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Table 1.

Gene expression ratios among different groups and their comparisons in PPD-stimulated PBMCs by microarray analysis with P value <0.05.

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Table 2.

Significantly regulated genes in PPD-stimulated PBMCs in pair-wise comparisons with ratio >4.

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Table 2 Expand

Figure 1.

Venn diagram of differentially expressed genes in PBMCs samples following PPD stimulation with P value <0.05 by Student's t-test and fold change >2.0 from: A, Pair-wise comparisons between three study groups (LTBI vs. HC; TB vs. HC; TB vs. LTBI); B, Transcription profiles of tuberculosis infection and active disease (TB&LTBI group vs. HC group; TB group vs. LTBI&HC group).

The total numbers of genes in panel A and B were 506 and 304 respectively.

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Figure 1 Expand

Figure 2.

Unsupervised hierarchical cluster analysis of 506 differentially expressed genes in the pair-wise comparisons.

There are 4 samples in each group. Pseudocolors indicate differential expression (red, up-regulation; green, down-regulation; black, no change in expression).

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Figure 2 Expand

Table 3.

Significantly regulated genes in PPD-stimulated PBMCs unique for tuberculosis infection and active disease with ratio >4.

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Figure 3.

Scatter plots of four discriminatively expressed genes between TB and LTBI by qPCR with P value <0.01.

Horizontal bar, median fold change of each group following PPD stimulation. ** significant difference: 0.001< P value <0.01.

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Figure 3 Expand

Figure 4.

The combination of CXCL10, ATP10A and TLR6 provides the best discrimination between TB patients and LTBI individuals.

The sensitivity and specificity of this three-gene panel was 80% and 89% respectively. 85% individuals were correctly classified. TB group, n = 25; LTBI group, n = 36. Rectangle: internal nodes; Oval and hexagon: terminal nodes showing the number finally determined as TB and LTBI, respectively.

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Table 4.

ROC analysis of selected genes for discrimination between TB group and LTBI group.

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Table 5.

demographic characteristics of the study populations.

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