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21三体综合征新生儿的TREC和KREC水平降低。

Decreased TREC and KREC levels in newborns with trisomy 21.

作者信息

Marakhonov Andrey, Mukhina Anna, Vlasova Elena, Efimova Irina, Balinova Natalya, Rodina Yulia, Pershin Dmitry, Markova Zhanna, Minzhenkova Marina, Shilova Nadezhda, Mudaeva Dzhaina, Saydaeva Djamila, Irbaieva Taisiya, Matulevich Svetlana, Belyashova Elena, Yakubovskiy Grigoriy, Tebieva Inna, Gabisova Yulia, Ikaev Murat, Irinina Nataliya, Nurgalieva Liya, Saifullina Elena, Belyaeva Tatiana, Romanova Olga, Voronin Sergey, Zinchenko Rena, Shcherbina Anna, Kutsev Sergey

机构信息

Research Centre for Medical Genetics, Moscow, Russia.

Oncology and Immunology, Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Moscow, Russia.

出版信息

Front Pediatr. 2024 Oct 17;12:1468635. doi: 10.3389/fped.2024.1468635. eCollection 2024.

Abstract

Newborn screening (NBS) for severe combined immunodeficiency (SCID) has been widely implemented to enable early detection and intervention. Trisomy 21, commonly known as Down syndrome (DS), poses unique challenges in NBS due to its frequent association with T and/or B cell lymphopenia. The pilot NBS screening program recently conducted in Russia was aimed to identify both severe T and B cell deficiencies by measuring TREC and KREC. This study aims to evaluate the incidence of DS in newborns who participated in the pilot program, assess their TREC and KREC values, and determine the proportion of DS newborns potentially identifiable through T/B lymphopenia NBS. We conducted a retrospective analysis of the data obtained during the pilot NBS program, involving 202,908 newborns from eight regions of Russia. The study identified 157 patients with trisomy 21 among the screened cohort, resulting in a DS birth prevalence of 1:1,284. Median TREC and KREC values did not significantly differ between full-term and pre-term subgroups of DS patients. TREC values in DS newborns were decreased and comparable to those of the extremely preterm newborns. DS newborns also demonstrated significant differences in KREC values as compared to the general cohort regardless of gestational age. Our data suggests abnormalities of T- and B-cell lineages development and requires further investigation. This article highlights the need for increased awareness of the intrinsic immunological defects associated with DS. The findings underscore the importance of continued follow-up and comprehensive support by healthcare teams for individuals with DS.

摘要

针对重症联合免疫缺陷(SCID)的新生儿筛查(NBS)已广泛实施,以实现早期检测和干预。21三体综合征,通常称为唐氏综合征(DS),由于其频繁与T和/或B细胞淋巴细胞减少相关,在NBS中带来了独特的挑战。最近在俄罗斯开展的试点NBS筛查项目旨在通过测量TREC和KREC来识别严重的T和B细胞缺陷。本研究旨在评估参与试点项目的新生儿中DS的发病率,评估他们的TREC和KREC值,并确定通过T/B淋巴细胞减少NBS可能识别出的DS新生儿比例。我们对试点NBS项目期间获得的数据进行了回顾性分析,该项目涉及来自俄罗斯八个地区的202,908名新生儿。研究在筛查队列中确定了157例21三体综合征患者,DS的出生患病率为1:1,284。DS患者的足月和早产亚组之间的TREC和KREC中位数无显著差异。DS新生儿的TREC值降低,与极早产新生儿相当。无论胎龄如何,DS新生儿与总体队列相比,KREC值也存在显著差异。我们的数据表明T和B细胞谱系发育异常,需要进一步研究。本文强调需要提高对与DS相关的内在免疫缺陷的认识。研究结果强调了医疗团队对DS患者持续随访和全面支持的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6950/11526121/944ca10b3ce3/fped-12-1468635-g001.jpg

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