Identification of a novel autoantigen eukaryotic initiation factor 3 associated with polymyositis
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
Grantová podpora
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-zdroje
- Klíčová slova
- autoantibodies, autoantigens, myositis,
- MeSH
- autoantigeny imunologie MeSH
- autoprotilátky krev MeSH
- biologické markery krev MeSH
- dospělí MeSH
- eukaryotický iniciační faktor 3 krev imunologie MeSH
- hmotnostní spektrometrie metody MeSH
- imunoprecipitace metody MeSH
- imunosupresiva aplikace a dávkování MeSH
- lidé středního věku MeSH
- lidé MeSH
- polymyozitida farmakoterapie imunologie patofyziologie MeSH
- progrese nemoci * MeSH
- referenční hodnoty MeSH
- retrospektivní studie MeSH
- revmatická horečka imunologie patofyziologie MeSH
- senzitivita a specificita MeSH
- Sjögrenův syndrom imunologie patofyziologie MeSH
- studie případů a kontrol MeSH
- stupeň závažnosti nemoci MeSH
- systémový lupus erythematodes imunologie patofyziologie MeSH
- western blotting metody MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- autoantigeny MeSH
- autoprotilátky MeSH
- biologické markery MeSH
- eukaryotický iniciační faktor 3 MeSH
- imunosupresiva 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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