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Updated: Jun 20, 2026

Application of Long-term cultured Interferon-γ Enzyme-linked Immunospot Assay for Assessing Effector and Memory T Cell Responses in Cattle
Published on: July 11, 2015
[Interferon-gamma release assay on suspicion of active tuberculosis?]
Andrea Browatzki1, Christian Niels Meyer
1Lunge- og Hjertemedicinsk Afdeling, Hvidovre Hospital, DK-2650 Hvidovre. browatzki@hotmail.com
Insights
The interferon-gamma release assay (IGRA) showed low sensitivity and a high false-positive rate for diagnosing active tuberculosis (TB). Physicians
Area of Science:
- Immunodiagnostics
- Infectious Disease Research
- Clinical Microbiology
Context:
- The study evaluates the interferon-gamma release assay (IGRA) in a clinical setting.
- Mycobacterium tuberculosis (TB) infection diagnosis presents challenges.
- IGRA is a newer diagnostic tool for TB detection.
Purpose:
- To assess the practical utility and clinical value of IGRA for suspected active TB.
- To analyze IGRA performance metrics including sensitivity, specificity, PPV, and NPV.
- To evaluate physician adherence to international guidelines when using IGRA.
Summary:
- A retrospective analysis of 91 patients tested with IGRA for M. tuberculosis infection was conducted.
- IGRA demonstrated 80% sensitivity and 85% specificity in patients with suspected active TB.
- The study found a high false-positive rate and low sensitivity for IGRA in active TB diagnosis, with suboptimal physician utilization.
Impact:
- Highlights potential limitations of IGRA in diagnosing active TB, including a high false-positive rate.
- Suggests suboptimal physician interpretation and application of IGRA, not aligning with international guidelines.
- Indicates IGRA may not be a reliable supplementary tool for active TB due to potential false results and diagnostic delays.
Introduction:
The purpose of this retrospective study was to outline the practical use and clinical value of the immunodiagnostic interferon-gamma release assay (IGRA) on suspicion of active Mycobacterium tuberculosis (TB) infection.
Material And Methods:
A retrospective study of all patients (n=91) tested with IGRA (Quantiferon-TB-Gold, Celletis International, Australia) for M. tuberculosis infection from 1 January 2005 to the 31 December 2006 at a Danish regional hospital.
Results:
In 74 patients suspected of active TB, the sensitivity of IGRA was 80% (8/10), the specificity was 85% (50/59), PPV was 47% (8/17) and NPV was 96% (50/52). The positive likelihood ratio (LR) was 5.3 and the negative LR was 0.24. Due to a suboptimal diagnostic setup, the diagnosis of lung cancer in one patient was delayed significantly by a positive IGRA.
Conclusion:
In the current study, IGRA had a high false-positive rate for diagnosing active TB and had a rather low sensitivity which is in line with recent meta analyses. The physicians' use and judgement of this new test seemed suboptimal, as the overwhelming use of IGRA for suspected active TB was not in concordance with international guidelines. IGRA does not differentiate between active and latent M. tuberculosis infection, and IGRA may seldomly be used as a supplementary evaluative tool (with many false negative and "false positive" results).
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