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. Author manuscript; available in PMC: 2020 Oct 15.
Published in final edited form as: J Immunol. 2019 Sep 20;203(8):2194–2209. doi: 10.4049/jimmunol.1900230

Table IV:

Top 20 upstream regulators not associated with Type I IFN, as based on impact of T-cell depletion on –log (adjusted p-values)

CD4 top upstream regulators CD8 top upstream regulators
Regulator Change in –(log p) with CD4 depletion Regulator Change in –(log p) with CD8 depletion
IFNG 40.37 TNF 11.03
LPS 35.31 IL27 7.98
Poly I:C RNA 34.72 IL10RA 5.69
CD40LG 28.06 NKX2 5.47
TNF 24.27 CpG nucleotide 5.30
TLR4 23.69 IFNG 5.28
STAT3 23.07 CREBBP 5.12
TLR3 21.19 NLRC5 5.02
TICAM 21.04 fluticasone 4.92
CD40 20.32 IL6 4.88
IL27 20.03 IL27RA 4.78
TLR9 19.49 PARP1 4.54
TLR7 19.21 MAPK1 3.90
STAT6 17.74 Mir-21 3.86
TRIM24 17.71 IL1RN 3.84
IL10 17.38 SOCS1 3.74
IL1B 17.12 STAT5A 3.67
TCR 16.94 GATA2 3.11
BTK 16.75 SMARCA4 3.07
NIKX2–3 16.35 KIT 2.97

Top 20 Mtb-induced upstream regulators of BAL cell gene expression not associated with Type I interferons. Results are expressed in terms of the decrease in significance (-log p-value) following depletion of CD4+ or CD8+ T cells. As shown, with the exceptions of IFNγ, TNFα, and IL-27 (indicated in bold) the lists do not overlap; further, the reductions in significance of the various regulations is far greater following depletion of CD4+ as compared to CD8+ T-cells.