Guidelines for implementation of population-based newborn screening for severe combined immunodeficiency

被引:51
作者
Comeau, Anne Marie [1 ]
Hale, Jaime E. [1 ]
Pai, Sung-Yun [2 ,3 ]
Bonilla, Francisco A. [2 ]
Notarangelo, Luigi D. [2 ]
Pasternack, Mark S. [4 ]
Meissner, H. Cody [5 ]
Cooper, Ellen Rae [6 ]
DeMaria, Alfred [7 ]
Sahai, Inderneel [1 ]
Eaton, Roger B. [1 ]
机构
[1] UMass Med Sch, New England Newborn Screening Program, Jamaica Plain, MA 02130 USA
[2] Childrens Hosp, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Massachusetts Gen Hosp, Boston, MA 02114 USA
[5] Tufts Med Ctr, Boston, MA USA
[6] Boston Med Ctr, Boston, MA USA
[7] Massachusetts Dept Publ Hlth, Boston, MA USA
关键词
STEM-CELL TRANSPLANTATION; DISEASES; DEFECTS;
D O I
10.1007/s10545-010-9103-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Severe combined immunodeficiency (SCID) is a Primary Immune Deficiency that is under consideration for population-based newborn screening (NBS) by many NBS programs, and has recently been recommended for inclusion in the US uniform panel of newborn screening conditions. A marker of SCID, the T cell receptor excision circle (TREC), is detectable in the newborn dried blood spot using a unique molecular assay as a primary screen. The New England Newborn Screening Program developed and validated a multiplex TREC assay in which both the TREC analyte and an internal control are acquired from a single punch and run in the same reaction. Massachusetts then implemented a statewide pilot SCID NBS program. The authors describe the rationale for a pilot SCID NBS program, a comprehensive strategy for successful implementation, the screening test algorithm, the screening follow-up algorithm and preliminary experience based on statewide screening in the first year. The Massachusetts experience demonstrates that SCID NBS is a program that can be implemented on a population basis with reasonable rates of false positives.
引用
收藏
页码:S273 / S281
页数:9
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