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滤泡素相互作用蛋白 1 缺乏症中 B 细胞缺失、无丙种球蛋白血症和肥厚型心肌病。

Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency.

机构信息

Pediatric Hematology Department, Fondazione Monza e Brianza per il Bambino e la sua Mamma (MBBM), University of Milano Bicocca, Monza, Italy.

Department of Pediatrics, Baylor College of Medicine, Houston, TX.

出版信息

Blood. 2021 Jan 28;137(4):493-499. doi: 10.1182/blood.2020006441.

Abstract

Agammaglobulinemia is the most profound primary antibody deficiency that can occur due to an early termination of B-cell development. We here investigated 3 novel patients, including the first known adult, from unrelated families with agammaglobulinemia, recurrent infections, and hypertrophic cardiomyopathy (HCM). Two of them also presented with intermittent or severe chronic neutropenia. We identified homozygous or compound-heterozygous variants in the gene for folliculin interacting protein 1 (FNIP1), leading to loss of the FNIP1 protein. B-cell metabolism, including mitochondrial numbers and activity and phosphatidylinositol 3-kinase/AKT pathway, was impaired. These defects recapitulated the Fnip1-/- animal model. Moreover, we identified either uniparental disomy or copy-number variants (CNVs) in 2 patients, expanding the variant spectrum of this novel inborn error of immunity. The results indicate that FNIP1 deficiency can be caused by complex genetic mechanisms and support the clinical utility of exome sequencing and CNV analysis in patients with broad phenotypes, including agammaglobulinemia and HCM. FNIP1 deficiency is a novel inborn error of immunity characterized by early and severe B-cell development defect, agammaglobulinemia, variable neutropenia, and HCM. Our findings elucidate a functional and relevant role of FNIP1 in B-cell development and metabolism and potentially neutrophil activity.

摘要

免疫球蛋白缺乏症是最严重的原发性抗体缺陷,可由 B 细胞发育早期终止引起。我们在此研究了 3 名来自无亲缘关系的家族的新患者,他们患有免疫球蛋白缺乏症、反复感染和肥厚型心肌病(HCM)。其中 2 名患者还存在间歇性或严重慢性中性粒细胞减少症。我们在滤泡素相互作用蛋白 1(FNIP1)基因中发现了纯合子或复合杂合变体,导致 FNIP1 蛋白缺失。B 细胞代谢,包括线粒体数量和活性以及磷脂酰肌醇 3-激酶/AKT 途径,受到损害。这些缺陷重现了 Fnip1-/-动物模型。此外,我们在 2 名患者中发现了单亲二倍体或拷贝数变异(CNV),扩大了这种新型先天性免疫缺陷的变异谱。结果表明,FNIP1 缺乏症可能由复杂的遗传机制引起,并支持外显子组测序和 CNV 分析在包括免疫球蛋白缺乏症和 HCM 在内的广泛表型患者中的临床应用。FNIP1 缺乏症是一种新型先天性免疫缺陷,其特征为早期和严重的 B 细胞发育缺陷、免疫球蛋白缺乏症、可变中性粒细胞减少症和 HCM。我们的研究结果阐明了 FNIP1 在 B 细胞发育和代谢以及潜在中性粒细胞活性中的功能和相关作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b887/7845007/c10bf73db4bd/bloodBLD2020006441absf1.jpg

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