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. 2021 Dec 2;10(12):1260. doi: 10.3390/biology10121260

Table 2.

Different assay performance of UCP-LFAs in high-dose and low-dose MTB infected rhesus macaques.

(a). AUCs of high-dose MTB infected RMs (n = 24)
wk3 wk6 wk9 wk12
SAA1 0.903 0.951 0.894 0.889
IP-10 0.858 0.984 1.000 0.956
IL-6 0.854 0.938 0.955 0.905
3BM 0.948 0.997 0.996 0.968
(b). AUCs of low-dose MTB infected RMs (n = 12)
wk2 wk4 wk6 wk8 wk10 wk12
SAA1 0.531 0.868 0.747 0.763 0.750 0.774
IP-10 0.646 0.944 0.944 0.883 0.870 0.952
IL-6 0.597 0.795 0.799 0.783 0.655 0.571
3BM 0.583 0.8958 0.875 0.858 0.964 0.821

SAA1, IP-10 and IL-6 levels were measured by UCP-LFA before and at several time points after (a) high-dose (500 CFU, n = 24) or (b) low-dose (15 CFU, n = 12) MTB Erdman infection. The ability to distinguish pre from postinfection states was evaluated per marker and for the 3BM (3 biomarkers) signature by ROC curve analysis over time, and the corresponding Area Under the Curve (AUC) was determined (ROC-AUC). Values above the cutoff per biomarker (described in Table 1b) were considered positive. 3BM signature was generated using the sum of all positive tests results from the individual markers. wk, week; RM, rhesus macaque; BM, biomarker.