Interleukin-9 blockage reduces early hepatic granuloma formation and fibrosis during Schistosoma japonicum infection in mice
Interleukin-9 blockage reduces early hepatic granuloma formation and fibrosis during Schistosoma japonicum infection in mice
复制标题
白细胞介素 9 阻断可减少小鼠日本血吸虫感染期间的早期肝肉芽肿形成和纤维化
DOI:
10.1111/imm.13111
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发表时间:
2019
期刊:
影响因子:
6.4
通讯作者:
Xia Chaoming
中科院分区:
文献类型:
--
作者:
Zhan Tingzheng;Ma Huihui;Jiang Suqin;Zhong Zirong;Wang Xiaoli;Li Chunxiang;Yu Dan;Liu Lei;Xu Jing;Xia Chaoming
Hepatic fibrosis induced by schistosomes is regulated by a complex network of cytokines. T helper type 9 (Th9) cells are a new type of effector T helper cells, which mainly secrete the specific cytokine interleukin‐9 (IL‐9). Interleukin‐9 has been shown to contribute to liver fibrosis in patients with chronic hepatitis B and in a mouse model due to carbon tetrachloride. However, the role of IL‐9 in schistosomiasis fibrosis remains unknown. In this study, we investigated the roles of IL‐9 in schistosomiasis throughin vivoandin vitrostudies. Thein vivostudies found that neutralization of IL‐9 reduced liver granulomatous inflammation and collagen deposition around parasite eggs. Thein vitrostudies found that the treatment of primary hepatic stellate cells with IL‐9 induced a significant increase of collagen andα‐smooth‐muscle actin. Moreover, we also described the dynamics and relevance of IL‐9 and IL‐4 in mice infected withSchistosoma japonicum. We found that IL‐9 might appear more quickly and at higher levels than IL‐4. Hence, our findings indicated that IL‐9 might play a role in regulating hepatic fibrosis in early‐stage schistosomiasis and become a promising approach for regulating hepatic fibrosis caused byS.japonicum.