新生儿对严重组合免疫缺陷的筛查

Chiara Azzari
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引用次数: 0

摘要

严重联合免疫缺陷症(SCID)是一组罕见的致命性疾病,在生命早期得到诊断是可以治愈的。新生儿SCID筛查的不同方法已被提出,从白细胞计数(便宜,但与低敏感性和特异性相关)到il - 7血浆水平评估(SCID患者通常增加)。最近,定量分析TRECs (VDJ重组的副产物)已被建议作为新生儿筛查的候选方法。TRECs分析具有良好的敏感性和特异性,但人均成本较高。串联质谱法绝对不昂贵,但目前它的使用仅限于少数SCID的变体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lo screening neonatale delle immunodeficienze severe combinate

Severe combined immunodeficiency (SCID) is a group of letal rare disease, which can be cured when diagnosed very early in the life. Different methods have been suggested for neonatal screening of SCID, from white blood cell count (inexpensive, but associated to low sensitivity and specificity), to IL7 plasma level evaluation (normally increased in SCID patients). Recently quantitative analysis of TRECs (by-product of VDJ recombination) has been suggested as the candidate method for neonatal screening. TRECs analysis has good sensitivity and specificity but it still has a high cost per patient. Tandem mass spectrometry is absolutely not-expensive but its use is, at present, limited to few variants of SCID.

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