Skip to main content
. 2022 Aug 16;13:949033. doi: 10.3389/fimmu.2022.949033

Table 2.

Immunomodulatory properties of secondary bile acids.

Bile acid Receptor involved Cellular mechanisms Effect on disease References
Innate immunity
DCA Unknown Reduces frequency of tuft cells. Increases biliary neutrophilia Might exacerbate obstructive cholestasis (37)
DCA TGR5 Reduces secretion of IL-1β, IL-6, IL-12p70, and TNF-α; Protects mice against experimental autoimmune uveitis (29)
TUDCA Unknown Reduces surface expression of co-stimulatory molecules (CD40, CD80 and CD86) and MHC-II;
Reduces differentiation of Th1/17
Reduces the expression of antigen presentation machinery in the gut;
Dampens innate inflammatory response to IFN-γ;
Attenuates T-cell activation
Ameliorates intestinal aGvHD disease (28)
isoDCA FXR Modulates dendritic cell function to induce Treg cells Unknown (31)
Adaptive immunity
LCA VDR Inhibits Th1 cell activation in vitro Unknown (32)
3-oxoLCA RORγt Inhibits Th17 cell differentiation in vitro and in vivo Unknown (33)
isoLCA
3-oxoLCA
/isoLCA
RORγt Inhibits Th17 cell differentiation in vitro and in vivo 3-oxoLCA/isoLCA levels reduced in IBD patients (34)
isoalloLCA or
isoalloLCA/3-oxoLCA
Unknown Enhances Treg cell differentiation in vitro or in vivo Unknown (33)
3-oxoLCA
/LCA
VDR Enhances Treg cell differentiation in vivo Ameliorates colitis-induced inflammation in mice (35)