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对血凝抑制结果呈低阳性或阴性的样本进行14种风疹IgG免疫测定的性能。

Performance of 14 rubella IgG immunoassays on samples with low positive or negative haemagglutination inhibition results.

作者信息

Huzly Daniela, Hanselmann Ingeborg, Neumann-Haefelin Dieter, Panning Marcus

机构信息

Institute of Virology, University Medical Center Freiburg, Germany.

Institute of Virology, University Medical Center Freiburg, Germany.

出版信息

J Clin Virol. 2016 Jan;74:13-8. doi: 10.1016/j.jcv.2015.11.022. Epub 2015 Nov 19.

Abstract

BACKGROUND

Rubella IgG testing is routinely done in prenatal care and seroepidemiological studies. Recently concern was raised that seropositivity rates were decreasing questioning vaccination policies. Manufacturers of rubella IgG assays and authors of seroepidemiological studies use different cut-offs for the definition of seropositivity. As rubella virus circulation is reduced since many years, seronegativity rates might be overestimated using an inappropriate cut-off.

OBJECTIVES

Using different cut-off definitions we compared fourteen current rubella IgG immunoassays for sensitivity and qualitative result concordance in samples with low positive or negative haemagglutination inhibition (HI) titre.

STUDY DESIGN

150 clinical samples from patients and health care workers were included in the study. All samples were measured in 14 different rubella IgG immunoassays. Seropositivity was defined using recombinant rubella IgG immunoblot as reference standard.

RESULTS

The concordance of qualitative results using the manufacturers cut-off definitions was 56.4% if grey-zone results were analysed separately and 69.8% if grey-zone results were defined as positive. Using universal cut-offs of 10 IU/ml or 15 IU/ml the concordance was 70% and 61.4% respectively. Using the different cut-off definitions up to 71 out of the 124 immunoblot-positive samples tested negative in the immunoassays. The mean coefficient of variation (CV) of quantitative results in positive samples was 51% (range 19-113%).

CONCLUSIONS

Determination of rubella immunity by measurement of rubella-IgG in a population with high vaccination coverage with current assays leads to a high number of false negative results. The value of routine rubella antibody testing in countries with high vaccination coverage should be discussed.

摘要

背景

风疹IgG检测常用于产前检查和血清流行病学研究。最近有人担心血清阳性率下降,对疫苗接种政策提出质疑。风疹IgG检测试剂盒制造商和血清流行病学研究作者对血清阳性的定义使用不同的临界值。由于多年来风疹病毒传播减少,使用不合适的临界值可能会高估血清阴性率。

目的

使用不同的临界值定义,我们比较了14种现有的风疹IgG免疫检测方法在血凝抑制(HI)滴度低阳性或阴性样本中的敏感性和定性结果一致性。

研究设计

研究纳入了150份来自患者和医护人员的临床样本。所有样本均采用14种不同的风疹IgG免疫检测方法进行检测。以重组风疹IgG免疫印迹作为参考标准定义血清阳性。

结果

如果分别分析灰区结果,使用制造商的临界值定义时定性结果的一致性为56.4%;如果将灰区结果定义为阳性,则一致性为69.8%。使用10 IU/ml或15 IU/ml的通用临界值时,一致性分别为70%和61.4%。使用不同的临界值定义,在124份免疫印迹阳性样本中,多达71份在免疫检测中呈阴性。阳性样本中定量结果的平均变异系数(CV)为51%(范围19 - 113%)。

结论

在疫苗接种覆盖率高的人群中,用当前检测方法通过检测风疹IgG来确定风疹免疫力会导致大量假阴性结果。在疫苗接种覆盖率高的国家,应讨论常规风疹抗体检测的价值。

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