Diagnostic benefits of adding EspC, EspF and Rv2348-B to the QuantiFERON Gold In-tube antigen combination

Interferon (IFN)-γ release assays (IGRAs) are used to diagnose latent tuberculosis (TB) infection (LTBI). To improve the accuracy of these tests, different approaches, such as alternative cytokine detection and using different antigens, are considered. Following this purpose, this study aims to eval...

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Veröffentlicht in:Scientific reports 2020-08, Vol.10 (1), p.13234, Article 13234
Hauptverfasser: Villar-Hernández, R., Blauenfeldt, T., García-García, E., Muriel-Moreno, B., De Souza-Galvão, M. L., Millet, J. P., Sabriá, F., Sánchez-Montalvá, A., Ruiz-Manzano, J., Pilarte, J., Jiménez, M. A., Centeno, C., Martos, C., Molina-Pinargote, I., González-Díaz, Y. D., Santiago, J., Cantos, A., Casas, I., Guerola, R. M., Prat, C., Andersen, P., Latorre, I., Ruhwald, M., Domínguez, J.
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container_start_page 13234
container_title Scientific reports
container_volume 10
creator Villar-Hernández, R.
Blauenfeldt, T.
García-García, E.
Muriel-Moreno, B.
De Souza-Galvão, M. L.
Millet, J. P.
Sabriá, F.
Sánchez-Montalvá, A.
Ruiz-Manzano, J.
Pilarte, J.
Jiménez, M. A.
Centeno, C.
Martos, C.
Molina-Pinargote, I.
González-Díaz, Y. D.
Santiago, J.
Cantos, A.
Casas, I.
Guerola, R. M.
Prat, C.
Andersen, P.
Latorre, I.
Ruhwald, M.
Domínguez, J.
description Interferon (IFN)-γ release assays (IGRAs) are used to diagnose latent tuberculosis (TB) infection (LTBI). To improve the accuracy of these tests, different approaches, such as alternative cytokine detection and using different antigens, are considered. Following this purpose, this study aims to evaluate the addition of EspC, EspF and Rv2348-B to those present in the QuantiFERON-TB Gold In-Tube (QFN-G-IT). We included 115 subjects: 74 active TB patients, 17 LTBI individuals and 24 healthy controls. Whole blood samples were collected in QFN-G-IT and in-house tubes containing different combinations of EspC, EspF and Rv2348-B, together with ESAT-6, CFP-10, and TB7.7. After overnight incubation at 37 ºC, plasma was harvested and IFN-γ quantified. IFN-γ levels in the QFN-G-IT and in-house tubes correlated very good (Spearman Rho(r) > 0.86). In-house antigen combinations distinguished healthy individuals from those with active TB and LTBI (specificities and sensitivities higher than 87.5% and 96.3%, respectively [AUC > 0.938]). Adding EspC, EspF and Rv2348-B, increased the sensitivity of the test, being the addition of EspC and Rv2348-B the combination that yielded a higher sensitivity with no specificity loss. Addition of these antigens could improve diagnosis in patients with impaired or immature immune response who are at high risk of developing TB.
doi_str_mv 10.1038/s41598-020-70204-w
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To improve the accuracy of these tests, different approaches, such as alternative cytokine detection and using different antigens, are considered. Following this purpose, this study aims to evaluate the addition of EspC, EspF and Rv2348-B to those present in the QuantiFERON-TB Gold In-Tube (QFN-G-IT). We included 115 subjects: 74 active TB patients, 17 LTBI individuals and 24 healthy controls. Whole blood samples were collected in QFN-G-IT and in-house tubes containing different combinations of EspC, EspF and Rv2348-B, together with ESAT-6, CFP-10, and TB7.7. After overnight incubation at 37 ºC, plasma was harvested and IFN-γ quantified. IFN-γ levels in the QFN-G-IT and in-house tubes correlated very good (Spearman Rho(r) &gt; 0.86). In-house antigen combinations distinguished healthy individuals from those with active TB and LTBI (specificities and sensitivities higher than 87.5% and 96.3%, respectively [AUC &gt; 0.938]). Adding EspC, EspF and Rv2348-B, increased the sensitivity of the test, being the addition of EspC and Rv2348-B the combination that yielded a higher sensitivity with no specificity loss. 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We included 115 subjects: 74 active TB patients, 17 LTBI individuals and 24 healthy controls. Whole blood samples were collected in QFN-G-IT and in-house tubes containing different combinations of EspC, EspF and Rv2348-B, together with ESAT-6, CFP-10, and TB7.7. After overnight incubation at 37 ºC, plasma was harvested and IFN-γ quantified. IFN-γ levels in the QFN-G-IT and in-house tubes correlated very good (Spearman Rho(r) &gt; 0.86). In-house antigen combinations distinguished healthy individuals from those with active TB and LTBI (specificities and sensitivities higher than 87.5% and 96.3%, respectively [AUC &gt; 0.938]). Adding EspC, EspF and Rv2348-B, increased the sensitivity of the test, being the addition of EspC and Rv2348-B the combination that yielded a higher sensitivity with no specificity loss. Addition of these antigens could improve diagnosis in patients with impaired or immature immune response who are at high risk of developing TB.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32764560</pmid><doi>10.1038/s41598-020-70204-w</doi><oa>free_for_read</oa></addata></record>
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subjects 692/53/2421
692/699/255/1856
Adult
Antigens
Antigens, Bacterial - immunology
Case-Control Studies
Early Diagnosis
ESAT-6 antigen
Female
Gold
Humanities and Social Sciences
Humans
Immune response
Interferon-gamma Release Tests
Latent Tuberculosis - diagnosis
Male
Middle Aged
multidisciplinary
Mycobacterium tuberculosis - immunology
Science
Science (multidisciplinary)
Sensitivity analysis
Sensitivity and Specificity
Spain
Tuberculin Test
Tuberculosis
Tuberculosis - diagnosis
Tuberculosis - immunology
γ-Interferon
title Diagnostic benefits of adding EspC, EspF and Rv2348-B to the QuantiFERON Gold In-tube antigen combination
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