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伴有难治性眼部发作的白塞病中的人类白细胞抗原

HLA antigens in Behçet's disease with refractory ocular attacks.

作者信息

Matsuki K, Juji T, Tokunaga K, Mochizuki M, Hayashi K, Fujino Y, Numaga J, Yamashita H

出版信息

Tissue Antigens. 1987 Apr;29(4):208-13. doi: 10.1111/j.1399-0039.1987.tb01578.x.

Abstract

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.

摘要

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。

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