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银屑病关节炎和银屑病中 HLA 二类分子及 T 细胞受体基因多态性

HLA class II and T cell receptor gene polymorphisms in psoriatic arthritis and psoriasis.

作者信息

Sakkas L I, Loqueman N, Bird H, Vaughan R W, Welsh K I, Panayi G S

机构信息

Division of Medicine, UMDS, Guy's Hospital, London, UK.

出版信息

J Rheumatol. 1990 Nov;17(11):1487-90.

PMID:2273489
Abstract

HLA-DRB, DQA and DQB genes as well as the T cell receptor (TcR) alpha, beta, and gamma genes were studied by Southern blot analysis of genomic DNA from patients with psoriatic arthritis (PsA) and psoriasis alone (Ps). A subtype of DR7, DR7a, was found in 38.8% of patients with PsA, 41.5% of patients with Ps, and in 8% of healthy individuals (N) (PsA vs N: pc = 0.0002, RR = 7.1; Ps vs N: pc = 0.0002, RR = 7.9). No association with TcR genes was found. Our findings suggest either that the DR7a allele may be in linkage disequilibrium with HLA-Cw6 or that it may be an important susceptibility factor for PsA and Ps.

摘要

通过对银屑病关节炎(PsA)患者及单纯银屑病(Ps)患者的基因组DNA进行Southern印迹分析,研究了HLA - DRB、DQA和DQB基因以及T细胞受体(TcR)α、β和γ基因。在38.8%的PsA患者、41.5%的Ps患者以及8%的健康个体(N)中发现了DR7的一个亚型DR7a(PsA与N相比:pc = 0.0002,RR = 7.1;Ps与N相比:pc = 0.0002,RR = 7.9)。未发现与TcR基因有关联。我们的研究结果表明,要么DR7a等位基因可能与HLA - Cw6处于连锁不平衡状态,要么它可能是PsA和Ps的一个重要易感因素。

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J Rheumatol. 1990 Nov;17(11):1487-90.
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Scid mouse model of psoriasis: a unique tool for drug development of autoreactive T-cell and th-17 cell-mediated autoimmune diseases.银屑病的重症联合免疫缺陷小鼠模型:用于自身反应性T细胞和Th17细胞介导的自身免疫性疾病药物开发的独特工具。
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