Singal D P, D'Souza M, Reid B, Bensen W G, Kassam Y B, Adachi J D
Departments of Pathology and Medicine, McMaster University, Hamilton, Ontario, Canada.
Lancet. 1987 Nov 14;2(8568):1118-20. doi: 10.1016/s0140-6736(87)91548-0.
With a cDNA probe for the DQ beta gene, two variants of the DR4-linked DQw3 (3.1 and 3.2) allele were analysed in patients with rheumatoid arthritis (RA), healthy individuals, and homozygous cell lines. The DQw3.1 allele, identified by 3.4 kb (HindIII), 2.3 kb (SstI), and 3.7 kb and 6.9 kb (BamHI) restriction fragment lengths, was expressed in 100% (of 18) DR4-positive patients, compared with only 19% (of 16) of DR4-positive controls including one of five homozygous cell lines. This DQ beta variant showed a highly significant association (relative risk = 78; p less than 10(-6) with RA and may therefore play an important part in susceptibility to RA.
采用DQβ基因的cDNA探针,对类风湿关节炎(RA)患者、健康个体及纯合细胞系中与DR4相关的DQw3(3.1和3.2)等位基因的两个变体进行了分析。通过3.4 kb(HindIII)、2.3 kb(SstI)以及3.7 kb和6.9 kb(BamHI)限制性片段长度鉴定出的DQw3.1等位基因,在18例DR4阳性患者中100%表达,而在包括5个纯合细胞系之一的16例DR4阳性对照中仅19%表达。这种DQβ变体与RA呈高度显著关联(相对风险=78;p<10-6),因此可能在RA易感性中起重要作用。