一名患有中枢神经系统念珠菌病的健康女性患有新型遗传性 CARD9 缺乏症。

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Ling-Hong Zhou , Wen-Jia Qiu , Chun-Xing Que , Jia-Hui Cheng , Rong-Sheng Zhu , Jun-Tian Huang , Ying-Kui Jiang , Hua-Zhen Zhao , Xuan Wang , Xun-Jia Cheng , Li-Ping Zhu
{"title":"一名患有中枢神经系统念珠菌病的健康女性患有新型遗传性 CARD9 缺乏症。","authors":"Ling-Hong Zhou ,&nbsp;Wen-Jia Qiu ,&nbsp;Chun-Xing Que ,&nbsp;Jia-Hui Cheng ,&nbsp;Rong-Sheng Zhu ,&nbsp;Jun-Tian Huang ,&nbsp;Ying-Kui Jiang ,&nbsp;Hua-Zhen Zhao ,&nbsp;Xuan Wang ,&nbsp;Xun-Jia Cheng ,&nbsp;Li-Ping Zhu","doi":"10.1016/j.clim.2024.110293","DOIUrl":null,"url":null,"abstract":"<div><p>Patients with caspase-associated recruitment domain-9 (<em>CARD9</em>) deficiency are more likely to develop invasive fungal disease that affect CNS. However, the understanding of how <em>Candida</em> invades and persists in CNS is still limited. We here reported a 24-year-old woman who were previously immunocompetent and diagnosed with CNS candidiasis. A novel autosomal recessive homozygous <em>CARD9</em> mutation (c.184 + 5G &gt; T) from this patient was identified using whole genomic sequencing. Furthermore, we extensively characterized the impact of this <em>CARD9</em> mutation on the host immune response in monocytes, neutrophils and CD4 + T cells, using single cell sequencing and in vitro experiments. Decreased pro-inflammatory cytokine productions of CD14 + monocyte, impaired Th17 cell differentiation, and defective neutrophil accumulation in CNS were found in this patient. In conclusion, this study proposed a novel mechanism of CNS candidiasis development. Patients with CNS candidiasis in absence of known immunodeficiencies should be analyzed for <em>CARD9</em> gene mutation as the cause of invasive fungal infection predisposition.</p></div>","PeriodicalId":10392,"journal":{"name":"Clinical immunology","volume":null,"pages":null},"PeriodicalIF":4.5000,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A novel inherited CARD9 deficiency in an otherwise healthy woman with CNS candidiasis\",\"authors\":\"Ling-Hong Zhou ,&nbsp;Wen-Jia Qiu ,&nbsp;Chun-Xing Que ,&nbsp;Jia-Hui Cheng ,&nbsp;Rong-Sheng Zhu ,&nbsp;Jun-Tian Huang ,&nbsp;Ying-Kui Jiang ,&nbsp;Hua-Zhen Zhao ,&nbsp;Xuan Wang ,&nbsp;Xun-Jia Cheng ,&nbsp;Li-Ping Zhu\",\"doi\":\"10.1016/j.clim.2024.110293\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Patients with caspase-associated recruitment domain-9 (<em>CARD9</em>) deficiency are more likely to develop invasive fungal disease that affect CNS. However, the understanding of how <em>Candida</em> invades and persists in CNS is still limited. We here reported a 24-year-old woman who were previously immunocompetent and diagnosed with CNS candidiasis. A novel autosomal recessive homozygous <em>CARD9</em> mutation (c.184 + 5G &gt; T) from this patient was identified using whole genomic sequencing. Furthermore, we extensively characterized the impact of this <em>CARD9</em> mutation on the host immune response in monocytes, neutrophils and CD4 + T cells, using single cell sequencing and in vitro experiments. Decreased pro-inflammatory cytokine productions of CD14 + monocyte, impaired Th17 cell differentiation, and defective neutrophil accumulation in CNS were found in this patient. In conclusion, this study proposed a novel mechanism of CNS candidiasis development. Patients with CNS candidiasis in absence of known immunodeficiencies should be analyzed for <em>CARD9</em> gene mutation as the cause of invasive fungal infection predisposition.</p></div>\",\"PeriodicalId\":10392,\"journal\":{\"name\":\"Clinical immunology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2024-06-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1521661624004029\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical immunology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1521661624004029","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

丙种球蛋白酶相关招募结构域-9(CARD9)缺乏症患者更容易患上影响中枢神经系统的侵袭性真菌病。然而,人们对念珠菌如何侵入中枢神经系统并在其中存活的了解仍然有限。我们在此报告了一名 24 岁女性的病例,她之前免疫功能正常,被诊断为中枢神经系统念珠菌病。通过全基因组测序,我们发现了该患者的一个新型常染色体隐性同基因 CARD9 突变(c.184 + 5G > T)。此外,我们还利用单细胞测序和体外实验,广泛研究了这种 CARD9 突变对单核细胞、中性粒细胞和 CD4 + T 细胞宿主免疫反应的影响。研究发现,该患者的 CD14 + 单核细胞促炎细胞因子生成减少,Th17 细胞分化受损,中性粒细胞在中枢神经系统的聚集出现缺陷。总之,这项研究提出了中枢神经系统念珠菌病的新发病机制。在没有已知免疫缺陷的情况下,中枢神经系统念珠菌病患者应进行CARD9基因突变分析,以确定侵袭性真菌感染易感性的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel inherited CARD9 deficiency in an otherwise healthy woman with CNS candidiasis

Patients with caspase-associated recruitment domain-9 (CARD9) deficiency are more likely to develop invasive fungal disease that affect CNS. However, the understanding of how Candida invades and persists in CNS is still limited. We here reported a 24-year-old woman who were previously immunocompetent and diagnosed with CNS candidiasis. A novel autosomal recessive homozygous CARD9 mutation (c.184 + 5G > T) from this patient was identified using whole genomic sequencing. Furthermore, we extensively characterized the impact of this CARD9 mutation on the host immune response in monocytes, neutrophils and CD4 + T cells, using single cell sequencing and in vitro experiments. Decreased pro-inflammatory cytokine productions of CD14 + monocyte, impaired Th17 cell differentiation, and defective neutrophil accumulation in CNS were found in this patient. In conclusion, this study proposed a novel mechanism of CNS candidiasis development. Patients with CNS candidiasis in absence of known immunodeficiencies should be analyzed for CARD9 gene mutation as the cause of invasive fungal infection predisposition.

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
Clinical immunology
Clinical immunology 医学-免疫学
CiteScore
12.30
自引率
1.20%
发文量
212
审稿时长
34 days
期刊介绍: Clinical Immunology publishes original research delving into the molecular and cellular foundations of immunological diseases. Additionally, the journal includes reviews covering timely subjects in basic immunology, along with case reports and letters to the editor.
×
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:481959085
Book学术官方微信