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一种与类风湿关节炎影像学进展相关的T细胞受体β链可变区多态性。

A T cell receptor beta chain variable region polymorphism associated with radiographic progression in rheumatoid arthritis.

作者信息

de Vries N, Prinsen C F, Mensink E B, van Riel P L, van't Hof M A, van de Putte L B

机构信息

Department of Internal Medicine, University Hospital Nijmegen, The Netherlands.

出版信息

Ann Rheum Dis. 1993 May;52(5):327-31. doi: 10.1136/ard.52.5.327.

Abstract

OBJECTIVE

In rheumatoid arthritis (RA) genetic factors influence susceptibility to disease and progression. Identifying these genetic factors may give more insight into the aetiology and pathogenesis of this disease. Furthermore, if these genetic markers can predict progression in an early stage of disease, timely institution of more aggressive treatment in patients with a bad prognosis may help to prevent joint damage. Several studies have shown that HLA-DRB1 alleles are associated with RA, whereas others have indicated that genes not linked to the HLA complex are also involved. Candidates for such genes are the T cell receptor (TCR) alpha/beta genes.

METHODS

The association of a polymorphism in a TCR beta chain variable region gene (TCR-V beta 8) with both risk for RA and radiographic progression of joint disease was analysed after a three year follow up. A cohort of 118 white patients with a duration of disease shorter than one year at entry, and 110 white controls were typed for this (BamHI) TCR-V beta 8 polymorphism.

RESULTS

The distribution of the two alleles, 2.0 and 23.0 kb, was identical in patients and controls. Radiographic progression (modified Sharp method) after a three year follow up, studied in 111 patients, was significantly less in the group possessing the 2.0 kb allele (p = 0.03).

CONCLUSION

This does not confirm the reported association of the (BamHI) TCR-V beta 8 2.0 kb allele with RA. By contrast with previous findings in smaller studies, in the present study this 2.0 kb allele was protective against radiographic progression. Because well known prognostic variables in RA were corrected for, the findings indicate that the TCR-V beta 8 polymorphism studied is a new prognostic marker for this disease.

摘要

目的

在类风湿关节炎(RA)中,遗传因素影响疾病易感性和病情进展。识别这些遗传因素可能会更深入地了解该疾病的病因和发病机制。此外,如果这些遗传标记能够在疾病早期预测病情进展,那么对预后不良的患者及时采取更积极的治疗措施可能有助于预防关节损伤。多项研究表明,HLA - DRB1等位基因与RA相关,而其他研究则表明与HLA复合体无关的基因也参与其中。此类基因的候选者是T细胞受体(TCR)α/β基因。

方法

在三年随访后,分析TCRβ链可变区基因(TCR - Vβ8)中的一种多态性与RA风险及关节疾病影像学进展之间的关联。对一组118例疾病病程在入组时短于一年的白人患者以及110例白人对照进行该(BamHI)TCR - Vβ8多态性分型。

结果

患者和对照中两种等位基因(2.0和23.0 kb)的分布相同。在111例患者中进行的三年随访后的影像学进展(改良Sharp法)研究显示,携带2.0 kb等位基因的组进展明显更少(p = 0.03)。

结论

这并未证实所报道的(BamHI)TCR - Vβ8 2.0 kb等位基因与RA的关联。与先前较小规模研究的结果相反,在本研究中该2.0 kb等位基因对影像学进展具有保护作用。由于对RA中已知的预后变量进行了校正,研究结果表明所研究的TCR - Vβ8多态性是该疾病的一种新的预后标志物。

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2
T cell genetics and rheumatoid arthritis (RA).T细胞遗传学与类风湿关节炎(RA)。
Clin Exp Immunol. 1998 Mar;111(3):469-71. doi: 10.1046/j.1365-2249.1998.00541.x.

本文引用的文献

1
Genetics of HLA-associated disease; rheumatoid arthritis.HLA相关疾病的遗传学;类风湿关节炎
Tissue Antigens. 1983 Sep;22(3):182-5. doi: 10.1111/j.1399-0039.1983.tb01189.x.

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