Table 3.
Significant PRCCs for inflammation outcomes. List of all the parameters/mechanisms (rows) that have a significant (i.e., p < 10−3) respect to outputs of the model that are directly related to inflammation (columns). See Appendix B for a detailed description of the outcomes analyzed here. A + (or −) indicates a positive (or negative) correlation between the parameter and the outcome. The magnitude/strength of the correlation is given by the number of + (or −). The table recapitulates, whenever possible, the dynamics over time. The outputs with * are selected as examples to illustrate PRCC time courses (see Figure 6). See Appendix A for details on the parameters listed below.
INFLAMMATION (LUNG) | |||||
---|---|---|---|---|---|
PARAMETERS | Total Activated Macrophages | Tot Pet Hot* | Caseation/Necrosis | TNF* | IL10* |
growthRateIntMtb | + early1 | + + early | |||
—chemokine threshold for Tγ recruitment | − − early | − early1 | + + + | ||
τTcyt−CC—chemokine threshold for Tcyt recruitment | − − early | − early then +1 | + + + | ||
τTreg−CC—chemokine threshold for Treg recruitment | −1 | + and then1 | + + early | − − − | |
k2—Naïve CD4 priming | + + | − early1 | +1 | ||
k4—CD4+ T precursor proliferation | + + + | +1 | |||
k13—CD8+ T precursor proliferation | − − − | − − − | + + + early − late | − − − | − − − |
k14—CD8+ T differentiation—effector | +1 | +1 | |||
k11—Naïve CD8 priming | − | + + early − late | −1 | −1 |
These PRCCs are below 0.3, so they are not shown in Figure 6.