Abstract

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.

Highlights

  • Interferon (IFN)-γ release assays (IGRAs) are used to diagnose latent tuberculosis (TB) infection (LTBI)

  • Considering the overall study population, antigen-specific IFN-γ levels detected in the QFN-G-IT and in-house QFN tubes was significantly higher in the Qiagen tube than in the in-house (p < 0.05) due to differences in the active TB group (Fig. 1A,C)

  • Healthy controls had a significantly lower amount of antigen-specific IFN-γ production compared to active TB and LTBI (p < 0.0001) but no statistically significant differences were detected between LTBI and active TB samples (p > 0.05) (Fig. 1C)

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Summary

Introduction

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). After whole blood stimulation and specific response analysis, the most frequently recognized antigens by active TB and LTBI individuals were ESAT-6, CFP-10 and EspC followed by Rv2348-B and EspF. Recognition of these antigens was determined as the ability to produce more than 50 pg/ml of IFN-γ after antigen-specific stimulation. EspC recognized cases that were not detected by CFP-10 or ESAT-6 (11% and 12%, respectively)

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