ASXL1缺失导致表观遗传功能障碍、联合免疫缺陷和ebv相关淋巴瘤。

IF 10.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-10-06 Epub Date: 2025-07-31 DOI:10.1084/jem.20240945
Maggie P Fu, Mehul Sharma, Pariya Yousefi, Sarah M Merrill, Ryan Tan, Simran Samra, Audi Setiadi, Liam Golding, Bhavi P Modi, Kate L Del Bel, Rebecca J Deyell, Jacob Rozmus, Wingfield Rehmus, Kyla J Hildebrand, Elliot James, Géraldine Blanchard-Rohner, Susan Lin, Kevin E Shopsowitz, Jefferson Terry, Anna F Lee, Britt I Drögemöller, Allison Matthews, Maja Tarailo-Graovac, Laura Sauvé, Hana Mitchell, Julie S Prendiville, Julia L MacIsaac, Kristy Dever, David T S Lin, Mandy Meijer, Colin J D Ross, Simon R M Dobson, Suzanne M Vercauteren, Wyeth W Wasserman, Clara D M van Karnebeek, Margaret L McKinnon, Michael S Kobor, Stuart E Turvey, Catherine M Biggs
{"title":"ASXL1缺失导致表观遗传功能障碍、联合免疫缺陷和ebv相关淋巴瘤。","authors":"Maggie P Fu, Mehul Sharma, Pariya Yousefi, Sarah M Merrill, Ryan Tan, Simran Samra, Audi Setiadi, Liam Golding, Bhavi P Modi, Kate L Del Bel, Rebecca J Deyell, Jacob Rozmus, Wingfield Rehmus, Kyla J Hildebrand, Elliot James, Géraldine Blanchard-Rohner, Susan Lin, Kevin E Shopsowitz, Jefferson Terry, Anna F Lee, Britt I Drögemöller, Allison Matthews, Maja Tarailo-Graovac, Laura Sauvé, Hana Mitchell, Julie S Prendiville, Julia L MacIsaac, Kristy Dever, David T S Lin, Mandy Meijer, Colin J D Ross, Simon R M Dobson, Suzanne M Vercauteren, Wyeth W Wasserman, Clara D M van Karnebeek, Margaret L McKinnon, Michael S Kobor, Stuart E Turvey, Catherine M Biggs","doi":"10.1084/jem.20240945","DOIUrl":null,"url":null,"abstract":"<p><p>Inborn errors of immunity (IEIs) are caused by deleterious variants in immune-related genes. ASXL1 is an epigenetic modifier not previously linked to an IEI. Clonal hematopoiesis and hematologic neoplasms often feature somatic ASXL1 variants, and Bohring-Opitz syndrome, a neurodevelopmental disorder, is caused by heterozygous truncating ASXL1 variants. We present an IEI caused by biallelic germline missense variants in ASXL1. The patient had a history of hematologic abnormalities and viral-associated complications, including chronic macrocytosis, persistent vaccine-strain rubella granulomas, and EBV-associated Hodgkin lymphoma. Immunophenotyping revealed loss of B cells, hypogammaglobulinemia, and impairments in cytotoxic T and NK cell populations. T cells exhibited skewing toward an exhausted memory phenotype, global DNA methylation loss, and increased epigenetic aging. These aberrations were ameliorated by wild-type ASXL1 transduction, confirming the patient variants' pathogenicity. This study defines a novel human IEI caused by ASXL1 deficiency, a diagnosis that should be considered in individuals with chronic viral infections, viral-associated malignancies, and combined immune deficiency.</p>","PeriodicalId":15760,"journal":{"name":"Journal of Experimental Medicine","volume":"222 10","pages":""},"PeriodicalIF":10.6000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphoma.\",\"authors\":\"Maggie P Fu, Mehul Sharma, Pariya Yousefi, Sarah M Merrill, Ryan Tan, Simran Samra, Audi Setiadi, Liam Golding, Bhavi P Modi, Kate L Del Bel, Rebecca J Deyell, Jacob Rozmus, Wingfield Rehmus, Kyla J Hildebrand, Elliot James, Géraldine Blanchard-Rohner, Susan Lin, Kevin E Shopsowitz, Jefferson Terry, Anna F Lee, Britt I Drögemöller, Allison Matthews, Maja Tarailo-Graovac, Laura Sauvé, Hana Mitchell, Julie S Prendiville, Julia L MacIsaac, Kristy Dever, David T S Lin, Mandy Meijer, Colin J D Ross, Simon R M Dobson, Suzanne M Vercauteren, Wyeth W Wasserman, Clara D M van Karnebeek, Margaret L McKinnon, Michael S Kobor, Stuart E Turvey, Catherine M Biggs\",\"doi\":\"10.1084/jem.20240945\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Inborn errors of immunity (IEIs) are caused by deleterious variants in immune-related genes. ASXL1 is an epigenetic modifier not previously linked to an IEI. Clonal hematopoiesis and hematologic neoplasms often feature somatic ASXL1 variants, and Bohring-Opitz syndrome, a neurodevelopmental disorder, is caused by heterozygous truncating ASXL1 variants. We present an IEI caused by biallelic germline missense variants in ASXL1. The patient had a history of hematologic abnormalities and viral-associated complications, including chronic macrocytosis, persistent vaccine-strain rubella granulomas, and EBV-associated Hodgkin lymphoma. Immunophenotyping revealed loss of B cells, hypogammaglobulinemia, and impairments in cytotoxic T and NK cell populations. T cells exhibited skewing toward an exhausted memory phenotype, global DNA methylation loss, and increased epigenetic aging. These aberrations were ameliorated by wild-type ASXL1 transduction, confirming the patient variants' pathogenicity. This study defines a novel human IEI caused by ASXL1 deficiency, a diagnosis that should be considered in individuals with chronic viral infections, viral-associated malignancies, and combined immune deficiency.</p>\",\"PeriodicalId\":15760,\"journal\":{\"name\":\"Journal of Experimental Medicine\",\"volume\":\"222 10\",\"pages\":\"\"},\"PeriodicalIF\":10.6000,\"publicationDate\":\"2025-10-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Experimental Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1084/jem.20240945\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/7/31 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1084/jem.20240945","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/31 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

先天性免疫错误(IEIs)是由免疫相关基因的有害变异引起的。ASXL1是一种表观遗传修饰子,以前与IEI没有关联。克隆造血和血液学肿瘤通常以体细胞ASXL1变异为特征,而bohling - opitz综合征是一种神经发育障碍,由杂合截断ASXL1变异引起。我们提出了由ASXL1的双等位种系错义变异引起的IEI。患者有血液学异常史和病毒相关并发症,包括慢性巨细胞增多症、持续性疫苗株风疹肉芽肿和ebv相关霍奇金淋巴瘤。免疫表型分析显示B细胞丢失,低γ球蛋白血症,细胞毒性T和NK细胞群受损。T细胞表现出向耗尽记忆表型倾斜,整体DNA甲基化丢失,并增加表观遗传老化。这些畸变通过野生型ASXL1转导得到改善,证实了患者变异的致病性。本研究定义了一种由ASXL1缺陷引起的新型人类IEI,这种诊断应该在慢性病毒感染、病毒相关恶性肿瘤和合并免疫缺陷的个体中考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphoma.

Inborn errors of immunity (IEIs) are caused by deleterious variants in immune-related genes. ASXL1 is an epigenetic modifier not previously linked to an IEI. Clonal hematopoiesis and hematologic neoplasms often feature somatic ASXL1 variants, and Bohring-Opitz syndrome, a neurodevelopmental disorder, is caused by heterozygous truncating ASXL1 variants. We present an IEI caused by biallelic germline missense variants in ASXL1. The patient had a history of hematologic abnormalities and viral-associated complications, including chronic macrocytosis, persistent vaccine-strain rubella granulomas, and EBV-associated Hodgkin lymphoma. Immunophenotyping revealed loss of B cells, hypogammaglobulinemia, and impairments in cytotoxic T and NK cell populations. T cells exhibited skewing toward an exhausted memory phenotype, global DNA methylation loss, and increased epigenetic aging. These aberrations were ameliorated by wild-type ASXL1 transduction, confirming the patient variants' pathogenicity. This study defines a novel human IEI caused by ASXL1 deficiency, a diagnosis that should be considered in individuals with chronic viral infections, viral-associated malignancies, and combined immune deficiency.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信