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回顾性分析纽约新生儿筛查严重联合免疫缺陷转诊中心。

Retrospective Analysis of a New York Newborn Screen Severe Combined Immunodeficiency Referral Center.

机构信息

Department of Pediatrics, Division of Allergy and Immunology, Montefiore Medical Center, 1525 Blondell Ave, Bronx, NY, 10461, USA.

出版信息

J Clin Immunol. 2020 Apr;40(3):456-465. doi: 10.1007/s10875-020-00757-y. Epub 2020 Jan 29.

Abstract

In 2010, the New York State (NYS) Newborn Screen (NBS) Program added the T cell receptor excision circle (TREC) assay to screen for severe combined immunodeficiency disorder (SCID). The objective of this study was to perform a retrospective chart review of 199 infants referred to a single institution for abnormal TREC on NYS NBS between 2010 and 2017. Statistical analysis included analysis of variance, logistic regression models, chi-square, and linear mixed models. One hundred ninety-nine infants were found to have a TREC value of fewer than 200 copies/μL on NYS NBS. Infants were stratified as primary immunodeficiency (PID) (n = 54), immunocompetent (n = 133), lost to follow-up (n = 8), or deceased (n = 4). PID included SCID (n = 3), DiGeorge (n = 6), idiopathic lymphopenia (IL) (n = 44), and other syndromes associated with lymphopenia (n = 3). The 3 SCID cases were identified and brought to treatment, although all experienced significant infections. The study population was found to be predominately non-Hispanic, African American, and male. There was a difference in the average TREC values among those with immunocompetence (83 copies/μL), IL (81 copies/μL), and PID (40 copies/μL) (p < 0.05). On follow-up of 40 patients with IL, patients typically did not have severe infections during first few years of life. This study demonstrates that TREC value can be used to stratify infants for further confirmatory testing to exclude PID. Risk factors, such as stressful prenatal/postnatal conditions, prematurity, race, and sex may affect TREC value but cannot explain all causes of lymphopenia. This study may assist providers in risk stratifying the likelihood of PID with an abnormal TREC and determining the extent of the initial work up that is necessary at the time of a newborn's presentation.

摘要

2010 年,纽约州(NYS)新生儿筛查(NBS)计划增加 T 细胞受体切除环(TREC)检测,以筛查严重联合免疫缺陷障碍(SCID)。本研究的目的是对 2010 年至 2017 年间在单一机构因 NYS NBS 上 TREC 异常而被转介的 199 名婴儿进行回顾性图表审查。统计分析包括方差分析、逻辑回归模型、卡方检验和线性混合模型。在 NYS NBS 上,发现 199 名婴儿的 TREC 值少于 200 拷贝/μL。婴儿分为原发性免疫缺陷(PID)(n=54)、免疫功能正常(n=133)、失访(n=8)或死亡(n=4)。PID 包括 SCID(n=3)、DiGeorge(n=6)、特发性淋巴细胞减少症(IL)(n=44)和其他与淋巴细胞减少症相关的综合征(n=3)。尽管所有患者均经历了严重感染,但仍确定并治疗了 3 例 SCID 病例。研究人群主要为非西班牙裔、非裔美国人和男性。免疫功能正常(83 拷贝/μL)、IL(81 拷贝/μL)和 PID(40 拷贝/μL)患者的平均 TREC 值存在差异(p<0.05)。在对 40 名 IL 患者进行随访后,患者通常在生命的前几年没有严重感染。本研究表明,TREC 值可用于对婴儿进行分层,以进行进一步的确认性检测以排除 PID。风险因素,如产前/产后压力大、早产、种族和性别可能会影响 TREC 值,但不能解释所有淋巴细胞减少症的原因。本研究可以帮助临床医生对 TREC 异常的婴儿进行 PID 风险分层,并确定在新生儿就诊时进行初始检查的必要性。

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