THE CENTROMERE KINESIN-LIKE PROTEIN, CENP-E - AN AUTOANTIGEN IN SYSTEMIC-SCLEROSIS

Citation
Jb. Rattner et al., THE CENTROMERE KINESIN-LIKE PROTEIN, CENP-E - AN AUTOANTIGEN IN SYSTEMIC-SCLEROSIS, Arthritis and rheumatism, 39(8), 1996, pp. 1355-1361
Citations number
39
Categorie Soggetti
Rheumatology
Journal title
ISSN journal
00043591
Volume
39
Issue
8
Year of publication
1996
Pages
1355 - 1361
Database
ISI
SICI code
0004-3591(1996)39:8<1355:TCKPC->2.0.ZU;2-V
Abstract
Objective, Autoantibodies directed against centromere proteins (CENPs) are a serologic feature in some patients with systemic sclerosis (SSc ), Previous studies have focused on autoantibodies to CENPs A, B, and C, CENP-E is a recently described 312-kd protein that also localizes t o the centromere, Therefore, we studied the presence of autoantibodies to recombinant CENP-E in patients with SSc, Methods, Sixty sera from patients with the SSc spectrum of diseases were screened for the prese nce of autoantibodies against CENP-E, by indirect immunofluorescence a nd immunoblotting using recombinant CENP-E protein, HLA class II allel es were determined by DNA oligotyping, Results, Among the SSc sera, 15 of 60 (25%) demonstrated antibody reactivity with recombinant CENP-E, and 14 of these 15 sera (93%) had antibodies directed against another CENP, Anti-CENP-E was seen in 13 of 30 sera,vith anti-CENP (43%), All patients with anti-CENP-E had a limited form of SSc, known as the CRE ST variant (calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, telangiectasias), When patients with anti-CENPs A, B, o r C were compared with patients with anti-CENP-E, no unique clinical f eatures in the anti-CENP-E positive group were identified, Ninety-thre e percent of the patients with anti-CENP-E had HLA-DQB1 alleles that h ad polar amino acids at position 26 (primarily DQB105), similar to pa tients with other CENP autoantibodies. Conclusion. Antibodies to CENP- E are common in patients with SSc, and are seen in higher frequency in sera from patients with a limited form, or CREST variant, of the dise ase.