Charmley P, Beall S S, Concannon P, Hood L, Gatti R A
Division of Biology, California Institute of Technology, Pasadena 91125.
J Neuroimmunol. 1991 Jun;32(3):231-40. doi: 10.1016/0165-5728(91)90193-b.
Multiple sclerosis (MS) has been associated with particular HLA haplotypes and has recently been reported to also be associated with the T cell receptor (TCR) beta-chain complex. We have tried to determine the source of the TCR-beta/MS association by exploiting the pattern of linkage disequilibrium within the TCR-beta complex. We describe a new DNA polymorphism with the TCR variable region gene segment V beta 15 which appears to localize between the constant region and V beta 11. When the distribution of V beta 11-V beta 15 haplotypes in MS patients was compared to healthy controls, the strength of the V beta 11-V beta 15 MS association (p = 0.107) was much less than the MS association with the adjacent V beta 8-V beta 11 haplotype (p = 0.0010). On the basis we exclude an MS susceptibility gene telomeric to V beta 11. The reported MS association with the TCR-beta gene complex therefore does not appear to be due to genes within the diversity, joining, or constant region but more likely involves a specific gene(s) within the variable region.
多发性硬化症(MS)与特定的人类白细胞抗原(HLA)单倍型有关,最近有报道称其也与T细胞受体(TCR)β链复合体相关。我们试图通过利用TCR-β复合体内的连锁不平衡模式来确定TCR-β/MS关联的来源。我们描述了一种新的DNA多态性,它存在于TCR可变区基因片段Vβ15中,该片段似乎定位在恒定区和Vβ11之间。当将MS患者中Vβ11-Vβ15单倍型的分布与健康对照进行比较时,Vβ11-Vβ15与MS的关联强度(p = 0.107)远低于MS与相邻的Vβ8-Vβ11单倍型的关联(p = 0.0010)。基于此,我们排除了Vβ11端粒处存在MS易感基因的可能性。因此,所报道的MS与TCR-β基因复合体的关联似乎并非由于多样性、连接或恒定区内的基因,而更可能涉及可变区内的特定基因。