Source:http://linkedlifedata.com/resource/pubmed/id/21447407
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2011-6-6
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pubmed:abstractText |
Ro52 antigen has recently been identified as TRIM21 protein, but the clinical significance of anti-Ro52/TRIM21 antibodies remains controversial. The aim of this multicentric study was to investigate the significance of anti-Ro52 antibodies without anti-SSA/Ro60 antibodies in various connective diseases. Sera were selected by each laboratory using its own method (ELISA, immunodot or Luminex technology), and then performed with ANA Screen BioPlex™ reagent (BIO-RAD). Among the 247 screened sera, 155/247 (63%) were confirmed as anti-Ro52 positive and anti-SSA/Ro60 negative. These sera were analyzed for the detection of other antibodies in relation with clinical settings. Isolated anti-Ro52 antibodies were detected in 89/155 (57%) sera. For the remaining sera (66/155), the main antibodies associations were Sm/SmRNP or Chromatin (n=38; 57%), Jo1 (n=17; 26%) and CenpB (n=9; 14%). Clinical data from the 155 patients showed high prevalence in autoimmune diseases (73%) including myositis or dermatomyositis (n=30), lupus (n=23); Sjögren and/or sicca syndrome (n=27); CREST or Systemic sclerosis (n=11) and autoimmune hepatitis (n=11). We found that pulmonary manifestations were often associated with the presence of anti-Ro52 antibodies (n=34, 22%), in addition with anti-tRNA synthetases, anti-SRP or anti-Ku antibodies (18/34) or isolated in half of cases (16/34). Separate detection of anti-Ro52 antibodies might be useful in related antisynthetase syndrome diagnosis. The presence of anti-Ro52 antibodies should probably precede development of autoimmune disease and must induce sequential follow-up of positive patients, particularly in interstitial lung disease progression.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1873-0183
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pubmed:author |
pubmed-author:AlyanakianM AMA,
pubmed-author:AndréCC,
pubmed-author:BengoufaDD,
pubmed-author:Chollet-MartinSS,
pubmed-author:ChretienPP,
pubmed-author:Dragon-DureyM AMA,
pubmed-author:GhillaniPP,
pubmed-author:GleizesAA,
pubmed-author:GoulvestreCC,
pubmed-author:JohanetCC,
pubmed-author:MussetLL,
pubmed-author:NicaisePP,
pubmed-author:ReamJ RJRJr,
pubmed-author:RouquetteA MAM,
pubmed-author:WeillBB
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pubmed:copyrightInfo |
Copyright © 2011 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
509-13
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pubmed:meshHeading |
pubmed-meshheading:21447407-Adolescent,
pubmed-meshheading:21447407-Adult,
pubmed-meshheading:21447407-Aged,
pubmed-meshheading:21447407-Aged, 80 and over,
pubmed-meshheading:21447407-Antibodies,
pubmed-meshheading:21447407-Autoantibodies,
pubmed-meshheading:21447407-Autoimmune Diseases,
pubmed-meshheading:21447407-Female,
pubmed-meshheading:21447407-Humans,
pubmed-meshheading:21447407-Lung Diseases,
pubmed-meshheading:21447407-Male,
pubmed-meshheading:21447407-Middle Aged,
pubmed-meshheading:21447407-Ribonucleoproteins,
pubmed-meshheading:21447407-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Clinical significance of anti-Ro52 (TRIM21) antibodies non-associated with anti-SSA 60kDa antibodies: results of a multicentric study.
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pubmed:affiliation |
Laboratoire d'Immunochimie, Groupe Hospitalier Pitié-Salpêtrière, Paris, France. pascale.ghillani-dalbin@psl.aphp.fr
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pubmed:publicationType |
Journal Article,
Multicenter Study
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