Functional T Cell Immunodeficiencies (with T Cells Present)

被引:41
|
作者
Notarangelo, Luigi D. [1 ,2 ]
机构
[1] Boston Childrens Hosp, Div Immunol, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Boston, MA 02115 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 31 | 2013年 / 31卷
关键词
intracellular signaling; immune dysregulation; lymphocytes; immune homeostasis; TEC-FAMILY KINASES; AUTOSOMAL-RECESSIVE FORM; PROTEIN-TYROSINE KINASE; CALCIUM SENSORS STIM1; OPERATED CA2+ ENTRY; EPSTEIN-BARR-VIRUS; HYPER-IGE SYNDROME; THYMOCYTE DEVELOPMENT; DOCK8; DEFICIENCY; PERIPHERAL-BLOOD;
D O I
10.1146/annurev-immunol-032712-095927
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Severe combined immunodeficiency (SCID) comprises a group of disorders that are fatal owing to genetic defects that abrogate T cell development. Numerous related defects have recently been identified that allow T cell development but that compromise T cell function by affecting proximal or distal steps in intracellular signaling. These functional T cell immunodeficiencies are characterized by immune dysregulation and increased risk of malignancies, in addition to infections. The study of patients with these rare conditions, and of corresponding animal models, illustrates the importance of intracellular signaling to maintain T cell homeostasis.
引用
收藏
页码:195 / 225
页数:31
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