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. 2019 Nov 14;10:2612. doi: 10.3389/fimmu.2019.02612

Table 3E.

Twenty new disease group-specific and 12 shared (more than 4 groups of diseases) Mφ reprogramming pathways have been identified in eight groups of 34 diseases and tumors.

A. Specific pathways (upregulated except #; unique for each group of diseases)
Autoimmune diseases Role of JAK1 and JAK3 in γc Cytokine Signaling
CNTF Signaling
Thrombopoietin Signaling
EGF Signaling
GM-CSF Signaling
Cardiovascular diseases IL-17A Signaling*
NRF2-Mediated Oxidative Stress Response
Parkinson's Signaling
Digestive inflammatory disease VDR/RXR Activation#
FXR/RXR Activation#
Infection disease Cyclins and Cell Cycle Regulation
Cell Cycle Regulation by BTG Family Proteins
Estrogen-mediated S-phase Entry
Role of CHK Proteins in Cell Cycle Checkpoint Control
Metabolic diseases Notch Signaling
Respiratory disease Adrenomedullin signaling pathway
Digestive tumors Oncostatin M Signaling
Cancer Drug Resistance By Drug Efflux (#, downregulated)
Other tumors IL-15 Production
Role of PKR in Interferon Induction and Response
B. Shared pathways (upregulated and shared by more than four major disease groups)
Altered T Cell and B Cell Signaling in Autoimmune Disease
Differential Regulation of Cytokine Production in Macrophages and T Heiper Cells by IL-17A and IL-17F
Neuroinflammation Signaling Pathway
Graft-vs.-Host Disease Signaling
IL-10 Signaling
Role of Cytokines in Mediating Communication between Immune Cells
Communication between Innate and Adaptive Immune Cells
Role of Hypercytokinemia/Hyperchemokinemia in the Pathogenesis of Disease
FLT3 Signaling in Hematopoietic Progenitor Cells
ERK/MAPK Signaling
JAK/Stat Signaling
Role of JAK1, JAK2 and TYK2 in Interferon Signaling
*

Some of the pathway names were simplified to avoid potential confusion.