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白塞病和葡萄膜炎-小柳原田病的免疫学方面

Immunological aspects of Behçet's and Vogt-Koyanagi-Harada's diseases.

作者信息

Ohno S

出版信息

Trans Ophthalmol Soc U K (1962). 1981 Sep;101 (Pt 3)(3):335-41.

PMID:6820735
Abstract

Immunogenetic studies showed that Behçet's disease has a primary association with HLA-B antigen (HLA-BW51) and the same association throughout the world, whereas, Vogt-Koyanagi-Harada's disease (VKH) is primarily associated with supertypic HLA-DR antigen (MT3), an HLA-D-linked B cell alloantigen in Japanese. Immunological investigation showed that the serum levels of gamma-interferon (IFN-gamma) were significantly increased in both Behçet's disease and VKH, IFN-gamma showed a significant decrease in the ocular exacerbation stage in Behçet's disease. The highest IFN titre was observed 1 to 2 months after the onset of the disease in VKH.

摘要

免疫遗传学研究表明,白塞病与HLA - B抗原(HLA - BW51)存在主要关联,且在全球范围内情况相同;而小柳原田病(VKH)主要与超型HLA - DR抗原(MT3)相关,MT3是日本人中一种与HLA - D连锁的B细胞同种异体抗原。免疫学调查显示,白塞病和VKH患者血清中的γ-干扰素(IFN - γ)水平均显著升高,在白塞病的眼部加重期IFN - γ显著降低。VKH患者在发病后1至2个月观察到最高的IFN滴度。

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