Beall S S, Concannon P, Charmley P, McFarland H F, Gatti R A, Hood L E, McFarlin D E, Biddison W E
Division of Biology, California Institute of Technology, Pasadena 91125.
J Neuroimmunol. 1989 Jan;21(1):59-66. doi: 10.1016/0165-5728(89)90159-8.
The T cell receptor (TcR) beta-chain germline gene repertoire of multiple sclerosis (MS) patients was compared to that of 100 normal individuals. No differences in the number of gene segments defined by probes representing 14 different human V beta subfamilies and the constant region genes were found. The distribution of haplotypes defined by restriction fragment length polymorphism (RFLP) alleles detected with V beta 8, V beta 11, and C beta probes in the MS patients was significantly different from that found in normal individuals. Because 84% of the MS patients were DR2+, the findings in these patients were compared to a second group of 43 normals who were DR2+. The distribution of TcR haplotypes in MS patients was also significantly different from that in the DR2+ normals. The data suggest that an MS susceptibility gene(s) may be located in the region of the TcR beta-chain gene complex.
将多发性硬化症(MS)患者的T细胞受体(TcR)β链种系基因库与100名正常个体的进行了比较。未发现代表14个不同人类Vβ亚家族的探针所定义的基因片段数量以及恒定区基因存在差异。用Vβ8、Vβ11和Cβ探针检测到的限制性片段长度多态性(RFLP)等位基因所定义的单倍型在MS患者中的分布与正常个体中的分布显著不同。由于84%的MS患者为DR2阳性,因此将这些患者的研究结果与另一组43名DR2阳性的正常个体进行了比较。MS患者中TcR单倍型的分布也与DR2阳性正常个体中的分布显著不同。数据表明,MS易感基因可能位于TcRβ链基因复合体区域。