Disease specificity of autoantibodies to cytosolic 5'-nucleotidase 1A in sporadic inclusion body myositis versus known autoimmune diseases
Language English Country United States Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
Grant support
18474
Arthritis Research UK - United Kingdom
MR/K000608/1
Medical Research Council - United Kingdom
MR/K006312/1
Medical Research Council - United Kingdom
MR/N003322/1
Medical Research Council - United Kingdom
PubMed
25714931
PubMed Central
PMC4699257
DOI
10.1136/annrheumdis-2014-206691
PII: S0003-4967(24)01913-7
Knihovny.cz E-resources
- Keywords
- Autoantibodies, Autoimmune Diseases, Dermatomyositis, Polymyositis,
- MeSH
- 5'-Nucleotidase immunology MeSH
- Autoimmune Diseases immunology MeSH
- Autoantibodies immunology MeSH
- Dermatomyositis diagnosis immunology MeSH
- Diabetes Mellitus, Type 1 immunology MeSH
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Myositis, Inclusion Body diagnosis immunology MeSH
- Neuromuscular Diseases immunology MeSH
- Polymyositis diagnosis immunology MeSH
- Arthritis, Rheumatoid immunology MeSH
- ROC Curve MeSH
- Multiple Sclerosis immunology MeSH
- Aged MeSH
- Sensitivity and Specificity MeSH
- Sjogren's Syndrome immunology MeSH
- Case-Control Studies MeSH
- Scleroderma, Systemic immunology MeSH
- Lupus Erythematosus, Systemic immunology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- 5'-Nucleotidase MeSH
- Autoantibodies MeSH
- NT5C1A protein, human MeSH Browser
OBJECTIVES: The diagnosis of inclusion body myositis (IBM) can be challenging as it can be difficult to clinically distinguish from other forms of myositis, particularly polymyositis (PM). Recent studies have shown frequent presence of autoantibodies directed against cytosolic 5'-nucleotidase 1A (cN-1A) in patients with IBM. We therefore, examined the autoantigenicity and disease specificity of major epitopes of cN-1A in patients with sporadic IBM compared with healthy and disease controls. METHODS: Serum samples obtained from patients with IBM (n=238), PM and dermatomyositis (DM) (n=185), other autoimmune diseases (n=246), other neuromuscular diseases (n=93) and healthy controls (n=35) were analysed for the presence of autoantibodies using immunodominant cN-1A peptide ELISAs. RESULTS: Autoantibodies directed against major epitopes of cN-1A were frequent in patients with IBM (37%) but not in PM, DM or non-autoimmune neuromuscular diseases (<5%). Anti-cN-1A reactivity was also observed in some other autoimmune diseases, particularly Sjögren's syndrome (SjS; 36%) and systemic lupus erythematosus (SLE; 20%). CONCLUSIONS: In summary, we found frequent anti-cN-1A autoantibodies in sera from patients with IBM. Heterogeneity in reactivity with the three immunodominant epitopes indicates that serological assays should not be limited to a distinct epitope region. The similar reactivities observed for SjS and SLE demonstrate the need to further investigate whether distinct IBM-specific epitopes exist.
Centre for Integrated Genomic Medical Research The University of Manchester Manchester UK
Department of Neurology Leiden University Medical Centre Leiden The Netherlands
Department of Neurology Neuromuscular Reference Centre Ghent University Hospital Ghent Belgium
MRC Centre for Neuromuscular Diseases University College London London UK
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