Cutting edge:: Roles of toll-like receptor 4 and IL-23 in IL-17 expression in response to Klebsiella pneumoniae infection

被引:376
作者
Happel, KI
Zheng, MQ
Young, E
Quinton, LJ
Lockhart, E
Ramsay, AJ
Shellito, JE
Schurr, JR
Bagby, GJ
Nelson, S
Kolls, JK
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Pulm & Crit Care Med Sect, New Orleans, LA 70112 USA
[2] Louisiana State Univ, Hlth Sci Ctr, Alcohol Res Ctr, New Orleans, LA 70112 USA
[3] Louisiana State Univ, Hlth Sci Ctr, Gene Therapy Program, New Orleans, LA 70112 USA
[4] Louisiana State Univ, Hlth Sci Ctr, Dept Physiol, New Orleans, LA 70112 USA
关键词
D O I
10.4049/jimmunol.170.9.4432
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Local production of IL-17 is a significant factor in effective host defense against Gram-negative bacteria. However, the proximal events mediating IL-17 elaboration by Tcells remain unclear. In this study, we show in vivo that intact Toll-like receptor 4 signaling in the lung is required for induction of both the p19 transcript of IL-23 and IL-17 protein elaboration in response to Klebsiella pneumoniae. Although IL-17 is widely considered a CD4(+) T cell product, we also demonstrate significant in vitro IL-17 production by CD8(+) T cells after culture in medium from dendritic cells exposed to these bacteria. The dominant portion of this IL-17-inducing activity for both CD4(+) and CD8(+) T cells is IL-23. These data demonstrate the critical signaling pathway for IL-17 induction in the host response to Gram-negative pulmonary infection and suggest a direct role for IL-23 in CD8(+) T cell IL-17 production.
引用
收藏
页码:4432 / 4436
页数:5
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