Transcriptional regulation of the mucosal immune system mediated by T-bet

被引:19
|
作者
Powell, N. [1 ,2 ]
Canavan, J. B. [1 ,2 ]
MacDonald, T. T. [2 ]
Lord, G. M. [1 ]
机构
[1] Kings Coll London, Guys Hosp, Natl Inst Hlth Res,Comprehens Biomed Res Ctr, Guys & St Thomas NHS Fdn Trust, London WC2R 2LS, England
[2] Barts & London Queen Marys Sch Med & Dent, Blizard Inst Cell & Mol Sci, Ctr Immunol & Infect Dis, London, England
基金
美国国家卫生研究院; 英国惠康基金; 英国医学研究理事会;
关键词
VERSUS-HOST-DISEASE; INFLAMMATORY-BOWEL-DISEASE; HELPER TYPE-1 CELLS; INTERFERON-GAMMA; IFN-GAMMA; CROHNS-DISEASE; CELIAC-DISEASE; ULCERATIVE-COLITIS; GENE-EXPRESSION; DENDRITIC CELLS;
D O I
10.1038/mi.2010.53
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune system faces the arduous task of defending the mucosal surfaces from invading pathogens, but must simultaneously repress responses against commensal organisms and other inert antigens that are abundant in the external environment, as inappropriate immune activation might expose the host to increased risk of autoimmunity. The behavior of individual immune cells is governed by the expression of transcription factors that are responsible for switching immune response genes on and off. T-bet (T-box expressed in T cells) has emerged as one of the key transcription factors responsible for controlling the fate of both innate and adaptive immune cells, and its expression in different immune cells found at mucosal surfaces is capable of dictating the critical balance between permitting robust host immunity and limiting susceptibility to autoimmunity and allergy.
引用
收藏
页码:567 / 577
页数:11
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