Innate IL-17 and IL-22 responses to enteric bacterial pathogens

被引:84
|
作者
Rubino, Stephen J. [1 ]
Geddes, Kaoru [2 ]
Girardin, Stephen E. [1 ]
机构
[1] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M6G 2T6, Canada
[2] Univ Toronto, Dept Immunol, Toronto, ON M6G 2T6, Canada
关键词
ROR-GAMMA-T; INDUCER-LIKE CELLS; LYMPHOID-CELLS; TH17; RESPONSES; HOST-DEFENSE; SEROTYPE TYPHIMURIUM; IMMUNE RECOGNITION; T(H)17 CELLS; DIFFERENTIATION; INFECTION;
D O I
10.1016/j.it.2012.01.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
With the identification of T helper (Th)17 cells, a specific subset of CD4 T cells expressing interleukin (IL)-17 and IL-22, research on the function of these cytokines initially largely focused on traditional adaptive immune responses. However, IL-17 and IL-22 enhance basic innate barrier defenses at mucosal surfaces, such as antimicrobial peptide production and neutrophil recruitment; both events that occur rapidly and precede adaptive phase immunity. At the intestinal mucosal surface, it is now clear that innate lymphoid cells are also important sources of IL-17 and IL-22 during early phases of infection. Here, we discuss the function of innate IL-17- and IL-22-producing lymphocytes during enteric bacterial infection and their regulation by the intestinal microbiota, Toll-like receptors (TLRs) and Nod-like receptors (NLRs).
引用
收藏
页码:112 / 118
页数:7
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