Table 1.
Diseases | Mechanisms and Functions | References |
---|---|---|
Multiple sclerosis/EAE | IRF7 inhibits the infiltration of macrophages and T cells, decreases the expression of CCL2, CXCL10, IL-1ß, IL17. | (141, 142) |
Rheumatoid arthritis | IRF7 inhibits proinflammatory cytokine, promotes anti-inflamamtory cytokine IL-1ß. | (143) |
Systemic lupus erythematosus (SLE) | IRF7 is a susceptibility locus, TRAP and Gfil prevent susceptibility to SLE by regulating nuclear transport of IRF7. | (106, 110, 144–154) |
Systemic sclerosis( SSc) | The overexpression of IRF7 forms complexes with smad3, mediates the fibrosis. | (43, 155–158) |
Autoimmune pancreatitis(AIP) | The IRF7-IFN-I-IL-33 axis mediates the development of AIP. | (159–162) |
Autoimmune thyroid diseases (AITD) | IRF7 SNP is associated with increased susceptibility to AITD. | (163–165) |
Diabetes | IRF7 interacts with Foxp3/CD8+T, affects the induction of TID, the STAT1-IRF7-MHC I complex axis accelerates the process of TID through IRF7-STAT2 cascade signals and promotes the proliferation of CD8+ T cells. IRF7 interacts with MCP-1 promotes the T2D development. | (166–172) |