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

Journal of Inherited Metabolic Disease - Tập 33 - Trang 273-281 - 2010
Anne Marie Comeau1, Jaime E. Hale1, Sung-Yun Pai2,3, Francisco A. Bonilla2, Luigi D. Notarangelo2, Mark S. Pasternack4, H. Cody Meissner5, Ellen Rae Cooper6, Alfred DeMaria7, Inderneel Sahai1, Roger B. Eaton1
1New England Newborn Screening Program, UMass Medical School, Jamaica Plain, USA
2Children’s Hospital, Boston, USA
3Dana-Farber Cancer Institute, Boston, USA
4Massachusetts General Hospital, Boston, USA
5Tufts Medical Center, Boston, USA
6Boston Medical Center, Boston, USA
7Massachusetts Department of Public Health, Boston, USA

Tóm tắt

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.

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