Goldberg M A, Arnett F C, Bias W B, Shulman L E
Arthritis Rheum. 1976 Mar-Apr;19(2):129-32. doi: 10.1002/art.1780190201.
Histocompatibility (HL-A) antigens were determined in 120 patients with systemic lupus erythematosus (SLE) and 120 matched controls. Increased frequencies of HL-A1 and HL-A8 were found. HL-A1 was more strongly associated with SLE in black patients (71 patients), whereas HL-A8 was more impressively associated with SLE in white patients (49 patients). In addition HL-A1 appeared more frequently in those with early onset of disease in both races; and HL-A1, HL-A8, and the HL-A1,8 phenotype seemed to be associated with severe SLE (renal and central nervous system involvement) in white patients. These data support the proposal that there are genetic influences in the pathogenesis and expression of SLE.
对120例系统性红斑狼疮(SLE)患者和120例匹配的对照者进行了组织相容性(HL - A)抗原检测。发现HL - A1和HL - A8的频率增加。HL - A1在黑人患者(71例)中与SLE的关联更强,而HL - A8在白人患者(49例)中与SLE的关联更显著。此外,HL - A1在两个种族中疾病早期发病者中出现得更频繁;并且HL - A1、HL - A8以及HL - A1,8表型似乎与白人患者的严重SLE(肾脏和中枢神经系统受累)有关。这些数据支持了SLE的发病机制和表达存在遗传影响这一观点。