Disease specificity of autoantibodies to cytosolic 5 '-nucleotidase 1A in sporadic inclusion body myositis versus known autoimmune diseases
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F16%3A10333045" target="_blank" >RIV/00216208:11110/16:10333045 - isvavai.cz</a>
Alternative codes found
RIV/00023728:_____/16:N0000023
Result on the web
<a href="http://dx.doi.org/10.1136/annrheumdis-2014-206691" target="_blank" >http://dx.doi.org/10.1136/annrheumdis-2014-206691</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1136/annrheumdis-2014-206691" target="_blank" >10.1136/annrheumdis-2014-206691</a>
Alternative languages
Result language
angličtina
Original language name
Disease specificity of autoantibodies to cytosolic 5 '-nucleotidase 1A in sporadic inclusion body myositis versus known autoimmune diseases
Original language description
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 Sjgren's syndrome (SjS; 36%) and systemic lupus erythematosus (SLE; 20%). Conclusions In summary, we found frequent anti-cN1A 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.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FE - Other fields of internal medicine
OECD FORD branch
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Result continuities
Project
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Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Annals of the Rheumatic Diseases
ISSN
0003-4967
e-ISSN
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Volume of the periodical
75
Issue of the periodical within the volume
4
Country of publishing house
GB - UNITED KINGDOM
Number of pages
6
Pages from-to
696-701
UT code for WoS article
000373403800021
EID of the result in the Scopus database
2-s2.0-84930014705