A deleterious role for Th9/IL-9 in hepatic fibrogenesis

作者:Qin, Shan-yu; Lu, Dong-hong; Guo, Xiao-yun; Luo, Wei; Hu, Bang-li; Huang, Xiao-li; Chen, Mei; Wang, Jia-xu; Ma, Shi-jia; Yang, Xian-wen; Jiang, Hai-xing*; Zhou, You
来源:Scientific Reports, 2016, 6(1): 18694.
DOI:10.1038/srep18694

摘要

helper 9 (Th9) cells, a recently recognized Th cell subset, are involved in autoimmune diseases. We aimed to investigate the role of Th9/interleukin-9 (IL-9) in the pathogenesis of hepatic fibrosis. Th9 and Th17 cells were quantified in chronic hepatitis B (CHB) patients with hepatic fibrosis, HBV-associated liver cirrhosis (LC) patients and healthy controls (HC). The percentages of Th9 and Th17 cells, concentrations of IL-9 and IL-17, as well as expression of IL-17, TNF-alpha, IL-6, IL-4, IL-21, TGF-beta 1 and IFN-gamma were significantly increased in plasma of CHB and LC patients compared with those in HC. Splenic Th9 and Th17 cells, plasma concentrations and liver expression of IL-9 and IL-17A were significantly elevated in mice with hepatic fibrosis compared with controls. Neutralization of IL-9 in mice ameliorated hepatic fibrosis, attenuated the activation of hepatic stellate cells, reduced frequencies of Th9, Th17 and Th1 cells in spleen, and suppressed expression of IL-9, IL-17A, IFN-gamma,TGF-beta 1, IL-6, IL-4 and TNF-alpha in plasma and liver respectively. Our data suggest a deleterious role of Th9/IL-9 in increasing hepatic fibrosis and exacerbating disease endpoints, indicating that Th9/IL9 based immunotherapy may be a promising approach for treating hepatic fibrosis.