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Whole Exome Sequencing Reveals Pathogenic Variants in ADA2 and FAS Causing DADA2 and ALPS.

作者信息

Ahn Terrie S, Kohn Lisa A

机构信息

Division of Clinical Immunology and Allergy, Department of Medicine, University of California, Los Angeles, 1245 16th St., Suite 303, Santa Monica, CA, 90404, USA.

出版信息

J Clin Immunol. 2023 Aug;43(6):1147-1151. doi: 10.1007/s10875-023-01484-w. Epub 2023 May 13.

DOI:10.1007/s10875-023-01484-w
PMID:37178281
Abstract
摘要

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引用本文的文献

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Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.显性负性ADA2突变导致杂合子携带者出现ADA2缺乏症。
J Exp Med. 2025 Nov 3;222(11). doi: 10.1084/jem.20250499. Epub 2025 Aug 27.
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Mimics and challenging presentations of DADA2.DADA2的模仿与具有挑战性的表现形式。
Clin Exp Immunol. 2025 Jan 21;219(1). doi: 10.1093/cei/uxaf017.
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Dominant negative mutations cause ADA2 deficiency in heterozygous carriers.显性负性突变导致杂合子携带者出现ADA2缺乏症。

本文引用的文献

1
Comprehensive analysis of ADA2 genetic variants and estimation of carrier frequency driven by a function-based approach.基于功能的方法对 ADA2 遗传变异的综合分析及携带者频率的估计。
J Allergy Clin Immunol. 2022 Jan;149(1):379-387. doi: 10.1016/j.jaci.2021.04.034. Epub 2021 May 15.
2
Deficiency of Adenosine Deaminase 2 (DADA2): Updates on the Phenotype, Genetics, Pathogenesis, and Treatment.腺苷脱氨酶 2 缺乏症(DADA2):表型、遗传学、发病机制和治疗的最新进展。
J Clin Immunol. 2018 Jul;38(5):569-578. doi: 10.1007/s10875-018-0525-8. Epub 2018 Jun 27.
3
Autoimmune lymphoproliferative syndrome due to FAS mutations outside the signal-transducing death domain: molecular mechanisms and clinical penetrance.
medRxiv. 2024 Dec 11:2024.12.09.24317629. doi: 10.1101/2024.12.09.24317629.
4
Genetic Testing in Patients with Autoimmune Lymphoproliferative Syndrome: Experience of 802 Patients at Cincinnati Children's Hospital Medical Center.自身免疫性淋巴组织增生综合征患者的基因检测:辛辛那提儿童医院医疗中心 802 例患者的经验。
J Clin Immunol. 2024 Jul 26;44(7):166. doi: 10.1007/s10875-024-01772-z.
由于信号转导死亡域之外的 FAS 突变导致的自身免疫性淋巴组织增生综合征:分子机制和临床外显率。
Genet Med. 2012 Jan;14(1):81-9. doi: 10.1038/gim.0b013e3182310b7d. Epub 2011 Oct 7.
4
FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndrome.FAS 部分功能不足是人类自身免疫性淋巴组织增生综合征的一种常见疾病机制。
J Immunol. 2011 May 15;186(10):6035-43. doi: 10.4049/jimmunol.1100021. Epub 2011 Apr 13.