Interleukin-22 mediates early host defense against attaching and effacing bacterial pathogens

被引:1520
作者
Zheng, Yan [1 ]
Valdez, Patricia A. [1 ]
Danilenko, Dimitry M. [2 ]
Hu, Yan [1 ]
Sa, Susan M. [2 ]
Gong, Qian [1 ]
Abbas, Alexander R. [3 ]
Modrusan, Zora [4 ]
Ghilardi, Nico [4 ]
de Sauvage, Frederic J. [4 ]
Ouyang, Wenjun [1 ]
机构
[1] Genentech Inc, Dept Immunol, San Francisco, CA 94080 USA
[2] Genentech Inc, Dept Pathol, San Francisco, CA 94080 USA
[3] Genentech Inc, Dept Bioinformat, San Francisco, CA 94080 USA
[4] Genentech Inc, Dept Mol Biol, San Francisco, CA 94080 USA
关键词
D O I
10.1038/nm1720
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Infections by attaching and effacing (A/E) bacterial pathogens, such as Escherichia coli O157:H7, pose a serious threat to public health. Using a mouse A/E pathogen, Citrobacter rodentium, we show that interleukin-22 (IL-22) has a crucial role in the early phase of host defense against C. rodentium. Infection of IL-22 knockout mice results in increased intestinal epithelial damage, systemic bacterial burden and mortality. We also find that IL-23 is required for the early induction of IL-22 during C. rodentium infection, and adaptive immunity is not essential for the protective role of IL-22 in this model. Instead, IL-22 is required for the direct induction of the Reg family of antimicrobial proteins, including RegIII beta and RegIII gamma, in colonic epithelial cells. Exogenous mouse or human RegIII gamma substantially improves survival of IL-22 knockout mice after C. rodentium infection. Together, our data identify a new innate immune function for IL-22 in regulating early defense mechanisms against A/E bacterial pathogens.
引用
收藏
页码:282 / 289
页数:8
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