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采用时间分辨荧光免疫分析法检测抗心磷脂抗体 IgG。

Detection of anticardiolipin antibody IgG by time-resolved fluoroimmunoassay.

机构信息

Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi 214023, China.

出版信息

Clin Rheumatol. 2012 Sep;31(9):1339-45. doi: 10.1007/s10067-012-2020-6. Epub 2012 Jun 10.

DOI:10.1007/s10067-012-2020-6
PMID:22684164
Abstract

In an effort to improve the quantitative detection of anticardiolipin antibodies (aCL) IgG so as to classify patients correctly as antiphospholipid syndrome (APS) positive, we developed a new immunoassay based on a sandwich time-resolved fluoroimmunoassay (TRFIA) using the complex of cardiolipin plus bovine β(2)GPI as antigen and Eu(3+)-labeled rabbit antihuman IgG as conjugate. The precision, sensitivity, specificity, and stability of the assay were evaluated, and comparison with the classical ELISA was also made. The aCL IgG TRFIA kit we established had a wider detectable range than three commercial ELISA ones from different manufacturers when a specimen was diluted, with strong positive result from 1:12.5 to 1:204,800. The average intra-assay and inter-assay CVs detected by the aCL IgG TRFIA was 3.14 and 3.70 %, respectively. The sensitivity was 0.1 GPL U/ml, and the clinical diagnostic specificity was 98 %. The established assay kit also behaved better in stability than the commercial ELISA ones. Additionally, the immunoassay we established correlated well with the ELISA, and the correlation coefficient was 0.975. We thus conclude that the TRFIA we developed for aCL IgG detection gives promise to a more sensitive and reliable diagnosis of APS and has potential value for large-scale screening programs.

摘要

为了提高抗心磷脂抗体(aCL)IgG 的定量检测水平,以便正确地将患者分类为抗磷脂综合征(APS)阳性,我们开发了一种新的免疫分析方法,该方法基于夹心时间分辨荧光免疫分析(TRFIA),使用心磷脂加牛β(2)GPI 复合物作为抗原,Eu(3+)标记的兔抗人 IgG 作为结合物。评估了该测定的精密度、灵敏度、特异性和稳定性,并与经典 ELISA 进行了比较。与来自不同制造商的三种商业 ELISA 相比,当稀释标本时,我们建立的 aCL IgG TRFIA 试剂盒具有更宽的检测范围,阳性结果强,范围为 1:12.5 至 1:204,800。aCL IgG TRFIA 的平均批内和批间 CV 分别为 3.14%和 3.70%。灵敏度为 0.1 GPL U/ml,临床诊断特异性为 98%。与商业 ELISA 相比,该试剂盒在稳定性方面表现更好。此外,我们建立的免疫分析与 ELISA 相关性良好,相关系数为 0.975。因此,我们得出结论,我们开发的用于检测 aCL IgG 的 TRFIA 有望更敏感、更可靠地诊断 APS,并具有大规模筛查计划的潜在价值。

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