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风湿试纸抗核抗体谱检测评估:一种用于同时检测抗自身抗原U1-核糖核蛋白(U1-RNP)、Sm、SS-A/Ro、SS-B/La以及天然DNA抗体的快速试纸检测方法。

Evaluation of the RheumaStrip ANA profile test: a rapid test strip procedure for simultaneously determining antibodies to autoantigens U1-ribonucleoprotein (U1-RNP), Sm, SS-A/Ro, SS-B/La, and to native DNA.

作者信息

Paxton H, Bendele T, O'Connor L, Haynes D C

机构信息

Maryland Medical Laboratory, Inc., Baltimore 21227.

出版信息

Clin Chem. 1990 May;36(5):792-7.

PMID:2140076
Abstract

The "LipoGen RheumaStrip ANA Profile" test method (LipoGen, Inc.) is a new assay format for autoantibody detection in which recombinant autoantigens are used. This enzyme immunoassay, in test-strip format, detects antibodies to autoantigens U1-ribonucleoprotein (U1-RNP), Sm, SS-A/Ro, SS-B/La, and to native DNA (nDNA). We evaluated 200 antinuclear antibody (ANA)-positive and 100 ANA-negative sera for the presence of antibodies to U1-RNP, Sm, SS-A/Ro, SS-B/La, and nDNA by the new test-strip procedure. These data correlated well with those obtained with either Ouchterlony double immunodiffusion for U1-RNP, Sm, SS-A/Ro, and SS-B/La or with Crithidia luciliae indirect immunofluorescence for anti-nDNA. Assay sensitivity and assay specificity of the ANA Profile method as compared with those of established procedures were respectively as follows: 89.8% and 98.8% for U1-RNP, 86.4% and 95.3% for Sm, 97.9% and 89.3% for SS-A/Ro, 98.3% and 86.3% for SS-B/La, and 97.5% and 93.1% for nDNA. Agreement between the ANA Profile test and these other test methodologies ranged from 88.7% for the SS-B/La test to 97.3% for the U1-RNP test. This new test procedure substantially decreases the time and effort required to perform these assays. Total hands-on time and overall assay time were decreased by 72% and 97%, respectively.

摘要

“LipoGen RheumaStrip ANA Profile”检测方法(LipoGen公司)是一种用于自身抗体检测的新检测形式,其中使用了重组自身抗原。这种试纸条形式的酶免疫测定法可检测针对自身抗原U1 - 核糖核蛋白(U1 - RNP)、Sm、SS - A/Ro、SS - B/La以及天然DNA(nDNA)的抗体。我们采用这种新的试纸条检测程序,对200份抗核抗体(ANA)阳性血清和100份ANA阴性血清进行检测,以确定其中是否存在针对U1 - RNP、Sm、SS - A/Ro、SS - B/La和nDNA的抗体。这些数据与通过欧氏双免疫扩散法检测U1 - RNP、Sm、SS - A/Ro和SS - B/La,以及通过利什曼原虫间接免疫荧光法检测抗nDNA所获得的数据高度相关。与既定检测方法相比,ANA Profile方法的检测灵敏度和检测特异性分别如下:U1 - RNP为89.8%和98.8%,Sm为86.4%和95.3%,SS - A/Ro为97.9%和89.3%,SS - B/La为98.3%和86.3%,nDNA为97.5%和93.1%。ANA Profile检测与其他检测方法之间的一致性范围从SS - B/La检测的88.7%到U1 - RNP检测的97.3%。这种新的检测程序大幅减少了进行这些检测所需的时间和精力。实际操作总时间和总体检测时间分别减少了72%和97%。

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