Table 2.
Innate Immunity [42,43,44,45,46] |
---|
Stimulation of the production by neutrophils, macrophages, and cells liningepithelial surfaces of CAMP and DEFB4 |
Increase in the antimicrobial effect against pathogens |
Induction of the intracellular pathogen recognition receptor NOD2 |
Enhancement in transcription of CAMP and DEFB4 |
Suppression of hepcidin antimicrobial peptide expression |
Reduction in ferroportin-mediated export of intracellular iron |
Adaptive Immunity [47] |
Differentiation and maturation of DC |
Expression on monocytes of molecules involved in antigen capture |
Reduction in pro-inflammatory Th1 response |
Increase anti-inflammatory Th2 response |
Increase in T regulatory cells |
Limitation of the number of CD4+ T cells |
CAMP, cathelicidin; DEFB4, β-defensin 2; DC, dendritic cells (DC).