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      A Three-Way Comparison of Tuberculin Skin Testing, QuantiFERON-TB Gold and T-SPOT. TB in Children

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          Abstract

          Background

          There are limited data comparing the performance of the two commercially available interferon gamma (IFN-γ) release assays (IGRAs) for the diagnosis of tuberculosis (TB) in children. We compared QuantiFERON-TB gold In Tube (QFT-IT), T-SPOT. TB and the tuberculin skin test (TST) in children at risk for latent TB infection or TB disease.

          Methods and Findings

          The results of both IGRAs were compared with diagnosis assigned by TST-based criteria and assessed in relation to TB contact history. Results from the TST and at least one assay were available for 96 of 100 children. Agreement between QFT-IT and T-SPOT. TB was high (93% agreement, κ = 0.83). QFT-IT and T-SPOT. TB tests were positive in 8 (89%) and 9 (100%) children with suspected active TB disease. There was moderate agreement between TST and either QFT-IT (75%, κ = 0.50) or T-SPOT. TB (75%, κ = 0.51). Among 38 children with TST-defined latent TB infection, QFT-IT gold and T-SPOT. TB assays were positive in 47% and 39% respectively. Three TST-negative children were positive by at least one IGRA. Children with a TB contact were more likely than children without a TB contact to have a positive IGRA (QFT-IT LR 3.9; T-SPOT. TB LR 3.9) and a positive TST (LR 1.4). Multivariate linear regression analysis showed that the magnitude of both TST induration and IGRA IFN-γ responses was significantly influenced by TB contact history, but only the TST was influenced by age.

          Conclusions

          Although a high level of agreement between the IGRAs was observed, they are commonly discordant with the TST. The correct interpretation of a negative assay in a child with a positive skin test in clinical practice remains challenging and highlights the need for longitudinal studies to determine the negative predictive value of IGRAs.

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          Most cited references36

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          Targeted tuberculin testing and treatment of latent tuberculosis infection. This official statement of the American Thoracic Society was adopted by the ATS Board of Directors, July 1999. This is a Joint Statement of the American Thoracic Society (ATS) and the Centers for Disease Control and Prevention (CDC). This statement was endorsed by the Council of the Infectious Diseases Society of America. (IDSA), September 1999, and the sections of this statement.

          (2000)
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            Meta-analysis: new tests for the diagnosis of latent tuberculosis infection: areas of uncertainty and recommendations for research.

            Until recently, the tuberculin skin test was the only test for detecting latent tuberculosis (TB) infection, but 2 ex vivo interferon-gamma release assays (IGRAs) are now commercially licensed. To estimate sensitivity, specificity, and reproducibility of IGRAs (commercial or research versions of QuantiFERON [QFT] and Elispot) for diagnosing latent TB infection in healthy and immune-suppressed persons. The authors searched MEDLINE and reviewed citations of all original articles and reviews for studies published in English. Studies had evaluated IGRAs using Mycobacterium tuberculosis-specific antigens (RD1 antigens) and overnight (16- to 24-h) incubation times. Reference standards had to be clearly defined without knowledge of test results. DATA EXTRACTION AND QUALITY ASSESSMENT: Specific criteria for quality assessment were developed for sensitivity, specificity, and reproducibility. When newly diagnosed active TB was used as a surrogate for latent TB infection, sensitivity of all tests was suboptimal, although it was higher with Elispot. No test distinguishes active TB from latent TB. Sensitivity of the tuberculin skin test and IGRAs was similar in persons who were categorized into clinical gradients of exposure. Pooled specificity was 97.7% (95% CI, 96% to 99%) and 92.5% (CI, 86% to 99%) for QFT and for Elispot, respectively. Both assays were more specific than the tuberculin skin test in samples vaccinated with bacille Calmette-Guérin. Elispot was more sensitive than the tuberculin skin test in 3 studies of immune-compromised samples. Discordant tuberculin skin test and IGRA reactions were frequent and largely unexplained, although some may be related to varied definitions of positive test results. Reversion of IGRA results from positive to negative was common in 2 studies in which it was assessed. Most studies used cross-sectional designs with the inherent limitation of no gold standard for latent TB infection, and most involved small samples with a widely varying likelihood of true-positive and false-positive test results. There is insufficient evidence on IGRA performance in children, immune-compromised persons, and the elderly. New IGRAs show considerable promise and have excellent specificity. Additional studies are needed to better define their performance in high-risk populations and in serial testing. Longitudinal studies are needed to define the predictive value of IGRAs.
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              Interpretation of repeated tuberculin tests. Boosting, conversion, and reversion.

              D. Menzies (1998)
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2008
                9 July 2008
                : 3
                : 7
                : e2624
                Affiliations
                [1 ]Department of Paediatrics, University of Melbourne, Royal Children's Hospital Melbourne, Parkville, Victoria, Australia
                [2 ]Murdoch Children's Research Institute, Royal Children's Hospital Melbourne, Parkville, Victoria, Australia
                [3 ]Infectious Diseases Unit, Department of General Medicine, Royal Children's Hospital Melbourne, Parkville, Victoria, Australia
                [4 ]Immigrant Health Service, Department of General Medicine, Royal Children's Hospital Melbourne, Parkville, Victoria, Australia
                [5 ]Department of Thoracic Medicine Royal Children's Hospital Melbourne, Parkville, Victoria, Australia
                University College London, United Kingdom
                Author notes

                Conceived and designed the experiments: SR TGC NC NR JPB. Performed the experiments: NR. Analyzed the data: SR TGC NC NR GAP. Contributed reagents/materials/analysis tools: SR NC. Wrote the paper: SR TGC NC NR GAP JPB. Performed experiments with laboratory scientist: NR. Wrote the first draft of the manuscript: TC. Enrolled patients: TC NR GP JB SR.

                Article
                08-PONE-RA-04202R2
                10.1371/journal.pone.0002624
                2440545
                18612425
                9220050b-e41b-4cad-94a8-fdca8eb9e71f
                Connell et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 4 April 2008
                : 6 June 2008
                Page count
                Pages: 8
                Categories
                Research Article
                Infectious Diseases
                Pediatrics and Child Health
                Infectious Diseases/HIV Infection and AIDS
                Infectious Diseases/Respiratory Infections
                Pediatrics and Child Health/Respiratory Pediatrics

                Uncategorized
                Uncategorized

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