Intestinal bacteria induce TSLP to promote mutualistic T-cell responses

被引:59
作者
Mosconi, I. [1 ,2 ]
Geuking, M. B. [3 ]
Zaiss, M. M. [1 ,2 ]
Massacand, J. C. [1 ,2 ]
Aschwanden, C. [1 ,2 ]
Chung, C. K. C. Kwong [3 ]
McCoy, K. D. [3 ]
Harris, N. L. [1 ,2 ]
机构
[1] Ecole Polytech Fed Lausanne, Swiss Vaccine Res Inst, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Global Hlth Inst, CH-1015 Lausanne, Switzerland
[3] Univ Bern, Inselspital, Maurice Muller Labs, Univ Klin Viszerale Chirurg & Med,DKF,Univ Hosp, CH-3010 Bern, Switzerland
关键词
THYMIC STROMAL LYMPHOPOIETIN; HUMAN EPITHELIAL-CELLS; DENDRITIC CELLS; INFLAMMATION; EXPRESSION; DIFFERENTIATION; MACROPHAGES; HOMEOSTASIS; COMMENSALS; IMMUNITY;
D O I
10.1038/mi.2013.12
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thymic stromal lymphopoietin (TSLP) is constitutively expressed in the intestine and is known to regulate inflammation in models of colitis. We show that steady-state TSLP expression requires intestinal bacteria and has an important role in limiting the expansion of colonic T helper type 17 (Th17) cells. Inappropriate expansion of the colonic Th17 cells occurred in response to an entirely benign intestinal microbiota, as determined following the colonization of germ-free C57BL/6 or TSLPR-/- mice with the altered Schaedler flora (ASF). TSLP-TSLPR (TSLP receptor) interactions also promoted the expansion of colonic Helios(-)Foxp3(+) regulatory T cells, necessary for the control of inappropriate Th17 responses following ASF bacterial colonization. In summary, these data reveal an important role for TSLP-TSLPR signaling in promoting steady-state mutualistic T-cell responses following intestinal bacterial colonization.
引用
收藏
页码:1157 / 1167
页数:11
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