Interleukin-22 mediates early host defense against attaching and effacing bacterial pathogens
Author(s) -
Yan Zheng,
Patricia Valdez,
Dimitry M. Danilenko,
Yan Hu,
M. Logan Susan,
Qihuang Gong,
Alexander R. Abbas,
Zora Modrušan,
Nico Ghilardi,
Frédéric J. de Sauvage,
Wenjun Ouyang
Publication year - 2008
Publication title -
nature medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.536
H-Index - 547
eISSN - 1546-170X
pISSN - 1078-8956
DOI - 10.1038/nm1720
Subject(s) - citrobacter rodentium , biology , microbiology and biotechnology , pathogen , immune system , innate immune system , immunity , immunology , acquired immune system , knockout mouse , enterobacteriaceae , escherichia coli , receptor , gene , biochemistry
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 RegIIIbeta and RegIIIgamma, in colonic epithelial cells. Exogenous mouse or human RegIIIgamma 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.
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