共 28 条
Vancomycin-resistant enterococci exploit antibiotic-induced innate immune deficits
被引:513
作者:
Brandl, Katharina
[1
]
Plitas, George
[2
]
Mihu, Coralia N.
[1
]
Ubeda, Carles
[1
]
Jia, Ting
[1
]
Fleisher, Martin
[3
]
Schnabl, Bernd
[4
]
DeMatteo, Ronald P.
[2
]
Pamer, Eric G.
[1
,3
]
机构:
[1] Mem Sloan Kettering Canc Ctr, Infect Dis Serv, Dept Med, Program Immunol,Sloan Kettering Inst, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Hepatobiliary Serv, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Clin Labs, New York, NY 10021 USA
[4] Columbia Univ, Dept Med, New York, NY 10032 USA
来源:
关键词:
D O I:
10.1038/nature07250
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Infection with antibiotic- resistant bacteria, such as vancomycin-resistant Enterococcus ( VRE), is a dangerous and costly complication of broad- spectrum antibiotic therapy(1,2). How antibiotic-mediated elimination of commensal bacteria promotes infection by antibiotic- resistant bacteria is a fertile area for speculation with few defined mechanisms. Here we demonstrate that antibiotic treatment of mice notably downregulates intestinal expression of RegIII gamma ( also known as Reg3g), a secreted C- type lectin that kills Gram- positive bacteria, including VRE. Downregulation of RegIII gamma markedly decreases in vivo killing of VRE in the intestine of antibiotic- treated mice. Stimulation of intestinal Toll- like receptor 4 by oral administration of lipopolysaccharide re-induces RegIII gamma, thereby boosting innate immune resistance of antibiotic-treated mice against VRE. Compromised mucosal innate immune defence, as induced by broad- spectrum antibiotic therapy, can be corrected by selectively stimulating mucosal epithelial Toll- like receptors, providing a potential therapeutic approach to reduce colonization and infection by antibiotic- resistant microbes.
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页码:804 / U8
页数:5
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