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Evaluation of a New IFN-γ Release Assay for Rapid Diagnosis of Active Tuberculosis in a High-Incidence Setting

Blood-based interferon-gamma (IFN-γ) release assays (IGRAs) have been proven to be useful in the diagnosis of Mycobacterium tuberculosis (Mtb) infection. However, IGRAs have not been recommended for clinical practice in most low-income settings due to cost-intensive limitations and shortage of clini...

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Autores principales: Li, Gen, Li, Feng, Zhao, Hui-Min, Wen, Han-Li, Li, Hai-Cong, Li, Chun-Ling, Ji, Ping, Xu, Peng, Wu, Kang, Hu, Zhi-Dong, Lu, Shui-Hua, Lowrie, Douglas B., Lv, Jian-Xin, Fan, Xiao-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386965/
https://www.ncbi.nlm.nih.gov/pubmed/28443247
http://dx.doi.org/10.3389/fcimb.2017.00117
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author Li, Gen
Li, Feng
Zhao, Hui-Min
Wen, Han-Li
Li, Hai-Cong
Li, Chun-Ling
Ji, Ping
Xu, Peng
Wu, Kang
Hu, Zhi-Dong
Lu, Shui-Hua
Lowrie, Douglas B.
Lv, Jian-Xin
Fan, Xiao-Yong
author_facet Li, Gen
Li, Feng
Zhao, Hui-Min
Wen, Han-Li
Li, Hai-Cong
Li, Chun-Ling
Ji, Ping
Xu, Peng
Wu, Kang
Hu, Zhi-Dong
Lu, Shui-Hua
Lowrie, Douglas B.
Lv, Jian-Xin
Fan, Xiao-Yong
author_sort Li, Gen
collection PubMed
description Blood-based interferon-gamma (IFN-γ) release assays (IGRAs) have been proven to be useful in the diagnosis of Mycobacterium tuberculosis (Mtb) infection. However, IGRAs have not been recommended for clinical practice in most low-income settings due to cost-intensive limitations and shortage of clinical data available. The established T-SPOT. TB assay containing Mtb-specific antigens ESAT-6 and CFP10 are widely used for immunodiagonsis of Mtb infection, but the high cost is one of the restricting factors against its clinical application in the developing countries. More recently, a cost-saving IGRA assay, TS-SPOT, was approved in China. This new assay contains an additional antigen Rv3615c. Rv3615c contains broadly recognized CD4(+) and CD8(+) epitopes, and T-cell responses to Rv3615c are as specific for Mtb infection as the responses to ESAT-6 and CFP10 in both Mtb-infected humans and M. bovis-infected cattle. Therefore, we assessed the likely effect of inclusion of Rv3615c as stimulus besides ESAT-6 and CFP10 in an IGRA assay and evaluated the performance of TS-SPOT for diagnosis of Mtb infection and active TB compared with T-SPOT.TB. We tested 155 active TB patients, 90 non-TB lung disease patients, and 55 healthy individuals. The results presented an improved positive rate for diagnosis of active TB and Mtb infection, that could be attributable to inclusion of Rv3615c in the mixture of stimulatory antigens. The diagnostic efficiency of TS-SPOT assay for active TB was as follows: sensitivity 80.00%, specificity 83.45%, positive predictive value (PPV) 83.78%, negative predictive value (NPV) 83.45%, positive likelihood ratio (LR+) 4.83, and negative likelihood ratio (LR−) 0.24. The results were similar to those of T-SPOT.TB, with an excellent agreement (κ = 0.91, 95% CI: 0.85–0.95) being observed between these two assays. The sensitivities of the TS-SPOT assay varied for patients with different forms of active TB, with the highest sensitivity for patients with culture-positive pulmonary TB (92.16%) and the lowest for those with tuberculosis meningitis (50.00%). Taken together, the current evidence indicates that this new TS-SPOT assay is a useful adjunct to the current tests for rapid diagnosis of active TB and Mtb infection in low-income and high-incidence settings due to its characteristics of cost-effectiveness and high-quality.
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spelling pubmed-53869652017-04-25 Evaluation of a New IFN-γ Release Assay for Rapid Diagnosis of Active Tuberculosis in a High-Incidence Setting Li, Gen Li, Feng Zhao, Hui-Min Wen, Han-Li Li, Hai-Cong Li, Chun-Ling Ji, Ping Xu, Peng Wu, Kang Hu, Zhi-Dong Lu, Shui-Hua Lowrie, Douglas B. Lv, Jian-Xin Fan, Xiao-Yong Front Cell Infect Microbiol Microbiology Blood-based interferon-gamma (IFN-γ) release assays (IGRAs) have been proven to be useful in the diagnosis of Mycobacterium tuberculosis (Mtb) infection. However, IGRAs have not been recommended for clinical practice in most low-income settings due to cost-intensive limitations and shortage of clinical data available. The established T-SPOT. TB assay containing Mtb-specific antigens ESAT-6 and CFP10 are widely used for immunodiagonsis of Mtb infection, but the high cost is one of the restricting factors against its clinical application in the developing countries. More recently, a cost-saving IGRA assay, TS-SPOT, was approved in China. This new assay contains an additional antigen Rv3615c. Rv3615c contains broadly recognized CD4(+) and CD8(+) epitopes, and T-cell responses to Rv3615c are as specific for Mtb infection as the responses to ESAT-6 and CFP10 in both Mtb-infected humans and M. bovis-infected cattle. Therefore, we assessed the likely effect of inclusion of Rv3615c as stimulus besides ESAT-6 and CFP10 in an IGRA assay and evaluated the performance of TS-SPOT for diagnosis of Mtb infection and active TB compared with T-SPOT.TB. We tested 155 active TB patients, 90 non-TB lung disease patients, and 55 healthy individuals. The results presented an improved positive rate for diagnosis of active TB and Mtb infection, that could be attributable to inclusion of Rv3615c in the mixture of stimulatory antigens. The diagnostic efficiency of TS-SPOT assay for active TB was as follows: sensitivity 80.00%, specificity 83.45%, positive predictive value (PPV) 83.78%, negative predictive value (NPV) 83.45%, positive likelihood ratio (LR+) 4.83, and negative likelihood ratio (LR−) 0.24. The results were similar to those of T-SPOT.TB, with an excellent agreement (κ = 0.91, 95% CI: 0.85–0.95) being observed between these two assays. The sensitivities of the TS-SPOT assay varied for patients with different forms of active TB, with the highest sensitivity for patients with culture-positive pulmonary TB (92.16%) and the lowest for those with tuberculosis meningitis (50.00%). Taken together, the current evidence indicates that this new TS-SPOT assay is a useful adjunct to the current tests for rapid diagnosis of active TB and Mtb infection in low-income and high-incidence settings due to its characteristics of cost-effectiveness and high-quality. Frontiers Media S.A. 2017-04-11 /pmc/articles/PMC5386965/ /pubmed/28443247 http://dx.doi.org/10.3389/fcimb.2017.00117 Text en Copyright © 2017 Li, Li, Zhao, Wen, Li, Li, Ji, Xu, Wu, Hu, Lu, Lowrie, Lv and Fan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Li, Gen
Li, Feng
Zhao, Hui-Min
Wen, Han-Li
Li, Hai-Cong
Li, Chun-Ling
Ji, Ping
Xu, Peng
Wu, Kang
Hu, Zhi-Dong
Lu, Shui-Hua
Lowrie, Douglas B.
Lv, Jian-Xin
Fan, Xiao-Yong
Evaluation of a New IFN-γ Release Assay for Rapid Diagnosis of Active Tuberculosis in a High-Incidence Setting
title Evaluation of a New IFN-γ Release Assay for Rapid Diagnosis of Active Tuberculosis in a High-Incidence Setting
title_full Evaluation of a New IFN-γ Release Assay for Rapid Diagnosis of Active Tuberculosis in a High-Incidence Setting
title_fullStr Evaluation of a New IFN-γ Release Assay for Rapid Diagnosis of Active Tuberculosis in a High-Incidence Setting
title_full_unstemmed Evaluation of a New IFN-γ Release Assay for Rapid Diagnosis of Active Tuberculosis in a High-Incidence Setting
title_short Evaluation of a New IFN-γ Release Assay for Rapid Diagnosis of Active Tuberculosis in a High-Incidence Setting
title_sort evaluation of a new ifn-γ release assay for rapid diagnosis of active tuberculosis in a high-incidence setting
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386965/
https://www.ncbi.nlm.nih.gov/pubmed/28443247
http://dx.doi.org/10.3389/fcimb.2017.00117
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