Matsuki K, Juji T, Tokunaga K, Mochizuki M, Hayashi K, Fujino Y, Numaga J, Yamashita H
Tissue Antigens. 1987 Apr;29(4):208-13. doi: 10.1111/j.1399-0039.1987.tb01578.x.
HLA class I, II, and III antigens were studied in Japanese patients with Behçet's disease with refractory ocular attacks. In addition to the increased frequency of B51, DQw3, especially TA10-negative DQw3, was increased and DQw1 was decreased significantly in this subgroup of Behçet's disease. As for complement markers, C4A Q0 was increased. A rare variant of BF S07 was first observed in Japanese. Although the mechanism for the DQw3 association is obscure, a possible hypothesis is that an immune-response or immune-suppression gene linked to the DQ antigens modulates the disease severity and the efficacy of treatments.
对患有难治性眼部发作的日本白塞病患者进行了 HLA I 类、II 类和 III 类抗原研究。除了 B51 频率增加外,DQw3,尤其是 TA10 阴性的 DQw3 在该亚组白塞病患者中增加,而 DQw1 显著降低。至于补体标志物,C4A Q0 增加。在日本人中首次观察到 BF S07 的一种罕见变体。虽然 DQw3 关联的机制尚不清楚,但一种可能的假说是,与 DQ 抗原相关的免疫反应或免疫抑制基因调节疾病严重程度和治疗效果。