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抗磷脂综合征患者中β2-糖蛋白I抗体的酶联免疫吸附测定(ELISA)特异性

Specificity of ELISA for antibody to beta 2-glycoprotein I in patients with antiphospholipid syndrome.

作者信息

Amengual O, Atsumi T, Khamashta M A, Koike T, Hughes G R

机构信息

Lupus/Arthritis Research Unit, Rayne Institute, St Thomas' Hospital, London.

出版信息

Br J Rheumatol. 1996 Dec;35(12):1239-43. doi: 10.1093/rheumatology/35.12.1239.

Abstract

The clinical significance of anti-beta 2 glycoprotein I (beta 2-GPI) antibodies was evaluated in patients with antiphospholipid syndrome (APS), primary and secondary to systemic lupus erythematosus (SLE). Anti-beta 2-GPI were tested in 120 patients (39 primary APS, 32 APS with SLE and 49 SLE without APS) by ELISA utilizing irradiated plates in the absence of cardiolipin. Anticardiolipin antibodies (aCL) and antiphosphatidylserine antibodies were also measured in the same patients using standardized assays. Anti-beta 2-GPI titres correlated strongly to those of aCL (r = 0.816, P = 0.0001), and to those of antiphosphatidylserine antibodies (r = 0.841, P = 0.0001). Anti-beta 2-GPI were detected in 53.5% of APS patients (38/71), but only in 4.1% of SLE patients without APS (2/49). In the latter group, 24.5% (12/49) of patients had a positive titre of aCL. The anti-beta 2-GPI assay showed higher specificity for APS than the aCL in APS (96 vs 75%, respectively, chi 2 = 6.75, P = 0.00094). Our findings suggest that the assay of anti-beta 2-GPI may improve the specificity for APS.

摘要

在抗磷脂综合征(APS)患者中评估了抗β2糖蛋白I(β2-GPI)抗体的临床意义,这些患者包括原发性抗磷脂综合征以及继发于系统性红斑狼疮(SLE)的继发性抗磷脂综合征。通过在无心磷脂的情况下使用辐照板的酶联免疫吸附测定(ELISA)法,对120例患者(39例原发性抗磷脂综合征、32例合并系统性红斑狼疮的抗磷脂综合征和49例无抗磷脂综合征的系统性红斑狼疮患者)检测了抗β2-GPI。还使用标准化检测方法对这些患者检测了抗心磷脂抗体(aCL)和抗磷脂酰丝氨酸抗体。抗β2-GPI滴度与抗心磷脂抗体滴度密切相关(r = 0.816,P = 0.0001),也与抗磷脂酰丝氨酸抗体滴度密切相关(r = 0.841,P = 0.0001)。53.5%的抗磷脂综合征患者(38/71)检测到抗β2-GPI,但无抗磷脂综合征的系统性红斑狼疮患者中仅4.1%(2/49)检测到。在后一组中,24.5%(12/49)的患者抗心磷脂抗体滴度呈阳性。在抗磷脂综合征中,抗β2-GPI检测比抗心磷脂抗体检测显示出更高的特异性(分别为96%和75%,χ2 = 6.75,P = 0.00094)。我们的研究结果表明,抗β2-GPI检测可能会提高抗磷脂综合征的特异性。

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