WSX-1 is required for resistance to Trypanosoma cruzi infection by regulation of proinflammatory cytokine production

被引:239
作者
Hamano, S
Himeno, K
Miyazaki, Y
Ishii, K
Yamanaka, A
Takeda, A
Zhang, M
Hisaeda, H
Mak, TW
Yoshimura, A
Yoshida, H [1 ]
机构
[1] Kyushu Univ, Med Inst Bioregulat, Div Mol & Cellular Immunol, Fukuoka 8128582, Japan
[2] Univ Toronto, Ontario Canc Inst, Toronto, ON M5G 2C1, Canada
[3] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2C1, Canada
[4] Univ Toronto, Dept Immunol, Toronto, ON M5G 2C1, Canada
[5] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3330012, Japan
[6] Kyushu Univ, Fac Med Sci, Dept Parasitol, Fukuoka 8128582, Japan
关键词
D O I
10.1016/S1074-7613(03)00298-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
WSX-1 is a class I cytokine receptor with homology to the IL-12 receptors and is essential for resistance to Leishmania major infection. In the present study, we demonstrated that WSX-1 was also required for resistance to Trypanosoma cruzi. WSX-1(-/-) mice exhibited prolonged parasitemia, severe liver injury, and increased mortality over wild-type mice. WSX-1(-/-) splenocytes produced enhanced levels of Th2 cytokines, which were responsible for the prolonged parasitemia. Massive necroinflammatory lesions were observed in the liver of infected WSX-1(-/-) mice, and IFN-gamma that was overproduced in WSX-1(-/-) mice compared with wild-type mice was responsible for the lesions. In addition, vast amounts of various proinflammatory cytokines, including IL-6 and TNF-alpha, were produced by liver mononuclear cells in WSX-1(-/-) mice. Thus, during T. cruzi infection, WSX-1 suppresses liver injury by regulating production of proinflammatory cytokines, while controlling parasitemia by suppression of Th2 responses, demonstrating its novel role as an inhibitory regulator of cytokine production.
引用
收藏
页码:657 / 667
页数:11
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