Abstract |
The presence of autoantibodies to the Ro52 protein in sera from patients with idiopathic inflammatory myopathies has recently been reported. These antibodies were found predominately in sera with the myositis-specific autoantibody anti- histidyl-tRNA synthetase (anti-Jo-1). In this report, we analysed sera from 216 patients to determine whether anti-Ro52 antibodies are associated with myositis autoantibodies other than anti-Jo-1. These included sera containing antibodies that recognize threonyl- or alanyl- tRNA synthetases, Mi-2, PM-Scl, signal recognition particle (SRP), as well as the systemic sclerosis-related antibodies anti- topoisomerase I (Scl-70) and anti-centromere. A high proportion of sera that contain anti- aminoacyl-tRNA synthetase antibodies, anti-SRP, or anti-PM-Scl antibodies were found to contain antibodies to the Ro52 protein. In contrast, in sera containing anti-Mi-2, anti-Scl-70 or anti-centromere antibodies, anti-Ro52 antibodies were absent or occurred infrequently. In addition, only one serum from 41 rheumatoid arthritis patients was positive for anti-Ro52 autoantibodies. These data indicate that anti-Ro52 antibodies are produced in particular subsets of myositis patients, and are not limited to sera with anti-Jo-1 antibodies.
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Authors | M B Frank, V McCubbin, E Trieu, Y Wu, D A Isenberg, I N Targoff |
Journal | Journal of autoimmunity
(J Autoimmun)
Vol. 12
Issue 2
Pg. 137-42
(Mar 1999)
ISSN: 0896-8411 [Print] England |
PMID | 10047434
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Copyright | Copyright 1999 Academic Press. |
Chemical References |
- Antibodies, Antinuclear
- Autoantibodies
- Autoantigens
- Jo-1 antibody
- RNA, Small Cytoplasmic
- RO60 protein, human
- Ribonucleoproteins
- SS-A antigen
- Amino Acyl-tRNA Synthetases
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Topics |
- Amino Acyl-tRNA Synthetases
(immunology)
- Antibodies, Antinuclear
(blood)
- Autoantibodies
(blood)
- Autoantigens
(chemistry, immunology)
- Humans
- Myositis
(immunology)
- RNA, Small Cytoplasmic
- Ribonucleoproteins
(chemistry, immunology)
- Scleroderma, Systemic
(immunology)
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