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多发性硬化易感性:T细胞受体β和γ基因区域多态性的人群及双胞胎研究。法国多发性硬化研究小组

Multiple sclerosis susceptibility: population and twin study of polymorphisms in the T-cell receptor beta and gamma genes region. French Group on Multiple Sclerosis.

作者信息

Briant L, Avoustin P, Clayton J, McDermott M, Clanet M, Cambon-Thomsen A

机构信息

Centre de Recherches sur le Polymorphisme Génétique des Populations Humaines, CRPG/CNRS UPR 8291, CHU Purpan, Toulouse, France.

出版信息

Autoimmunity. 1993;15(1):67-73. doi: 10.3109/08916939309004841.

Abstract

Multiple sclerosis (MS) is a demyelinating auto-immune disease of the central nervous system with a suspected genetic component. Previous publications have demonstrated that MS susceptibility is influenced by Major Histocompatibility Complex (MHC) genes and recent studies have focused on additional susceptibility genes. The accumulation of activated T-cells in demyelinating MS lesions, the possible auto-immune mechanism of this disease and the functional relationship between MHC and T cell receptor (TCR) molecules support the hypothesis that TCR genes are good candidates to influence MS development. Published results in this domain are conflicting and still a matter of controversy. In the present study we analysed the influence of V beta, C beta, P lambda G3 and V gamma gene polymorphisms defined by Restriction Fragments Length Polymorphism (RFLP) on 48 pairs of monozygotic and dizygotic twins with at least one of each pair affected, and also in 63 unrelated MS patients for V gamma gene polymorphism. These results have been compared with those in the non affected twins and with data from a control group (Beall et al., 1989) regarding C beta and V beta polymorphisms and with a local control population for V gamma. No significant correlation between C beta, V gamma or P lambda G3 polymorphisms and MS was found, only a non significant tendency to reduced P lambda G3 allele sharing among dizygotic non concordant twin pairs was observed. However one V beta 11, 25 kb allele and a haplotype defined by V beta 11 and C beta alleles showed a correlation with MS susceptibility of borderline significance.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

多发性硬化症(MS)是一种中枢神经系统的脱髓鞘自身免疫性疾病,疑似具有遗传因素。先前的出版物表明,MS易感性受主要组织相容性复合体(MHC)基因影响,最近的研究则聚焦于其他易感性基因。脱髓鞘性MS病变中活化T细胞的积累、该疾病可能的自身免疫机制以及MHC与T细胞受体(TCR)分子之间的功能关系支持了TCR基因是影响MS发展的良好候选基因这一假说。该领域已发表的结果相互矛盾,仍是一个有争议的问题。在本研究中,我们分析了由限制性片段长度多态性(RFLP)定义的Vβ、Cβ、PλG3和Vγ基因多态性对48对单卵和双卵双胞胎(每对中至少有一人患病)的影响,还分析了63例无亲缘关系的MS患者的Vγ基因多态性。这些结果与未患病双胞胎的结果进行了比较,并与一个对照组(Beall等人,1989年)关于Cβ和Vβ多态性的数据以及一个当地对照组人群关于Vγ的数据进行了比较。未发现Cβ、Vγ或PλG3多态性与MS之间存在显著相关性,仅在双卵不一致双胞胎对中观察到PλG3等位基因共享减少的不显著趋势。然而,一个Vβ11、25kb等位基因以及由Vβ11和Cβ等位基因定义的单倍型与MS易感性显示出临界显著的相关性。(摘要截断于250字)

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