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在先前确定为抗核抗体阴性的样本中检测和鉴定显著的抗核抗体。

Detection and identification of significant ANAs in previously determined ANA negative samples.

作者信息

Kidd Kara, Cusi Karen, Mueller Ruth, Goodner Megan, Boyes Bob, Hoy Eric

机构信息

Immuno Concepts, NA Ltd, Sacramento, CA, USA.

出版信息

Clin Lab. 2005;51(9-10):517-21.

Abstract

BACKGROUND

An antinuclear antibody (ANA) substrate transfected with the cDNA to hyperexpress the 60 kD SS-A/Ro antigen (HEp-2000) has been shown to detect anti-SS-A/Ro antibodies missed by standard HEp-2 and other immunoassays. Despite this evidence, many laboratories remain convinced that with experienced technicians, standard HEp-2 is acceptable for ANA detection.

AIM

To challenge the ability of HEp-2000 to detect anti-SS-A/Ro antibodies in samples previously determined to be ANA negative using standard HEp-2.

METHODS

Three hundred and seventy-one pre-screened "negative" ANA samples were provided by a university hospital laboratory in Germany. These samples were tested on the HEp-2000 substrate at a dilution of 1:40 by indirect immunofluorescence (IIF). Samples that screened positive for a nuclear pattern were titered (range of 1:40-1:640) and all ANA-positive patterns were identified. Samples containing at least one positive ANA pattern at a dilution greater than or equal to 1:160 were further tested. Samples that produced a speckled pattern were tested for antibodies to the extractable nuclear antigens (ENA) and samples that showed homogeneous staining were tested for antibodies to dsDNA, and if negative, were then tested for anti-histone antibodies.

RESULTS

Ninety-one patient samples were positive with titers > or =1:160. Speckled patterns were the most common finding (30 samples) followed by speckled/homogeneous mixed patterns (19 samples) and samples demonstrating the SS-A/Ro pattern (16 samples) either alone or in combination with other ANA patterns. The remaining 26 positive samples consisted of various other ANA patterns. The most commonly identified ENAs were SS-A/Ro (14 samples), Scl-70 (11 samples) and SSB (6 samples). No antibodies to dsDNA were identified in 23 positive samples with homogeneous staining patterns, though 17 of these samples tested positive for antibodies to histone.

CONCLUSIONS

HEp-2000 detected anti-SS-A/Ro antibodies in 16 (4%) of the "ANA negative" samples. In addition to improved sensitivity for anti-SS-A antibodies, HEp-2000 demonstrated improved sensitivity over standard HEp-2 substrate for other significant ANAs including anti-Scl-70, anti-histone, and anti-SS-B antibodies.

摘要

背景

转染了编码60kD SS-A/Ro抗原的cDNA以实现该抗原高表达的抗核抗体(ANA)底物(HEp-2000)已被证明能够检测出标准HEp-2及其他免疫检测方法遗漏的抗SS-A/Ro抗体。尽管有此证据,但许多实验室仍坚信,对于经验丰富的技术人员而言,标准HEp-2用于ANA检测是可以接受的。

目的

挑战HEp-2000检测先前使用标准HEp-2判定为ANA阴性的样本中抗SS-A/Ro抗体的能力。

方法

德国一家大学医院实验室提供了371份预先筛选的“阴性”ANA样本。这些样本以1:40的稀释度在HEp-2000底物上通过间接免疫荧光法(IIF)进行检测。筛选出核型阳性的样本进行滴度测定(范围为1:40 - 1:640),并识别所有ANA阳性模式。对稀释度大于或等于1:160时至少呈现一种阳性ANA模式的样本进行进一步检测。出现斑点状模式的样本检测可提取核抗原(ENA)抗体,呈现均匀染色的样本检测双链DNA(dsDNA)抗体,若为阴性,则检测抗组蛋白抗体。

结果

91份患者样本滴度≥1:160呈阳性。斑点状模式是最常见的结果(30份样本),其次是斑点状/均匀混合模式(19份样本)以及单独或与其他ANA模式组合出现SS-A/Ro模式的样本(16份样本)。其余26份阳性样本由各种其他ANA模式组成。最常识别出的ENA是SS-A/Ro(14份样本)、Scl-70(11份样本)和SSB(6份样本)。在23份呈现均匀染色模式的阳性样本中未检测到dsDNA抗体,不过其中17份样本组蛋白抗体检测呈阳性。

结论

HEp-2000在16份(4%)“ANA阴性”样本中检测到了抗SS-A/Ro抗体。除了提高抗SS-A抗体的敏感性外,HEp-2000在检测包括抗Scl-70、抗组蛋白和抗SS-B抗体在内的其他重要ANA时,相较于标准HEp-2底物也表现出更高的敏感性。

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