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. 2018 Feb 20;9:298. doi: 10.3389/fimmu.2018.00298

Table 1.

Comparison of H3K4me3-related GO-terms in β-trained monocytes and monocytes of SLE patients.

Go-term β-Glucan-induced trained immunity
SLE
p-Value p-Value
M1 Sugar binding 3.9E−2 0.72
M2 Carboxylic acid metabolic process 7.9E−5 4.5E−2
Cellular ketone metabolic process 1.3E−4 0.32
Oxidoreductase 1.4E−3 4.3E−2
Lipid metabolic process 5.4E−6 3.2E−3
M3 Signal transducer activity 2.4E−3 3.7E−2
Receptor activity 2.1E−2 1.2E−2
M4 Cofactor binding 3.5E−3 0.16
M5 Immune response 3.00E−19 3.7E−2
Response to wounding 5.00E−17 1.3E−2
Chemotaxis 5.2E−7 0.79
Cytokine activity 8.00E−12 5.3E−2
Chemokine activity 3.7E−9 9.3E−2

H3K4me3 modulations were related to gene promoter site. Related GO-terms of the major epigenetically modulated promoter sites in in vitro β-glucan-trained monocytes, defined as M clusters (10), were compared with the same GO-terms in monocytes of SLE patients (78) and adjusted p-values are shown.