• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
The potential role for infections in the pathogenesis of autoimmune Addison's disease.感染在自身免疫性艾迪生病发病机制中的潜在作用。
Clin Exp Immunol. 2019 Jan;195(1):52-63. doi: 10.1111/cei.13207. Epub 2018 Sep 30.
2
The purification and application of biologically active recombinant steroid cytochrome P450 21-hydroxylase: the major autoantigen in autoimmune Addison's disease.生物活性重组甾体细胞色素P450 21-羟化酶的纯化与应用:自身免疫性艾迪生病的主要自身抗原
J Autoimmun. 2009 Aug;33(1):58-67. doi: 10.1016/j.jaut.2009.02.018. Epub 2009 Mar 28.
3
Adrenal-cortex autoantibodies and steroid-producing cells autoantibodies in patients with Addison's disease: comparison of immunofluorescence and immunoprecipitation assays.艾迪生病患者的肾上腺皮质自身抗体和类固醇生成细胞自身抗体:免疫荧光法与免疫沉淀法的比较
J Clin Endocrinol Metab. 1999 Feb;84(2):618-22. doi: 10.1210/jcem.84.2.5459.
4
Autoantibodies to steroidogenic enzymes in autoimmune polyglandular syndrome, Addison's disease, and premature ovarian failure.自身免疫性多内分泌腺综合征、艾迪生病和卵巢早衰中针对类固醇生成酶的自身抗体。
J Clin Endocrinol Metab. 1996 May;81(5):1871-6. doi: 10.1210/jcem.81.5.8626850.
5
II. Adrenal cortex and steroid 21-hydroxylase autoantibodies in children with organ-specific autoimmune diseases: markers of high progression to clinical Addison's disease.二、器官特异性自身免疫性疾病患儿的肾上腺皮质与类固醇21-羟化酶自身抗体:临床Addison病高进展风险的标志物
J Clin Endocrinol Metab. 1997 Mar;82(3):939-42. doi: 10.1210/jcem.82.3.3849.
6
T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency.自身免疫性原发性肾上腺功能不全患者对类固醇细胞色素 P450 21-羟化酶的 T 细胞反应。
J Clin Endocrinol Metab. 2009 Dec;94(12):5117-24. doi: 10.1210/jc.2009-1115. Epub 2009 Nov 4.
7
Adrenal autoantibodies and organ-specific autoimmunity in patients with Addison's disease.艾迪生病患者的肾上腺自身抗体与器官特异性自身免疫
Clin Endocrinol (Oxf). 1996 Oct;45(4):453-60. doi: 10.1046/j.1365-2265.1996.8040813.x.
8
Autoimmune Addison's disease--evidence for a role of steroid 21-hydroxylase autoantibodies in adrenal insufficiency.自身免疫性Addison病——类固醇21-羟化酶自身抗体在肾上腺功能不全中作用的证据
J Clin Endocrinol Metab. 1994 Nov;79(5):1517-21. doi: 10.1210/jcem.79.5.7962352.
9
Autoantibody responses in autoimmune ovarian insufficiency and in Addison's disease are IgG1 dominated and suggest a predominant, but not exclusive, Th1 type of response.自身免疫性卵巢功能不全和艾迪生病中的自身抗体反应以 IgG1 为主,提示以 Th1 型反应为主,但并非排他性的。
Eur J Endocrinol. 2010 Aug;163(2):309-17. doi: 10.1530/EJE-10-0257. Epub 2010 May 24.
10
The effect of types I and III interferons on adrenocortical cells and its possible implications for autoimmune Addison's disease.Ⅰ型和Ⅲ型干扰素对肾上腺皮质细胞的影响及其对自身免疫性艾迪生病的可能意义。
Clin Exp Immunol. 2014 Jun;176(3):351-62. doi: 10.1111/cei.12291.

引用本文的文献

1
Secrets and lies of host-microbial interactions: MHC restriction and trans-regulation of T cell trafficking conceal the role of microbial agents on the edge between health and multifactorial/complex diseases.宿主-微生物相互作用的秘密和谎言:MHC 限制和 T 细胞迁移的反调节掩盖了微生物因子在健康和多因素/复杂疾病之间边缘的作用。
Cell Mol Life Sci. 2024 Jan 13;81(1):40. doi: 10.1007/s00018-023-05040-y.
2
Autoimmune primary adrenal insufficiency -current diagnostic approaches and future perspectives.自身免疫性原发性肾上腺功能不全——当前的诊断方法和未来展望。
Front Endocrinol (Lausanne). 2023 Nov 10;14:1285901. doi: 10.3389/fendo.2023.1285901. eCollection 2023.
3
Endocrine Autoimmunity in Pregnancy.妊娠期内分泌自身免疫。
Front Immunol. 2022 Jun 29;13:907561. doi: 10.3389/fimmu.2022.907561. eCollection 2022.
4
The genetics of autoimmune Addison disease: past, present and future.自身免疫性艾迪生病的遗传学:过去、现在和未来。
Nat Rev Endocrinol. 2022 Jul;18(7):399-412. doi: 10.1038/s41574-022-00653-y. Epub 2022 Apr 11.
5
Primary Adrenal Insufficiency After COVID-19 Infection.新型冠状病毒肺炎感染后的原发性肾上腺皮质功能减退症
AACE Clin Case Rep. 2022 Mar-Apr;8(2):51-53. doi: 10.1016/j.aace.2021.11.001. Epub 2021 Nov 14.
6
COVID-19 and the Endocrine System: A Comprehensive Review on the Theme.新型冠状病毒肺炎与内分泌系统:关于该主题的全面综述
J Clin Med. 2021 Jun 29;10(13):2920. doi: 10.3390/jcm10132920.
7
Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease.自身免疫性艾迪生病患者中罕见的Toll样受体3变异体的鉴定与特征分析。
J Transl Autoimmun. 2019 May 28;1:100005. doi: 10.1016/j.jtauto.2019.100005. eCollection 2019 Apr.
8
USP29 maintains the stability of cGAS and promotes cellular antiviral responses and autoimmunity.USP29 维持 cGAS 的稳定性,并促进细胞抗病毒反应和自身免疫。
Cell Res. 2020 Oct;30(10):914-927. doi: 10.1038/s41422-020-0341-6. Epub 2020 May 26.
9
Pathogen infection and autoimmune disease.病原体感染与自身免疫性疾病。
Clin Exp Immunol. 2019 Jan;195(1):10-14. doi: 10.1111/cei.13239.

本文引用的文献

1
Autoimmune Polyendocrine Syndromes.自身免疫性多内分泌综合征
N Engl J Med. 2018 Mar 22;378(12):1132-1141. doi: 10.1056/NEJMra1713301.
2
Autoantibodies in Autoimmune Hepatitis: Can Epitopes Tell Us about the Etiology of the Disease?自身免疫性肝炎中的自身抗体:抗原表位能否告诉我们疾病的病因?
Front Immunol. 2018 Feb 16;9:163. doi: 10.3389/fimmu.2018.00163. eCollection 2018.
3
CMV-associated adrenal insufficiency in a renal transplant recipient.一名肾移植受者的巨细胞病毒相关性肾上腺功能不全
IDCases. 2017 Dec 26;11:44-45. doi: 10.1016/j.idcr.2017.12.009. eCollection 2018.
4
Characteristics of Korean Patients with Primary Adrenal Insufficiency: A Registry-Based Nationwide Survey in Korea.韩国原发性肾上腺皮质功能减退症患者的特征:一项基于韩国全国登记系统的调查
Endocrinol Metab (Seoul). 2017 Dec;32(4):466-474. doi: 10.3803/EnM.2017.32.4.466.
5
Transcription Factor IRF4 Promotes CD8 T Cell Exhaustion and Limits the Development of Memory-like T Cells during Chronic Infection.转录因子 IRF4 促进慢性感染期间 CD8 T 细胞耗竭并限制记忆样 T 细胞的发育。
Immunity. 2017 Dec 19;47(6):1129-1141.e5. doi: 10.1016/j.immuni.2017.11.021. Epub 2017 Dec 12.
6
Heritability of Addison's disease and prevalence of associated autoimmunity in a cohort of 112,100 Swedish twins.112100 名瑞典双胞胎队列中 Addison 病的遗传率和相关自身免疫的患病率。
Endocrine. 2017 Dec;58(3):521-527. doi: 10.1007/s12020-017-1441-z. Epub 2017 Oct 16.
7
Infectious and non-infectious complications in primary immunodeficiency disorders: an autopsy study from North India.原发性免疫缺陷病的感染性和非感染性并发症:来自印度北部的一项尸检研究
J Clin Pathol. 2018 May;71(5):425-435. doi: 10.1136/jclinpath-2017-204708. Epub 2017 Sep 28.
8
BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency.BACH2免疫缺陷表明超级增强子与单倍剂量不足之间存在关联。
Nat Immunol. 2017 Jul;18(7):813-823. doi: 10.1038/ni.3753. Epub 2017 May 22.
9
Primary adrenal insufficiency is associated with impaired natural killer cell function: a potential link to increased mortality.原发性肾上腺皮质功能减退与自然杀伤细胞功能受损有关:这是死亡率增加的一个潜在关联。
Eur J Endocrinol. 2017 Apr;176(4):471-480. doi: 10.1530/EJE-16-0969.
10
Clinical and Immunological Characteristics of Autoimmune Addison Disease: A Nationwide Swedish Multicenter Study.自身免疫性艾迪生病的临床和免疫学特征:一项瑞典全国性多中心研究
J Clin Endocrinol Metab. 2017 Feb 1;102(2):379-389. doi: 10.1210/jc.2016-2522.

感染在自身免疫性艾迪生病发病机制中的潜在作用。

The potential role for infections in the pathogenesis of autoimmune Addison's disease.

机构信息

Department of Clinical Science, University of Bergen, Bergen, Norway.

K.G. Jebsen Senter for Autoimmune Sykdommer, University of Bergen, Bergen, Norway.

出版信息

Clin Exp Immunol. 2019 Jan;195(1):52-63. doi: 10.1111/cei.13207. Epub 2018 Sep 30.

DOI:10.1111/cei.13207
PMID:30144040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6300649/
Abstract

Autoimmune Addison's disease (AAD), or primary adrenocortical insufficiency, is a classical organ-specific autoimmune disease with 160 years of history. AAD is remarkably homogeneous with one major dominant self-antigen, the cytochrome P450 21-hydroxylase enzyme, which is targeted by both autoantibodies and autoreactive T cells. Like most autoimmune diseases, AAD is thought to be caused by an unfortunate combination of genetic and environmental factors. While the number of genetic associations with AAD is increasing, almost nothing is known about environmental factors. A major environmental factor commonly proposed for autoimmune diseases, based partly on experimental and clinical data and partly on shared pathways between anti-viral immunity and autoimmunity, is viral infections. However, there are few reports associating viral infections to AAD, and it has proved difficult to establish which immunological processes that could link any viral infection with the initiation or progression of AAD. In this review, we will summarize the current knowledge on the underlying mechanisms of AAD and take a closer look on the potential involvement of viruses.

摘要

自身免疫性艾迪生病(AAD),又称原发性肾上腺皮质功能不全,是一种具有 160 年历史的经典器官特异性自身免疫性疾病。AAD 具有高度一致性,其主要自身抗原为细胞色素 P450 21-羟化酶,该抗原可被自身抗体和自身反应性 T 细胞靶向。与大多数自身免疫性疾病一样,AAD 被认为是遗传和环境因素不幸结合的结果。尽管与 AAD 相关的遗传关联数量正在增加,但几乎不了解环境因素。病毒感染是一种常见的环境因素,部分基于实验和临床数据,部分基于抗病毒免疫和自身免疫之间的共同途径,被普遍提出与自身免疫性疾病有关。然而,很少有报道将病毒感染与 AAD 相关联,并且很难确定哪些免疫过程可以将任何病毒感染与 AAD 的发生或进展联系起来。在这篇综述中,我们将总结目前关于 AAD 潜在机制的知识,并更仔细地研究病毒的潜在作用。