An alternate pathway for type 1 T cell differentiation

被引:26
作者
Feng, CG
Watanabe, S
Maruyama, S
Suzuki, G
Sato, M
Furuta, T
Kojima, S
Taki, S
Asano, Y [1 ]
机构
[1] Ehime Univ, Sch Med, Dept Microbiol & Immunol, Shigenobu, Ehime 7910295, Japan
[2] Natl Inst Radiol Sci, Chiba 2638555, Japan
[3] Inst Med Sci, Dept Parasitol, Tokyo 1080071, Japan
[4] Univ Tokyo, Fac Med, Dept Immunol, Tokyo 1130033, Japan
关键词
IFN-regulatory factor-1; IL-12; Leishmania major; Listeria monocytogenes; Plasmodium berghei; T cell subsets;
D O I
10.1093/intimm/11.8.1185
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IFN-regulatory factor-1 (IRF-1) gene-disrupted mice are defective in IL-12 and IL-18 gene expression at the transcriptional and post-translational level respectively, The mutant mouse mounts a type 2 T cell response upon bacterial infection because of the impaired induction of the IL-12 p40 gene and IFN-gamma-producing type 1 T cells are not induced. We showed here, however, that different pathogens activate a novel pathway for inducing IFN-gamma-producing type 1 T cells even in an IRF-1-deficient mouse. This pathway is independent of IL-12 and IL-18, and is mediated by a distinct function of macrophage lineage cells. Macrophages of the mutant mice fail to activate the IL-12-dependent pathway, but they function in the IL-12-independent pathway in Plasmodium-infected mice. This leads to the hypothesis that the IL-12-independent novel pathway for inducing IFN-gamma-producing T cells is distinct from the classical type 1/type 2 T cell subset differentiation pathway.
引用
收藏
页码:1185 / 1194
页数:10
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