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Accuracy of multitarget indirect enzyme-linked immunoassay assay for detection of tuberculosis antibody

BACKGROUND: Diagnosis of tuberculosis (TB) is still difficult. The development of rapid and sensitive laboratory tools for the diagnosis of tuberculosis is a priority. This study aimed to develop an indirect enzyme-linked immunoassay (ELISA) assay for detection of TB antibody and explore its diagnos...

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Autores principales: Hu, Yang, Liu, Ming, Hu, Haili, Yang, Hua, Qin, Lianhua, Hu, Zhongyi, Zhu, Changtai, Liu, Zhonghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743715/
https://www.ncbi.nlm.nih.gov/pubmed/35071425
http://dx.doi.org/10.21037/atm-21-5598
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author Hu, Yang
Liu, Ming
Hu, Haili
Yang, Hua
Qin, Lianhua
Hu, Zhongyi
Zhu, Changtai
Liu, Zhonghua
author_facet Hu, Yang
Liu, Ming
Hu, Haili
Yang, Hua
Qin, Lianhua
Hu, Zhongyi
Zhu, Changtai
Liu, Zhonghua
author_sort Hu, Yang
collection PubMed
description BACKGROUND: Diagnosis of tuberculosis (TB) is still difficult. The development of rapid and sensitive laboratory tools for the diagnosis of tuberculosis is a priority. This study aimed to develop an indirect enzyme-linked immunoassay (ELISA) assay for detection of TB antibody and explore its diagnostic value in patients with pulmonary tuberculosis (PTB) via a multi-center clinical evaluation. METHODS: The specific antigen, fusion antigen, and specific antibody peptide were obtained using molecular cloning and phage peptide library screening. An indirect ELISA assay was developed using multiple target materials. Further, the assay was validated in six institutions with clinically confirmed TB patients, non-TB patients with pulmonary disease, and healthy controls as research subjects. RESULTS: An indirect ELISA assay was developed with 16 kD antigen, 11,488 (CFP10-MPT48-TB8.4) fusion antigen, and TB18 and pl2 as target antigens against TB antibody. The results of this multicenter study showed that the sensitivity, specificity, and the area under the receiver operating characteristic curve (AUC) of the assay were 48.25% [95% confidence interval (CI): 45.5–51.1%], 92.20% (95% CI: 90.7–93.5%) and 0.724 (95% CI: 0.707–0.741), respectively, and the cut-off value was 0.119. According to the meta-analysis, the combined ROC was 0.736 (95% CI: 0.692–0.779), I(2)=83.73%. The sensitivity of the sputum-positive PTB group (culture or smear positive) was 58.75% (95% CI: 52.96–65.00%); the sensitivity in sputum-negative group (culture or smear negative) was 37.38% (95% CI: 32.71–42.52%), respectively; the sensitivity of the sputum-positive group was significantly higher than that of sputum-negative group (OR =1.57, 95% CI: 1.29–1.92, P<0.001). CONCLUSIONS: Multitarget indirect ELISA assay based on specific-TB antigen, fusion antigen, and antibody peptide is of value for the diagnosis of PTB and can be used as an auxiliary rapid diagnostic tool to improve the sensitivity of sputum-negative TB.
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spelling pubmed-87437152022-01-21 Accuracy of multitarget indirect enzyme-linked immunoassay assay for detection of tuberculosis antibody Hu, Yang Liu, Ming Hu, Haili Yang, Hua Qin, Lianhua Hu, Zhongyi Zhu, Changtai Liu, Zhonghua Ann Transl Med Original Article BACKGROUND: Diagnosis of tuberculosis (TB) is still difficult. The development of rapid and sensitive laboratory tools for the diagnosis of tuberculosis is a priority. This study aimed to develop an indirect enzyme-linked immunoassay (ELISA) assay for detection of TB antibody and explore its diagnostic value in patients with pulmonary tuberculosis (PTB) via a multi-center clinical evaluation. METHODS: The specific antigen, fusion antigen, and specific antibody peptide were obtained using molecular cloning and phage peptide library screening. An indirect ELISA assay was developed using multiple target materials. Further, the assay was validated in six institutions with clinically confirmed TB patients, non-TB patients with pulmonary disease, and healthy controls as research subjects. RESULTS: An indirect ELISA assay was developed with 16 kD antigen, 11,488 (CFP10-MPT48-TB8.4) fusion antigen, and TB18 and pl2 as target antigens against TB antibody. The results of this multicenter study showed that the sensitivity, specificity, and the area under the receiver operating characteristic curve (AUC) of the assay were 48.25% [95% confidence interval (CI): 45.5–51.1%], 92.20% (95% CI: 90.7–93.5%) and 0.724 (95% CI: 0.707–0.741), respectively, and the cut-off value was 0.119. According to the meta-analysis, the combined ROC was 0.736 (95% CI: 0.692–0.779), I(2)=83.73%. The sensitivity of the sputum-positive PTB group (culture or smear positive) was 58.75% (95% CI: 52.96–65.00%); the sensitivity in sputum-negative group (culture or smear negative) was 37.38% (95% CI: 32.71–42.52%), respectively; the sensitivity of the sputum-positive group was significantly higher than that of sputum-negative group (OR =1.57, 95% CI: 1.29–1.92, P<0.001). CONCLUSIONS: Multitarget indirect ELISA assay based on specific-TB antigen, fusion antigen, and antibody peptide is of value for the diagnosis of PTB and can be used as an auxiliary rapid diagnostic tool to improve the sensitivity of sputum-negative TB. AME Publishing Company 2021-12 /pmc/articles/PMC8743715/ /pubmed/35071425 http://dx.doi.org/10.21037/atm-21-5598 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Hu, Yang
Liu, Ming
Hu, Haili
Yang, Hua
Qin, Lianhua
Hu, Zhongyi
Zhu, Changtai
Liu, Zhonghua
Accuracy of multitarget indirect enzyme-linked immunoassay assay for detection of tuberculosis antibody
title Accuracy of multitarget indirect enzyme-linked immunoassay assay for detection of tuberculosis antibody
title_full Accuracy of multitarget indirect enzyme-linked immunoassay assay for detection of tuberculosis antibody
title_fullStr Accuracy of multitarget indirect enzyme-linked immunoassay assay for detection of tuberculosis antibody
title_full_unstemmed Accuracy of multitarget indirect enzyme-linked immunoassay assay for detection of tuberculosis antibody
title_short Accuracy of multitarget indirect enzyme-linked immunoassay assay for detection of tuberculosis antibody
title_sort accuracy of multitarget indirect enzyme-linked immunoassay assay for detection of tuberculosis antibody
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743715/
https://www.ncbi.nlm.nih.gov/pubmed/35071425
http://dx.doi.org/10.21037/atm-21-5598
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