Antibodies to beta(2)-glycoprotein I - A specific marker for the antiphospholipid syndrome

被引:84
作者
Guerin, J
Feighery, C
Sim, RB
Jackson, J
机构
[1] ST JAMES HOSP, DEPT IMMUNOL, DUBLIN 8, IRELAND
[2] UNIV OXFORD, DEPT BIOCHEM, MRC, IMMUNOCHEM UNIT, OXFORD OX1 3QU, ENGLAND
[3] DUBLIN INST TECHNOL, DUBLIN, IRELAND
[4] ST JAMES HOSP, DEPT IMMUNOL, DUBLIN 8, IRELAND
关键词
beta(2)-glycoprotein I; antiphospholipid syndrome; ELISA; cardiolipin; thrombosis;
D O I
10.1046/j.1365-2249.1997.4601357.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The antiphospholipid syndrome is a disorder characterized by recurrent thrombosis and the presence of antibodies specific to phospholipids. However, the diagnosis of this syndrome is hampered by the lack of a specific laboratory test. In this study an ELISA for the measurement of antibodies to solid-phase beta(2)-glycoprotein I (beta(2)-GPI) was established and compared with anticardiolipin antibodies for diagnosis of antiphospholipid syndrome. Significantly elevated levels of antibodies to beta(2)-GPI were found in all patients with definite antiphospholipid syndrome (median = 91 AU). Marginally elevated levels of antibodies to beta(2)-GPI were observed in 5% of patients with systemic lupus erythematosus (SLE; median = 4 AU), 1% with stroke (median = 3 AU), 13% with infectious mononucleosis (median = 3 AU), 10% with HIV infection (median = 3 AU) and 8% with VDRL false-positive serology for syphilis (median = 4 AU), but not in patients with rheumatoid factor, syphilis or carotid artery stenosis. In contrast, significantly raised levels of anticardiolipin antibodies were observed in 100% of patients with definite antiphospholipid syndrome, 30% with SLE, 88% with HIV infection, 94% with syphilis, 62% with infectious mononucleosis, 9% with rheumatoid factor-positive sera, 74% VDRL false-positive serology for syphilis, 47% with stroke and 0% with carotid artery stenosis. This solid-phase assay for antibodies to beta(2)-GPI is highly specific for the antiphospholipid syndrome and represents an advance in the laboratory diagnosis of this disorder.
引用
收藏
页码:304 / 309
页数:6
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