SAP controls T cell responses to virus and terminal differentiation of TH2 cells

被引:211
作者
Wu, CB
Nguyen, KB
Pien, GC
Wang, NH
Gullo, C
Howie, D
Sosa, MR
Edwards, MJ
Borrow, P
Satoskar, AR
Sharpe, AH
Biron, CA
Terhorst, C [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Div Immunol, Boston, MA 02115 USA
[2] Brown Univ, Div Biol & Med, Dept Mol Microbiol & Immunol, Providence, RI 02912 USA
[3] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[4] Edward Jenner Inst Vaccine Res, Newbury RG20 7NN, Berks, England
[5] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[6] Harvard Univ, Sch Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/87713
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
SH2DIA, which encodes signaling lymphocyte activation molecule (SLAM)-associated protein (SAP), is altered in patients with X-linked lymphoproliferative disease (XLP), a primary immunodeficiency, SAP-deficient mice infected with lymphocytic choriomeningitis virus had greatly increased numbers of CD8(+) and CD4(+) interferon-gamma -producing spleen and liver cells compared to wild-type mice. The immune responses of SAP-deficient mice to infection with Leishmania major together with in vitro studies showed that activated SAP-deficient T cells had an impaired ability to differentiate into T helper 2 cells,The aberrant immune responses in SAP-deficient mice show that SAP controls several distinct key T cell signal transduction pathways, which explains in pare the complexity of the XLP phenotypes.
引用
收藏
页码:410 / 414
页数:5
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