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22q11.2 缺失综合征患儿的 T 细胞受体切除环(TREC)水平及其后期疾病特征。

Neonatal Levels of T-cell Receptor Excision Circles (TREC) in Patients with 22q11.2 Deletion Syndrome and Later Disease Features.

机构信息

Department of Pediatric Research, Women and Children's Division, Oslo University Hospital Rikshospitalet, Oslo, Norway,

出版信息

J Clin Immunol. 2015 May;35(4):408-15. doi: 10.1007/s10875-015-0153-5. Epub 2015 Mar 27.

Abstract

PURPOSE

Newborns with severe T-cell lymphopenia, including those with 22q11.2 deletion syndrome (DS), have low numbers of T-cell receptor excision circles (TRECs). The aim of this study was to determine a possible correlation between neonatal TRECs in 22q11.2DS and the development of different phenotypes to elucidate the prognostic value of TREC in this disease.

METHODS

In this national survey including 46 patients with 22q11.2DS born after 2005, TREC levels were determined using stored newborn screening blood spots on filter cards. Patients were grouped into quartiles according to their TREC values, except the two infants with thymus aplasia.

RESULTS

The two patients with thymic aplasia had no detectable TREC. The rest had no severe clinical immunodeficiency. There was a significant correlation between low TRECs and the proportion of patients with CD3(+)CD4(+)T-cells below the 5th percentile of healthy infants (p = 0.027) as well as the proportion with an abnormal thymus feature either no thymus or remnant thymus as observed during heart surgery (p = 0.022). Significantly lower TRECs (p = 0.019) were found in patients with cardiac defects compared to no such defects. Patients within the lowest quartile of TREC values (<71 TRECs/μL, n = 11) had more frequent severe cardiac defects than the other quartiles (p = 0.010). Eight of these patients in the lowest quartile needed an operation/intervention within two weeks after birth or died because of a cardiac defect.

CONCLUSION

The low TREC values not only correlate with decreased T-cell immunity, but also with the occurrence of heart defects in the patients.

摘要

目的

严重 T 细胞淋巴细胞减少症新生儿,包括 22q11.2 缺失综合征(DS)患者,其 T 细胞受体切除环(TREC)数量较低。本研究旨在确定 22q11.2DS 新生儿 TRECs 与不同表型的发展之间是否存在可能的相关性,以阐明该疾病中 TRECs 的预后价值。

方法

本研究为全国性调查,纳入 2005 年后出生的 46 例 22q11.2DS 患者,使用储存在滤纸片上的新生儿筛查血斑来测定 TRECs 水平。除了两名患有胸腺发育不全的婴儿外,患者根据 TRECs 值分为四组。

结果

两名患有胸腺发育不全的婴儿无法检测到 TRECs。其余患者均无严重的临床免疫缺陷。低 TRECs 与 CD3(+)CD4(+)T 细胞比例低于健康婴儿第 5 百分位数的患者比例(p=0.027)以及在心脏手术期间观察到的异常胸腺特征(无胸腺或残留胸腺)的患者比例显著相关(p=0.022)。与无心脏缺陷的患者相比,心脏缺陷患者的 TRECs 显著降低(p=0.019)。TREC 值最低四分位数(<71 TRECs/μL,n=11)的患者比其他四分位数更频繁出现严重的心脏缺陷(p=0.010)。这 11 名最低四分位数的患者中有 8 人在出生后两周内需要手术/干预,或因心脏缺陷而死亡。

结论

低 TRECs 值不仅与 T 细胞免疫功能下降相关,而且与患者心脏缺陷的发生相关。

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