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

被引:0
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作者
K Mark Ansel
Rebecca J Greenwald
Suneet Agarwal
Craig H Bassing
Silvia Monticelli
Jeneen Interlandi
Ivana M Djuretic
Dong U Lee
Arlene H Sharpe
Frederick W Alt
Anjana Rao
机构
[1] Harvard Medical School,Department of Pathology
[2] CBR Institute for Biomedical Research,Department of Pathology
[3] Brigham and Women's Hospital,Department of Genetics
[4] Harvard Medical School,Division of Biotechnologies applied to Medical Sciences
[5] University of Milan,undefined
[6] Howard Hughes Medical Institute and the Children's Hospital,undefined
来源
Nature Immunology | 2004年 / 5卷
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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-γ also produced abundant interleukin 4 in vitro and in vivo. Despite mounting a vigorous interferon-γ 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.
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页码:1251 / 1259
页数:8
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