Simian immunodeficiency virus-induced mucosal interleukin-17 deficiency promotes Salmonella dissemination from the gut

被引:450
作者
Raffatellu, Manuela [1 ]
Santos, Renato L. [1 ]
Verhoeven, David E. [1 ]
George, Michael D. [1 ]
Wilson, R. Paul [1 ]
Winter, Sebastian E. [1 ]
Godinez, Ivan [1 ]
Sankaran, Sumathi [1 ]
Paixao, Tatiane A. [1 ]
Gordon, Melita A. [2 ]
Kolls, Jay K. [3 ]
Dandekar, Satya [1 ]
Baumler, Andreas J. [1 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Med Microbiol & Immunol, Davis, CA 95616 USA
[2] Univ Liverpool, Fac Med, Div Gastroenterol, Liverpool L69 3BX, Merseyside, England
[3] Childrens Hosp Pittsburgh, Pittsburgh, PA 15213 USA
关键词
D O I
10.1038/nm1743
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
Salmonella typhimurium causes a localized enteric infection in immunocompetent individuals, whereas HIV- infected individuals develop a life- threatening bacteremia. Here we show that simian immunodeficiency virus (SIV) infection results in depletion of T helper type 17 (T(H)17) cells in the ileal mucosa of rhesus macaques, thereby impairing mucosal barrier functions to S. typhimurium dissemination. In SIV- negative macaques, the gene expression profile induced by S. typhimurium in ligated ileal loops was dominated by T(H)17 responses, including the expression of interleukin- 17 (IL- 17) and IL- 22. T(H)17 cells were markedly depleted in SIV- infected rhesus macaques, resulting in blunted T(H)17 responses to S. typhimurium infection and increased bacterial dissemination. IL- 17 receptor - deficient mice showed increased systemic dissemination of S. typhimurium from the gut, suggesting that IL- 17 deficiency causes defects in mucosal barrier function. We conclude that SIV infection impairs the IL- 17 axis, an arm of the mucosal immune response preventing systemic microbial dissemination from the gastrointestinal tract.
引用
收藏
页码:421 / 428
页数:8
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