• 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

IL12B 和 IL23R 多态性与斑秃有关。

IL12B and IL23R polymorphisms are associated with alopecia areata.

机构信息

Biology Department, East Tehran Branch, Islamic Azad University, Tehran, Iran.

Skin Research Centre, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Genes Immun. 2020 May;21(3):203-210. doi: 10.1038/s41435-020-0100-1. Epub 2020 May 1.

DOI:10.1038/s41435-020-0100-1
PMID:32355229
Abstract

Alopecia areata is an autoimmune disease in which activation of autoreactive T cells and inflammatory immune signals target the hair follicles autoantigens. Although cytokines are involved in regulating autoimmune inflammation, the specific involvement of these molecules in the pathogenesis of alopecia areata has been remained unsettled. Here, a possible influence of IL12B, IL17A, and IL23R variations on susceptibility to alopecia areata in Iranian patients was investigated. Genotyping of IL12B (rs3212227), IL17A (rs2275913), and IL23R (rs10889677) variants were performed by extracting genomic DNA from patients and controls. Gene expression was analyzed by real-time RT-PCR. The frequency of IL12B and IL23R gene polymorphisms is significantly higher in the patients than controls, while no significant difference was found for IL17A. Stratification of the patients with respect to age at disease onset indicated that CC genotype of IL12B (rs3212227) and AA genotype of IL23R (rs10889677) gene polymorphisms are significantly associated with late-onset alopecia areata disease. In contrast to IL17A and IL23R, IL12B gene expression levels elevated in patients to that of controls, but genotypes had no effect on levels of gene expression. Overall, our data confirmed that the IL12B and IL23R polymorphisms are associated with the risk to develop alopecia areata in our population.

摘要

斑秃是一种自身免疫性疾病,其中自身反应性 T 细胞和炎症免疫信号的激活靶向毛囊自身抗原。虽然细胞因子参与调节自身免疫炎症,但这些分子在斑秃发病机制中的具体参与仍未确定。在这里,研究了 IL12B、IL17A 和 IL23R 变异对伊朗患者斑秃易感性的可能影响。通过从患者和对照中提取基因组 DNA 来进行 IL12B(rs3212227)、IL17A(rs2275913)和 IL23R(rs10889677)变异的基因分型。通过实时 RT-PCR 分析基因表达。与对照组相比,患者中 IL12B 和 IL23R 基因多态性的频率显着升高,而 IL17A 则没有显着差异。根据疾病发病年龄对患者进行分层表明,IL12B(rs3212227)的 CC 基因型和 IL23R(rs10889677)的 AA 基因型与斑秃的迟发性发病显着相关。与 IL17A 和 IL23R 相反,患者的 IL12B 基因表达水平高于对照组,但基因型对基因表达水平没有影响。总体而言,我们的数据证实了 IL12B 和 IL23R 多态性与我们人群中斑秃发病风险相关。

相似文献

1
IL12B and IL23R polymorphisms are associated with alopecia areata.IL12B 和 IL23R 多态性与斑秃有关。
Genes Immun. 2020 May;21(3):203-210. doi: 10.1038/s41435-020-0100-1. Epub 2020 May 1.
2
Investigation of interleukin-12, interleukin-17 and interleukin-23 receptor gene polymorphisms in alopecia areata.斑秃患者白细胞介素-12、白细胞介素-17和白细胞介素-23受体基因多态性的研究
J Int Med Res. 2015 Aug;43(4):526-34. doi: 10.1177/0300060514549784. Epub 2015 May 27.
3
Meta-analysis of the IL23R and IL12B polymorphisms in multiple sclerosis.白细胞介素23受体(IL23R)和白细胞介素12B(IL12B)基因多态性在多发性硬化症中的荟萃分析。
Int J Neurosci. 2016;126(3):205-12. doi: 10.3109/00207454.2015.1007508. Epub 2015 Jun 16.
4
Genetic variation at IL12B, IL23R and IL23A is associated with psoriasis severity, psoriatic arthritis and type 2 diabetes mellitus.白细胞介素12B、白细胞介素23受体和白细胞介素23A的基因变异与银屑病严重程度、银屑病关节炎和2型糖尿病有关。
J Dermatol Sci. 2014 Sep;75(3):167-72. doi: 10.1016/j.jdermsci.2014.05.010. Epub 2014 Jun 11.
5
IL23R and IL12B polymorphisms in Spanish IBD patients: no evidence of interaction.西班牙炎症性肠病患者中白细胞介素23受体(IL23R)和白细胞介素12B(IL12B)基因多态性:无相互作用证据
Inflamm Bowel Dis. 2008 Sep;14(9):1192-6. doi: 10.1002/ibd.20463.
6
Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis.白细胞介素基因多态性与斑秃:系统评价和荟萃分析。
Medicine (Baltimore). 2024 Feb 23;103(8):e37300. doi: 10.1097/MD.0000000000037300.
7
IL17A and IL23R gene polymorphisms affect the clinical features and prognosis of patients with multiple myeloma.白细胞介素17A(IL17A)和白细胞介素23受体(IL23R)基因多态性影响多发性骨髓瘤患者的临床特征和预后。
Hematol Oncol. 2018 Feb;36(1):196-201. doi: 10.1002/hon.2469. Epub 2017 Aug 7.
8
Association of IL17 and IL23R gene polymorphisms with rheumatic heart disease in South Indian population.印度南部人群中白细胞介素17(IL17)和白细胞介素23受体(IL23R)基因多态性与风湿性心脏病的关联
Immunol Invest. 2018 Oct;47(7):754-764. doi: 10.1080/08820139.2018.1493053. Epub 2018 Jul 9.
9
IL12B and IL23R gene SNPs in Japanese psoriasis.日本银屑病患者的 IL12B 和 IL23R 基因 SNPs 研究。
Immunogenetics. 2013 Nov;65(11):823-8. doi: 10.1007/s00251-013-0721-x. Epub 2013 Aug 17.
10
A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes.一项大规模基因关联研究证实了白细胞介素12B(IL12B),并导致将白细胞介素23受体(IL23R)鉴定为银屑病风险基因。
Am J Hum Genet. 2007 Feb;80(2):273-90. doi: 10.1086/511051. Epub 2006 Dec 21.

引用本文的文献

1
Evaluating the Causal Relationship Between Human Blood Metabolites and the Susceptibility to Alopecia Areata.评估人体血液代谢物与斑秃易感性之间的因果关系。
J Cosmet Dermatol. 2025 May;24(5):e70248. doi: 10.1111/jocd.70248.
2
Cellular and Molecular Determinants of Biologic Drugs Resistance and Therapeutic Failure in Inflammatory Bowel Disease.炎症性肠病中生物药物耐药性和治疗失败的细胞与分子决定因素
Int J Mol Sci. 2024 Feb 28;25(5):2789. doi: 10.3390/ijms25052789.
3
Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis.

本文引用的文献

1
Alopecia areata is characterized by dysregulation in systemic type 17 and type 2 cytokines, which may contribute to disease-associated psychological morbidity.斑秃的特征是全身17型和2型细胞因子失调,这可能导致与疾病相关的心理发病率。
Br J Dermatol. 2020 Jan;182(1):130-137. doi: 10.1111/bjd.18008. Epub 2019 Jul 17.
2
TNF-α -308G/A gene polymorphism in bullous pemphigoid and alopecia areata.大疱性类天疱疮和斑秃中TNF-α -308G/A基因多态性
Hum Antibodies. 2018;26(4):201-207. doi: 10.3233/HAB-180339.
3
Cytokine Targeted Therapeutics for Alopecia Areata: Lessons from Atopic Dermatitis and Other Inflammatory Skin Diseases.
白细胞介素基因多态性与斑秃:系统评价和荟萃分析。
Medicine (Baltimore). 2024 Feb 23;103(8):e37300. doi: 10.1097/MD.0000000000037300.
4
Family aggregation and prevalence of other autoimmune diseases in SAPHO syndrome.SAPHO综合征中的家族聚集性及其他自身免疫性疾病的患病率
Heliyon. 2023 Nov 2;9(11):e21541. doi: 10.1016/j.heliyon.2023.e21541. eCollection 2023 Nov.
5
Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata.斑秃中Th1和Th17相关细胞因子的遗传特异性失调
Biomolecules. 2023 Aug 23;13(9):1285. doi: 10.3390/biom13091285.
6
Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review.《斑秃的临床与遗传方面:最新综述》。
Genes (Basel). 2023 Jun 28;14(7):1362. doi: 10.3390/genes14071362.
7
Evaluation of A7488G polymorphism in -infected patients: a case-control study.对感染患者中A7488G多态性的评估:一项病例对照研究。
Ann Med Surg (Lond). 2023 May 18;85(6):2298-2303. doi: 10.1097/MS9.0000000000000816. eCollection 2023 Jun.
8
Genetic association of IL2RA, IL17RA, IL23R, and IL31RA single nucleotide polymorphisms with alopecia areata.IL2RA、IL17RA、IL23R和IL31RA单核苷酸多态性与斑秃的遗传关联。
Saudi J Biol Sci. 2022 Nov;29(11):103460. doi: 10.1016/j.sjbs.2022.103460. Epub 2022 Sep 27.
9
Genetic Association between Interleukin Genes and Alopecia Areata in Jordanian Patients.约旦患者白细胞介素基因与斑秃之间的遗传关联。
Oman Med J. 2022 Sep 30;37(5):e421. doi: 10.5001/omj.2022.92. eCollection 2022 Sep.
10
The Immunogenetics of Alopecia areata.斑秃的免疫遗传学。
Adv Exp Med Biol. 2022;1367:19-59. doi: 10.1007/978-3-030-92616-8_2.
斑秃的细胞因子靶向治疗:来自特应性皮炎和其他炎症性皮肤病的经验教训。
J Investig Dermatol Symp Proc. 2018 Jan;19(1):S62-S64. doi: 10.1016/j.jisp.2017.10.005.
4
Comorbidities in patients with alopecia areata.斑秃患者的合并症。
J Am Acad Dermatol. 2017 Apr;76(4):755-757. doi: 10.1016/j.jaad.2016.12.007.
5
IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis.白细胞介素-23受体突变与溃疡性结肠炎相关:一项系统评价和荟萃分析。
Oncotarget. 2017 Jan 17;8(3):4849-4863. doi: 10.18632/oncotarget.13607.
6
Common variants in IL-17A/IL-17RA axis contribute to predisposition to and progression of congestive heart failure.白细胞介素-17A/白细胞介素-17受体A轴的常见变异体导致充血性心力衰竭的易感性和进展。
Medicine (Baltimore). 2016 Jul;95(27):e4105. doi: 10.1097/MD.0000000000004105.
7
Association of Interleukin-23 receptor gene polymorphisms with susceptibility to Crohn's disease: A meta-analysis.白细胞介素-23受体基因多态性与克罗恩病易感性的关联:一项荟萃分析。
Sci Rep. 2015 Dec 18;5:18584. doi: 10.1038/srep18584.
8
Genetic Polymorphisms of IL-17F and TRAF3IP2 Could Be Predictive Factors of the Long-Term Effect of Infliximab against Crohn's Disease.IL-17F和TRAF3IP2的基因多态性可能是英夫利昔单抗治疗克罗恩病长期疗效的预测因素。
Biomed Res Int. 2015;2015:416838. doi: 10.1155/2015/416838. Epub 2015 Oct 19.
9
The role of lymphocytes in the development and treatment of alopecia areata.淋巴细胞在斑秃发病及治疗中的作用。
Expert Rev Clin Immunol. 2015;11(12):1335-51. doi: 10.1586/1744666X.2015.1085306. Epub 2015 Sep 7.
10
Alopecia areata profiling shows TH1, TH2, and IL-23 cytokine activation without parallel TH17/TH22 skewing.斑秃特征分析显示 TH1、TH2 和 IL-23 细胞因子激活,而无平行的 TH17/TH22 偏倚。
J Allergy Clin Immunol. 2015 Nov;136(5):1277-87. doi: 10.1016/j.jaci.2015.06.032. Epub 2015 Aug 24.