Immune Regulatory Genes Are Major Genetic Factors to Behcet Disease: Systematic Review.

Q4 Medicine Open Rheumatology Journal Pub Date : 2018-06-29 eCollection Date: 2018-01-01 DOI:10.2174/1874312901812010070
Yan Deng, Weifeng Zhu, Xiaodong Zhou
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引用次数: 6

Abstract

Behcet's disease (BD) is a chronic refractory multi-system autoimmune disorder that occurs in a genetically susceptible host. Multiple genetic factors have been identified that may contribute to the pathogenesis of BD. The major genes with polymorphisms associated with BD include HLA-B and -A, CIITA, ERAP1, MICA, IL10, IL12A, IL12RB2, IL23R, MEFV, IRF8, TNFAIP3, REL, TLR4, NOD1,2, CCR1,CCR3, GIMAP1,2,4, KLRC4, STAT4, NCOA5, FOXP3, PSORS1C1, FUT2, UBAC2, SUMO4, ADO-EGR2, CEBPB-PTPN1, and JPKL-CNTN5. These genes encode proteins involved mainly in immune regulation and inflammation, and some in transcription and post-translational modification. A complete view of these BD-associated genes may provide a clue to this complex disease in terms of its pathogenesis and exploring potentially targeted therapies for BD.

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免疫调节基因是白塞病的主要遗传因素:系统综述。
白塞氏病(BD)是一种发生在遗传易感宿主体内的慢性难治性多系统自身免疫性疾病。多种遗传因素可能与双相障碍的发病机制有关,与双相障碍相关的主要多态性基因包括HLA-B和-A、CIITA、ERAP1、MICA、IL10、IL12A、IL12RB2、IL23R、MEFV、IRF8、TNFAIP3、REL、TLR4、NOD1、2、CCR1、CCR3、GIMAP1、2,4、KLRC4、STAT4、NCOA5、FOXP3、PSORS1C1、FUT2、UBAC2、SUMO4、do - egr2、CEBPB-PTPN1和JPKL-CNTN5。这些基因编码的蛋白质主要参与免疫调节和炎症,部分参与转录和翻译后修饰。全面了解这些与双相障碍相关的基因可能为了解这种复杂疾病的发病机制和探索双相障碍的潜在靶向治疗提供线索。
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来源期刊
Open Rheumatology Journal
Open Rheumatology Journal Medicine-Rheumatology
CiteScore
0.80
自引率
0.00%
发文量
2
期刊介绍: ENTHAM Open publishes a number of peer-reviewed, open access journals. These free-to-view online journals cover all major disciplines of science, medicine, technology and social sciences. BENTHAM Open provides researchers a platform to rapidly publish their research in a good-quality peer-reviewed journal. All peer-reviewed accepted submissions meeting high research and ethical standards are published with free access to all.
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