Presence of autoantibodies to the glycolytic enzyme α‐enolase in sera from patients with early rheumatoid arthritis
Open Access
- 8 May 2002
- journal article
- research article
- Published by Wiley in Arthritis & Rheumatism
- Vol. 46 (5) , 1196-1201
- https://doi.org/10.1002/art.10252
Abstract
Objective To identify a new autoantigen/autoantibody population in rheumatoid arthritis (RA) sera. Methods Following a population‐based recruitment effort, 255 patients with very early arthritis (median disease duration 4 months) were studied using different clinical, biologic, and radiologic assessments. After a followup period of 1 year, patients were classified as having RA (n = 145), non‐RA rheumatic diseases (n = 70), and undifferentiated arthritis (n = 40). Patients' sera were analyzed by one‐dimensional (1D) and 2D Western blotting. The recognized 50‐kd protein was analyzed by matrix‐assisted laser desorption ionization–time‐of‐flight (MALDI‐TOF) mass spectrometry (MS). RA serum reactivities were evaluated against the recombinant protein synthesized by an in vitro coupled transcription–translation system. Results On 1D Western blots, 36 of the 145 RA sera bound to a 50‐kd polypeptide. On 2D Western blots, anti–50‐kd+ RA sera recognized a triplet of isoelectric point 6.5–7.0 and a molecular mass of 50 kd. The 3 spots of the triplet were analyzed by MALDI‐TOF MS and were shown to correspond to human α‐enolase. A goat anti‐enolase antiserum, which recognized a band comigrating with the 50‐kd antigen on 1D Western blots, gave a labeling pattern on 2D Western blots similar to that observed with anti–50‐kd+ RA sera. Among the 36 RA sera that identified α‐enolase in protein maps, only 8 recognized the recombinant (unmodified) α‐enolase. The specificity of anti–α ‐enolase antibodies for RA was 97.1%. Half of the anti–α ‐enolase–positive RA patients were negative for both rheumatoid factor and antifilaggrin antibodies. The presence of anti–α‐enolase antibodies was the greatest predictive factor of radiologic progression in the first 66 RA patients included. Conclusion Autoantibodies to α‐enolase, an enzyme of the glycolytic pathway, are present in the sera of patients with very early RA and have potential diagnostic and prognostic value for RA.Keywords
Funding Information
- Inserm
- Fondation de la Recherche Médicale
- Programme Hospitalier de Recherche Clinique VERA-O (Very Early Rheumatoid Arthritis Outcome)
- Association de Recherche sur la Polyarthrite
This publication has 12 references indexed in Scilit:
- Autoantibodies to GPI in rheumatoid arthritis: linkage between an animal model and human diseaseNature Immunology, 2001
- Multifunctional α-enolase: its role in diseasesCellular and Molecular Life Sciences, 2001
- Rheumatoid factors, anti-filaggrin antibodies and low in vitro interleukin-2 and interferon-γ production are useful immunological markers for early diagnosis of community cases of rheumatoid arthritis. A preliminary studyJoint Bone Spine, 2001
- Two-dimensional electrophresis and mass spectrometry identification of proteins bound by a murine monoclonal anti-cardiolipin antibody: A powerful technique to characterize the cross-reactivity of a single autoantibodyElectrophoresis, 2000
- The immunologic homunculus in rheumatoid arthritisArthritis & Rheumatism, 1999
- Arthritis Provoked by Linked T and B Cell Recognition of a Glycolytic EnzymeScience, 1999
- Serum samples of patients with rheumatoid arthritis contain a specific autoantibody to “denatured” aldolase A in the osteoblast-like cell line, MG-63Annals of the Rheumatic Diseases, 1999
- Citrulline is an essential constituent of antigenic determinants recognized by rheumatoid arthritis-specific autoantibodies.Journal of Clinical Investigation, 1998
- EFFECTS OF HYDROXYCHLOROQUINE AND SULPHASALAZINE ON PROGRESSION OF JOINT DAMAGE IN RHEUMATOID ARTHRITISThe Lancet, 1989
- Glycolytic activity in human synovial lining cells in rheumatoid arthritis.Annals of the Rheumatic Diseases, 1979