Evaluation of the Performance of QuantiFERON-TB Gold Plus Assay in Human Immunodeficiency Virus Infection

Introduction: Individuals co-infected with human immunodeficiency virus (HIV) and Mycobacterium tuberculosis have an increased risk of the reactivation of latent tuberculosis (TB) infection (LTBI) to active TB. The addition of peptides to stimulate CD8+ T cells is expected to increase the sensitivit...

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Main Authors: Melike YAŞAR DUMAN, Cengiz ÇAVUŞOĞLU, İmre ALTUĞLU, Ayşin ZEYTİNOĞLU, Ayşe Deniz GÖKENGİN, Tansu Gülbahar AYDOĞAN, Mehmet Nurullah ORMAN
Format: Article
Language:Turkish
Published: Galenos Yayinevi 2022-08-01
Series:Mediterranean Journal of Infection, Microbes and Antimicrobials
Subjects:
Online Access:https://mjima.org/abstract.php?id=325
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author Melike YAŞAR DUMAN
Cengiz ÇAVUŞOĞLU
İmre ALTUĞLU
Ayşin ZEYTİNOĞLU
Ayşe Deniz GÖKENGİN
Tansu Gülbahar AYDOĞAN
Mehmet Nurullah ORMAN
author_facet Melike YAŞAR DUMAN
Cengiz ÇAVUŞOĞLU
İmre ALTUĞLU
Ayşin ZEYTİNOĞLU
Ayşe Deniz GÖKENGİN
Tansu Gülbahar AYDOĞAN
Mehmet Nurullah ORMAN
author_sort Melike YAŞAR DUMAN
collection DOAJ
description Introduction: Individuals co-infected with human immunodeficiency virus (HIV) and Mycobacterium tuberculosis have an increased risk of the reactivation of latent tuberculosis (TB) infection (LTBI) to active TB. The addition of peptides to stimulate CD8+ T cells is expected to increase the sensitivity of the QuantiFERON®-TB Gold Plus (QFT-Plus) assay in detecting LTBI and TB infection in patients. This study aimed to determine the prevalence of LTBI in patients with HIV infection in our region and to evaluate the possible factors that may interfere with the performance of the QFT-Plus assay in HIV infection. Materials and Methods: The study included 132 HIV-positive and 133 HIV-negative cases presented to the Ege University Medical Faculty Hospital between January 2016 and December 2019. Demographic and clinical data and laboratory/culture results were obtained from the mycobacteriology laboratory and hospital database. Results: QFT-Plus positivity rates were 30.1% (40/133) in the HIV-negative and 21.2% (28/132) in HIV-positive groups. The indeterminate results of the HIV-positive and HIV-negative groups were 4.5% and 3%, respectively. The CD4+ T cell count was below 200/mm3 in five of the six patients in the HIV-positive group with indeterminate results, and the median lymphocyte count was significantly lower. Although no significant difference was found between the median lymphocyte counts of the HIV-positive and HIV-negative group, the positivity rates and secreted interferon (IFN)-ɣ levels were lower, and the indeterminate results were higher in the HIV-positive group than in the HIV-negative group, but the difference was not significant. The rate of QFT-Plus positivity was 32.4% in patients with a viral load below 10,000 copies/ml and 16.1% in patients with a viral load above 10,000 copies/ml (p=0.047). Conclusion: The positivity rates and secreted IFN-ɣ levels were lower, and the indeterminate results were higher in the HIV-positive group than in the HIV-negative group. The addition of TB2 tube to the QFT-Plus assay could contribute to the sensitivity of the test in both HIV-positive and HIV-negative individuals with LTBI.
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spelling doaj.art-519ab2e6de79462d88badc5e4cb2a06a2023-02-15T16:07:20ZturGalenos YayineviMediterranean Journal of Infection, Microbes and Antimicrobials2147-673X2022-08-0111110.4274/mjima.galenos.2022.2021.27Evaluation of the Performance of QuantiFERON-TB Gold Plus Assay in Human Immunodeficiency Virus InfectionMelike YAŞAR DUMAN0https://orcid.org/0000-0001-8913-2314Cengiz ÇAVUŞOĞLU1https://orcid.org/0000-0001-7152-5216İmre ALTUĞLU2https://orcid.org/0000-0002-8280-6037Ayşin ZEYTİNOĞLU3https://orcid.org/0000-0003-4174-9539Ayşe Deniz GÖKENGİN4https://orcid.org/0000-0003-0704-2302Tansu Gülbahar AYDOĞAN5https://orcid.org/0000-0002-3959-426XMehmet Nurullah ORMAN6https://orcid.org/0000-0003-3544-9329Ege University Faculty of Medicine, Department of Medical Microbiology, İzmir, TurkeyEge University Faculty of Medicine, Department of Medical Microbiology, İzmir, TurkeyEge University Faculty of Medicine, Department of Medical Microbiology, İzmir, TurkeyEge University Faculty of Medicine, Department of Medical Microbiology, İzmir, TurkeyEge University Faculty of Medicine, Department of Infectious Diseases and Clinical Microbiology, İzmir, TurkeyEge University Faculty of Medicine, Department of Medical Microbiology, İzmir, TurkeyEge University Faculty of Medicine, Department of Biostatistics and Medical Informatics, İzmir, TurkeyIntroduction: Individuals co-infected with human immunodeficiency virus (HIV) and Mycobacterium tuberculosis have an increased risk of the reactivation of latent tuberculosis (TB) infection (LTBI) to active TB. The addition of peptides to stimulate CD8+ T cells is expected to increase the sensitivity of the QuantiFERON®-TB Gold Plus (QFT-Plus) assay in detecting LTBI and TB infection in patients. This study aimed to determine the prevalence of LTBI in patients with HIV infection in our region and to evaluate the possible factors that may interfere with the performance of the QFT-Plus assay in HIV infection. Materials and Methods: The study included 132 HIV-positive and 133 HIV-negative cases presented to the Ege University Medical Faculty Hospital between January 2016 and December 2019. Demographic and clinical data and laboratory/culture results were obtained from the mycobacteriology laboratory and hospital database. Results: QFT-Plus positivity rates were 30.1% (40/133) in the HIV-negative and 21.2% (28/132) in HIV-positive groups. The indeterminate results of the HIV-positive and HIV-negative groups were 4.5% and 3%, respectively. The CD4+ T cell count was below 200/mm3 in five of the six patients in the HIV-positive group with indeterminate results, and the median lymphocyte count was significantly lower. Although no significant difference was found between the median lymphocyte counts of the HIV-positive and HIV-negative group, the positivity rates and secreted interferon (IFN)-ɣ levels were lower, and the indeterminate results were higher in the HIV-positive group than in the HIV-negative group, but the difference was not significant. The rate of QFT-Plus positivity was 32.4% in patients with a viral load below 10,000 copies/ml and 16.1% in patients with a viral load above 10,000 copies/ml (p=0.047). Conclusion: The positivity rates and secreted IFN-ɣ levels were lower, and the indeterminate results were higher in the HIV-positive group than in the HIV-negative group. The addition of TB2 tube to the QFT-Plus assay could contribute to the sensitivity of the test in both HIV-positive and HIV-negative individuals with LTBI.https://mjima.org/abstract.php?id=325quantiferon-tb gold plusactive tuberculosishuman immunodeficiency viruslatent tuberculosis infectionmycobacterium tuberculosis
spellingShingle Melike YAŞAR DUMAN
Cengiz ÇAVUŞOĞLU
İmre ALTUĞLU
Ayşin ZEYTİNOĞLU
Ayşe Deniz GÖKENGİN
Tansu Gülbahar AYDOĞAN
Mehmet Nurullah ORMAN
Evaluation of the Performance of QuantiFERON-TB Gold Plus Assay in Human Immunodeficiency Virus Infection
Mediterranean Journal of Infection, Microbes and Antimicrobials
quantiferon-tb gold plus
active tuberculosis
human immunodeficiency virus
latent tuberculosis infection
mycobacterium tuberculosis
title Evaluation of the Performance of QuantiFERON-TB Gold Plus Assay in Human Immunodeficiency Virus Infection
title_full Evaluation of the Performance of QuantiFERON-TB Gold Plus Assay in Human Immunodeficiency Virus Infection
title_fullStr Evaluation of the Performance of QuantiFERON-TB Gold Plus Assay in Human Immunodeficiency Virus Infection
title_full_unstemmed Evaluation of the Performance of QuantiFERON-TB Gold Plus Assay in Human Immunodeficiency Virus Infection
title_short Evaluation of the Performance of QuantiFERON-TB Gold Plus Assay in Human Immunodeficiency Virus Infection
title_sort evaluation of the performance of quantiferon tb gold plus assay in human immunodeficiency virus infection
topic quantiferon-tb gold plus
active tuberculosis
human immunodeficiency virus
latent tuberculosis infection
mycobacterium tuberculosis
url https://mjima.org/abstract.php?id=325
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