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Evaluation of the IP-10 mRNA release assay for diagnosis of TB in HIV-infected individuals
HIV-infected individuals are susceptible to Mycobacterium tuberculosis (M.tb) infection and are at high risk of developing active tuberculosis (TB). Interferon-gamma release assays (IGRAs) are auxiliary tools in the diagnosis of TB. However, the performance of IGRAs in HIV-infected individuals is su...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272546/ https://www.ncbi.nlm.nih.gov/pubmed/37333845 http://dx.doi.org/10.3389/fcimb.2023.1152665 |
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author | Tang, Yang Yu, Yanhua Wang, Quan Wen, Zilu Song, Ruixue Li, Yu Zhou, Yingquan Ma, Ruiying Jia, Hongyan Bai, Shaoli Abdulsalam, Harimulati Du, Boping Sun, Qi Xing, Aiying Pan, Liping Wang, Jianyun Song, Yanzheng |
author_facet | Tang, Yang Yu, Yanhua Wang, Quan Wen, Zilu Song, Ruixue Li, Yu Zhou, Yingquan Ma, Ruiying Jia, Hongyan Bai, Shaoli Abdulsalam, Harimulati Du, Boping Sun, Qi Xing, Aiying Pan, Liping Wang, Jianyun Song, Yanzheng |
author_sort | Tang, Yang |
collection | PubMed |
description | HIV-infected individuals are susceptible to Mycobacterium tuberculosis (M.tb) infection and are at high risk of developing active tuberculosis (TB). Interferon-gamma release assays (IGRAs) are auxiliary tools in the diagnosis of TB. However, the performance of IGRAs in HIV-infected individuals is suboptimal, which limits clinical application. Interferon-inducible protein 10 (IP-10) is an alternative biomarker for identifying M.tb infection due to its high expression after stimulation with M.tb antigens. However, whether IP-10 mRNA constitutes a target for the diagnosis of TB in HIV-infected individuals is unknown. Thus, we prospectively enrolled HIV-infected patients with suspected active TB from five hospitals between May 2021 and May 2022, and performed the IGRA test (QFT-GIT) alongside the IP-10 mRNA release assay on peripheral blood. Of the 216 participants, 152 TB patients and 48 non-TB patients with a conclusive diagnosis were included in the final analysis. The number of indeterminate results of IP-10 mRNA release assay (13/200, 6.5%) was significantly lower than that of the QFT-GIT test (42/200, 21.0%) (P = 0.000026). IP-10 mRNA release assay had a sensitivity of 65.3% (95%CI 55.9% – 73.8%) and a specificity of 74.2% (95%CI 55.4% – 88.1%), respectively; while the QFT-GIT test had a sensitivity of 43.2% (95%CI 34.1% – 52.7%) and a specificity of 87.1% (95%CI 70.2% – 96.4%), respectively. The sensitivity of the IP-10 mRNA release assay was significantly higher than that of QFT-GIT test (P = 0.00062), while no significant difference was detected between the specificities of these two tests (P = 0.198). The IP-10 mRNA release assay showed a lower dependence on CD4(+) T cells than that of QFT-GIT test. This was evidenced by the fact that the QFT-GIT test had a higher number of indeterminate results and a lower sensitivity when the CD4(+) T cells counts were decreased (P < 0.05), while no significant difference in the number of indeterminate results and sensitivity were observed for the IP-10 mRNA release assay among HIV-infected individuals with varied CD4(+)T cells counts (P > 0.05). Therefore, our study suggested that M.tb specific IP-10 mRNA is a better biomarker for diagnosis of TB in HIV-infected individuals. |
format | Online Article Text |
id | pubmed-10272546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102725462023-06-17 Evaluation of the IP-10 mRNA release assay for diagnosis of TB in HIV-infected individuals Tang, Yang Yu, Yanhua Wang, Quan Wen, Zilu Song, Ruixue Li, Yu Zhou, Yingquan Ma, Ruiying Jia, Hongyan Bai, Shaoli Abdulsalam, Harimulati Du, Boping Sun, Qi Xing, Aiying Pan, Liping Wang, Jianyun Song, Yanzheng Front Cell Infect Microbiol Cellular and Infection Microbiology HIV-infected individuals are susceptible to Mycobacterium tuberculosis (M.tb) infection and are at high risk of developing active tuberculosis (TB). Interferon-gamma release assays (IGRAs) are auxiliary tools in the diagnosis of TB. However, the performance of IGRAs in HIV-infected individuals is suboptimal, which limits clinical application. Interferon-inducible protein 10 (IP-10) is an alternative biomarker for identifying M.tb infection due to its high expression after stimulation with M.tb antigens. However, whether IP-10 mRNA constitutes a target for the diagnosis of TB in HIV-infected individuals is unknown. Thus, we prospectively enrolled HIV-infected patients with suspected active TB from five hospitals between May 2021 and May 2022, and performed the IGRA test (QFT-GIT) alongside the IP-10 mRNA release assay on peripheral blood. Of the 216 participants, 152 TB patients and 48 non-TB patients with a conclusive diagnosis were included in the final analysis. The number of indeterminate results of IP-10 mRNA release assay (13/200, 6.5%) was significantly lower than that of the QFT-GIT test (42/200, 21.0%) (P = 0.000026). IP-10 mRNA release assay had a sensitivity of 65.3% (95%CI 55.9% – 73.8%) and a specificity of 74.2% (95%CI 55.4% – 88.1%), respectively; while the QFT-GIT test had a sensitivity of 43.2% (95%CI 34.1% – 52.7%) and a specificity of 87.1% (95%CI 70.2% – 96.4%), respectively. The sensitivity of the IP-10 mRNA release assay was significantly higher than that of QFT-GIT test (P = 0.00062), while no significant difference was detected between the specificities of these two tests (P = 0.198). The IP-10 mRNA release assay showed a lower dependence on CD4(+) T cells than that of QFT-GIT test. This was evidenced by the fact that the QFT-GIT test had a higher number of indeterminate results and a lower sensitivity when the CD4(+) T cells counts were decreased (P < 0.05), while no significant difference in the number of indeterminate results and sensitivity were observed for the IP-10 mRNA release assay among HIV-infected individuals with varied CD4(+)T cells counts (P > 0.05). Therefore, our study suggested that M.tb specific IP-10 mRNA is a better biomarker for diagnosis of TB in HIV-infected individuals. Frontiers Media S.A. 2023-06-02 /pmc/articles/PMC10272546/ /pubmed/37333845 http://dx.doi.org/10.3389/fcimb.2023.1152665 Text en Copyright © 2023 Tang, Yu, Wang, Wen, Song, Li, Zhou, Ma, Jia, Bai, Abdulsalam, Du, Sun, Xing, Pan, Wang and Song https://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) and the copyright owner(s) 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 | Cellular and Infection Microbiology Tang, Yang Yu, Yanhua Wang, Quan Wen, Zilu Song, Ruixue Li, Yu Zhou, Yingquan Ma, Ruiying Jia, Hongyan Bai, Shaoli Abdulsalam, Harimulati Du, Boping Sun, Qi Xing, Aiying Pan, Liping Wang, Jianyun Song, Yanzheng Evaluation of the IP-10 mRNA release assay for diagnosis of TB in HIV-infected individuals |
title | Evaluation of the IP-10 mRNA release assay for diagnosis of TB in HIV-infected individuals |
title_full | Evaluation of the IP-10 mRNA release assay for diagnosis of TB in HIV-infected individuals |
title_fullStr | Evaluation of the IP-10 mRNA release assay for diagnosis of TB in HIV-infected individuals |
title_full_unstemmed | Evaluation of the IP-10 mRNA release assay for diagnosis of TB in HIV-infected individuals |
title_short | Evaluation of the IP-10 mRNA release assay for diagnosis of TB in HIV-infected individuals |
title_sort | evaluation of the ip-10 mrna release assay for diagnosis of tb in hiv-infected individuals |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272546/ https://www.ncbi.nlm.nih.gov/pubmed/37333845 http://dx.doi.org/10.3389/fcimb.2023.1152665 |
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