Hao Q, Saida T, Kawakami H, Mine H, Maruya E, Inoko H, Saji H
Department of Neurology, Utano National Hospital, Kyoto, Japan.
Hum Immunol. 1992 Oct;35(2):116-24. doi: 10.1016/0198-8859(92)90019-j.
The distribution of HLA-A, B, C, DR and DRB1, DQB1, DPB1 alleles was studied in 60 Japanese patients with clinically definite multiple sclerosis (MS) using serologic and genomic analysis. We found significant associations with HLA-Cw3 (p = 0.002, pc = 0.012, RR = 3.2), DR2 (p = 0.007, RR = 2.6), and DQB1*0602 (p = 0.04, RR = 4.0) in Japanese patients for the first time. The combined presence of Cw3 and DR2 gave a higher risk than each antigen alone. The reported increase in the frequency of DPw4 in Japanese MS patients [12] could not be confirmed by our genomic study. The frequencies of all of the residues in each variable region of the amino acid sequences of DQ beta and DP beta chains were not different between the MS patients and the controls. These results suggest that MS susceptibility may result from polygenic influences and from the presence of environmental factors.
采用血清学和基因组分析方法,对60例临床确诊的日本多发性硬化症(MS)患者的HLA - A、B、C、DR以及DRB1、DQB1、DPB1等位基因分布情况进行了研究。我们首次发现,日本MS患者与HLA - Cw3(p = 0.002,pc = 0.012,RR = 3.2)、DR2(p = 0.007,RR = 2.6)和DQB1*0602(p = 0.04,RR = 4.0)存在显著关联。Cw3和DR2同时存在时的风险高于单独任何一种抗原。我们的基因组研究未能证实此前报道的日本MS患者中DPw4频率增加[12]。MS患者与对照组之间,DQβ链和DPβ链氨基酸序列各可变区中所有残基的频率并无差异。这些结果表明,MS易感性可能源于多基因影响以及环境因素的存在。