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