Deletion of a conserved Il4 silencer impairs T helper type 1-mediated immunity

被引:99
|
作者
Ansel, KM
Greenwald, RJ
Agarwal, S
Bassing, CH
Monticelli, S
Interlandi, J
Djuretic, IM
Lee, DU
Sharpe, AH
Walt, F
Rao, A [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[2] CBR Inst Biomed Res, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[5] Univ Milan, Div Biotechnol Appl Med Sci, I-20133 Milan, Italy
[6] Howard Hughes Med Inst, Boston, MA 02115 USA
[7] Childrens Hosp, Boston, MA 02115 USA
关键词
D O I
10.1038/ni1135
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Helper T cell differentiation involves silencing as well as activation of gene expression. We have identified a conserved silencer of the gene encoding interleukin 4 (Il4) marked by DNase I hypersensitivity (HS IV) and permissive chromatin structure in all helper T cells. Deletion of HS IV increased Il4 and Il13 transcription by naive T cells and led to T helper type 2 skewing in vitro. HS IV controlled Il4 silencing during T helper type 1 differentiation, as HS IV-deficient T helper type 1 cells that expressed interferon-gamma also produced abundant interleukin 4 in vitro and in vivo. Despite mounting a vigorous interferon-gamma response, HS IV-deficient mice were more susceptible to Leishmania major infection than were wild-type littermate control mice, showing a critical function for Il4 silencing in T helper type 1-mediated immunity.
引用
收藏
页码:1251 / 1259
页数:9
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