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一种新型 EROS(CYBC1)突变导致慢性肉芽肿病。

A novel mutation in EROS (CYBC1) causes chronic granulomatous disease.

机构信息

Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, United Kingdom.

Aster Medcity Hospital, Kochi, Kerala, India.

出版信息

Clin Immunol. 2023 Oct;255:109761. doi: 10.1016/j.clim.2023.109761. Epub 2023 Sep 8.

Abstract

Chronic Granulomatous Disease (CGD) is an inborn error of immunity characterised by opportunistic infection and sterile granulomatous inflammation. CGD is caused by a failure of reactive oxygen species (ROS) production by the phagocyte NADPH oxidase. Mutations in the genes encoding phagocyte NADPH oxidase subunits cause CGD. We and others have described a novel form of CGD (CGD5) secondary to lack of EROS (CYBC1), a highly selective chaperone for gp91phox. EROS-deficient cells express minimal levels of gp91phox and its binding partner p22phox, but EROS also controls the expression of other proteins such as P2X7. The full nature of CGD5 is currently unknown. We describe a homozygous frameshift mutation in CYBC1 leading to CGD. Individuals who are heterozygous for this mutation are found in South Asian populations (allele frequency = 0.00006545), thus it is not a private mutation. Therefore, it is likely to be the underlying cause of other cases of CGD.

摘要

慢性肉芽肿病(CGD)是一种遗传性免疫缺陷病,其特征为机会性感染和非化脓性肉芽肿性炎症。CGD 是由于吞噬细胞 NADPH 氧化酶产生活性氧(ROS)的失败引起的。吞噬细胞 NADPH 氧化酶亚基的基因突变导致 CGD。我们和其他人已经描述了一种新型的 CGD(CGD5)继发于 EROS(CYBC1)缺乏,这是 gp91phox 的高度选择性伴侣。缺乏 EROS 的细胞表达最低水平的 gp91phox 和其结合伴侣 p22phox,但 EROS 还控制其他蛋白质的表达,如 P2X7。CGD5 的全部性质目前尚不清楚。我们描述了一个导致 CGD 的 CYBC1 纯合移码突变。在南亚人群中发现了这种突变的杂合子(等位基因频率为 0.00006545),因此它不是一个私人突变。因此,它很可能是其他 CGD 病例的潜在原因。

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