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日本 STAT3 功能获得性变异患者的临床和免疫学异质性。

Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3.

机构信息

Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.

Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima, Japan.

出版信息

J Clin Immunol. 2021 May;41(4):780-790. doi: 10.1007/s10875-021-00975-y. Epub 2021 Jan 26.

Abstract

PURPOSE

Germline loss-of-function variants in the signal transducer and activator of transcription 3 (STAT3) gene result in autosomal dominant hyper IgE syndrome, whereas somatic gain-of-function (GOF) variants in STAT3 are associated with some malignancies. In addition, germline GOF variants in STAT3 are linked to disorders involving autoimmunity and lymphoproliferation. In this study, we describe five Japanese families with germline GOF variants in STAT3, including three novel variants. We also present the clinical and immunological characteristics of these patients.

METHODS

Eight patients from five families were enrolled in this study. We performed genetic and immunological analyses, and collected the associated clinical information.

RESULTS

We identified five heterozygous variants in STAT3 using whole-exome sequencing and target gene sequencing. Two of these (E286G and T716M) were previously reported and three (K348E, E415G, and G618A) were novel. A STAT3 reporter assay revealed that all of the variants were GOF. However, the immunological and clinical characteristics among the patients were highly variable.

CONCLUSION

Patients with STAT3 GOF variants exhibited clinical and immunological heterogeneity with incomplete penetrance.

摘要

目的

信号转导子和转录激活因子 3(STAT3)基因的胚系失活变异导致常染色体显性高免疫球蛋白 E 综合征,而 STAT3 的体细胞获得性功能(GOF)变异与一些恶性肿瘤有关。此外,STAT3 的胚系 GOF 变异与涉及自身免疫和淋巴增生的疾病有关。在这项研究中,我们描述了五个具有 STAT3 胚系 GOF 变异的日本家族,包括三个新变异。我们还介绍了这些患者的临床和免疫学特征。

方法

本研究纳入了五个家族的 8 名患者。我们进行了基因和免疫学分析,并收集了相关的临床信息。

结果

我们通过全外显子测序和靶基因测序鉴定了 STAT3 的五个杂合变异。其中两个(E286G 和 T716M)是先前报道的,三个(K348E、E415G 和 G618A)是新的。STAT3 报告基因检测显示所有变异均具有 GOF。然而,患者之间的免疫和临床特征高度可变。

结论

具有 STAT3 GOF 变异的患者表现出不完全外显的临床和免疫学异质性。

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