Identification of a novel autoantigen eukaryotic initiation factor 3 associated with polymyositis
Language English Country England, Great Britain Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
Grant support
18474
Versus Arthritis - United Kingdom
MR/N003322/1
Medical Research Council - United Kingdom
PubMed
31728542
PubMed Central
PMC7188460
DOI
10.1093/rheumatology/kez406
PII: 5571130
Knihovny.cz E-resources
- Keywords
- autoantibodies, autoantigens, myositis,
- MeSH
- Autoantigens immunology MeSH
- Autoantibodies blood MeSH
- Biomarkers blood MeSH
- Adult MeSH
- Eukaryotic Initiation Factor-3 blood immunology MeSH
- Mass Spectrometry methods MeSH
- Immunoprecipitation methods MeSH
- Immunosuppressive Agents administration & dosage MeSH
- Middle Aged MeSH
- Humans MeSH
- Polymyositis drug therapy immunology physiopathology MeSH
- Disease Progression * MeSH
- Reference Values MeSH
- Retrospective Studies MeSH
- Rheumatic Fever immunology physiopathology MeSH
- Sensitivity and Specificity MeSH
- Sjogren's Syndrome immunology physiopathology MeSH
- Case-Control Studies MeSH
- Severity of Illness Index MeSH
- Lupus Erythematosus, Systemic immunology physiopathology MeSH
- Blotting, Western methods MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Autoantigens MeSH
- Autoantibodies MeSH
- Biomarkers MeSH
- Eukaryotic Initiation Factor-3 MeSH
- Immunosuppressive Agents MeSH
OBJECTIVES: To describe the prevalence and clinical associations of autoantibodies to a novel autoantigen, eukaryotic initiation factor 3 (eIF3), detected in idiopathic inflammatory myositis. METHODS: Sera or plasma from 678 PM patients were analysed for autoantigen specificity by radio-labelled protein immunoprecipitation (IPP). Samples immunoprecipitating the same novel autoantigens were further analysed by indirect immunofluorescence and IPP using pre-depleted cell extracts. The autoantigen was identified through a combination of IPP and MALDI-TOF mass spectrometry, and confirmed using commercial antibodies and IPP-western blots. Additional samples from patients with DM (668), DM-overlap (80), PM-overlap (191), systemic sclerosis (150), systemic lupus erythematosus (200), Sjogren's syndrome (40), rheumatoid arthritis (50) and healthy controls (150) were serotyped by IPP as disease or healthy controls. RESULTS: IPP revealed a novel pattern in three PM patients (0.44%) that was not found in disease-specific or healthy control sera. Indirect immunofluorescence demonstrated a fine cytoplasmic speckled pattern for all positive patients. Mass spectrometry analysis of the protein complex identified the target autoantigen as eIF3, a cytoplasmic complex with a role in the initiation of translation. Findings were confirmed by IPP-Western blotting. The three anti-eIF3-positive patients had no history of malignancy or interstitial lung disease, and had a favourable response to treatment. CONCLUSION: We report a novel autoantibody in 0.44% of PM patients directed against a cytoplasmic complex of proteins identified as eIF3. Although our findings need further confirmation, anti-eIF3 appears to correlate with a good prognosis and a favourable response to treatment.
Department of Musculoskeletal Biology 2 University of Liverpool Liverpool UK
Department of Rheumatology Leighton Hospital Crewe
Department of Rheumatology Manchester Royal Infirmary Manchester UK
Immunology Department of Internal Medicine University of Debrecen Debrecen Hungary
Pharmacy and Pharmacology University of Bath Bath
Rheumatology Charles University Prague Czech Republic
University Hospital Birmingham Queen Elizabeth Hospital Birmingham
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