Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Paris, France.
University of Paris, Imagine Institute, Paris, France.
J Exp Med. 2020 Jun 1;217(6). doi: 10.1084/jem.20191804.
Autosomal dominant hyper-IgE syndrome (AD-HIES) is typically caused by dominant-negative (DN) STAT3 mutations. Patients suffer from cold staphylococcal lesions and mucocutaneous candidiasis, severe allergy, and skeletal abnormalities. We report 12 patients from 8 unrelated kindreds with AD-HIES due to DN IL6ST mutations. We identified seven different truncating mutations, one of which was recurrent. The mutant alleles encode GP130 receptors bearing the transmembrane domain but lacking both the recycling motif and all four STAT3-recruiting tyrosine residues. Upon overexpression, the mutant proteins accumulate at the cell surface and are loss of function and DN for cellular responses to IL-6, IL-11, LIF, and OSM. Moreover, the patients' heterozygous leukocytes and fibroblasts respond poorly to IL-6 and IL-11. Consistently, patients with STAT3 and IL6ST mutations display infectious and allergic manifestations of IL-6R deficiency, and some of the skeletal abnormalities of IL-11R deficiency. DN STAT3 and IL6ST mutations thus appear to underlie clinical phenocopies through impairment of the IL-6 and IL-11 response pathways.
常染色体显性遗传高免疫球蛋白 E 综合征(AD-HIES)通常由显性负 STAT3 突变引起。患者患有冷葡萄球菌病和粘膜皮肤念珠菌病、严重过敏和骨骼异常。我们报告了 8 个无关家族的 12 名 AD-HIES 患者,其病因是 DN IL6ST 突变。我们鉴定了 7 种不同的截断突变,其中一种是复发性的。突变等位基因编码 GP130 受体,具有跨膜结构域,但缺乏再循环基序和所有四个招募 STAT3 的酪氨酸残基。这些突变蛋白在细胞表面过度表达,并且功能丧失和对 IL-6、IL-11、LIF 和 OSM 的细胞反应呈显性负。此外,患者的杂合白细胞和成纤维细胞对 IL-6 和 IL-11 的反应较差。一致地,STAT3 和 IL6ST 突变患者表现出 IL-6R 缺乏的感染和过敏表现,以及 IL-11R 缺乏的一些骨骼异常。因此,DN STAT3 和 IL6ST 突变似乎通过损害 IL-6 和 IL-11 反应途径导致临床表型的相似性。