In contrast, in the injured or fibrotic liver, HSC exist in a predominantly activated state and acquire proliferative capacity themselves.5 We hypothesize that HSC activated in

vivo also up-regulate B7-H4 expression, and then dominate Sirolimus ic50 the liver environment with T cell inhibitory signals leading to attenuation of the immune response. T cell responses can be divided into two major stages: (1) primary and (2) recall responses. Antigen-specific primary T cell responses have been shown in the liver.38 Similarly, T cells activated in the peripheral lymphoid tissues that traffic through the liver have poor survival, earning the liver the reputation as a graveyard for activated T cells.39 It has been shown that the coinhibitory molecule B7-H1 expressed on hepatocytes promotes priming but inhibits recall T cell responses.40 In contrast, we report here that B7-H4 on AHSC inhibits both priming and recall CD8+ T cell responses. Inhibiting https://www.selleckchem.com/products/LBH-589.html T cell responses at different stages highlights the key role of HSC in modulating intrahepatic immunity in fibrosis. Here we provide evidence that B7-H4 expression on AHSC-induced T cell inactivation or anergy that could be reversed

by exogenous IL-2. The rescue mechanism from B7-H4 is similar to B7-H1-mediated T cell inhibition because the B7-H1 (PD-L1)-PD-1 inhibitory pathway can also be overcome by provision of exogenous IL-2.41 This may have interesting implications in chronic viral diseases such as HCV

infection, as the inhibitory effects of B7-H4 on T cells may be perpetuated or amplified by a relative deficiency of IL-2.42, 43 Still unknown is the cellular regulation of B7-H4 in AHSC, although our studies are starting to offer some intriguing clues. In tumor macrophages the upregulation of B7-H4 is dependent on IL-6 and IL-10.32 Janus kinase (JAK) Interestingly, AHSC also secrete IL-6; however, whereas QHSC can be isolated from IL-6 knockout mice, these cells do not seem to proliferate or transition to an activated state (data not shown). Altogether, it will be of further interest to investigate whether B7-H4 expression on HSC results in, is coincidental with, or is a consequence of HSC proliferation and activation. In summary, our results demonstrate that AHSC inhibit T cell responses in a B7-H4-dependent manner. In the tumor microenvironment, B7-H4 attenuates T cell responses and the tumors use this mechanism to evade the T cell immunity. In the present study, our results suggest that AHSC proliferate, perpetuate fibrosis, and inhibit intrahepatic T cell immunity. AHSC expressed B7-H4 provides a novel link between liver fibrosis and impaired intrahepatic immunity and highlights the potential importance of targeting interventions toward the AHSC in hepatotropic infections such as HCV.