Egyptian Journal of Chest Disease and Tuberculosis (Oct 2012)

Role of Quantiferon TB gold assays in monitoring the efficacy of antituberculosis therapy

  • N. Helmy,
  • S. Abdel latif,
  • M.M. Kamel,
  • W. Ashour,
  • E. El Kattan

DOI
https://doi.org/10.1016/j.ejcdt.2012.09.011
Journal volume & issue
Vol. 61, no. 4
pp. 329 – 336

Abstract

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Rationale: The impact of antituberculous treatment on (IFN)-γ response to mycobacterial tuberculosis antigens have been widely investigated but the results have been controversial. Aim of work: To evaluate the role of Quantiferon TB gold assays as one of the interferon-gamma release assays (IGRAs) for monitoring the efficacy of antituberculosis therapy in patients with active disease. Subjects and methods: Thirty patients with active pulmonary TB were enrolled in this cross-sectional study where they were subjected to history taking, clinical examination, chest X-ray, direct smear examination of sputum samples for AFB using Ziehl–Neelson stain performed on three visits; up on enrollment, 2 and 6 months later. Lowenstein Jensen medium cultures of sputum samples were done for isolation of Mycobacterium tuberculosis on first visit. All patients in the study group were subjected to QuantiFERON-TB Gold estimation on the three visits. Results: The mean sensitivity and specificity of QFT-G test was 85.9% and 62.6% respectively. Using χ2 analysis, there was a statistically significant association between QFT-G results and culture results upon enrollment and Acid fast bacilli positivity on second and third visits. Studying the changes in QFT-G results throughout the whole study period revealed a statistically significant decrease in number of QFT-G positive cases from 24/29 patients (82.8%) at first visit to 4/25 patients (16%) at the third visit. All 21/25 patients (84%) who became QFT-G negative at the end of the study had a complete clinical and microbiological recovery of the TB disease. Conclusion: The analysis of QFT-G assay results showed that in the majority of our TB patients there was a correlation between clinical treatment outcome and changes of IFN-γ response to M. tuberculosis-specific antigens.

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