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The diagnosis of active and latent tuberculosis remains a challenge. Although a new approach based on detecting Mycobacterium
tuberculosis-specific T-cells has been introduced, it cannot distinguish between latent infection and active disease. The aim of this
study was to evaluate the diagnostic potential of interleukin-2 (IL-2) as biomarker after specific antigen stimulation with PE35 and
PPE68 for the discrimination of active and latent tuberculosis infection (LTBI). The production of IL-2 was measured in the antigenstimulated
whole-blood supernatants following stimulation with recombinant PE35 and PPE68. The discrimination performance
(assessed by the area under ROC curve) for IL-2 following stimulation with recombinant PE35 and PPE68 between LTBI and patients
with active TB were 0.837 [95% confidence interval (CI) 0.72-0.97] for LTBI diagnosis and 0.75 (95% CI 0.63-0.89) for active TB
diagnosis, respectively. Applying the 6.4 pg/mL cut-off for IL-2 induced by PE35 in the present study population resulted in sensitivity
of 78%, specificity of 83%, PPV of 83% and NPV of 78% for the discrimination of active TB and LTBI. In addition, a sensitivity of
81%, specificity of 71%, PPV of 68 and 83% of NPV was reported based on the 4.4 pg/mL cut-off for IL-2 induced by PPE68. This
study confirms IL-2 induced by PE35 and PPE68 as a sensitive and specific biomarker and highlights IL-2 as new promising adjunct
markers for discriminating of LTBI and active TB disease.