抗β -糖蛋白I,抗凝血酶原和抗心磷脂抗体在系统性红斑狼疮和抗磷脂综合征患者的纵向研究。

British journal of rheumatology Pub Date : 1998-10-01
M Inanç, S Donohoe, C T Ravirajan, E L Radway-Bright, I Mackie, S Machin, D A Isenberg
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引用次数: 0

摘要

目的:测定研究期间有初始或复发性血栓/神经系统(T/N)事件的系统性红斑狼疮(SLE)和抗磷脂综合征(APS)患者的系列样本中抗β 2糖蛋白- 1(抗β 2 gpi)和抗凝血酶原(抗prot)抗体水平,以及抗β 2 gpi抗体的IgG亚类分布。探讨这些抗体与β 2gpi抗原、抗心磷脂抗体(aCL)、抗双链DNA (ds)、C3水平及疾病活动性的相关性。方法:在长期随访的队列中,从7例SLE患者中鉴定出50份血清样本,这些患者在随访期间发生了T/N事件。ELISA法检测抗beta2GPI IgG、抗prot、aCL、抗beta2GPI IgG亚类及beta2GPI抗原水平。比较相应疾病活动性[不列颠群岛狼疮评估组(British islands Lupus Assessment Group, BILAG)]、抗dsdna和C3水平。结果:6例患者T/N事件前后IgG抗β 2gpi抗体水平升高,但波动幅度小于aCL抗体水平。T/N事件前后抗β 2gpi抗体的主要亚类是IgG2。所有病例IgG抗prot抗体均为阴性。抗β 2gpi与aCL抗体之间存在显著但较弱的相关性。疾病活动性与抗beta2GPI抗体IgG和beta2GPI抗原水平无相关性。β 2gpi抗原水平有波动,部分患者出现T/N事件后有升高趋势。结论:研究期间发生T/N事件的患者大部分存在抗β 2gpi IgG抗体,而不存在抗prot IgG抗体。在随访期间,发现许多IgG acl阴性样本具有IgG抗β 2gpi活性。抗β 2gpi IgG的主要亚类是IgG2,这可能在APS的发病机制中起重要作用。一些SLE患者在T/N事件后发现β 2gpi抗原水平升高。IgG抗β 2gpi抗体可作为具有aCL抗体和狼疮抗凝剂的SLE和APS患者未来T/N事件的辅助标记物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-beta2-glycoprotein I, anti-prothrombin and anticardiolipin antibodies in a longitudinal study of patients with systemic lupus erythematosus and the antiphospholipid syndrome.

Objective: To determine anti-beta2 glycoprotein-I (anti-beta2GPI) and anti-prothrombin (anti-ProT) antibody levels, and the IgG subclass distribution of anti-beta2GPI antibodies, in serial samples from patients with systemic lupus erythematosus (SLE) and antiphospholipid syndrome (APS) having initial or recurrent thrombotic/neurological (T/N) events during the study period. To investigate the correlations between these antibodies and beta2GPI antigen, anticardiolipin antibody (aCL), anti-double-stranded (ds) DNA, C3 levels and disease activity.

Methods: Fifty serum samples were identified from seven patients with SLE who had had T/N events during the follow-up from a cohort under long-term follow-up. IgG anti-beta2GPI, anti-ProT, aCL, IgG subclasses of anti-beta2GPI and beta2GPI antigen levels were determined by ELISA. Corresponding disease activity [British Isles Lupus Assessment Group (BILAG)], anti-dsDNA and C3 levels were compared.

Results: IgG anti-beta2GPI antibody levels were elevated in six of the patients before and after the T/N events with less marked fluctuations than aCL antibody levels. The predominant subclass of anti-beta2GPI antibodies was IgG2 before and after the T/N events. IgG anti-ProT antibodies were negative in all cases. There was a significant but weak correlation between anti-beta2GPI and aCL antibodies. No correlation was found between disease activity and IgG anti-beta2GPI antibody and beta2GPI antigen levels. There were fluctuations in beta2GPI antigen levels and a trend to increase after T/N events was observed in some patients.

Conclusion: Most of the patients with a T/N event during the study period had IgG anti-beta2GPI, but not IgG anti-ProT antibodies. Many IgG aCL-negative samples were found to have IgG anti-beta2GPI activity during the follow-up period. The predominant subclass of IgG anti-beta2GPI was IgG2, which may have importance in the pathogenesis of APS. beta2GPI antigen levels were found to be increased in some patients with SLE after T/N events. IgG anti-beta2GPI antibodies may be used as an adjunctive marker of future T/N events in patients with SLE and APS with aCL antibodies and lupus anticoagulant.

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