THE ANTIPHOSPHOLIPID COFACTOR SYNDROMES - A PRIMARY VARIANT WITH ANTIBODIES TO BETA-2-GLYCOPROTEIN-I BUT NO ANTIBODIES DETECTABLE IN STANDARD ANTIPHOSPHOLIPID ASSAYS/

Citation
Ar. Cabral et al., THE ANTIPHOSPHOLIPID COFACTOR SYNDROMES - A PRIMARY VARIANT WITH ANTIBODIES TO BETA-2-GLYCOPROTEIN-I BUT NO ANTIBODIES DETECTABLE IN STANDARD ANTIPHOSPHOLIPID ASSAYS/, The American journal of medicine, 101(5), 1996, pp. 472-481
Citations number
60
Categorie Soggetti
Medicine, General & Internal
ISSN journal
00029343
Volume
101
Issue
5
Year of publication
1996
Pages
472 - 481
Database
ISI
SICI code
0002-9343(1996)101:5<472:TACS-A>2.0.ZU;2-U
Abstract
BACKGROUND: Most systemic lupus erythematosus (SLE) patients with two or more clinical manifestations of the antiphospholipid syndrome (APS) and negative antiphospholipid antibodies (aPL) have antibodies to bet a(2)-glycoprotein-I (a beta(2)GP-I). Herein we describe a similar set of circumstances, but in patients without evidence of SLE. PATIENTS AN D METHODS: We studied 6 patients with recurrent venous and/or arterial thromboses without aPL as detected by routine assays nor clinical or serological evidence of other autoimmune disease. Immunogloublin (Ig) G and IgM antibodies to bovine and human phospholipid-free beta(2)GP-I were studied by Western blot test and by enzyme-linked immunosorbent assay (ELISA) utilizing radiated and nonirradiated plates. We also tes ted antibodies to cardiolipin, phosphatidylserine, and phosphatidyleth anolamine by ELISA. As controls, 54 normal sera were studied. RESULTS: All 6 patients had recurrent arterial and/or venous thromboses. Three also had thrombocytopenia, 1 had livedo reticularis, and 2 had valvul ar heart disease. None of the patients had aPL, but all had serum IgG reactivity against human and bovine beta(2)GP-I (P <0.001 versus contr ols for both). Titers of antibovine beta(2)GP-I were higher when studi ed in irradiated plates but were also higher than normal in nonirradia ted plates (P <0.001). These antibodies did not recognize human or bov ine beta(2)GP-I bound to cardiolipin in solid phase. We confirmed by W estern blot that these autoantibodies recognize human beta(2)GP-I. We found no IgM a beta(2)GP-I. CONCLUSIONS: We describe a primary conditi on akin to the antiphospholipid syndrome with negative aPL, but with s erum IgG antibodies to human and bovine beta(2)GP-I. These antibodies recognize beta(2)GP-I epitopes that are not accessible when beta(2)GP- I is bound to cardiolipin. (C) 1996 by Excerpta Medica, Inc.