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. 2017 Jan 23;17:94. doi: 10.1186/s12879-017-2205-3

Table 2.

Genes having the highest differential expression associated with immune response-related pathways

Gene symbol Description p-value Fold change Associated pathway
S100A8 S100 calcium binding protein A8 1.62E-03 5.934 IL12 signalling and production in macrophages
Production of nitric oxide and reactive oxygen species
MMP9 Matrix metallopeptidase 9 3.07E-03 4.501 IL8 signalling
Leukocyte extravasation signalling
CXCR2 Chemokine (C-X-C motif) receptor 2 3.39E-04 3.401 IL8 signalling
IFITM1 Interferon induced transmembrane protein 1 2.13E-03 2.375 IFN signalling
CCR3 Chemokine (C-C motif) receptor 3 Gene 1.31E-03 1.655 CCR3 signalling in eosinophils
Chemokine signalling
ACTA2 Actin, alpha 2, smooth muscle, aorta 1.77E-03 1.640 Crosstalk between DC and NK cells
Leukocyte extravasation signalling
Integrin signalling
TAB1 Mitogen-activated protein kinase 7 interacting protein 1 2.82E-03 1.276 iNOS signalling
NF-kB signalling
IL10 signalling
Toll-like receptor signalling
CD40LG CD40 ligand 1.41E-03 −1.740 T helper cell differentiation
CD40 signalling
IL12 signalling and production in macrophages
NF-kB signalling
JUN Jun oncogene 4.08E-03 −1.587 CD28 signalling in T helper cells
IL12 signalling and production in macrophages
Production of nitric oxide and reactive oxygen species
T-cell receptor signalling
iNOS signalling
IL8 signalling
IL10 signalling
PLCG1 phospholipase C, gamma 1 5.33E-03 −1.541 iCOS-iCOSL signalling in T-helper cells
PCK signalling in T-lymphocytes
Production of nitric oxide and reactive oxygen species
Phospholipase C signalling
IL15 signalling
PRKCQ protein kinase C, theta 3.14E-03 −1.461 T-cell receptor signalling
CCR5 signalling in macrophages
Natural killer cells signalling
Apoptosis signalling
B-cell receptor signalling
PRKD3 protein kinase D3 6.26E-03 −1.440 Calcium-induced T-lymphocyte apoptosis
LPS stimulated MAPK signalling
CCR5 signalling in macrophages
CCR3 signalling in eosinophils
CXCR4 signalling

The genes analysed here were used when comparing non-immunised mice to mice immunised with a combination of T-cell-epitope-containing peptides (T14 + T15 + T16)