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Can Interferon-Γ Release Assays Be Useful for Monitoring the Response to Anti-Tuberculosis Treatment?: A Systematic Review and Meta-Analysis Publisher Pubmed



Pourakbari B1 ; Mamishi S1, 2 ; Benvari S3 ; Sauzullo I4 ; Bedini A5 ; Valentini P6 ; Keicho N7 ; Mahmoudi S1
Authors
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Authors Affiliations
  1. 1. Pediatric Infectious Disease Research Center, Children’s Medical Center Hospital, Tehran University of Medical Sciences, Dr. Gharib Street, Keshavarz Boulevard, Tehran, Iran
  2. 2. Department of Infectious Diseases, Pediatrics Center of Excellence, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Microbiology, Faculty of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran
  4. 4. Department of Public Health and Infectious Diseases, Sapienza University, Rome, Italy
  5. 5. Clinic of Infectious Diseases, Azienda Ospedaliero-Universitaria, Policlinico of Modena, Modena, Italy
  6. 6. Institute of Pediatrics, Universita Cattolica del Sacro Cuore, Fondazione Policlinico Universitario Gemelli, Rome, Italy
  7. 7. The Research Institute of Tuberculosis, Japan Anti-Tuberculosis Association, Kiyose, Tokyo, Japan

Source: Archivum Immunologiae et Therapiae Experimentalis Published:2020


Abstract

The number of studies which evaluated interferon-gamma release assays (IGRAs) results after anti-tuberculosis (TB) treatment has been rapidly increasing. The aim of this study was to investigate the potential use of IGRAs (QFT-GIT, T-SPOT.TB, QFT-Plus) in assessing the response to anti-TB treatment. We searched all studies in English language published from 1 October 2011 to 18 November 2018 in PubMed, Web of Science, and Scopus. Our search included the term “tuberculosis treatment AND interferon-γ release assay”. We included studies evaluating the performance of commercial IGRAs (including QFT-GIT, T-SPOT.TB and QFT-Plus) before and after the anti-TB treatment. We performed subgroup analysis based on the age (children, adults), type of TB (active, latent, active and latent, and contacts exposed to MDR defined as MDR LTBI), type of IGRAs (QFT-GIT and T-SPOT.TB), and follow-up interval (2, 3, 4, 6, 9 months). Of the 18 included studies, 12 used QFT-GIT for assessment of IGRA performance after therapy, 1 used T-SPOT.TB, and 3 used both QFT-GIT and T-SPOT.TB. Since then, only two studies have assessed the QFT-Plus performance during therapy. According to the results of the meta-analysis, the pooled rate of positive IGRAs (QFT-GIT and T-SPOT.TB) following anti-TB therapy was estimated at 76% [95% CI 70–81%] and no difference was found compared to the pooled positive rate of IGRAs before initiation of therapy which was 76% [95% CI 60–89%]. The subgroup analysis showed that the pooled rate of positive IGRAs (QFT-GIT and T-SPOT.TB) after anti-TB therapy was significantly higher in monitoring active TB subjects [80% (95% CI 74–88%)] than LTBI [71% (95% CI 70–81%)]. Available data are now sufficient to suggest that monitoring changes in the IGRAs (QFT-GIT and T-SPOT.TB) response during anti-TB treatment may have limited use in evaluating the effectiveness of treatment, while the monitoring changes in QFT-Plus during anti-tubercular treatment are recommended to determine treatment efficacy or for treatment monitoring. Further research is needed to establish the efficacy of this new assay as marker on a larger scale for treatment monitoring. © 2020, L. Hirszfeld Institute of Immunology and Experimental Therapy, Wroclaw, Poland.
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