25 To determine whether IL30 requires the other subunit, EBI3, to form a heterodimer for maximizing inhibition of IL12 toxicity, we compared the efficacy of IL30 to either EBI3 or IL27. Interestingly, IL30 is more potent

than IL27 or EBI3 in inhibiting IL12-induced toxicity in the liver, including the reduction of the number of liver lesions (Fig. 5A,B) and alanine aminotransferase (ALT) / aspartate aminotransferase (AST) levels (Supporting BEZ235 datasheet Fig. 4), suggesting that IL30 may act independently of IL27. To further this hypothesis, we used EBI3 knockout (EBI3−/−) mice. As expected, IL30 reverses IL12 hepatotoxicity in EBI3−/− mice, whereas reconstitution of IL27 or overexpression of EBI3 does not affect liver toxicity Ferroptosis mutation (Fig. 5A,B). One potential mechanism that explains the protective role of IL30 in the absence of EBI3 could be that IL30 competes or is more efficient than IL27 in occupying WSX1, therefore initiating downstream signaling independently of IL27. To confirm this hypothesis, the effect of IL30 on IL12-mediated toxicity was tested in WSX1−/− mice. If IL30 signals through WSX1 and competes with IL27 for signaling, then the lack of WSX1

would demolish the ability of IL30 to inhibit liver toxicity. The same as is found in wildtype mice, IL30 inhibits the number of liver lesions and the amount of the liver transaminases released in the serum in WSX1−/− mice (Fig. 5A,B; Supporting Fig. 4). These results confirm that the hepatoprotective selleck kinase inhibitor role of IL30 is independent of the IL27 pathway. Because IL12 induces IL30 expression by way of IFN-γ, we then asked whether IL30 might inhibit IL12 toxicity by way of inhibition of IFN-γ expression. As such, we determined whether IL30 inhibits IL12-mediated IFN-γ expression

in wildtype, EBI3−/−, and WSX1−/− mice. As expected, IL30 inhibits circulating IFN-γ levels (Fig. 6A). This observation once more confirms the IL27- and WSX1-independent function of IL30. Of interest here is that the number of lesions induced by IL12 is lower in the EBI3−/− and WSX1−/− when compared with wildtype mice (Fig. 5B), although the level of IL12-mediated IFN-γ induction is heightened in the absence of WSX1 or EBI3. This discrepancy could be explained by the increased induction of IL30 in these mice (Supporting Fig. 5), which counteracts the toxic effect from increased IFN-γ and reduces toxicity in livers. To further confirm that IFN-γ plays a key role in IL12-mediated liver injury and IL30 inhibits IFN-γ expression, both proinflammatory cytokines were coadministered into mice. As expected, coadministration of IL12 and IFN-γ enhanced toxicity of the liver when compared with IL12 alone (Fig. 6B,C), further demonstrating IFN-γ’s role in hepatotoxicity. Meanwhile, the addition of IL30 significantly reduced the number of lesions in the liver (Fig. 6C).