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Usefulness of interferon-γ release assay for the diagnosis of latent tuberculosis infection in young children

PURPOSE: Latent tuberculosis infection (LTBI) in young children may progress to severe active tuberculosis (TB) disease and serve as a reservoir for future transmission of TB disease. There are limited data on interferon-γ release assay (IGRA) performance in young children, which our research aims t...

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Autores principales: Yun, Ki Wook, Kim, Young Kwang, Kim, Hae Ryun, Lee, Mi Kyung, Lim, In Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958703/
https://www.ncbi.nlm.nih.gov/pubmed/27462354
http://dx.doi.org/10.3345/kjp.2016.59.6.256
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author Yun, Ki Wook
Kim, Young Kwang
Kim, Hae Ryun
Lee, Mi Kyung
Lim, In Seok
author_facet Yun, Ki Wook
Kim, Young Kwang
Kim, Hae Ryun
Lee, Mi Kyung
Lim, In Seok
author_sort Yun, Ki Wook
collection PubMed
description PURPOSE: Latent tuberculosis infection (LTBI) in young children may progress to severe active tuberculosis (TB) disease and serve as a reservoir for future transmission of TB disease. There are limited data on interferon-γ release assay (IGRA) performance in young children, which our research aims to address by investigating the usefulness of IGRA for the diagnosis of LTBI. METHODS: We performed a tuberculin skin test (TST) and IGRA on children who were younger than 18 years and were admitted to Chung-Ang University Hospital during May 2011–June 2015. Blood samples for IGRA were collected, processed, and interpreted according to manufacturer protocol. RESULTS: Among 149 children, 31 (20.8%) and 10 (6.7%) were diagnosed with LTBI and active pulmonary TB, respectively. In subjects lacking contact history with active TB patients, TST and IGRA results were positive in 41.4% (29 of 70) and 12.9% (9 of 70) subjects, respectively. The agreement (kappa) of TST and IGRA was 0.123. The control group, consisting of non-TB-infected subjects, showed no correlation between age and changes in interferon-γ concentration after nil antigen, TB-specific antigen, or mitogen stimulation in IGRAs (P=0.384, P=0.176, and P=0.077, respectively). In serial IGRAs, interferon-γ response to TB antigen increased in IGRA-positive LTBI subjects, but did not change considerably in initially IGRA-negative LTBI or control subjects. CONCLUSION: The lack of decrease in interferon-γ response in young children indicates that IGRA could be considered for this age group. Serial IGRA tests might accurately diagnose LTBI in children lacking contact history with active TB patients.
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spelling pubmed-49587032016-07-26 Usefulness of interferon-γ release assay for the diagnosis of latent tuberculosis infection in young children Yun, Ki Wook Kim, Young Kwang Kim, Hae Ryun Lee, Mi Kyung Lim, In Seok Korean J Pediatr Original Article PURPOSE: Latent tuberculosis infection (LTBI) in young children may progress to severe active tuberculosis (TB) disease and serve as a reservoir for future transmission of TB disease. There are limited data on interferon-γ release assay (IGRA) performance in young children, which our research aims to address by investigating the usefulness of IGRA for the diagnosis of LTBI. METHODS: We performed a tuberculin skin test (TST) and IGRA on children who were younger than 18 years and were admitted to Chung-Ang University Hospital during May 2011–June 2015. Blood samples for IGRA were collected, processed, and interpreted according to manufacturer protocol. RESULTS: Among 149 children, 31 (20.8%) and 10 (6.7%) were diagnosed with LTBI and active pulmonary TB, respectively. In subjects lacking contact history with active TB patients, TST and IGRA results were positive in 41.4% (29 of 70) and 12.9% (9 of 70) subjects, respectively. The agreement (kappa) of TST and IGRA was 0.123. The control group, consisting of non-TB-infected subjects, showed no correlation between age and changes in interferon-γ concentration after nil antigen, TB-specific antigen, or mitogen stimulation in IGRAs (P=0.384, P=0.176, and P=0.077, respectively). In serial IGRAs, interferon-γ response to TB antigen increased in IGRA-positive LTBI subjects, but did not change considerably in initially IGRA-negative LTBI or control subjects. CONCLUSION: The lack of decrease in interferon-γ response in young children indicates that IGRA could be considered for this age group. Serial IGRA tests might accurately diagnose LTBI in children lacking contact history with active TB patients. The Korean Pediatric Society 2016-06 2016-06-30 /pmc/articles/PMC4958703/ /pubmed/27462354 http://dx.doi.org/10.3345/kjp.2016.59.6.256 Text en Copyright © 2016 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yun, Ki Wook
Kim, Young Kwang
Kim, Hae Ryun
Lee, Mi Kyung
Lim, In Seok
Usefulness of interferon-γ release assay for the diagnosis of latent tuberculosis infection in young children
title Usefulness of interferon-γ release assay for the diagnosis of latent tuberculosis infection in young children
title_full Usefulness of interferon-γ release assay for the diagnosis of latent tuberculosis infection in young children
title_fullStr Usefulness of interferon-γ release assay for the diagnosis of latent tuberculosis infection in young children
title_full_unstemmed Usefulness of interferon-γ release assay for the diagnosis of latent tuberculosis infection in young children
title_short Usefulness of interferon-γ release assay for the diagnosis of latent tuberculosis infection in young children
title_sort usefulness of interferon-γ release assay for the diagnosis of latent tuberculosis infection in young children
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958703/
https://www.ncbi.nlm.nih.gov/pubmed/27462354
http://dx.doi.org/10.3345/kjp.2016.59.6.256
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