana1, Eduardo L. Cançado2, Débora R. Terrabuio2, Francisco Tustumi1, Elaine P. Leon1, Clovis Artur Silva3, Eduardo F. Borba Neto1 and Eloisa Bonfa1, 1Rheumatology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil, 2Gastroenterology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil, 3Paediatric Rheumatology International Trials Organization (PRINTO), Istituto Giannina Gaslini, Genova, Italy

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Auto-immunity, autoantibodies, hepatitis and systemic lupus erythematosus (SLE)

  • Tweet
  • Email
  • Print
Session Information

Title: Miscellaneous Rheumatic and Inflammatory I

Session Type: Abstract Submissions (ACR)

Background/Purpose: Anti-ribosomal P proteins antibody (anti-rib P) is a highly specific marker for systemic lupus erythematosus (SLE) and it is associated with liver involvement in this disease. Similarities between autoimmune hepatitis (AIH) and SLE-associated hepatitis raised the possibility that anti-rib P antibodies may also have relevance in AIH. This study was therefore undertaken to evaluate the frequency and clinical significance of anti-rib P antibodies in a large AIH cohort before treatment.

Methods: Ninety-six patients with AIH diagnosed according to the Revised Original Pretreatment Scoring System of the International Autoimmune Hepatitis Group were studied. Charts were reviewed for demographic, clinical, treatment and laboratorial parameters. 82 healthy individuals were included as control. Available frozen sera samples from AIH patients obtained at diagnosis were tested for IgG anti-rib P by ELISA using a commercial kit employing synthetic 22 amino acid C-terminal peptide as antigen and reactivity was confirmed by immunoblotting using rat liver ribosomal fraction. All sera were screened for other lupus specific autoantibodies, anti-dsDNA and anti-Sm. Three patients positive for anti-dsDNA (n=1) and anti-Sm (n=2) were excluded.

Results: Moderate to high titers (>40U) of anti-rib P antibody were found in 9.7% (9/93) AIH patients and in none of the controls (p=0.003). Mean antibody titer was 93.6 ± 33.1 units. Positive results by ELISA were confirmed by immunoblotting. Patients with positive results for anti-rib P were referred to the Rheumatology Outpatient Clinic for a more detailed clinical evaluation. No sign of lupus was found in all of them. At presentation, AIH patients with and without anti-rib P antibodies had similar demographic/clinical features, including the frequency of cirrhosis (44% vs. 28%, p=0.44), hepatic laboratorial findings (p>0.05), corticosteroid and azathioprine therapy frequencies (100% vs. 99%, p=0.17 and 78% vs. 92%, p=0.17, respectively). The long follow up period was also comparable in those with and without anti-rib P antibodies (10.7± 5.1 vs. 10.3 ± 5.2 years, p=0.68). Importantly, at the final observation AIH patients with anti-rib P had a significantly higher frequency of cirrhosis compared to negative group (100% vs. 60%, p=0.04) despite no difference in the frequency of drugs at the last visit (p>0.05).

 Conclusion: The novel demonstration of anti-rib P in AIH patients without clinical and laboratorial evidence of SLE suggests a common underlying mechanism targeting liver in these two diseases. In addition, this antibody seems to predict a group of patients with worse AIH prognosis.


Disclosure:

A. L. Calich,
None;

V. S. T. Viana,
None;

E. L. Cançado,
None;

D. R. Terrabuio,
None;

F. Tustumi,
None;

E. P. Leon,
None;

C. A. Silva,

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPQ) ,

2,

Federico Foundation Grants,

2;

E. F. Borba Neto,
None;

E. Bonfa,

Grants,

2.

  • Tweet
  • Email
  • Print

« Back to 2012 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/anti-ribosomal-p-antibodies-in-a-large-cohort-of-autoimmune-hepatitis-with-no-evidence-of-lupus-a-common-underlying-mechanism-targeting-liver/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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.).

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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology