Ishihara M, Ohno S, Ishida T, Ando H, Naruse T, Nose Y, Inoko H
Department of Ophthalmology, Yokohama City University School of Medicine, Kanagawa, Japan.
Tissue Antigens. 1994 Apr;43(4):238-41. doi: 10.1111/j.1399-0039.1994.tb02331.x.
Previous HLA serological studies showed positive associations of the DR52 antigen, the DR52-associated antigens (DR3, DR5 and DR6) and the DR8 antigen with sarcoidosis. To investigate the HLA alleles that may contribute to the genetic susceptibility to sarcoidosis at the DNA level, HLA-DRB1, -DRB3, -DQA1 and DQB1 genotyping using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was performed in 63 Japanese patients with sarcoidosis. The frequencies of the DR52-associated DRB1 alleles (DRB111, DRB112 and DRB114 except DRB11302), DRB108, DRB30101, DQA10501 and DQB10301 were significantly increased in patients compared with healthy controls. The significant increase of DRB30101, DQA10501 and DQB10301 could be explained by linkage disequilibrium with the DR52-associated DRB1 alleles. It must be noted that the DR8 haplotype, which does not possess the DRB3 gene, also showed a significant increase in sarcoidosis. These results suggest that the HLA-alleles responsible for the susceptibility to sarcoidosis are located at the HLA-DRB1 locus rather than the HLA-DRB3, -DQA1 and -DQB1 loci. In contrast, DRB11302 may confer resistance to the disease.
以往的HLA血清学研究表明,DR52抗原、DR52相关抗原(DR3、DR5和DR6)以及DR8抗原与结节病呈正相关。为了在DNA水平上研究可能导致结节病遗传易感性的HLA等位基因,我们对63例日本结节病患者采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法进行了HLA-DRB1、-DRB3、-DQA1和DQB1基因分型。与健康对照相比,患者中DR52相关的DRB1等位基因(DRB111、DRB112和除DRB11302外的DRB114)、DRB108、DRB30101、DQA10501和DQB10301的频率显著增加。DRB30101、DQA10501和DQB10301的显著增加可以用与DR52相关的DRB1等位基因的连锁不平衡来解释。必须指出的是,不具有DRB3基因的DR8单倍型在结节病中也显示出显著增加。这些结果表明,导致结节病易感性的HLA等位基因位于HLA-DRB1位点,而不是HLA-DRB3、-DQA1和-DQB1位点。相反,DRB11302可能赋予对该病的抗性。