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SH2D1A 新变异致 X 连锁淋巴增殖性疾病 1 型患者致死性 HLH:病例报告

英文原题:Fatal HLH in patients with X-linked lymphoproliferative disease 1 due to a novel variant in SH2D1A: case report.

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Fatal HLH in patients with X-linked lymphoproliferative disease 1 due to a novel variant in SH2D1A: case report.

PubMed 2025/05/19(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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研究概要

我们鉴定出一个与 XLP1 中致死性 HLH 相关的新型 SH2D1A 变异。

中文摘要

报告一例与新型SH2D1A变异相关的致死性HLH病例,说明临床表现的多样性及合并感染的潜在作用。

分析3名幼年死于HLH的兄弟的临床和实验室资料。采用576基因IEI检测面板进行遗传学评估(西班牙Veritas,在Jeffrey Modell基金会支持下)。存活的兄弟姐妹及父母在乌克兰LeoGENE科学医学遗传中心接受检测。

一名1岁男童因持续发热4天及肝脾肿大、贫血、中性粒细胞减少、转氨酶升高和低蛋白血症入院。免疫表型显示CD4⁺细胞减少、CD8⁺ T细胞增加、NK细胞计数降低及免疫球蛋白水平升高。患者EBV病毒血症水平高,且SARS-CoV-2血清学标志物阳性。尽管接受强化治疗,HLH仍迅速进展,患者于35天内死亡。基因检测发现一种新型、可能致病的SH2D1A半合子变异c.175delC(p.Thr59Glnfs*22),此前未在受累患者或gnomAD数据库中报告。家族史显示,两名年长的男性兄弟分别在11个月和1岁9个月时死于快速进展的疾病,表现包括发热、肝脾肿大、皮炎、肠炎、贫血、血小板减少和转氨酶升高。第二名患病兄弟EBV血清学检测阳性。该家庭另有一名健康姐妹和一名健康兄弟,二者EBV IgG阳性,但未检出病毒血症。携带者检测证实母亲和姐妹为杂合携带者;两名男性兄弟(其中一名出生仅1个月)未受累。

我们发现一种与XLP1致死性HLH相关的新型SH2D1A变异。结果提示,在EBV暴露前尽早进行遗传学诊断对改善患者结局十分重要。包括SARS-CoV-2在内的合并感染是否会触发XLP1相关HLH,仍需进一步研究。

展开英文摘要原文

Present a clinical case of fatal HLH associated with a novel SH2D1A variant, highlighting the variability of clinical presentation and the potential role of co-infections.

We analyzed clinical and laboratory data of three brothers who died from HLH in early age. Genetic evaluation was performed using a 576-gene panel for IEI (Veritas, Spain, supported by the Jeffrey Modell Foundation). Alive siblings and parents were tested in Scientific Medical Genetic Center LeoGENE, Ukraine.

A 1-year-old boy was admitted with a persistent 4-day fever and clinical signs of hepatosplenomegaly, anemia, neutropenia, hypertransaminasemia, and hypoproteinemia. Immunophenotyping revealed decreased CD4, increased CD8 T cells, reduced NK cell counts, and elevated immunoglobulin levels. This patient demonstrated high EBV viremia and positive serological markers for SARS-CoV-2. Despite intensive treatment, HLH progressed rapidly, leading to fatality within 35 days. Genetic testing identified a novel, likely pathogenic hemizygous SH2D1A variant, c.175delC (p.Thr59Glnfs*22), not previously reported in affected individuals or the gnomAD database. Family history shows that two older male siblings died at 11 months and 1 year 9 months from a rapidly developed disease presented by fever, hepatosplenomegaly, dermatitis, enterocolitis, anemia, thrombocytopenia, and hypertransaminasemia. The second affected sibling tested positive for EBV serology. The family also included a healthy sister and brother, both with positive EBV serology (IgG) but no detectable viremia. Carrier testing confirmed that the mother and sister are heterozygous carriers, while two male siblings (one of them was born 1 month ago) are unaffected.

We identified a novel SH2D1A variant associated with fatal HLH in XLP1. Our findings highlight the importance of early genetic diagnosis before EBV exposure to improve patient outcomes. The potential role of co-infections, including SARS-CoV-2, in triggering HLH in XLP1 remains an area for further investigation.

论文信息

作者
Boyarchuk O、Volokha A、Yarema N、Dyvoniak O、Tomashivska T、Shymanska I、Makukh H、Walter JE
第一作者单位
Department of Children's Diseases and Pediatric Surgery, I.Horbachevsky Ternopil National Medical University, Ternopil, Ukraine.
通讯作者单位
Division of Pediatric Allergy and Immunology, Department of Pediatrics, University of South Florida, St. Petersburg, FL, United States.United States
文献类型
病例报告
期刊
Frontiers in immunology2025
原文标识
PubMed 40458416 · DOI 10.3389/fimmu.2025.1602107