Farid N R, Sampson L, Noel E P, Barnard J M, Mandeville R, Larsen B, Marshall W H, Carter N D
J Clin Invest. 1979 Jan;63(1):108-13. doi: 10.1172/JCI109263.
An association between Graves' disease and the human leukocyte antigen (HLA) system has previously been reported. The disease was more strongly associated with the HLA D locus antigen Dw3 than with HLA B8. Products of the HLA D locus are determined by the interaction of test cells with standard typing lymphocytes, a technically difficult procedure. Recently, it has been possible to type serologically for D locus related (DRw) specificities on peripheral bone marrow-derived (B) lymphocytes. Blood B lymphocytes from 50 unrelated controls and 41 patients with Graves' disease were typed for seven HLA DRw specificities. 28 patients with Graves' disease (68%) were positive for DRw3, in contrast to 14 controls (28%); whereas only 21 patients (50%) were HLA B8 positive, compared with 13 (26%) controls. Thus, positivity for DRw3 afforded a relative risk for Graves' disease of 5.5, whereas that for HLA B8 amounted to 3.0. Additionally, a family with multiple cases of Graves' disease in which the disease was previously shown to be inherited with the haplotype, was linked to DRw2, which suggests that the susceptibility to the disease was inherited in association with that antigen. Two HLA B/glyoxalase recombination events were observed in this family; in both instances HLA DRw followed HLA B. This study thus demonstrates that the disease susceptibility gene for Graves' disease is in strong linkage disequilibrium with DRw3; however, it may be associated with other DRw specificities and inherited within family units in association with them.
此前已有报道称格雷夫斯病与人类白细胞抗原(HLA)系统之间存在关联。该疾病与HLA D位点抗原Dw3的关联比与HLA B8的关联更强。HLA D位点的产物由测试细胞与标准分型淋巴细胞的相互作用决定,这是一个技术上困难的过程。最近,已经能够在外周血骨髓来源的(B)淋巴细胞上进行与D位点相关(DRw)特异性的血清学分型。对50名无关对照和41名格雷夫斯病患者的血液B淋巴细胞进行了7种HLA DRw特异性分型。28名格雷夫斯病患者(68%)DRw3呈阳性,相比之下,14名对照(28%)呈阳性;而只有21名患者(50%)HLA B8呈阳性,对照中有13名(26%)呈阳性。因此,DRw3阳性使格雷夫斯病的相对风险为5.5,而HLA B8阳性的相对风险为3.0。此外,一个有多例格雷夫斯病的家族,此前已证明该疾病与单倍型一起遗传,与DRw2相关联,这表明该疾病的易感性与该抗原一起遗传。在这个家族中观察到两个HLA B/乙二醛酶重组事件;在这两种情况下,HLA DRw都跟随HLA B。因此,这项研究表明,格雷夫斯病的疾病易感基因与DRw3处于强连锁不平衡状态;然而,它可能与其他DRw特异性相关,并在家族单位内与它们一起遗传。