Long-Term Follow-up of STAT5B Deficiency in Three Argentinian Patients: Clinical and Immunological Features

被引:36
|
作者
Bezrodnik, Liliana [1 ]
Di Giovanni, Daniela [1 ]
Soledad Caldirola, Maria [1 ]
Esnaola Azcoiti, Maria [1 ]
Torgerson, Troy [2 ,3 ,4 ]
Isabel Gaillard, Maria [1 ]
机构
[1] Dr Ricardo Gutierrez Childrens Hosp, RA-1330 Gallo, Capital Federal, Argentina
[2] Seattle Childrens Res Inst, Seattle, WA USA
[3] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[4] Seattle Childrens Res Inst, Ctr Immun & Immunotherapies, Diagnost Immunol Lab, Seattle, WA USA
关键词
Stat5B; primary immunodeficiency; growth hormone; lymphocytic interstitial pneumonitis; dysregulatory syndrome; regulatory T cells; GROWTH-HORMONE INSENSITIVITY; REGULATORY T-CELLS; IMMUNE DYSREGULATION; MUTATION; POLYENDOCRINOPATHY; IMMUNODEFICIENCY; ENTEROPATHY; HOMEOSTASIS; DYSFUNCTION; ACTIVATION;
D O I
10.1007/s10875-015-0145-5
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 signal transducer and activator of transcription (STAT) family of proteins regulate gene transcription in response to a variety of cytokines. STAT5B, in particular, plays an important role in T cells, where it is a key mediator of interleukin-2 (IL-2) induced responses. STAT5B deficiency causes a rare autosomal recessive disorder reported in only a handful of individuals. There are currently ten published cases of STAT5B deficiency, four of which are Argentinians. Aim This is a report of more than 10 years follow up of the clinical and immunological features of three Argentinian STAT5B deficient patients. Conclusion More than a decade of follow-up demonstrates that STAT5B deficiency is associated with various clinical pathologies that cause significant morbidity. Early diagnosis is critical for the prevention and improvement of clinical outcomes for STAT5B deficient patients.
引用
收藏
页码:264 / 272
页数:9
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