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Detection of endothelial cell‐reactive immunoglobulin in patients with anti‐phospholipid antibodies
Author(s) -
McCrae Keith R.,
DeMichele Angela,
Samuels Philip,
Roth Denise,
Kuo Alice,
Meng Qianghua,
Rauch Joyce,
Cines Douglas B.
Publication year - 1991
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1991.tb08087.x
Subject(s) - antibody , immunology , endothelial stem cell , cardiolipin , von willebrand factor , autoantibody , medicine , immunoglobulin g , lupus anticoagulant , population , pathogenesis , chemistry , phospholipid , platelet , biochemistry , in vitro , environmental health , membrane
Individuals with anti‐phospholipid antibodies are at increased risk for the development of thrombosis and fetal loss. The pathogenesis of these syndromes is unknown, but may involve antibody‐mediated alterations in endothelial cell coagulant activity. To address this possibility, we determined the incidence of endothelial cell‐reactive antibodies in 76 patients whose plasma contained anti‐phospholipid antibodies, but who had no clinically‐evident immune disorder. Plasma from 47 patients deposited significantly more immunoglobulin on cultured endothelial cells than control plasma. Positive tests were more frequent in patients with a history of thrombosis than in those without (17/19 v 23/48; P =0.004). However, we observed no correlation between immunoglobulin deposition on cardiolipin and endothelial cells by individual plasmas. Furthermore, endothelial cell reactivity was not diminished by adsorption of anti‐cardiolipin antibodies from patient sera using liposomes. Immunoglobulin fractions prepared from 5/6 patient sera immuno‐precipitated a ≈ 70 kDa endothelial cell surface protein; 4/5 of these fractions also induced the release of von Willebrand factor from endothelial cells. These results demonstrate that plasma from many patients with anti‐phospholipid antibodies, but no clinically‐evident autoimmune disease, also contains endothelial cell‐reactive antibodies. Detection of such antibodies might help identify individuals in this patient population at greatest risk for thrombosis.