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本文引用的文献

1
Screening for Latent Tuberculosis Infection in Adults: US Preventive Services Task Force Recommendation Statement.成人潜伏性结核感染的筛查:美国预防服务工作组建议声明
JAMA. 2023 May 2;329(17):1487-1494. doi: 10.1001/jama.2023.4899.
2
Comparing the diagnostic performance of QuantiFERON-TB Gold Plus with QFT-GIT, T-SPOT.TB and TST: a systematic review and meta-analysis.比较 QuantiFERON-TB Gold Plus 与 QFT-GIT、T-SPOT.TB 和 TST 的诊断性能:系统评价和荟萃分析。
BMC Infect Dis. 2023 Jan 20;23(1):40. doi: 10.1186/s12879-023-08008-2.
3
Novel Automation of an Enzyme-Linked Immunosorbent Spot Assay Testing Method: Comparable Diagnostic Performance of the T-SPOT. Test Using Manual Density Gradient Cell Isolation versus Automated Positive Selection with the T-Cell Kit.新型酶联免疫斑点分析检测方法的自动化:使用手动密度梯度细胞分离与 T 细胞试剂盒自动化阳性选择进行 T-SPOT.试验的可比诊断性能。
J Clin Microbiol. 2022 Sep 21;60(9):e0055122. doi: 10.1128/jcm.00551-22. Epub 2022 Aug 30.
4
Tuberculosis Infection in Children and Adolescents: Testing and Treatment.儿童和青少年结核病感染:检测与治疗。
Pediatrics. 2021 Dec 1;148(6). doi: 10.1542/peds.2021-054663.
5
The Impact of Borderline Quantiferon-TB Gold Plus Results for Latent Tuberculosis Screening under Routine Conditions in a Low-Endemicity Setting.在低流行地区常规条件下,边缘型 Quantiferon-TB Gold Plus 结果对潜伏性结核病筛查的影响。
J Clin Microbiol. 2021 Nov 18;59(12):e0137021. doi: 10.1128/JCM.01370-21. Epub 2021 Sep 22.
6
Comparison of three tests for latent tuberculosis infection in high-risk people in the USA: an observational cohort study.美国高危人群中三种潜伏性结核病感染检测方法的比较:一项观察性队列研究。
Lancet Infect Dis. 2022 Jan;22(1):85-96. doi: 10.1016/S1473-3099(21)00145-6. Epub 2021 Sep 6.
7
Impact of T-Cell Xtend on T-SPOT. Assay in High-Risk Individuals after Delayed Blood Sample Processing.T 细胞扩增技术对延迟血样处理的高危人群 T-SPOT.assay 的影响。
J Clin Microbiol. 2021 Apr 20;59(5). doi: 10.1128/JCM.00120-21.
8
Interferon-γ Release Assays in Children <15 Years of Age.15 岁以下儿童的干扰素-γ 释放试验。
Pediatrics. 2020 Jan;145(1). doi: 10.1542/peds.2019-1930.
9
Comparing QuantiFERON-TB Gold Plus with Other Tests To Diagnose Mycobacterium tuberculosis Infection.比较 Quantiferon-TB Gold Plus 与其他检测方法诊断结核分枝杆菌感染。
J Clin Microbiol. 2019 Oct 23;57(11). doi: 10.1128/JCM.00985-19. Print 2019 Nov.
10
Treatment of latent infection to achieve tuberculosis elimination in low-incidence countries.低发病国家消除结核病策略中的潜伏感染治疗。
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两种用于儿童结核病感染的γ-干扰素释放试验的比较

Comparison of Two Interferon-Gamma Release Assays for Pediatric Tuberculosis Infection.

作者信息

Gaensbauer James T, Reves Randall R, Katz Dolly, Ahmed Amina, Venkatappa Thara

机构信息

Mayo Clinic Center for Tuberculosis, Mayo Clinic, Rochester, MN, United States.

Division of Pediatric Infectious Diseases, Department of Pediatrics and Adolescent Medicine, Mayo Clinic, Rochester, MN, United States.

出版信息

J Pediatric Infect Dis Soc. 2025 Jan 20;14(1). doi: 10.1093/jpids/piae135.

DOI:10.1093/jpids/piae135
PMID:39749968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11851244/
Abstract

INTRODUCTION

Identifying tuberculosis infection (TBI) using interferon-gamma release assays (IGRAs) is a primary component of clinical and public health efforts to prevent pediatric tuberculosis (TB). Pediatric data comparing the 2 IGRAs in the United States are very limited. We compared the performance of the 2 IGRAs among a large pediatric cohort tested for TBI and assessed whether discordance might be due to quantitative results close to test cutoff values.

METHODS

Children aged 0-15 years with both T-SPOT.TB (T-SPOT) and QuantiFERON-TB Gold In-Tube (QFT-GIT) tests were identified from a US multicenter study enrolling people at elevated risk of TBI or progression to TB disease. Results were compared using McNemar's Chi-square tests with stratification by age category and testing reason. Percent agreement and kappa statistics were also calculated. We characterized quantitative test results among children with discordant QFT-GIT-positive/T-SPOT-negative results.

RESULTS

Among 3793 children, a higher number had positive QFT-GIT than T-SPOT (10.1% vs 7.4%, P < .001). This difference was noted for all age categories except <2 years, and for children with close-contact and non-close contact test indications. Among discordant QFT-GIT-positive/T-SPOT-negative children, lowering the positive threshold for T-SPOT to include borderline spot counts (5-7) did not eliminate the discordance, nor were QFT-GIT antigen-minus-nil results concentrated in the range just above the standard cutoff of 0.35 IU/mL.

CONCLUSIONS

In a large pediatric cohort tested for TBI, QFT-GIT had a higher proportion of positive results than T-SPOT, and discordance was not related to quantitative results close to the established diagnostic cutoffs.

摘要

引言

使用干扰素-γ释放试验(IGRAs)来识别结核感染(TBI)是预防儿童结核病(TB)的临床和公共卫生工作的主要组成部分。在美国,比较这两种IGRAs的儿科数据非常有限。我们在一个接受TBI检测的大型儿科队列中比较了这两种IGRAs的性能,并评估了结果不一致是否可能是由于定量结果接近检测临界值所致。

方法

从一项美国多中心研究中确定年龄在0至15岁且同时进行了T-SPOT.TB(T-SPOT)和结核菌素释放试验(QFT-GIT)检测的儿童,该研究纳入了TBI或进展为结核病风险较高的人群。使用McNemar卡方检验按年龄类别和检测原因进行分层比较结果。还计算了一致率和kappa统计量。我们对QFT-GIT阳性/T-SPOT阴性结果不一致的儿童的定量检测结果进行了特征分析。

结果

在3793名儿童中,QFT-GIT阳性的人数多于T-SPOT阳性的人数(10.1%对7.4%,P<0.001)。除2岁以下儿童外,所有年龄类别以及有密切接触和非密切接触检测指征的儿童均存在这种差异。在QFT-GIT阳性/T-SPOT阴性结果不一致的儿童中,将T-SPOT的阳性阈值降低以纳入临界斑点计数(5-7)并不能消除不一致性,QFT-GIT抗原减去零结果也没有集中在略高于0.35 IU/mL标准临界值的范围内。

结论

在一个接受TBI检测的大型儿科队列中,QFT-GIT阳性结果的比例高于T-SPOT,且结果不一致与接近既定诊断临界值的定量结果无关。