一大批先天性免疫错误儿科患者的遗传特征:单中心经验

IF 7.2 2区 医学 Q1 IMMUNOLOGY
Natalia Kuzmenko, Maxim Alexenko, Anna Mukhina, Yulia Rodina, Mariia Fadeeva, Dmitrii Pershin, Amina Kieva, Elena Raykina, Miсhael Maschan, Galina Novichkova, Anna Shcherbina
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引用次数: 0

摘要

超过 450 种基因缺陷会导致先天性免疫错误(IEI)。它们在特定人群中的发病率受国家特征和其他因素的影响。我们介绍了对 1809 名俄罗斯 IEI 儿童进行基因检测的结果。在 1809 名受检者中,有 1112 人(61.5%)发现了证实 IEI 的基因缺陷。这些缺陷包括 118 个单个基因的变异(87.9% 的患者)和 6 条染色体的畸变(11.8%)。值得注意的是,有三名患者携带不止一个 IEI 基因的致病变异。大缺失占所有缺陷的 5%。在 799 个原始变异中,有 350 个(44%)以前未被描述过。在 20% 的患者中发现了罕见的基因缺陷(每个基因有 10 个或更少患者)。在 967 名有生殖系变异的患者中,29% 为常染色体显性遗传,34% 为 X 连锁遗传,37% 为常染色体隐性遗传。四名非随机 X 失活的女性表现出 X 连锁疾病的症状(BTK、WAS、CYBB、IKBKG 基因缺陷)。尽管俄罗斯的近亲结婚率相对较低,但仍有 47.9% 的常染色体隐性基因缺陷是在同卵状态下发现的。值得注意的是,其中 28% 的病例携带 NBN 基因的 "斯拉夫 "突变或其他基因的已知热点突变。IEI 遗传形式的多样性和新描述变体的高频率凸显了俄罗斯 IEI 群体的遗传异质性。在这个庞大的群体中发现的新变异将丰富基因数据库。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genetic Characteristics of a Large Pediatric Cohort of Patients with Inborn Errors of Immunity: Single-Center Experience.

Genetic Characteristics of a Large Pediatric Cohort of Patients with Inborn Errors of Immunity: Single-Center Experience.

More than 450 genetic defects result in inborn errors of immunity (IEI). Their individual prevalence in specific cohorts is influenced by national characteristics and other factors. We present results of genetic testing conducted in 1809 Russian children with IEI. Genetic defects confirming IEI were found in 1112 out of 1809 (61.5%) probands. These defects included variants in 118 single genes (87.9% of patients) and aberrations in 6 chromosomes (11.8%). Notably, three patients harbored pathogenic variants in more than one IEI gene. Large deletions constituted 5% of all defects. Out of the 799 original variants, 350 (44%) have not been described previously. Rare genetic defects (10 or fewer patients per gene) were identified in 20% of the patients. Among 967 probands with germline variants, defects were inherited in an autosomal dominant manner in 29%, X-linked in 34%, and autosomal recessive in 37%. Four females with non-random X-inactivation exhibited symptoms of X-linked diseases (BTK, WAS, CYBB, IKBKG gene defects). Despite a relatively low rate of consanguinity in Russia, 47.9% of autosomal recessive gene defects were found in a homozygous state. Notably, 28% of these cases carried "Slavic" mutation of the NBN gene or known hot-spot mutations in other genes. The diversity of IEI genetic forms and the high frequency of newly described variants underscore the genetic heterogeneity within the Russian IEI group. The new variants identified in this extensive cohort will enrich genetic databases.

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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
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