1). Analysis of 15 normal, uninfected PPD-negative healthy donors revealed no detectable cytokine expressing CD4+ T cells after stimulation with the M. tuberculosis proteins, ESAT-6, Ag85B and 16 kDa (Table 1), thus confirming specificity of intracellular cytokine

staining. Following stimulation with Staphylococcal enterotoxin PF-562271 purchase fragment B (SEB), the proportion of 3+ CD4+ T cells, which produced IFN-γ, IL-2 and TNF-α simultaneously, was very low and did not differ statistically between TB patients and subjects with LTBI (data not shown). Similarly, there was no statistically significant difference in the proportions of 2+ CD4+ T cells (IFN-γ+IL-2+, IFN-γ+TNF-α+ and/or IL-2+TNF-α+) between TB patients and LTBI subjects, but the latter had a significantly FG-4592 purchase lower proportion of 1+ TNF-α+ CD4+ T cells (data not shown). There were a number of differences between TB patients and subjects

with LTBI following stimulation with ESAT-6, Ag85B and the 16-kDa antigen (Fig. 2). Most notably, and in contrast with the previously reported results in chronic viral infections, we found a significantly higher proportion of 3+ CD4+ T cells simultaneously secreting IFN-γ, IL-2 and TNF-α in patients with TB, as compared with LTBI subjects, upon stimulation with any of the three tested M. tuberculosis antigens (Fig. 2). Using a threshold of 0.01% to avoid systematic biases incurred by zeroing negative values (frequency

values <0.01% were set to zero), we found that 3+ CD4+ T cells were detectable in very few LTBI subjects (3/18, 3/18 and 2/18 in response to Ag85B, ESAT-6 and 16 kDa, respectively), but were frequently detected in most TB patients (17/20, 18/20 and 17/20, in response to Ag85B, ESAT-6 Forskolin molecular weight and 16 kDa, respectively; see also Table 1 for comparison). In contrast, LTBI subjects had significantly higher (12- to 15-fold) proportions of 2+ CD4+ T cells that produced IL-2 and IFN-γ (IFN-γ+IL-2+) in response to Ag85B, ESAT-6 and 16 kDa, compared with TB patients (Fig. 2). Moreover, LTBI subjects also had higher proportions of 1+ CD4+ T cells that produced IFN-γ only (IFN-γ+), compared with TB patients, although this difference attained statistical significance only in response to Ag85B. Proportions of any other 2+ or 1+ cytokine secreting CD4+ T-cell subsets did not differ between TB patients and subjects with LTBI after short-term antigen stimulation (Fig. 2). This suggests that the type of response is not determined by the type of antigen, but is rather homogenous against the whole pathogen. It has been previously reported that LTBI individuals with a negative short-term (24 h) IFN-γ release test (IGRA) may turn to a positive response after long-term (6 days) stimulation 21.