HETEROGENEITY OF THE ANTI-RO(SSA) RESPONSE IN RHEUMATIC DISEASES

Citation
Fj. Lopezlongo et al., HETEROGENEITY OF THE ANTI-RO(SSA) RESPONSE IN RHEUMATIC DISEASES, Journal of rheumatology, 21(8), 1994, pp. 1450-1456
Citations number
57
Categorie Soggetti
Rheumatology
Journal title
ISSN journal
0315162X
Volume
21
Issue
8
Year of publication
1994
Pages
1450 - 1456
Database
ISI
SICI code
0315-162X(1994)21:8<1450:HOTARI>2.0.ZU;2-G
Abstract
Objective. The immune response to the Ro(SSA) antigen is heterogeneous . Anti-Ro(SSA) postie e sera may contain antibodies recognizing either a 60 or a 52 kDa polypeptide component of the Ro(SSA) particle. Thus we sought to determine the profile of anti-Ro(SSA) antibodies defined by immunoblotting in patients with rheumatic diseases. Methods. Immuno blotting against human placenta extract and ELISA against recombinant Ro(SSA) antigen as confirmatory tests were done to detect anti-Ro(SSA) antibodies in 563 sera from patients with systemic lupus erythematosu s (SLE), Sjogren's syndrome (SS), rheumatoid arthritis (RA) and other connective tissue diseases. Results. Anti-52 kDa antibodies were more common in primary patients with SS (9/22; 40.9 %) than in patients wit h SLE (29/135; 21.4 %) or patients with RA (7/315; 2.2 %). Anti-60 kDs antibodies were more frequent in patients with SLE (26/135; 19.2 %) t han in patients with primary SS (2/22; 9 %) or RA (17/315; 5.3 %). Non e of the 22 patients with primary SS had only antibodies to the 60 kDa polypeptide. Among the 153 patients whose sera were positive by ELISA , 73 (47.7 %) were negative by immunoblotting. The most frequent diagn oses in these sera were RA and SLE. The anti-52 kDa sera had higher op tical density values compared to anti-60 kDa sera. Conclusions. Our ob servations indicate the existence of qualitatively and quantitatively different anti-Ro(SSA) responses in the rheumatic diseases. The major responses are anti-52 kDa antibodies in primary SS, both anti-52 and a nti-60 kDa antibodies in SLE, and anti-60 kDa antibodies in RA and oth er connective tissue diseases.