Nonsevere combined immunodeficiency T-cell lymphopenia identified through newborn screening

被引:8
|
作者
Patrawala, Meera [1 ]
Kobrynski, Lisa [1 ]
机构
[1] Emory Univ, Sch Med, Dept Pediat, Allergy Immunol Sect,Childrens Healthcare Atlanta, Atlanta, GA 30322 USA
关键词
newborn screening; T-cell lymphopenia; T-cell receptor excision circle; TERMINAL DELETION; JACOBSEN SYNDROME; TREC; TRANSPLANTATION; MECHANISMS; DISEASE; CHARGE; 11Q;
D O I
10.1097/ACI.0000000000000586
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose of review Although severe combined immunodeficiency (SCID) is the primary target condition for newborn screening (NBS), over 25 secondary targets, conditions other than SCID, have been identified. There is no standard method for evaluating neonates with non-SCID T-cell lymphopenia (TCL) and no standard approaches to treatment. We will describe these conditions and discuss recommendations for evaluating and follow-up of non-SCID TCL detected by NBS. Recent findings The birth prevalence of non-SCID TCL detected through SCID NBS is higher than SCID and can be a burden on NBS programs. We will present some publications discussing outcomes and comorbidities in these patients. NBS for SCID has been very successful in identifying infants with SCID at birth to institute early life saving therapies. TCL due to other conditions can cause significant immune deficiency and treatment is dependent on the cause of the defect, as well as the magnitude of the immunodeficiency. Data collection from NBS programs should include assessment of various therapies and clinical outcomes. Better systems for recording long-term outcomes of SCID NBS including both SCID and non-SCID conditions should become a priority for NBS programs. This will help to advance the goal of NBS programs: improve outcomes in the most cost-effective manner.
引用
收藏
页码:586 / 593
页数:8
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