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结核感染T细胞检测(管内法)结果的临界范围。

A borderline range for Quantiferon Gold In-Tube results.

作者信息

Jonsson Jerker, Westman Anna, Bruchfeld Judith, Sturegård Erik, Gaines Hans, Schön Thomas

机构信息

The Public Health Agency of Sweden, Solna, Sweden.

Unit of Infectious Diseases, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

出版信息

PLoS One. 2017 Nov 2;12(11):e0187313. doi: 10.1371/journal.pone.0187313. eCollection 2017.

Abstract

OBJECTIVE

Interferon gamma release assays like Quantiferon Gold In-Tube (QFT) are used to identify individuals infected with Mycobacterium tuberculosis. A dichotomous cut-off (0.35 IU/ml) defines a positive QFT without considering test variability. Our objective was to evaluate the introduction of a borderline range under routine conditions.

METHODS

Results of routine QFT samples from Sweden (2009-2014) were collected. A borderline range (0.20-0.99 IU/ml) was introduced in 2010 recommending a follow-up sample. The association between borderline results and incident active TB within 3 to 24 months was investigated through linkage with the national TB-register.

RESULTS

Using the recommended QFT cut-off, 75.1% tests were negative, 21.4% positive and 3.5% indeterminate. In total, 9% (3656/40773) were within the borderline range. In follow-up samples, individuals with initial results between 0.20-0.34 IU/ml and 0.35-0.99 IU/ml displayed negative results below the borderline range (<0.20 IU/ml) in 66.1% (230/348) and 42.5% (285/671) respectively, and none developed incident TB. Among 6712 individuals with a positive initial test >0.99 IU/ml, 65 (0.97%) developed incident TB within 3-24 months.

CONCLUSIONS

We recommend retesting of subjects with QFT results in the range 0.20-0.99 IU/ml to enhance reliability and validity of the test. Half of the subjects in the borderline range will be negative at a level <0.20 IU/ml when retested and have a very low risk of developing incident active TB.

摘要

目的

像管内定量γ-干扰素释放试验(QFT)这样的检测方法被用于识别感染结核分枝杆菌的个体。一个二分法临界值(0.35国际单位/毫升)定义QFT阳性,而未考虑检测变异性。我们的目的是在常规条件下评估引入一个临界范围。

方法

收集了瑞典(2009 - 2014年)常规QFT样本的结果。2010年引入了一个临界范围(0.20 - 0.99国际单位/毫升),并建议进行后续样本检测。通过与国家结核病登记处的关联,研究了临界结果与3至24个月内新发活动性结核病之间的关联。

结果

使用推荐的QFT临界值,75.1%的检测为阴性,21.4%为阳性,3.5%为不确定。总共有9%(3656/40773)在临界范围内。在后续样本中,初始结果在0.20 - 0.34国际单位/毫升和0.35 - 0.99国际单位/毫升之间的个体,分别有66.1%(共230/348)和42.5%(共285/671)在后续检测中显示结果低于临界范围(<0.20国际单位/毫升)且为阴性,并且均未发生新发结核病。在6712名初始检测结果>0.99国际单位/毫升呈阳性的个体中,有65名(0.97%)在3至24个月内发生了新发结核病。

结论

我们建议对QFT结果在0.20 - 0.99国际单位/毫升范围内的受试者进行重新检测,以提高检测的可靠性和有效性。临界范围内一半的受试者在重新检测时结果会低于0.20国际单位/毫升且为阴性,发生新发活动性结核病的风险非常低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ed/5667766/4e613a0e9967/pone.0187313.g001.jpg

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